Stefan M. Pulst - Publications

Neurology University of Utah, Salt Lake City, UT 
spinocerebellar ataxias, Parkinson disease

183 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Dansithong W, Paul S, Scoles DR, Pulst SM, Huynh DP. Generation of SNCA Cell Models Using Zinc Finger Nuclease (ZFN) Technology for Efficient High-Throughput Drug Screening. Plos One. 10: e0136930. PMID 26317803 DOI: 10.1371/journal.pone.0136930  1
2015 Gibson SB, Kasarskis EJ, Hu N, Pulst SM, Mendiondo MS, Matthews DE, Mitsumoto H, Tandan R, Simmons Z, Kryscio RJ, Bromberg MB. Relationship of creatine kinase to body composition, disease state, and longevity in ALS. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-5. PMID 26312548 DOI: 10.3109/21678421.2015.1062516  1
2015 Sun X, Li PP, Zhu S, Cohen R, Marque LO, Ross CA, Pulst SM, Chan HY, Margolis RL, Rudnicki DD. Nuclear retention of full-length HTT RNA is mediated by splicing factors MBNL1 and U2AF65. Scientific Reports. 5: 12521. PMID 26218986 DOI: 10.1038/srep12521  1
2015 Scoles DR, Ho MH, Dansithong W, Pflieger LT, Petersen LW, Thai KK, Pulst SM. Repeat Associated Non-AUG Translation (RAN Translation) Dependent on Sequence Downstream of the ATXN2 CAG Repeat. Plos One. 10: e0128769. PMID 26086378 DOI: 10.1371/journal.pone.0128769  1
2015 Dansithong W, Paul S, Figueroa KP, Rinehart MD, Wiest S, Pflieger LT, Scoles DR, Pulst SM. Ataxin-2 regulates RGS8 translation in a new BAC-SCA2 transgenic mouse model. Plos Genetics. 11: e1005182. PMID 25902068 DOI: 10.1371/journal.pgen.1005182  1
2015 Cirulli ET, Lasseigne BN, Petrovski S, Sapp PC, Dion PA, Leblond CS, Couthouis J, Lu YF, Wang Q, Krueger BJ, Ren Z, Keebler J, Han Y, Levy SE, Boone BE, ... ... Pulst SM, et al. Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways. Science (New York, N.Y.). 347: 1436-41. PMID 25700176 DOI: 10.1126/science.aaa3650  1
2015 Lo RY, Figueroa KP, Pulst SM, Lin CY, Perlman S, Wilmot G, Gomez C, Schmahmann J, Paulson H, Shakkottai VG, Ying S, Zesiewicz T, Bushara K, Geschwind M, Xia G, et al. Coenzyme Q10 and spinocerebellar ataxias. Movement Disorders : Official Journal of the Movement Disorder Society. 30: 214-20. PMID 25449974 DOI: 10.1002/mds.26088  1
2015 Moscovich M, Okun MS, Favilla C, Figueroa KP, Pulst SM, Perlman S, Wilmot G, Gomez C, Schmahmann J, Paulson H, Shakkottai V, Ying S, Zesiewicz T, Kuo SH, Mazzoni P, et al. Clinical evaluation of eye movements in spinocerebellar ataxias: a prospective multicenter study. Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society. 35: 16-21. PMID 25259863 DOI: 10.1097/WNO.0000000000000167  1
2014 Neuenschwander AG, Thai KK, Figueroa KP, Pulst SM. Amyotrophic lateral sclerosis risk for spinocerebellar ataxia type 2 ATXN2 CAG repeat alleles: a meta-analysis. Jama Neurology. 71: 1529-34. PMID 25285812 DOI: 10.1001/jamaneurol.2014.2082  1
2014 Gallego-Iradi C, Bickford JS, Khare S, Hall A, Nick JA, Salmasinia D, Wawrowsky K, Bannykh S, Huynh DP, Rincon-Limas DE, Pulst SM, Nick HS, Fernandez-Funez P, Waters MF. KCNC3(R420H), a K(+) channel mutation causative in spinocerebellar ataxia 13 displays aberrant intracellular trafficking. Neurobiology of Disease. 71: 270-9. PMID 25152487 DOI: 10.1016/j.nbd.2014.08.020  1
2014 Nguyen TT, Oh SS, Weaver D, Lewandowska A, Maxfield D, Schuler MH, Smith NK, Macfarlane J, Saunders G, Palmer CA, Debattisti V, Koshiba T, Pulst S, Feldman EL, Hajnóczky G, et al. Loss of Miro1-directed mitochondrial movement results in a novel murine model for neuron disease. Proceedings of the National Academy of Sciences of the United States of America. 111: E3631-40. PMID 25136135 DOI: 10.1073/pnas.1402449111  1
2014 Narayanaswami P, Showers D, Levi B, Showers M, Jones EC, Busis NA, Comella CL, Pulst SM, Hosey JP, Griggs RC. State neurologic societies and the AAN: Strengthening neurology for the future. Neurology. Clinical Practice. 4: 247-255. PMID 25110622 DOI: 10.1212/CPJ.0000000000000034  1
2014 Tezenas du Montcel S, Durr A, Bauer P, Figueroa KP, Ichikawa Y, Brussino A, Forlani S, Rakowicz M, Schöls L, Mariotti C, van de Warrenburg BP, Orsi L, Giunti P, Filla A, Szymanski S, ... ... Pulst SM, et al. Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes. Brain : a Journal of Neurology. 137: 2444-55. PMID 24972706 DOI: 10.1093/brain/awu174  1
2014 Pulst SM, Pflieger LT. Coexpression networks predict ataxia genes. Jama Neurology. 71: 825-8. PMID 24861589 DOI: 10.1001/jamaneurol.2014.757  1
2014 Matilla-Dueñas A, Ashizawa T, Brice A, Magri S, McFarland KN, Pandolfo M, Pulst SM, Riess O, Rubinsztein DC, Schmidt J, Schmidt T, Scoles DR, Stevanin G, Taroni F, Underwood BR, et al. Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxias. Cerebellum (London, England). 13: 269-302. PMID 24307138 DOI: 10.1007/s12311-013-0539-y  1
2014 Gibson SB, Figueroa KP, Bromberg MB, Pulst SM, Cannon-Albright L. Familial clustering of ALS in a population-based resource. Neurology. 82: 17-22. PMID 24306004 DOI: 10.1212/01.wnl.0000438219.39061.da  1
2014 Dai Y, Zheng K, Clark J, Swerdlow RH, Pulst SM, Sutton JP, Shinobu LA, Simon DK. Rapamycin drives selection against a pathogenic heteroplasmic mitochondrial DNA mutation. Human Molecular Genetics. 23: 637-47. PMID 24101601 DOI: 10.1093/hmg/ddt450  1
2013 Ashizawa T, Figueroa KP, Perlman SL, Gomez CM, Wilmot GR, Schmahmann JD, Ying SH, Zesiewicz TA, Paulson HL, Shakkottai VG, Bushara KO, Kuo SH, Geschwind MD, Xia G, Mazzoni P, ... ... Pulst SM, et al. Clinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational study. Orphanet Journal of Rare Diseases. 8: 177. PMID 24225362 DOI: 10.1186/1750-1172-8-177  1
2013 Tazen S, Figueroa K, Kwan JY, Goldman J, Hunt A, Sampson J, Gutmann L, Pulst SM, Mitsumoto H, Kuo SH. Amyotrophic lateral sclerosis and spinocerebellar ataxia type 2 in a family with full CAG repeat expansions of ATXN2. Jama Neurology. 70: 1302-4. PMID 23959108 DOI: 10.1001/jamaneurol.2013.443  1
2013 Bürk K, Strzelczyk A, Reif PS, Figueroa KP, Pulst SM, Zühlke C, Oertel WH, Hamer HM, Rosenow F. Mesial temporal lobe epilepsy in a patient with spinocerebellar ataxia type 13 (SCA13). The International Journal of Neuroscience. 123: 278-82. PMID 23215817 DOI: 10.3109/00207454.2012.755180  1
2013 Hansen ST, Pulst SM. Response to ethanol induced ataxia between C57BL/6J and 129X1/SvJ mouse strains using a treadmill based assay. Pharmacology, Biochemistry, and Behavior. 103: 582-8. PMID 23103202 DOI: 10.1016/j.pbb.2012.10.010  1
2013 Hansen ST, Meera P, Otis TS, Pulst SM. Changes in Purkinje cell firing and gene expression precede behavioral pathology in a mouse model of SCA2. Human Molecular Genetics. 22: 271-83. PMID 23087021 DOI: 10.1093/hmg/dds427  1
2012 Pulst SM, Otis TS. Repolarization matters: mutations in the Kv4.3 potassium channel cause SCA19/22. Annals of Neurology. 72: 829-31. PMID 23280833 DOI: 10.1002/ana.23803  1
2012 Hekman KE, Yu GY, Brown CD, Zhu H, Du X, Gervin K, Undlien DE, Peterson A, Stevanin G, Clark HB, Pulst SM, Bird TD, White KP, Gomez CM. A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insult. Human Molecular Genetics. 21: 5472-83. PMID 23001565 DOI: 10.1093/hmg/dds392  1
2012 Kareus SA, Figueroa KP, Cannon-Albright LA, Pulst SM. Shared predispositions of parkinsonism and cancer: a population-based pedigree-linked study. Archives of Neurology. 69: 1572-7. PMID 22945795 DOI: 10.1001/archneurol.2012.2261  1
2012 Scoles DR, Pflieger LT, Thai KK, Hansen ST, Dansithong W, Pulst SM. ETS1 regulates the expression of ATXN2. Human Molecular Genetics. 21: 5048-65. PMID 22914732 DOI: 10.1093/hmg/dds349  1
2011 Fischbeck KH, Pulst SM. Amyotrophic lateral sclerosis and spinocerebellar ataxia 2. Neurology. 76: 2050-1. PMID 21562249 DOI: 10.1212/WNL.0b013e31821f4498  1
2011 Figueroa KP, Waters MF, Garibyan V, Bird TD, Gomez CM, Ranum LP, Minassian NA, Papazian DM, Pulst SM. Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13). Plos One. 6: e17811. PMID 21479265 DOI: 10.1371/journal.pone.0017811  1
2010 Figueroa KP, Minassian NA, Stevanin G, Waters M, Garibyan V, Forlani S, Strzelczyk A, Bürk K, Brice A, Dürr A, Papazian DM, Pulst SM. KCNC3: phenotype, mutations, channel biophysics-a study of 260 familial ataxia patients. Human Mutation. 31: 191-6. PMID 19953606 DOI: 10.1002/humu.21165  1
2009 Figueroa KP, Farooqi S, Harrup K, Frank J, O'Rahilly S, Pulst SM. Genetic variance in the spinocerebellar ataxia type 2 (ATXN2) gene in children with severe early onset obesity. Plos One. 4: e8280. PMID 20016785 DOI: 10.1371/journal.pone.0008280  1
2009 Pulst SM. Neurodegenerative disease. Genetic discrimination in Huntington disease. Nature Reviews. Neurology. 5: 525-6. PMID 19794509 DOI: 10.1038/nrneurol.2009.153  1
2009 Sikorska M, Sandhu JK, Simon DK, Pathiraja V, Sodja C, Li Y, Ribecco-Lutkiewicz M, Lanthier P, Borowy-Borowski H, Upton A, Raha S, Pulst SM, Tarnopolsky MA. Identification of ataxia-associated mtDNA mutations (m.4052T>C and m.9035T>C) and evaluation of their pathogenicity in transmitochondrial cybrids. Muscle & Nerve. 40: 381-94. PMID 19626676 DOI: 10.1002/mus.21355  1
2009 Liu J, Tang TS, Tu H, Nelson O, Herndon E, Huynh DP, Pulst SM, Bezprozvanny I. Deranged calcium signaling and neurodegeneration in spinocerebellar ataxia type 2. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 9148-62. PMID 19625506 DOI: 10.1523/JNEUROSCI.0660-09.2009  1
2009 Huynh DP, Maalouf M, Silva AJ, Schweizer FE, Pulst SM. Dissociated fear and spatial learning in mice with deficiency of ataxin-2. Plos One. 4: e6235. PMID 19617910 DOI: 10.1371/journal.pone.0006235  1
2009 Bhidayasiri R, Pulst SM. Juvenile parkinsonism. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 13: 290-2. PMID 18571951 DOI: 10.1016/j.ejpn.2008.04.010  1
2008 Waters MF, Pulst SM. Sca13. Cerebellum (London, England). 7: 165-9. PMID 18592334 DOI: 10.1007/s12311-008-0039-7  1
2007 Al-Ramahi I, Pérez AM, Lim J, Zhang M, Sorensen R, de Haro M, Branco J, Pulst SM, Zoghbi HY, Botas J. dAtaxin-2 mediates expanded Ataxin-1-induced neurodegeneration in a Drosophila model of SCA1. Plos Genetics. 3: e234. PMID 18166084 DOI: 10.1371/journal.pgen.0030234  1
2007 Ng H, Pulst SM, Huynh DP. Ataxin-2 mediated cell death is dependent on domains downstream of the polyQ repeat. Experimental Neurology. 208: 207-15. PMID 17949716 DOI: 10.1016/j.expneurol.2007.07.023  1
2007 Simon DK, Zheng K, Velázquez L, Santos N, Almaguer L, Figueroa KP, Pulst SM. Mitochondrial complex I gene variant associated with early age at onset in spinocerebellar ataxia type 2. Archives of Neurology. 64: 1042-4. PMID 17620498 DOI: 10.1001/archneur.64.7.1042  1
2007 Pulst SM. Ataxia rating scales in the balance. Nature Clinical Practice. Neurology. 3: 119. PMID 17342188 DOI: 10.1038/ncpneuro0446  1
2007 Huynh DP, Nguyen DT, Pulst-Korenberg JB, Brice A, Pulst SM. Parkin is an E3 ubiquitin-ligase for normal and mutant ataxin-2 and prevents ataxin-2-induced cell death. Experimental Neurology. 203: 531-41. PMID 17097639 DOI: 10.1016/j.expneurol.2006.09.009  1
2007 Paulson HL, Pulst SM. Chapter 5 Polyglutamine Ataxias: In Vitro and In Vivo Models Blue Books of Neurology. 31: 145-169. DOI: 10.1016/S1877-184X(09)70079-6  1
2007 Brice A, Pulst SM. Preface Blue Books of Neurology. 31: xvii-xviii. DOI: 10.1016/S1877-184X(09)70073-5  1
2006 Willeumier K, Pulst SM, Schweizer FE. Proteasome inhibition triggers activity-dependent increase in the size of the recycling vesicle pool in cultured hippocampal neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 11333-41. PMID 17079661 DOI: 10.1523/JNEUROSCI.1684-06.2006  1
2006 Waters MF, Minassian NA, Stevanin G, Figueroa KP, Bannister JP, Nolte D, Mock AF, Evidente VG, Fee DB, Müller U, Dürr A, Brice A, Papazian DM, Pulst SM. Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes. Nature Genetics. 38: 447-51. PMID 16501573 DOI: 10.1038/ng1758  1
2006 Scoles DR, Yong WH, Qin Y, Wawrowsky K, Pulst SM. Schwannomin inhibits tumorigenesis through direct interaction with the eukaryotic initiation factor subunit c (eIF3c). Human Molecular Genetics. 15: 1059-70. PMID 16497727 DOI: 10.1093/hmg/ddl021  1
2006 Kiehl TR, Nechiporuk A, Figueroa KP, Keating MT, Huynh DP, Pulst SM. Generation and characterization of Sca2 (ataxin-2) knockout mice. Biochemical and Biophysical Research Communications. 339: 17-24. PMID 16293225 DOI: 10.1016/j.bbrc.2005.10.186  1
2005 Bhidayasiri R, Perlman SL, Pulst SM, Geschwind DH. Late-onset Friedreich ataxia: phenotypic analysis, magnetic resonance imaging findings, and review of the literature. Archives of Neurology. 62: 1865-9. PMID 16344344 DOI: 10.1001/archneur.62.12.1865  1
2005 Waters MF, Fee D, Figueroa KP, Nolte D, Müller U, Advincula J, Coon H, Evidente VG, Pulst SM. An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus? Neurology. 65: 1111-3. PMID 16135769 DOI: 10.1212/01.wnl.0000177490.05162.41  1
2005 Scoles DR, Qin Y, Nguyen V, Gutmann DH, Pulst SM. HRS inhibits EGF receptor signaling in the RT4 rat schwannoma cell line. Biochemical and Biophysical Research Communications. 335: 385-92. PMID 16083858 DOI: 10.1016/j.bbrc.2005.07.083  1
2005 Bhidayasiri R, Pulst SM. Dystonia (DYT) genetic loci. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 9: 367-70. PMID 16055360 DOI: 10.1016/j.ejpn.2005.05.002  1
2005 Pulst SM, Santos N, Wang D, Yang H, Huynh D, Velazquez L, Figueroa KP. Spinocerebellar ataxia type 2: polyQ repeat variation in the CACNA1A calcium channel modifies age of onset. Brain : a Journal of Neurology. 128: 2297-303. PMID 16000334 DOI: 10.1093/brain/awh586  1
2005 Konakova M, Pulst SM. Dystonia-associated forms of torsinA are deficient in ATPase activity. Journal of Molecular Neuroscience : Mn. 25: 105-17. PMID 15781971 DOI: 10.1385/JMN:25:1:105  1
2005 Pulst SM. Spinocerebellar ataxia type 2 (SCA2) Movement Disorders. 631-636. DOI: 10.1016/B978-012088382-0/50055-4  1
2005 Oh MK, Scoles DR, Pulst SM. DNA Microarray analysis of immediate response to EGF treatment in rat schwannoma cells Biotechnology and Bioprocess Engineering. 10: 444-450.  1
2004 Glass AS, Huynh DP, Franck T, Woitalla D, Müller T, Pulst SM, Berg D, Krüger R, Riess O. Screening for mutations in synaptotagmin XI in Parkinson's disease. Journal of Neural Transmission. Supplementum. 21-8. PMID 15354386  1
2004 Fee DB, So YT, Barraza C, Figueroa KP, Pulst SM. Phenotypic variability associated with Arg26Gln mutation in caveolin3. Muscle & Nerve. 30: 375-8. PMID 15318349 DOI: 10.1002/mus.20092  1
2004 Matsuura T, Fang P, Lin X, Khajavi M, Tsuji K, Rasmussen A, Grewal RP, Achari M, Alonso ME, Pulst SM, Zoghbi HY, Nelson DL, Roa BB, Ashizawa T. Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10. American Journal of Human Genetics. 74: 1216-24. PMID 15127363 DOI: 10.1086/421526  1
2004 Oberlin SR, Konakova M, Pulst S, Chesselet MF. Development and anatomic localization of torsinA. Advances in Neurology. 94: 61-5. PMID 14509655  1
2003 Figueroa KP, Pulst SM. Identification and expression of the gene for human ataxin-2-related protein on chromosome 16. Experimental Neurology. 184: 669-78. PMID 14769358 DOI: 10.1016/S0014-4886(03)00287-5  1
2003 Pulst SM. Neurogenetics: single gene disorders. Journal of Neurology, Neurosurgery, and Psychiatry. 74: 1608-14. PMID 14638875 DOI: 10.1136/jnnp.74.12.1608  1
2003 Oh MK, Scoles DR, Haipek C, Strand AD, Gutmann DH, Olson JM, Pulst SM. Genetic heterogeneity of stably transfected cell lines revealed by expression profiling with oligonucleotide microarrays. Journal of Cellular Biochemistry. 90: 1068-78. PMID 14624465 DOI: 10.1002/jcb.10712  1
2003 Huynh DP, Scoles DR, Nguyen D, Pulst SM. The autosomal recessive juvenile Parkinson disease gene product, parkin, interacts with and ubiquitinates synaptotagmin XI. Human Molecular Genetics. 12: 2587-97. PMID 12925569 DOI: 10.1093/hmg/ddg269  1
2003 Huynh DP, Yang HT, Vakharia H, Nguyen D, Pulst SM. Expansion of the polyQ repeat in ataxin-2 alters its Golgi localization, disrupts the Golgi complex and causes cell death. Human Molecular Genetics. 12: 1485-96. PMID 12812977 DOI: 10.1093/hmg/ddg175  1
2003 Berendt M, Dam M, Licht BG, Hyson LL, Licht MH, Harper KM, Pulst SM. Re: Clinical presentations of naturally occurring canine seizures: Similarities to human seizures (multiple letters) Epilepsy and Behavior. 4: 198-201. PMID 12697147 DOI: 10.1016/S1525-5050(02)00686-8  1
2003 Nance MA, Bird TD, Pulst SM. Ethical Issues in Genetic Testing for Movement Disorders Genetics of Movement Disorders. 541-550. DOI: 10.1016/B978-012566652-7/50047-2  1
2003 Pauls DL, Pulst SM, State MW. Genetics of Gilles de la Tourette Syndrome Genetics of Movement Disorders. 491-501. DOI: 10.1016/B978-012566652-7/50044-7  1
2003 Vakharia H, Oh MK, Pulst SM. Spinocerebellar Ataxia 11 (SCA11) Genetics of Movement Disorders. 117-119. DOI: 10.1016/B978-012566652-7/50014-9  1
2003 Pulst SM. Spinocerebellar Ataxia 2 (SCA2) Genetics of Movement Disorders. 45-56. DOI: 10.1016/B978-012566652-7/50006-X  1
2003 Pulst SM. Inherited Ataxias: An Introduction Genetics of Movement Disorders. 19-34. DOI: 10.1016/B978-012566652-7/50004-6  1
2003 Pulst SM. Introduction to Medical Genetics and Methods of DNA Testing Genetics of Movement Disorders. 1-18. DOI: 10.1016/B978-012566652-7/50003-4  1
2003 Pulst SM. Genetics of Movement Disorders Genetics of Movement Disorders. 1-561.  1
2002 Adams CR, Figueroa KP, Zu L, Anderson TL, Graves MC, Garcia CA, Pulst SM. Bethlem myopathy in a black creole pedigree. Journal of Clinical Neuromuscular Disease. 4: 7-10. PMID 19078680  1
2002 Scoles DR, Nguyen VD, Qin Y, Sun CX, Morrison H, Gutmann DH, Pulst SM. Neurofibromatosis 2 (NF2) tumor suppressor schwannomin and its interacting protein HRS regulate STAT signaling. Human Molecular Genetics. 11: 3179-89. PMID 12444102  1
2002 Sun CX, Haipek C, Scoles DR, Pulst SM, Giovannini M, Komada M, Gutmann DH. Functional analysis of the relationship between the neurofibromatosis 2 tumor suppressor and its binding partner, hepatocyte growth factor-regulated tyrosine kinase substrate. Human Molecular Genetics. 11: 3167-78. PMID 12444101  1
2002 Bhidayasiri R, Pulst SM. Segmental unilateral lentiginosis in generalized neurofibromatosis type 1. Archives of Neurology. 59: 1331-2. PMID 12164732 DOI: 10.1001/archneur.59.8.1331  1
2002 Grewal RP, Achari M, Matsuura T, Durazo A, Tayag E, Zu L, Pulst SM, Ashizawa T. Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10. Archives of Neurology. 59: 1285-90. PMID 12164725 DOI: 10.1001/archneur.59.8.1285  1
2002 Scoles DR, Chen M, Pulst SM. Effects of Nf2 missense mutations on schwannomin interactions. Biochemical and Biophysical Research Communications. 290: 366-74. PMID 11779178 DOI: 10.1006/bbrc.2001.6178  1
2001 Konakova M, Pulst SM. Immunocytochemical characterization of torsin proteins in mouse brain. Brain Research. 922: 1-8. PMID 11730696 DOI: 10.1016/S0006-8993(01)03014-1  1
2001 Cholfin JA, Sobrido MJ, Perlman S, Pulst SM, Geschwind DH. The SCA12 mutation as a rare cause of spinocerebellar ataxia. Archives of Neurology. 58: 1833-5. PMID 11708992  1
2001 Pulst SM. Genomes, neuroscience, and neurology. Archives of Neurology. 58: 1755-7. PMID 11708979  1
2001 Huynh DP, Dy M, Nguyen D, Kiehl TR, Pulst SM. Differential expression and tissue distribution of parkin isoforms during mouse development. Brain Research. Developmental Brain Research. 130: 173-81. PMID 11675120 DOI: 10.1016/S0165-3806(01)00234-6  1
2001 Figueroa KP, Chan P, Schöls L, Tanner C, Riess O, Perlman SL, Geschwind DH, Pulst SM. Association of moderate polyglutamine tract expansions in the slow calcium-activated potassium channel type 3 with ataxia. Archives of Neurology. 58: 1649-53. PMID 11594924  1
2001 Sobrido MJ, Cholfin JA, Perlman S, Pulst SM, Geschwind DH. SCA8 repeat expansions in ataxia: a controversial association. Neurology. 57: 1310-2. PMID 11591855  1
2001 Kiehl TR, Shibata H, Vo T, Huynh DP, Pulst SM. Identification and expression of a mouse ortholog of A2BP1. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 12: 595-601. PMID 11471052 DOI: 10.1007/s00335-001-2056-4  1
2001 Konakova M, Huynh DP, Yong W, Pulst SM. Cellular distribution of torsin A and torsin B in normal human brain. Archives of Neurology. 58: 921-7. PMID 11405807  1
2001 So YT, Zu L, Barraza C, Figueroa KP, Pulst SM. Rippling muscle disease: evidence for phenotypic and genetic heterogeneity. Muscle & Nerve. 24: 340-4. PMID 11353417 DOI: 10.1002/1097-4598(200103)24:3<340::AID-MUS1003>3.0.CO;2-X  1
2001 Gutmann DH, Haipek CA, Burke SP, Sun CX, Scoles DR, Pulst SM. The NF2 interactor, hepatocyte growth factor-regulated tyrosine kinase substrate (HRS), associates with merlin in the "open" conformation and suppresses cell growth and motility. Human Molecular Genetics. 10: 825-34. PMID 11285248  1
2001 Costa RM, Yang T, Huynh DP, Pulst SM, Viskochil DH, Silva AJ, Brannan CI. Learning deficits, but normal development and tumor predisposition, in mice lacking exon 23a of Nf1. Nature Genetics. 27: 399-405. PMID 11279521 DOI: 10.1038/86898  1
2001 Bruder CE, Hirvelä C, Tapia-Paez I, Fransson I, Segraves R, Hamilton G, Zhang XX, Evans DG, Wallace AJ, Baser ME, Zucman-Rossi J, Hergersberg M, Boltshauser E, Papi L, Rouleau GA, ... ... Pulst SM, et al. High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH. Human Molecular Genetics. 10: 271-82. PMID 11159946  1
2001 Kiehl TR, Olson JM, Pulst SM. The hereditary disease array group (HDAG) - Microarrays, models and mechanisms: A collaboration update Current Genomics. 2: 221-229. DOI: 10.2174/1389202013350878  1
2001 Pulst SM. Current Genomics: Foreword Current Genomics. 2: xxx.  1
2000 Kiehl TR, Shibata H, Pulst SM. The ortholog of human ataxin-2 is essential for early embryonic patterning in C. elegans. Journal of Molecular Neuroscience : Mn. 15: 231-41. PMID 11303786 DOI: 10.1385/JMN:15:3:231  1
2000 Huynh DP, Scoles DR, Ho TH, Del Bigio MR, Pulst SM. Parkin is associated with actin filaments in neuronal and nonneural cells. Annals of Neurology. 48: 737-44. PMID 11079537 DOI: 10.1002/1531-8249(200011)48:5<737::AID-ANA7>3.0.CO;2-D  1
2000 Matsuura T, Yamagata T, Burgess DL, Rasmussen A, Grewal RP, Watase K, Khajavi M, McCall AE, Davis CF, Zu L, Achari M, Pulst SM, Alonso E, Noebels JL, Nelson DL, et al. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10. Nature Genetics. 26: 191-4. PMID 11017075 DOI: 10.1038/79911  1
2000 Pulst SM. Ethical issues in DNA testing. Muscle & Nerve. 23: 1503-7. PMID 11003784 DOI: 10.1002/1097-4598(200010)23:10<1503::AID-MUS5>3.0.CO;2-V  1
2000 Lim DJ, Rubenstein AE, Evans DG, Jacks T, Seizinger BG, Baser ME, Beebe D, Brackmann DE, Chiocca EA, Fehon RG, Giovannini M, Glazer R, Gusella JF, Gutmann DH, Korf B, ... ... Pulst SM, et al. Advances in neurofibromatosis 2 (NF2): a workshop report. Journal of Neurogenetics. 14: 63-106. PMID 10992163  1
2000 Huynh DP, Figueroa K, Hoang N, Pulst SM. Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human. Nature Genetics. 26: 44-50. PMID 10973246 DOI: 10.1038/79162  1
2000 Hayes S, Turecki G, Brisebois K, Lopes-Cendes I, Gaspar C, Riess O, Ranum LP, Pulst SM, Rouleau GA. CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2). Human Molecular Genetics. 9: 1753-8. PMID 10915763  1
2000 Scoles DR, Huynh DP, Chen MS, Burke SP, Gutmann DH, Pulst SM. The neurofibromatosis 2 tumor suppressor protein interacts with hepatocyte growth factor-regulated tyrosine kinase substrate. Human Molecular Genetics. 9: 1567-74. PMID 10861283  1
2000 Shibata H, Huynh DP, Pulst SM. A novel protein with RNA-binding motifs interacts with ataxin-2. Human Molecular Genetics. 9: 1303-13. PMID 10814712  1
2000 Pulst SM, Filla A. Ataxias on the march from Quebec to Tunisia. Neurology. 54: 1400-1. PMID 10751244  1
2000 Pulst SM. NF2 in monozygotic twins. Surgical Neurology. 53: 95; author reply 96. PMID 10697243 DOI: 10.1016/S0090-3019(99)00173-1  1
1999 Simon DK, Pulst SM, Sutton JP, Browne SE, Beal MF, Johns DR. Familial multisystem degeneration with parkinsonism associated with the 11778 mitochondrial DNA mutation. Neurology. 53: 1787-93. PMID 10563629  1
1999 Kuo AA, Pulst SM, Eliashiv DS, Adams CR. Electrical inexcitability of nerves and muscles in severe infantile spinal muscular atrophy. Journal of Neurology, Neurosurgery, and Psychiatry. 67: 122. PMID 10454872  1
1999 Pulst SM. Genetic linkage analysis. Archives of Neurology. 56: 667-72. PMID 10369304 DOI: 10.1001/archneur.56.6.667  1
1999 Huynh DP, Del Bigio MR, Ho DH, Pulst SM. Expression of ataxin-2 in brains from normal individuals and patients with Alzheimer's disease and spinocerebellar ataxia 2. Annals of Neurology. 45: 232-41. PMID 9989626 DOI: 10.1002/1531-8249(199902)45:2<232::AID-ANA14>3.0.CO;2-7  1
1999 Zu L, Figueroa KP, Grewal R, Pulst SM. Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22. American Journal of Human Genetics. 64: 594-9. PMID 9973298 DOI: 10.1086/302247  1
1998 Grewal RP, Tayag E, Figueroa KP, Zu L, Durazo A, Nunez C, Pulst SM. Clinical and genetic analysis of a distinct autosomal dominant spinocerebellar ataxia. Neurology. 51: 1423-6. PMID 9818872  1
1998 Buttner N, Geschwind D, Jen JC, Perlman S, Pulst SM, Baloh RW. Oculomotor phenotypes in autosomal dominant ataxias. Archives of Neurology. 55: 1353-7. PMID 9779665 DOI: 10.1001/archneur.55.10.1353  1
1998 Mautner VF, Schröder S, Pulst SM, Ostertag H, Kluwe L. [Neurofibromatosis versus schwannomatosis]. Fortschritte Der Neurologie-Psychiatrie. 66: 271-7. PMID 9676422 DOI: 10.1055/s-2007-995262  1
1998 Nechiporuk T, Huynh DP, Figueroa K, Sahba S, Nechiporuk A, Pulst SM. The mouse SCA2 gene: cDNA sequence, alternative splicing and protein expression. Human Molecular Genetics. 7: 1301-9. PMID 9668173  1
1998 Scoles DR, Huynh DP, Morcos PA, Coulsell ER, Robinson NG, Tamanoi F, Pulst SM. Neurofibromatosis 2 tumour suppressor schwannomin interacts with betaII-spectrin. Nature Genetics. 18: 354-9. PMID 9537418 DOI: 10.1038/ng0498-354  1
1998 Sahba S, Nechiporuk A, Figueroa KP, Nechiporuk T, Pulst SM. Genomic structure of the human gene for spinocerebellar ataxia type 2 (SCA2) on chromosome 12q24.1. Genomics. 47: 359-64. PMID 9480749 DOI: 10.1006/geno.1997.5131  1
1998 Gouw LG, Castañeda MA, McKenna CK, Digre KB, Pulst SM, Perlman S, Lee MS, Gomez C, Fischbeck K, Gagnon D, Storey E, Bird T, Jeri FR, Ptácek LJ. Analysis of the dynamic mutation in the SCA7 gene shows marked parental effects on CAG repeat transmission. Human Molecular Genetics. 7: 525-32. PMID 9467013 DOI: 10.1093/hmg/7.3.525  1
1997 Riess O, Laccone FA, Gispert S, Schöls L, Zühlke C, Vieira-Saecker AM, Herlt S, Wessel K, Epplen JT, Weber BH, Kreuz F, Chahrokh-Zadeh S, Meindl A, Lunkes A, Aguiar J, ... ... Pulst SM, et al. SCA2 trinucleotide expansion in German SCA patients. Neurogenetics. 1: 59-64. PMID 10735276  1
1997 Geschwind DH, Perlman S, Figueroa KP, Karrim J, Baloh RW, Pulst SM. Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlations. Neurology. 49: 1247-51. PMID 9371902  1
1997 Adams C, Starkman S, Pulst SM. Clinical and molecular analysis of a pedigree of southern Italian ancestry with spinocerebellar ataxia type 2. Neurology. 49: 1163-6. PMID 9339711  1
1997 Nechiporuk T, Nechiporuk A, Sahba S, Figueroa K, Shibata H, Chen XN, Korenberg JR, de Jong P, Pulst SM. A high-resolution PAC and BAC map of the SCA2 region. Genomics. 44: 321-9. PMID 9325053 DOI: 10.1006/geno.1997.4886  1
1997 Schöls L, Gispert S, Vorgerd M, Menezes Vieira-Saecker AM, Blanke P, Auburger G, Amoiridis G, Meves S, Epplen JT, Przuntek H, Pulst SM, Riess O. Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds. Archives of Neurology. 54: 1073-80. PMID 9311350  1
1997 Huynh DP, Vinters HV, Ho DH, Ho VV, Pulst SM. Neuronal expression and intracellular localization of presenilins in normal and Alzheimer disease brains. Journal of Neuropathology and Experimental Neurology. 56: 1009-17. PMID 9291942  1
1997 Sutton JP, Pulst SM. Atypical parkinsonism in a family of Portuguese ancestry: absence of CAG repeat expansion in the MJD1 gene. Neurology. 48: 1285-90. PMID 9153459  1
1997 Geschwind DH, Perlman S, Figueroa CP, Treiman LJ, Pulst SM. The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia. American Journal of Human Genetics. 60: 842-50. PMID 9106530  1
1997 Huynh DP, Mautner V, Baser ME, Stavrou D, Pulst SM. Immunohistochemical detection of schwannomin and neurofibromin in vestibular schwannomas, ependymomas and meningiomas. Journal of Neuropathology and Experimental Neurology. 56: 382-90. PMID 9100669  1
1997 Pulst SM, Riccardi V, Mautner V. Spinal schwannomatosis. Neurology. 48: 787-8. PMID 9065571  1
1996 Huynh DP, Ho VV, Pulst SM. Characterization and expression of presenilin 1 in mouse brain. Neuroreport. 7: 2423-8. PMID 8981396  1
1996 Huynh DP, Tran TM, Nechiporuk T, Pulst SM. Expression of neurofibromatosis 2 transcript and gene product during mouse fetal development. Cell Growth & Differentiation : the Molecular Biology Journal of the American Association For Cancer Research. 7: 1551-61. PMID 8930405  1
1996 Baser ME, Mautner VF, Ragge NK, Nechiporuk A, Riccardi VM, Klein J, Sainz J, Pulst SM. Presymptomatic diagnosis of neurofibromatosis 2 using linked genetic markers, neuroimaging, and ocular examinations. Neurology. 47: 1269-77. PMID 8909442  1
1996 Pulst SM, Nechiporuk A, Nechiporuk T, Gispert S, Chen XN, Lopes-Cendes I, Pearlman S, Starkman S, Orozco-Diaz G, Lunkes A, DeJong P, Rouleau GA, Auburger G, Korenberg JR, Figueroa C, et al. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2. Nature Genetics. 14: 269-76. PMID 8896555 DOI: 10.1038/ng1196-269  1
1996 Baser ME, Ragge NK, Riccardi VM, Janus T, Gantz B, Pulst SM. Phenotypic variability in monozygotic twins with neurofibromatosis 2. American Journal of Medical Genetics. 64: 563-7. PMID 8870923 DOI: 10.1002/(SICI)1096-8628(19960906)64:4<563::AID-AJMG7>3.0.CO;2-Q  1
1996 Nechiporuk T, Nechiporuk A, Guan X, Frederick R, Figueroa K, Chumakov I, Korenberg JR, de Jong PJ, Pulst SM. Identification of three new microsatellite markers in the spinocerebellar ataxia type 2 (SCA2) region and 1.2 Mb physical map. Human Genetics. 97: 462-7. PMID 8834243 DOI: 10.1007/s004390050073  1
1996 Scoles DR, Baser ME, Pulst SM. A missense mutation in the neurofibromatosis 2 gene occurs in patients with mild and severe phenotypes. Neurology. 47: 544-6. PMID 8757035  1
1996 Mautner VF, Lindenau M, Baser ME, Hazim W, Tatagiba M, Haase W, Samii M, Wais R, Pulst SM. The neuroimaging and clinical spectrum of neurofibromatosis 2. Neurosurgery. 38: 880-5; discussion 88. PMID 8727812 DOI: 10.1097/00006123-199605000-00004  1
1996 Huynh DP, Pulst SM. Neurofibromatosis 2 antisense oligodeoxynucleotides induce reversible inhibition of schwannomin synthesis and cell adhesion in STS26T and T98G cells. Oncogene. 13: 73-84. PMID 8700556  1
1996 Nechiporuk A, Lopes-Cendes I, Nechiporuk T, Starkman S, Andermann E, Rouleau GA, Weissenbach JS, Kort E, Pulst SM. Genetic mapping of the spinocerebellar ataxia type 2 gene on human chromosome 12. Neurology. 46: 1731-5. PMID 8649579  1
1996 Sainz J, Figueroa K, Baser ME, Pulst SM. Identification of three neurofibromatosis type 2 (NF2) gene mutations in vestibular schwannomas. Human Genetics. 97: 121-3. PMID 8557252  1
1995 Kim UJ, Shizuya H, Sainz J, Garnes J, Pulst SM, de Jong P, Simon MI. Construction and utility of a human chromosome 22-specific Fosmid library. Genetic Analysis : Biomolecular Engineering. 12: 81-4. PMID 8574898 DOI: 10.1016/1050-3862(95)00122-0  1
1995 Sainz J, Figueroa K, Baser ME, Mautner VF, Pulst SM. High frequency of nonsense mutations in the NF2 gene caused by C to T transitions in five CGA codons. Human Molecular Genetics. 4: 137-9. PMID 7711726 DOI: 10.1093/hmg/4.1.137  1
1995 Kluwe L, Pulst SM, Köppen J, Mautner VF. A 163-bp deletion in the neurofibromatosis 2 (NF2) gene associated with variant phenotypes [corrected]. Human Genetics. 95: 443-6. PMID 7705843 DOI: 10.1007/BF00208973  1
1995 Mautner VF, Tatagiba M, Lindenau M, Fünsterer C, Pulst SM, Baser ME, Kluwe L, Zanella FE. Spinal tumors in patients with neurofibromatosis type 2: MR imaging study of frequency, multiplicity, and variety. Ajr. American Journal of Roentgenology. 165: 951-5. PMID 7676998 DOI: 10.2214/ajr.165.4.7676998  1
1995 Ragge NK, Baser ME, Klein J, Nechiporuk A, Sainz J, Pulst SM, Riccardi VM. Ocular abnormalities in neurofibromatosis 2. American Journal of Ophthalmology. 120: 634-41. PMID 7485365  1
1995 Kluwe L, Pulst SM, Köppen J, Mautner VF. A 163-bp deletion at the C-terminus of the schwannomin gene associated with variable phenotypes of neurofibromatosis type 2 Human Genetics. 96: 254. DOI: 10.1007/BF00207396  1
1994 Huynh DP, Nechiporuk T, Pulst SM. Differential expression and tissue distribution of type I and type II neurofibromins during mouse fetal development. Developmental Biology. 161: 538-51. PMID 8314000 DOI: 10.1006/dbio.1994.1052  0.44
1994 Huynh DP, Nechiporuk T, Pulst SM. Alternative transcripts in the mouse neurofibromatosis type 2 (NF2) gene are conserved and code for schwannomins with distinct C-terminal domains. Human Molecular Genetics. 3: 1075-9. PMID 7981675  1
1994 Sainz J, Huynh DP, Figueroa K, Ragge NK, Baser ME, Pulst SM. Mutations of the neurofibromatosis type 2 gene and lack of the gene product in vestibular schwannomas. Human Molecular Genetics. 3: 885-91. PMID 7951231  1
1993 Sainz J, Baser ME, Ragge NK, Nelson RA, Pulst SM. Loss of alleles in vestibular schwannomas: use of microsatellite markers on chromosome 22. Archives of Otolaryngology--Head & Neck Surgery. 119: 1285-8. PMID 17431981 DOI: 10.1001/archotol.1993.01880240015003  1
1993 Pulst SM, Rouleau GA, Marineau C, Fain P, Sieb JP. Familial meningioma is not allelic to neurofibromatosis 2. Neurology. 43: 2096-8. PMID 8413972  1
1993 Rouleau GA, Merel P, Lutchman M, Sanson M, Zucman J, Marineau C, Hoang-Xuan K, Demczuk S, Desmaze C, Plougastel B, Pulst SM, Lenoir G, Bijlsma E, Fashold R, Dumanski J, et al. Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2 Nature. 363: 515-521. PMID 8379998  1
1993 Nechiporuk A, Fain P, Kort E, Nee LE, Frommelt E, Polinsky RJ, Korenberg JR, Pulst SM. Linkage of familial Alzheimer disease to chromosome 14 in two large early-onset pedigrees: effects of marker allele frequencies on lod scores. American Journal of Medical Genetics. 48: 63-6. PMID 8357039 DOI: 10.1002/ajmg.1320480113  1
1993 Mautner VF, Tatagiba M, Guthoff R, Samii M, Pulst SM. Neurofibromatosis 2 in the pediatric age group. Neurosurgery. 33: 92-6. PMID 8355853  1
1993 Sainz J, Rasmussen M, Nechiporuk A, Vissing H, Cheng X, Korenberg JR, Pulst SM. Dinucleotide repeat polymorphism at the D22S351 locus. Human Molecular Genetics. 2: 1749. PMID 8268946 DOI: 10.1093/hmg/2.10.1749  1
1993 Pulst SM, Nechiporuk A, Starkman S. Anticipation in spinocerebellar ataxia type 2. Nature Genetics. 5: 8-10. PMID 8220431 DOI: 10.1038/ng0993-8c  1
1993 Sainz J, Nechiporuk A, Kim UJ, Simon MI, Pulst SM. CA-repeat polymorphism at the D22S430 locus adjacent to NF2. Human Molecular Genetics. 2: 2203. PMID 8111404 DOI: 10.1093/hmg/2.12.2203  1
1993 Mautner VF, Pulst SM. Non-classifiable neurofibromatoses | NICHTKLASSIFIZIERBARE NEUROFIBROMATOSE Aktuelle Neurologie. 20: 123-127.  1
1992 Huynh DP, Lin CT, Pulst SM. Expression of neurofibromin, the neurofibromatosis 1 gene product: studies in human neuroblastoma cells and rat brain. Neuroscience Letters. 143: 233-6. PMID 1436672 DOI: 10.1016/0304-3940(92)90272-9  1
1992 Kamino K, Orr HT, Payami H, Wijsman EM, Alonso ME, Pulst SM, Anderson L, O'dahl S, Nemens E, White JA. Linkage and mutational analysis of familial Alzheimer disease kindreds for the APP gene region. American Journal of Human Genetics. 51: 998-1014. PMID 1415269  1
1992 Falik-Borenstein TC, Pribyl TM, Pulst SM, Van Dyke DL, Weiss L, Chu ML, Kraus J, Marshak D, Korenberg JR. Stable ring chromosome 21: molecular and clinical definition of the lesion. American Journal of Medical Genetics. 42: 22-8. PMID 1308361 DOI: 10.1002/ajmg.1320420107  1
1991 Korenberg JR, Kalousek DK, Anneren G, Pulst SM, Hall JG, Epstein CJ, Cox DR. Deletion of chromosome 21 and normal intelligence: molecular definition of the lesion. Human Genetics. 87: 112-8. PMID 2066097 DOI: 10.1007/BF00204163  1
1991 Pulst SM, Pribyl T, Barker DF, Riccardi VM, Ren M, Yaari H, Korenberg JR. Molecular analysis of a patient with neurofibromatosis 1 and achondroplasia. American Journal of Medical Genetics. 40: 84-7. PMID 1909491 DOI: 10.1002/ajmg.1320400117  1
1991 Pulst SM, Yang-Feng T, Korenberg JR. Relative order and location of DNA sequences on chromosome 21 linked to familial Alzheimer disease. American Journal of Medical Genetics. 41: 454-9. PMID 1776637 DOI: 10.1002/ajmg.1320410415  1
1991 Pulst SM, Riccardi VM, Fain P, Korenberg JR. Familial spinal neurofibromatosis: clinical and DNA linkage analysis. Neurology. 41: 1923-7. PMID 1745350  1
1991 Mautner VF, Laute S, Schneider E, Pulst SM. [Neurofibromatosis: current clinical and molecular genetic aspects from the neurologic viewpoint]. Der Nervenarzt. 62: 340-8. PMID 1678877  1
1991 Pulst SM, Fain P, Cohn V, Nee LE, Polinsky RJ, Korenberg JR. Exclusion of linkage to the pericentromeric region of chromosome 21 in the Canadian pedigree with familial Alzheimer disease. Human Genetics. 87: 159-61. PMID 1676700 DOI: 10.1007/BF00204173  1
1990 Pulst SM, Deen DF. Potentiation of BCNU-induced cytotoxicity and sister chromatid exchanges by dibromodulcitol in vitro. Anticancer Research. 10: 1647-50. PMID 2285238  1
1990 Pulst SM, Graham JM, Fain P, Barker D, Pribyl T, Korenberg JR. The achondroplasia gene is not linked to the locus for neurofibromatosis 1 on chromosome 17. Human Genetics. 85: 12-4. PMID 2162805 DOI: 10.1007/BF00276318  1
1990 Korenberg JR, Kawashima H, Pulst SM, Ikeuchi T, Ogasawara N, Yamamoto K, Schonberg SA, West R, Allen L, Magenis E. Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype. American Journal of Human Genetics. 47: 236-46. PMID 2143053  1
1990 Pulst SM, Korenberg JR. Panel of aneuploid cell lines for physical mapping of the proximal long arm of human chromosome 21. American Journal of Medical Genetics. Supplement. 7: 137-40. PMID 2127362  1
1990 Pulst SM. Prenatal diagnosis of the neurofibromatoses. Clinics in Perinatology. 17: 829-44. PMID 1981029  1
1990 Pulst SM, Korenberg JR, Ren M, Greenwald J. A new HaeIII polymorphism at the D21S13 locus. Human Genetics. 85: 671. PMID 1977689 DOI: 10.1007/BF00193597  1
1990 Pulst SM, Korenberg JR, Greenwald J, Carbone M. A new EcoRI polymorphism at the D21S13 locus. Human Genetics. 84: 580. PMID 1970976 DOI: 10.1007/BF00210815  1
1989 Brown RO, Pulst SM, Mayeri E. Neuroendocrine bag cells of Aplysia are activated by bag cell peptide-containing neurons in the pleural ganglion. Journal of Neurophysiology. 61: 1142-52. PMID 2746315  1
1989 Korenberg JR, Pulst SM, Neve RL, West R. The Alzheimer amyloid precursor protein maps to human chromosome 21 bands q21.105-q21.05. Genomics. 5: 124-7. PMID 2527801 DOI: 10.1016/0888-7543(89)90095-5  1
1989 Pulst SM. [Diagnosis of von Recklinghausen's neurofibromatosis]. Deutsche Medizinische Wochenschrift (1946). 114: 647-8. PMID 2495918  1
1988 Pulst SM, Gusman D, Mayeri E. Immunostaining for peptides of the egg-laying hormone/bag cell peptide precursor protein in the head ganglia of Aplysia. Neuroscience. 27: 363-71. PMID 3200446 DOI: 10.1016/0306-4522(88)90244-8  1
1987 Pulst SM, Rothman BS, Mayeri E. Presence of immunoreactive alpha-bag cell peptide[1-8] in bag cell neurons of Aplysia suggests novel carboxypeptidase processing of neuropeptides. Neuropeptides. 10: 249-59. PMID 3683775 DOI: 10.1016/0143-4179(87)90075-8  1
1986 Pulst SM, Levin VA, Deen DF. In Vitro Cytotoxic Effects of Dibromodulcitol in 9L Rat Brain Tumor Cells. Pharmaceutical Research. 3: 302-6. PMID 24271715 DOI: 10.1023/A:1016319620508  1
1986 Pulst SM, Gusman D, Rothman BS, Mayeri E. Coexistence of egg-laying hormone and alpha-bag cell peptide in bag cell neurons of Aplysia indicates that they are a peptidergic multitransmitter system. Neuroscience Letters. 70: 40-5. PMID 2877421 DOI: 10.1016/0304-3940(86)90434-9  1
1984 Pulst SM. [Neurologic complications in acquired immunodeficiency syndrome (AIDS). A clinical, computer tomographic and neuropathologic case presentation with a review of the literature]. Der Nervenarzt. 55: 407-12. PMID 6090962  1
1983 Pulst SM, Walshe TM, Romero JA. Carbon monoxide poisoning with features of Gilles de la Tourette's syndrome. Archives of Neurology. 40: 443-4. PMID 6574730 DOI: 10.1001/archneur.1983.04050070073019  1
1983 Pulst SM, Lombroso CT. External ophthalmoplegia, alpha and spindle coma in imipramine overdose: case report and review of the literature. Annals of Neurology. 14: 587-90. PMID 6418060 DOI: 10.1002/ana.410140516  1
1982 Wolpers Ch. M, Pulst SM. Carotid thrombosis following blunt trauma to the neck. Report of 2 cases | DIE KAROTISTHROMBOSE NACH STUMPFEM HALSTRAUMA IM STRASSENVERKEHR. ZWEI FALLBERICHTE Aktuelle Neurologie. 9: 83-87.  1
1982 Pulst SM, Sayk J. Survival time of patients with gliomas and glioblastomas under antiepileptic therapy | ZUR UBERLEBENSZEIT VON PATIENTEN MIT GLIOMEN/GLIOBLASTOMEN UNTER ANTIEPILEPTIKA Nervenarzt. 53: 612-613.  1
1981 Pulst SM. Infrared-thermography in the diagnosis of sympathetic lesions | DIE INFRAROT THERMOGRAPHIE ZUR DIAGNOSTIK VON SYMPATHIKUSLASIONEN Aktuelle Neurologie. 8: 43-47.  1
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