| Year |
Citation |
Score |
| 2022 |
Schmitz M, Villar-Piqué A, Hermann P, Escaramís G, Calero M, Chen C, Kruse N, Cramm M, Golanska E, Sikorska B, Liberski PP, Pocchiari M, Lange P, Stehmann C, Sarros S, ... ... Geschwind MD, et al. Diagnostic accuracy of cerebrospinal fluid biomarkers in genetic prion diseases. Brain : a Journal of Neurology. PMID 35288744 DOI: 10.1093/brain/awab350 |
0.303 |
|
| 2020 |
Jones E, Hummerich H, Viré E, Uphill J, Dimitriadis A, Speedy H, Campbell T, Norsworthy P, Quinn L, Whitfield J, Linehan J, Jaunmuktane Z, Brandner S, Jat P, Nihat A, ... ... Geschwind MD, et al. Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study. The Lancet. Neurology. 19: 840-848. PMID 32949544 DOI: 10.1016/S1474-4422(20)30273-8 |
0.331 |
|
| 2020 |
Yang CY, Lai RY, Amokrane N, Lin CY, Figueroa KP, Pulst SM, Perlman S, Wilmot G, Gomez CM, Schmahmann JD, Paulson H, Shakkottai VG, Rosenthal LS, Ying SH, Zesiewicz T, ... ... Geschwind M, et al. Dysphagia in spinocerebellar ataxias type 1, 2, 3 and 6. Journal of the Neurological Sciences. 415: 116878. PMID 32454319 DOI: 10.1016/J.Jns.2020.116878 |
0.366 |
|
| 2020 |
Gan SR, Figueroa KP, Xu HL, Perlman S, Wilmot G, Gomez CM, Schmahmann J, Paulson H, Shakkottai VG, Ying SH, Zesiewicz T, Bushara K, Geschwind MD, Xia G, Subramony SH, et al. The impact of ethnicity on the clinical presentations of spinocerebellar ataxia type 3. Parkinsonism & Related Disorders. 72: 37-43. PMID 32105964 DOI: 10.1016/J.Parkreldis.2020.02.004 |
0.413 |
|
| 2019 |
Ngo KJ, Rexach JE, Lee H, Petty LE, Perlman S, Valera JM, Deignan JL, Mao Y, Aker M, Posey JE, Jhangiani SN, Coban-Akdemir ZH, Boerwinkle E, Muzny D, Nelson AB, ... ... Geschwind MD, et al. A Diagnostic Ceiling for Exome Sequencing in Cerebellar Ataxia and Related Neurological Disorders. Human Mutation. PMID 31692161 DOI: 10.1002/Humu.23946 |
0.357 |
|
| 2019 |
Aguilar-Calvo P, Sevillano AM, Bapat J, Soldau K, Sandoval DR, Altmeppen HC, Linsenmeier L, Pizzo DP, Geschwind MD, Sanchez H, Appleby BS, Cohen ML, Safar JG, Edland SD, Glatzel M, et al. Shortening heparan sulfate chains prolongs survival and reduces parenchymal plaques in prion disease caused by mobile, ADAM10-cleaved prions. Acta Neuropathologica. PMID 31673874 DOI: 10.1007/S00401-019-02085-X |
0.323 |
|
| 2019 |
Minikel EV, Vallabh SM, Orseth MC, Brandel JP, Haïk S, Laplanche JL, Zerr I, Parchi P, Capellari S, Safar J, Kenny J, Fong JC, Takada LT, Ponto C, Hermann P, ... ... Geschwind MD, et al. Age at onset in genetic prion disease and the design of preventive clinical trials. Neurology. PMID 31171647 DOI: 10.1212/Wnl.0000000000007745 |
0.366 |
|
| 2019 |
Staffaroni AM, Kramer AO, Casey M, Kang H, Rojas JC, Orrú CD, Caughey B, Allen IE, Kramer JH, Rosen HJ, Blennow K, Zetterberg H, Geschwind MD. Association of Blood and Cerebrospinal Fluid Tau Level and Other Biomarkers With Survival Time in Sporadic Creutzfeldt-Jakob Disease. Jama Neurology. PMID 31058916 DOI: 10.1001/Jamaneurol.2019.1071 |
0.323 |
|
| 2019 |
Vallabh SM, Nobuhara CK, Llorens F, Zerr I, Parchi P, Capellari S, Kuhn E, Klickstein J, Safar JG, Nery FC, Swoboda KJ, Geschwind MD, Zetterberg H, Arnold SE, Minikel EV, et al. Prion protein quantification in human cerebrospinal fluid as a tool for prion disease drug development. Proceedings of the National Academy of Sciences of the United States of America. PMID 30936307 DOI: 10.1073/Pnas.1901947116 |
0.332 |
|
| 2019 |
Vitali P, Palesi F, Cotta Ramusino M, Pan M, Costa A, Gandini Wheeler-Kingshott C, Ceroni M, Micieli G, Anzalone N, Giaccone G, Tagliavini F, Geschwind M. Early cortical and late striatal diffusion restriction on 3T MRI in a long-lived sporadic creutzfeldt-jakob disease case. Journal of Magnetic Resonance Imaging : Jmri. PMID 30912188 DOI: 10.1002/Jmri.26711 |
0.312 |
|
| 2019 |
Lai RY, Tomishon D, Figueroa KP, Pulst SM, Perlman S, Wilmot G, Gomez CM, Schmahmann JD, Paulson H, Shakkottai VG, Ying SH, Zesiewicz T, Bushara K, Geschwind M, Xia G, et al. Tremor in the Degenerative Cerebellum: Towards the Understanding of Brain Circuitry for Tremor. Cerebellum (London, England). PMID 30830673 DOI: 10.1007/S12311-019-01016-6 |
0.387 |
|
| 2018 |
Villar-Piqué A, Schmitz M, Lachmann I, Karch A, Calero O, Stehmann C, Sarros S, Ladogana A, Poleggi A, Santana I, Ferrer I, Mitrova E, Žáková D, Pocchiari M, Baldeiras I, ... ... Geschwind MD, et al. Cerebrospinal Fluid Total Prion Protein in the Spectrum of Prion Diseases. Molecular Neurobiology. PMID 30062673 DOI: 10.1007/S12035-018-1251-1 |
0.396 |
|
| 2018 |
Geschwind MD, Murray K. Differential diagnosis with other rapid progressive dementias in human prion diseases. Handbook of Clinical Neurology. 153: 371-397. PMID 29887146 DOI: 10.1016/B978-0-444-63945-5.00020-9 |
0.424 |
|
| 2018 |
Ngo K, Aker M, Petty LE, Chen J, Cavalcanti F, Nelson AB, Hassin-Baer S, Geschwind MD, Perlman S, Italiano D, Laganà A, Cavallaro S, Coppola G, Below JE, Fogel BL. Expanding the global prevalence of spinocerebellar ataxia type 42. Neurology. Genetics. 4: e232. PMID 29629410 DOI: 10.1212/Nxg.0000000000000232 |
0.353 |
|
| 2017 |
Kuo PH, Gan SR, Wang J, Lo RY, Figueroa KP, Tomishon D, Pulst SM, Perlman S, Wilmot G, Gomez CM, Schmahmann JD, Paulson H, Shakkottai VG, Ying SH, Zesiewicz T, ... ... Geschwind MD, et al. Dystonia and ataxia progression in spinocerebellar ataxias. Parkinsonism & Related Disorders. PMID 29089256 DOI: 10.1016/J.Parkreldis.2017.10.007 |
0.304 |
|
| 2017 |
Kim MO, Takada LT, Wong K, Forner SA, Geschwind MD. Genetic PrP Prion Diseases. Cold Spring Harbor Perspectives in Biology. PMID 28778873 DOI: 10.1101/Cshperspect.A033134 |
0.4 |
|
| 2017 |
Erkkinen MG, Kim MO, Geschwind MD. Clinical Neurology and Epidemiology of the Major Neurodegenerative Diseases. Cold Spring Harbor Perspectives in Biology. PMID 28716886 DOI: 10.1101/Cshperspect.A033118 |
0.423 |
|
| 2017 |
Takada LT, Kim MO, Cleveland RW, Wong K, Forner SA, Gala II, Fong JC, Geschwind MD. Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 174: 36-69. PMID 27943639 DOI: 10.1002/Ajmg.B.32505 |
0.38 |
|
| 2016 |
Luo L, Wang J, Lo RY, Figueroa KP, Pulst SM, Kuo PH, Perlman S, Wilmot G, Gomez CM, Schmahmann JD, Paulson H, Shakkottai VG, Ying SH, Zesiewicz T, Bushara K, ... Geschwind M, et al. The Initial Symptom and Motor Progression in Spinocerebellar Ataxias. Cerebellum (London, England). PMID 27848087 DOI: 10.1007/S12311-016-0836-3 |
0.338 |
|
| 2016 |
Kim H, Kim JH, Possin KL, Winer J, Geschwind MD, Xu D, Hess CP. Surface-based morphometry reveals caudate subnuclear structural damage in patients with premotor Huntington disease. Brain Imaging and Behavior. PMID 27730480 DOI: 10.1007/S11682-016-9616-4 |
0.31 |
|
| 2016 |
Fong JC, Rojas JC, Bang J, Legati A, Rankin KP, Forner S, Miller ZA, Karydas AM, Coppola G, Grouse CK, Ralph J, Miller BL, Geschwind MD. Genetic Prion Disease Caused by PRNP Q160X Mutation Presenting with an Orbitofrontal Syndrome, Cyclic Diarrhea, and Peripheral Neuropathy. Journal of Alzheimer's Disease : Jad. PMID 27716661 DOI: 10.3233/Jad-160300 |
0.381 |
|
| 2016 |
Geschwind MD, Paras N. Deutetrabenazine for Treatment of Chorea in Huntington Disease. Jama. 316: 33-5. PMID 27380339 DOI: 10.1001/Jama.2016.8011 |
0.33 |
|
| 2016 |
Graus F, Titulaer MJ, Balu R, Benseler S, Bien CG, Cellucci T, Cortese I, Dale RC, Gelfand JM, Geschwind M, Glaser CA, Honnorat J, Höftberger R, Iizuka T, Irani SR, et al. A clinical approach to diagnosis of autoimmune encephalitis. The Lancet. Neurology. PMID 26906964 DOI: 10.1016/S1474-4422(15)00401-9 |
0.337 |
|
| 2015 |
Savard M, Irani SR, Guillemette A, Gosselin-Lefebvre S, Geschwind M, Jansen GH, Gould PV, Laforce R. Creutzfeldt-Jakob Disease-Like Periodic Sharp Wave Complexes in Voltage-Gated Potassium Channel-Complex Antibodies Encephalitis: A Case Report. Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society. PMID 26375660 DOI: 10.1097/Wnp.0000000000000171 |
0.327 |
|
| 2015 |
Tousseyn T, Bajsarowicz K, Sánchez H, Gheyara A, Oehler A, Geschwind M, DeArmond B, DeArmond SJ. Prion Disease Induces Alzheimer Disease-Like Neuropathologic Changes. Journal of Neuropathology and Experimental Neurology. 74: 873-888. PMID 26226132 DOI: 10.1097/Nen.0000000000000228 |
0.357 |
|
| 2015 |
Cali I, Miller CJ, Parisi JE, Geschwind MD, Gambetti P, Schonberger LB. Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone. Acta Neuropathologica Communications. 3: 37. PMID 26108478 DOI: 10.1186/S40478-015-0214-2 |
0.362 |
|
| 2015 |
Kim MO, Geschwind MD. Clinical update of Jakob-Creutzfeldt disease. Current Opinion in Neurology. 28: 302-10. PMID 25923128 DOI: 10.1097/Wco.0000000000000197 |
0.424 |
|
| 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 |
0.303 |
|
| 2015 |
Hurth K, Tarawneh R, Ghoshal N, Benzinger TL, Clifford DB, Geschwind M, Morris JC, Galvin JE, Schmidt RE, Cairns NJ. Whipple's disease masquerades as dementia with Lewy bodies. Alzheimer Disease and Associated Disorders. 29: 85-9. PMID 23995819 DOI: 10.1097/Wad.0B013E3182A715Da |
0.381 |
|
| 2014 |
Caverzasi E, Mandelli ML, DeArmond SJ, Hess CP, Vitali P, Papinutto N, Oehler A, Miller BL, Lobach IV, Bastianello S, Geschwind MD, Henry RG. White matter involvement in sporadic Creutzfeldt-Jakob disease. Brain : a Journal of Neurology. 137: 3339-54. PMID 25367029 DOI: 10.1093/Brain/Awu298 |
0.302 |
|
| 2014 |
Minikel EV, Zerr I, Collins SJ, Ponto C, Boyd A, Klug G, Karch A, Kenny J, Collinge J, Takada LT, Forner S, Fong JC, Mead S, Geschwind MD. Ascertainment bias causes false signal of anticipation in genetic prion disease. American Journal of Human Genetics. 95: 371-82. PMID 25279981 DOI: 10.1016/J.Ajhg.2014.09.003 |
0.364 |
|
| 2014 |
Irani SR, Gelfand JM, Bettcher BM, Singhal NS, Geschwind MD. Effect of rituximab in patients with leucine-rich, glioma-inactivated 1 antibody-associated encephalopathy. Jama Neurology. 71: 896-900. PMID 24842754 DOI: 10.1001/Jamaneurol.2014.463 |
0.301 |
|
| 2014 |
Caverzasi E, Henry RG, Vitali P, Lobach IV, Kornak J, Bastianello S, Dearmond SJ, Miller BL, Rosen HJ, Mandelli ML, Geschwind MD. Application of quantitative DTI metrics in sporadic CJD. Neuroimage. Clinical. 4: 426-35. PMID 24624328 DOI: 10.1016/J.Nicl.2014.01.011 |
0.347 |
|
| 2014 |
Uflacker A, Doraiswamy PM, Rechitsky S, See T, Geschwind M, Tur-Kaspa I. Preimplantation Genetic Diagnosis (PGD) for Genetic Prion Disorder Due to F198S Mutation in the PRNP Gene Jama Neurology. 71: 484-486. PMID 24493558 DOI: 10.1001/Jamaneurol.2013.5884 |
0.342 |
|
| 2014 |
Geschwind MD. Doxycycline for Creutzfeldt-Jakob disease: a failure, but a step in the right direction. The Lancet. Neurology. 13: 130-2. PMID 24411710 DOI: 10.1016/S1474-4422(14)70001-8 |
0.348 |
|
| 2014 |
You SC, Geschwind MD, Sha SJ, Apple A, Satris G, Wood KA, Johnson ET, Gooblar J, Feuerstein JS, Finkbeiner S, Kang GA, Miller BL, Hess CP, Kramer JH, Possin KL. Executive functions in premanifest Huntington's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 29: 405-9. PMID 24375511 DOI: 10.1002/Mds.25762 |
0.322 |
|
| 2014 |
Uflacker A, Doraiswamy M, Rechitsky S, See T, Geschwind M, Tur-Kaspa I. Preimplantation Genetic Diagnosis for a Genetic Prion Disease American Journal of Geriatric Psychiatry. 22. DOI: 10.1016/J.Jagp.2013.12.076 |
0.319 |
|
| 2013 |
Kim MO, Cali I, Oehler A, Fong JC, Wong K, See T, Katz JS, Gambetti P, Bettcher BM, Dearmond SJ, Geschwind MD. Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases. Acta Neuropathologica Communications. 1: 80. PMID 24330864 DOI: 10.1186/2051-5960-1-80 |
0.343 |
|
| 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, 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 |
0.357 |
|
| 2013 |
Bechtel K, Geschwind MD. Ethics in prion disease. Progress in Neurobiology. 110: 29-44. PMID 23906487 DOI: 10.1016/J.Pneurobio.2013.07.001 |
0.385 |
|
| 2013 |
Vossel KA, Beagle AJ, Rabinovici GD, Shu H, Lee SE, Naasan G, Hegde M, Cornes SB, Henry ML, Nelson AB, Seeley WW, Geschwind MD, Gorno-Tempini ML, Shih T, Kirsch HE, et al. Seizures and epileptiform activity in the early stages of Alzheimer disease. Jama Neurology. 70: 1158-66. PMID 23835471 DOI: 10.1001/Jamaneurol.2013.136 |
0.341 |
|
| 2013 |
Biglan KM, Zhang Y, Long JD, Geschwind M, Kang GA, Killoran A, Lu W, McCusker E, Mills JA, Raymond LA, Testa C, Wojcieszek J, Paulsen JS. Refining the diagnosis of Huntington disease: the PREDICT-HD study. Frontiers in Aging Neuroscience. 5: 12. PMID 23565093 DOI: 10.3389/Fnagi.2013.00012 |
0.313 |
|
| 2013 |
Lee SE, Tartaglia MC, Yener G, Genç S, Seeley WW, Sanchez-Juan P, Moreno F, Mendez MF, Klein E, Rademakers R, López de Munain A, Combarros O, Kramer JH, Kenet RO, Boxer AL, ... Geschwind MD, et al. Neurodegenerative disease phenotypes in carriers of MAPT p.A152T, a risk factor for frontotemporal dementia spectrum disorders and Alzheimer disease. Alzheimer Disease and Associated Disorders. 27: 302-9. PMID 23518664 DOI: 10.1097/Wad.0B013E31828Cc357 |
0.416 |
|
| 2013 |
Johnson DY, Dunkelberger DL, Henry M, Haman A, Greicius MD, Wong K, DeArmond SJ, Miller BL, Gorno-Tempini ML, Geschwind MD. Sporadic Jakob-Creutzfeldt disease presenting as primary progressive aphasia. Jama Neurology. 70: 254-7. PMID 23400721 DOI: 10.1001/2013.Jamaneurol.139 |
0.445 |
|
| 2013 |
McIntyre D, Geschwind M, Zerr I, Metz R, Droste D, Diederich N, Beyenburg S. Report on cluster of three autopsy confirmed cases of sporadic Creutzfeldt–/INS;Jakob disease from Luxembourg including videos, imaging, genetics and neuropathology Journal of the Neurological Sciences. 333. DOI: 10.1016/J.Jns.2013.07.1277 |
0.312 |
|
| 2012 |
Paterson RW, Torres-Chae CC, Kuo AL, Ando T, Nguyen EA, Wong K, DeArmond SJ, Haman A, Garcia P, Johnson DY, Miller BL, Geschwind MD. Differential diagnosis of Jakob-Creutzfeldt disease. Archives of Neurology. 69: 1578-82. PMID 23229042 DOI: 10.1001/2013.Jamaneurol.79 |
0.401 |
|
| 2012 |
Coppola G, Chinnathambi S, Lee JJ, Dombroski BA, Baker MC, Soto-Ortolaza AI, Lee SE, Klein E, Huang AY, Sears R, Lane JR, Karydas AM, Kenet RO, Biernat J, Wang LS, ... ... Geschwind MD, et al. Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases. Human Molecular Genetics. 21: 3500-12. PMID 22556362 DOI: 10.1093/Hmg/Dds161 |
0.368 |
|
| 2012 |
Tartaglia MC, Johnson DY, Thai JN, Cattaruzza T, Wong K, Garcia P, Dearmond SJ, Miller BL, Geschwind MD. Clinical overlap between Jakob-Creutzfeldt disease and Lewy body disease. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 39: 304-10. PMID 22547509 DOI: 10.1017/S0317167100013421 |
0.345 |
|
| 2012 |
Forner S, Wong K, Bostrom A, Takada L, Tartaglia C, Haman A, Torres-Chae C, Raudabaugh B, Devereux G, Miller B, Geschwind M. CSF Biomarkers Findings in a Large Rapidly Progressive Dementia Cohort (S14.004) Neurology. 78. DOI: 10.1212/Wnl.78.1_Meetingabstracts.S14.004 |
0.305 |
|
| 2012 |
Tartaglia C, Lee S, Geschwind M, Perry D, Afaisen S, Khan B, Wu T, Rodriguez H, Ketelle R, Steele J, Miller B. Neuropsychiatric Features of Parkinsonism Dementia Complex and Other Neurodegenerative Diseases on Guam (P05.040) Neurology. 78. DOI: 10.1212/Wnl.78.1_Meetingabstracts.P05.040 |
0.411 |
|
| 2012 |
Lee S, Tartaglia C, Geschwind M, Perry D, Afaisen S, Wu T, Khan B, Steele J, Miller B. Hetereogeneity of Neurodegenerative Diseases on Guam (P05.037) Neurology. 78. DOI: 10.1212/Wnl.78.1_Meetingabstracts.P05.037 |
0.373 |
|
| 2011 |
Perry DC, Geschwind MD. Thorough work-up and new diagnostic criteria needed for CJD. Nature Reviews. Neurology. 7: 479-80. PMID 21892213 DOI: 10.1038/Nrneurol.2011.118 |
0.361 |
|
| 2011 |
Lee SE, Rabinovici GD, Mayo MC, Wilson SM, Seeley WW, DeArmond SJ, Huang EJ, Trojanowski JQ, Growdon ME, Jang JY, Sidhu M, See TM, Karydas AM, Gorno-Tempini ML, Boxer AL, ... ... Geschwind MD, et al. Clinicopathological correlations in corticobasal degeneration. Annals of Neurology. 70: 327-40. PMID 21823158 DOI: 10.1002/Ana.22424 |
0.375 |
|
| 2011 |
Vitali P, Maccagnano E, Caverzasi E, Henry RG, Haman A, Torres-Chae C, Johnson DY, Miller BL, Geschwind MD. Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias. Neurology. 76: 1711-9. PMID 21471469 DOI: 10.1212/Wnl.0B013E31821A4439 |
0.341 |
|
| 2010 |
Tartaglia MC, Thai JN, See T, Kuo A, Harbaugh R, Raudabaugh B, Cali I, Sattavat M, Sanchez H, DeArmond SJ, Geschwind MD. Pathologic evidence that the T188R mutation in PRNP is associated with prion disease. Journal of Neuropathology and Experimental Neurology. 69: 1220-7. PMID 21107135 DOI: 10.1097/Nen.0B013E3181Ffc39C |
0.408 |
|
| 2010 |
Benetti F, Geschwind MD, Legname G. De novo prions. F1000 Biology Reports. 2. PMID 20948787 DOI: 10.3410/B2-46 |
0.336 |
|
| 2010 |
Zou WQ, Puoti G, Xiao X, Yuan J, Qing L, Cali I, Shimoji M, Langeveld JP, Castellani R, Notari S, Crain B, Schmidt RE, Geschwind M, Dearmond SJ, Cairns NJ, et al. Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein. Annals of Neurology. 68: 162-72. PMID 20695009 DOI: 10.1002/Ana.22094 |
0.388 |
|
| 2010 |
Yang TI, Jung DS, Ahn BY, Jeong BH, Cho HJ, Kim YS, Na DL, Geschwind MD, Kim EJ. Familial Creutzfeldt-Jakob disease with V180I mutation. Journal of Korean Medical Science. 25: 1097-100. PMID 20592908 DOI: 10.3346/Jkms.2010.25.7.1097 |
0.377 |
|
| 2010 |
Kieburtz K, McDermott MP, Voss TS, Corey-Bloom J, Deuel LM, Dorsey ER, Factor S, Geschwind MD, Hodgeman K, Kayson E, Noonberg S, Pourfar M, Rabinowitz K, Ravina B, Sanchez-Ramos J, et al. A randomized, placebo-controlled trial of latrepirdine in Huntington disease. Archives of Neurology. 67: 154-60. PMID 20142523 DOI: 10.1001/Archneurol.2009.334 |
0.317 |
|
| 2009 |
Rosenbloom MH, Smith S, Akdal G, Geschwind MD. Immunologically mediated dementias. Current Neurology and Neuroscience Reports. 9: 359-67. PMID 19664365 DOI: 10.1007/S11910-009-0053-2 |
0.35 |
|
| 2009 |
Choi EM, Geschwind MD, Deering C, Pomeroy K, Kuo A, Miller BL, Safar JG, Prusiner SB. Prion proteins in subpopulations of white blood cells from patients with sporadic Creutzfeldt-Jakob disease. Laboratory Investigation; a Journal of Technical Methods and Pathology. 89: 624-35. PMID 19434060 DOI: 10.1038/Labinvest.2009.30 |
0.303 |
|
| 2009 |
Geschwind MD. Clinical trials for prion disease: difficult challenges, but hope for the future. The Lancet. Neurology. 8: 304-6. PMID 19278901 DOI: 10.1016/S1474-4422(09)70050-X |
0.426 |
|
| 2009 |
Geschwind MD, Potter CA, Sattavat M, Garcia PA, Rosen HJ, Miller BL, DeArmond SJ. Correlating DWI MRI with pathologic and other features of Jakob-Creutzfeldt disease. Alzheimer Disease and Associated Disorders. 23: 82-87. PMID 19266702 DOI: 10.1097/Wad.0B013E31818323Ef |
0.34 |
|
| 2008 |
Geschwind MD, Tan KM, Lennon VA, Barajas RF, Haman A, Klein CJ, Josephson SA, Pittock SJ. Voltage-gated potassium channel autoimmunity mimicking creutzfeldt-jakob disease. Archives of Neurology. 65: 1341-6. PMID 18852349 DOI: 10.1001/Archneur.65.10.1341 |
0.402 |
|
| 2008 |
Vitali P, Migliaccio R, Agosta F, Rosen HJ, Geschwind MD. Neuroimaging in dementia. Seminars in Neurology. 28: 467-83. PMID 18843575 DOI: 10.1055/S-0028-1083695 |
0.37 |
|
| 2008 |
Webb TE, Poulter M, Beck J, Uphill J, Adamson G, Campbell T, Linehan J, Powell C, Brandner S, Pal S, Siddique D, Wadsworth JD, Joiner S, Alner K, Petersen C, ... ... Geschwind MD, et al. Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series. Brain : a Journal of Neurology. 131: 2632-46. PMID 18757886 DOI: 10.1093/Brain/Awn202 |
0.406 |
|
| 2008 |
Geschwind MD, Shu H, Haman A, Sejvar JJ, Miller BL. Rapidly progressive dementia. Annals of Neurology. 64: 97-108. PMID 18668637 DOI: 10.1002/Ana.21430 |
0.356 |
|
| 2008 |
Valcour V, Haman A, Cornes S, Lawall C, Parsa AT, Glaser C, Yagi S, Tihan T, Bhatnagar J, Geschwind M. A case of enteroviral meningoencephalitis presenting as rapidly progressive dementia. Nature Clinical Practice. Neurology. 4: 399-403. PMID 18477991 DOI: 10.1038/Ncpneuro0804 |
0.351 |
|
| 2007 |
Geschwind MD, Haman A, Miller BL. Rapidly progressive dementia. Neurologic Clinics. 25: 783-807, vii. PMID 17659190 DOI: 10.1016/J.Ncl.2007.04.001 |
0.322 |
|
| 2007 |
Boxer AL, Rabinovici GD, Kepe V, Goldman J, Furst AJ, Huang SC, Baker SL, O'neil JP, Chui H, Geschwind MD, Small GW, Barrio JR, Jagust W, Miller BL. Amyloid imaging in distinguishing atypical prion disease from Alzheimer disease. Neurology. 69: 283-90. PMID 17636066 DOI: 10.1212/01.Wnl.0000265815.38958.B6 |
0.35 |
|
| 2007 |
Josephson SA, Papanastassiou AM, Berger MS, Barbaro NM, McDermott MW, Hilton JF, Miller BL, Geschwind MD. The diagnostic utility of brain biopsy procedures in patients with rapidly deteriorating neurological conditions or dementia. Journal of Neurosurgery. 106: 72-5. PMID 17236490 DOI: 10.3171/Jns.2007.106.1.72 |
0.345 |
|
| 2007 |
Chang CC, Eggers SD, Johnson JK, Haman A, Miller BL, Geschwind MD. Anti-GAD antibody cerebellar ataxia mimicking Creutzfeldt-Jakob disease. Clinical Neurology and Neurosurgery. 109: 54-7. PMID 16621241 DOI: 10.1016/J.Clineuro.2006.01.009 |
0.348 |
|
| 2006 |
Lewis AM, Yu M, DeArmond SJ, Dillon WP, Miller BL, Geschwind MD. Human growth hormone-related iatrogenic Creutzfeldt-Jakob disease with abnormal imaging. Archives of Neurology. 63: 288-90. PMID 16476821 DOI: 10.1001/Archneur.63.2.288 |
0.363 |
|
| 2006 |
Rabinovici GD, Wang PN, Levin J, Cook L, Pravdin M, Davis J, DeArmond SJ, Barbaro NM, Martindale J, Miller BL, Geschwind MD. First symptom in sporadic Creutzfeldt-Jakob disease. Neurology. 66: 286-7. PMID 16434680 DOI: 10.1212/01.Wnl.0000196440.00297.67 |
0.318 |
|
| 2006 |
Boxer AL, Geschwind MD, Belfor N, Gorno-Tempini ML, Schauer GF, Miller BL, Weiner MW, Rosen HJ. Patterns of brain atrophy that differentiate corticobasal degeneration syndrome from progressive supranuclear palsy. Archives of Neurology. 63: 81-6. PMID 16401739 DOI: 10.1001/Archneur.63.1.81 |
0.363 |
|
| 2005 |
Safar JG, Geschwind MD, Deering C, Didorenko S, Sattavat M, Sanchez H, Serban A, Vey M, Baron H, Giles K, Miller BL, Dearmond SJ, Prusiner SB. Diagnosis of human prion disease. Proceedings of the National Academy of Sciences of the United States of America. 102: 3501-6. PMID 15741275 DOI: 10.1073/Pnas.0409651102 |
0.388 |
|
| 2004 |
Goldman JS, Miller BL, Safar J, de Tourreil S, Martindale JL, Prusiner SB, Geschwind MD. When sporadic disease is not sporadic: the potential for genetic etiology. Archives of Neurology. 61: 213-6. PMID 14967768 DOI: 10.1001/Archneur.61.2.213 |
0.391 |
|
| 2003 |
Geschwind MD, Martindale J, Miller D, DeArmond SJ, Uyehara-Lock J, Gaskin D, Kramer JH, Barbaro NM, Miller BL. Challenging the clinical utility of the 14-3-3 protein for the diagnosis of sporadic Creutzfeldt-Jakob disease. Archives of Neurology. 60: 813-6. PMID 12810484 DOI: 10.1001/Archneur.60.6.813 |
0.386 |
|
| 2003 |
Martindale J, Geschwind MD, De Armond S, Young G, Dillon WP, Henry R, Uyehara-Lock JH, Gaskin DA, Miller BL. Sporadic Creutzfeldt-Jakob disease mimicking variant Creutzfeldt-Jakob disease. Archives of Neurology. 60: 767-70. PMID 12756143 DOI: 10.1001/Archneur.60.5.767 |
0.42 |
|
| 2003 |
Martindale JL, Geschwind MD, Miller BL. Psychiatric and neuroimaging findings in Creutzfeldt-Jakob disease. Current Psychiatry Reports. 5: 43-6. PMID 12686001 DOI: 10.1007/S11920-003-0008-2 |
0.428 |
|
| 2002 |
Greicius MD, Geschwind MD, Miller BL. Presenile dementia syndromes: an update on taxonomy and diagnosis. Journal of Neurology, Neurosurgery, and Psychiatry. 72: 691-700. PMID 12023408 DOI: 10.1136/Jnnp.72.6.691 |
0.4 |
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