| Year |
Citation |
Score |
| 2024 |
Yska HAF, Turk BR, Fatemi A, Goodman J, Voermans M, Amos D, Amanat M, van de Stadt S, Engelen M, Smith-Fine A, Keller J. International validation of meaningfulness of postural sway and gait to assess myeloneuropathy in adults with adrenoleukodystrophy. Journal of Inherited Metabolic Disease. PMID 38795020 DOI: 10.1002/jimd.12753 |
0.709 |
|
| 2022 |
Turk BR, Poisson LM, Nemeth CL, Goodman J, Moser AB, Jones RO, Fatemi A, Singh J. MicroRNA and metabolomics signatures for adrenomyeloneuropathy disease severity. Jimd Reports. 63: 593-603. PMID 36341174 DOI: 10.1002/jmd2.12323 |
0.711 |
|
| 2022 |
Engelen M, van Ballegoij WJC, Mallack EJ, Van Haren KP, Köhler W, Salsano E, van Trotsenburg ASP, Mochel F, Sevin C, Regelman MO, Tritos NA, Halper A, Lachmann RH, Davison J, Raymond GV, ... ... Fatemi A, et al. International Recommendations for the Diagnosis and Management of Patients With Adrenoleukodystrophy: A Consensus-Based Approach. Neurology. PMID 36175155 DOI: 10.1212/WNL.0000000000201374 |
0.732 |
|
| 2022 |
Smith Fine A, Kaufman M, Goodman J, Turk B, Bastian A, Lin D, Fatemi A, Keller J. Wearable sensors detect impaired gait and coordination in LBSL during remote assessments. Annals of Clinical and Translational Neurology. 9: 468-477. PMID 35257509 DOI: 10.1002/acn3.51509 |
0.7 |
|
| 2020 |
Mallack EJ, Turk BR, Yan H, Price C, Mlis MD, Moser AB, Becker C, Hollandsworth K, Adang L, Vanderver A, Van Haren K, Ruzhnikov M, Kurtzberg J, Maegawa G, Orchard PJ, ... ... Fatemi A, et al. MRI Surveillance of Boys with X-linked Adrenoleukodystrophy Identified by Newborn Screening: Meta-analysis and Consensus Guidelines. Journal of Inherited Metabolic Disease. PMID 33373467 DOI: 10.1002/jimd.12356 |
0.725 |
|
| 2020 |
Sripathy SR, Wang Y, Moses RL, Fatemi A, Batista DA, Maher BJ. Generation of 10 patient-specific induced pluripotent stem cells (iPSCs) to model Pitt-Hopkins Syndrome. Stem Cell Research. 48: 102001. PMID 32971458 DOI: 10.1016/J.Scr.2020.102001 |
0.313 |
|
| 2020 |
Nemeth CL, Tomlinson SN, Sharma R, Sharma A, Kannan S, Kannan RM, Fatemi A. Glial restricted precursor delivery of dendrimer N-acetylcysteine promotes migration and differentiation following transplant in mouse white matter injury model. Nanoscale. PMID 32724988 DOI: 10.1039/C9Nr10804A |
0.306 |
|
| 2020 |
Guillen Sacoto MJ, Tchasovnikarova IA, Torti E, Forster C, Andrew EH, Anselm I, Baranano KW, Briere LC, Cohen JS, Craigen WJ, Cytrynbaum C, Ekhilevitch N, Elrick MJ, Fatemi A, Fraser JL, et al. De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial Dysmorphism. American Journal of Human Genetics. PMID 32693025 DOI: 10.1016/J.Ajhg.2020.06.013 |
0.33 |
|
| 2020 |
Turk BR, Theda C, Fatemi A, Moser AB. X-linked adrenoleukodystrophy: Pathology, pathophysiology, diagnostic testing, newborn screening and therapies. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 80: 52-72. PMID 31909500 DOI: 10.1002/Jdn.10003 |
0.745 |
|
| 2019 |
Fine AS, Nemeth CL, Kaufman ML, Fatemi A. Mitochondrial aminoacyl-tRNA synthetase disorders: an emerging group of developmental disorders of myelination. Journal of Neurodevelopmental Disorders. 11: 29. PMID 31839000 DOI: 10.1186/S11689-019-9292-Y |
0.36 |
|
| 2019 |
Turk BR, Theda C, Fatemi A, Moser AB. X-linked Adrenoleukodystrophy: Pathology, Pathophysiology, Diagnostic Testing, Newborn Screening, and Therapies. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. PMID 31778737 DOI: 10.1016/j.ijdevneu.2019.11.002 |
0.735 |
|
| 2019 |
Page KM, Stenger EO, Connelly JA, Shyr D, West T, Wood S, Case L, Kester M, Shim S, Hammond L, Hammond M, Webb C, Biffi A, Bambach B, Fatemi A, et al. Hematopoietic Stem Cell Transplantation to Treat Leukodystrophies: Clinical Practice Guidelines from the Hunter's Hope Leukodystrophy Care Network. Biology of Blood and Marrow Transplantation : Journal of the American Society For Blood and Marrow Transplantation. PMID 31499213 DOI: 10.1016/J.Bbmt.2019.09.003 |
0.313 |
|
| 2019 |
Nemeth CL, Fine AS, Fatemi A. Translational challenges in advancing regenerative therapy for treating neurological disorders using nanotechnology. Advanced Drug Delivery Reviews. 148: 60-67. PMID 31100303 DOI: 10.1016/J.Addr.2019.05.003 |
0.347 |
|
| 2019 |
Casasnovas C, Ruiz M, Schlüter A, Naudí A, Fourcade S, Veciana M, Castañer S, Albertí A, Bargalló N, Johnson M, Raymond GV, Fatemi A, Moser AB, Villarroya F, Portero-Otín M, et al. Biomarker Identification, Safety, and Efficacy of High-Dose Antioxidants for Adrenomyeloneuropathy: a Phase II Pilot Study. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. PMID 31077039 DOI: 10.1007/S13311-019-00735-2 |
0.349 |
|
| 2019 |
Pant DC, Dorboz I, Schlüter A, Fourcade S, Launay N, Joya J, Aguilera-Albesa S, Yoldi ME, Casasnovas C, Willis MJ, Ruiz M, Ville D, Lesca G, Siquier-Pernet K, Desguerre I, ... ... Fatemi A, et al. Loss of the sphingolipid desaturase DEGS1 causes hypomyelinating leukodystrophy. The Journal of Clinical Investigation. PMID 30620337 DOI: 10.1172/Jci123959 |
0.35 |
|
| 2018 |
Niño DF, Zhou Q, Yamaguchi Y, Martin LY, Wang S, Fulton WB, Jia H, Lu P, Prindle T, Zhang F, Crawford J, Hou Z, Mori S, Chen LL, Guajardo A, ... Fatemi A, et al. Cognitive impairments induced by necrotizing enterocolitis can be prevented by inhibiting microglial activation in mouse brain. Science Translational Medicine. 10. PMID 30541786 DOI: 10.1126/Scitranslmed.Aan0237 |
0.335 |
|
| 2018 |
Gordon-Lipkin E, Cohen JS, Srivastava S, Soares BP, Levey E, Fatemi A. ST3GAL5-Related Disorders: A Deficiency in Ganglioside Metabolism and a Genetic Cause of Intellectual Disability and Choreoathetosis. Journal of Child Neurology. 883073818791099. PMID 30185102 DOI: 10.1177/0883073818791099 |
0.319 |
|
| 2018 |
Wojcik MH, Okada K, Prabhu SP, Nowakowski DW, Ramsey K, Balak C, Rangasamy S, Brownstein CA, Schmitz-Abe K, Cohen JS, Fatemi A, Shi J, Grant EP, Narayanan V, Ho HH, et al. De novo variant in KIF26B is associated with pontocerebellar hypoplasia with infantile spinal muscular atrophy. American Journal of Medical Genetics. Part A. PMID 30151950 DOI: 10.1002/Ajmg.A.40493 |
0.319 |
|
| 2018 |
Gordon-Lipkin E, Fatemi A. Current Therapeutic Approaches in Leukodystrophies: A Review. Journal of Child Neurology. 33: 861-868. PMID 30112967 DOI: 10.1177/0883073818792313 |
0.355 |
|
| 2018 |
Turk BR, Nemeth CL, Marx JS, Tiffany C, Jones RO, Theisen BE, Murray CF, Kambhampati SP, Ramireddy R, Singh S, Rosen MR, Kaufman M, Watkins PA, Kannan S, Kannan RM, ... Fatemi A, et al. Dendrimer N-acetylcysteine modulates monophagocytic response in adrenoleukodystrophy. Annals of Neurology. PMID 30069915 DOI: 10.1002/Ana.25303 |
0.72 |
|
| 2018 |
Doman SE, Girish A, Nemeth CL, Drummond GT, Carr P, Garcia MS, Johnston MV, Kannan S, Fatemi A, Zhang J, Wilson MA. Early Detection of Hypothermic Neuroprotection Using T2-Weighted Magnetic Resonance Imaging in a Mouse Model of Hypoxic Ischemic Encephalopathy. Frontiers in Neurology. 9: 304. PMID 29867720 DOI: 10.3389/Fneur.2018.00304 |
0.483 |
|
| 2018 |
Zarate YA, Smith-Hicks CL, Greene C, Abbott MA, Siu VM, Calhoun ARUL, Pandya A, Li C, Sellars EA, Kaylor J, Bosanko K, Kalsner L, Basinger A, Slavotinek AM, Perry H, ... ... Fatemi A, et al. Natural history and genotype-phenotype correlations in 72 individuals with SATB2-associated syndrome. American Journal of Medical Genetics. Part A. PMID 29436146 DOI: 10.1002/Ajmg.A.38630 |
0.328 |
|
| 2018 |
Srivastava S, Desai S, Cohen J, Smith-Hicks C, Barañano K, Fatemi A, Naidu S. Monogenic disorders that mimic the phenotype of Rett syndrome. Neurogenetics. PMID 29322350 DOI: 10.1007/S10048-017-0535-3 |
0.324 |
|
| 2017 |
Powis Z, Farwell Hagman KD, Mroske C, McWalter K, Cohen JS, Colombo R, Serretti A, Fatemi A, David KL, Reynolds J, Immken LD, Nagakura H, Cunniff C, Payne K, Barbaro-Dieber T, et al. Expansion and further delineation of the SETD5 phenotype leading to global developmental delay, variable dysmorphic features, and reduced penetrance. Clinical Genetics. PMID 28881385 DOI: 10.1111/Cge.13132 |
0.307 |
|
| 2017 |
Adang LA, Sherbini O, Ball L, Bloom M, Darbari A, Amartino H, DiVito D, Eichler F, Escolar M, Evans SH, Fatemi A, Fraser J, Hollowell L, Jaffe N, Joseph C, et al. Revised consensus statement on the preventive and symptomatic care of patients with leukodystrophies. Molecular Genetics and Metabolism. PMID 28863857 DOI: 10.1016/J.Ymgme.2017.08.006 |
0.585 |
|
| 2017 |
Nemeth CL, Drummond GT, Mishra MK, Zhang F, Carr P, Garcia MS, Doman S, Fatemi A, Johnston MV, Kannan RM, Kannan S, Wilson MA. Uptake of dendrimer-drug by different cell types in the hippocampus after hypoxic-ischemic insult in neonatal mice: Effects of injury, microglial activation and hypothermia. Nanomedicine : Nanotechnology, Biology, and Medicine. PMID 28669854 DOI: 10.1016/J.Nano.2017.06.014 |
0.473 |
|
| 2017 |
Theisen BE, Rumyantseva A, Cohen JS, Alcaraz WA, Shinde DN, Tang S, Srivastava S, Pevsner J, Trifunovic A, Fatemi A. Deficiency of WARS2, encoding mitochondrial tryptophanyl tRNA synthetase, causes severe infantile onset leukoencephalopathy. American Journal of Medical Genetics. Part A. PMID 28650581 DOI: 10.1002/Ajmg.A.38339 |
0.309 |
|
| 2017 |
Turk BR, Moser AB, Fatemi A. Therapeutic strategies in adrenoleukodystrophy. Wiener Medizinische Wochenschrift (1946). 167: 219-226. PMID 28493141 DOI: 10.1007/S10354-016-0534-2 |
0.755 |
|
| 2017 |
Turk BR, Theisen BE, Nemeth CL, Marx JS, Shi X, Rosen M, Jones RO, Moser AB, Watkins PA, Raymond GV, Tiffany C, Fatemi A. Antioxidant Capacity and Superoxide Dismutase Activity in Adrenoleukodystrophy. Jama Neurology. PMID 28288261 DOI: 10.1001/jamaneurol.2016.5715 |
0.725 |
|
| 2017 |
Ismail FY, Fatemi A, Johnston M. The Quest for Neuroprotection for Injuries in the Developing Brain Journal of International Child Neurology Association. DOI: 10.17724/Jicna.2017.79 |
0.499 |
|
| 2016 |
Poretti A, Meoded A, Fatemi A. Diffusion tensor imaging: A biomarker of outcome in Krabbe's disease. Journal of Neuroscience Research. 94: 1108-15. PMID 27638596 DOI: 10.1002/Jnr.23769 |
0.349 |
|
| 2016 |
Cohen JS, Srivastava S, Farwell Hagman KD, Shinde DN, Huether R, Darcy D, Wallerstein R, Houge G, Berland S, Monaghan KG, Poretti A, Wilson AL, Chung WK, Fatemi A. Further evidence that de novo missense and truncating variants in ZBTB18 cause intellectual disability with variable features. Clinical Genetics. PMID 27598823 DOI: 10.1111/Cge.12861 |
0.326 |
|
| 2016 |
Ismail FY, Fatemi A, Johnston MV. Cerebral plasticity: Windows of opportunity in the developing brain. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. PMID 27567276 DOI: 10.1016/J.Ejpn.2016.07.007 |
0.469 |
|
| 2016 |
Rodan LH, Cohen J, Fatemi A, Gillis T, Lucente D, Gusella J, Picker JD. A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin gene. European Journal of Human Genetics : Ejhg. PMID 27329733 DOI: 10.1038/Ejhg.2016.74 |
0.314 |
|
| 2016 |
Sweda R, Phillips AW, Marx JS, Johnston M, Wilson MA, Fatemi A. GLIAL RESTRICTED PRECURSORS PROTECT NEONATAL BRAIN SLICES FROM HYPOXIC-ISCHEMIC CELL DEATH WITHOUT DIRECT TISSUE CONTACT. Stem Cells and Development. PMID 27149035 DOI: 10.1089/scd.2015.0378 |
0.435 |
|
| 2016 |
Breu M, Zhang J, Porambo M, Pletnikov MV, Goeral K, Kakara M, Johnston MV, Fatemi A. Diffusion Tensor Imaging Abnormalities in the Cerebral White Matter Correlate with Sex-Dependent Neurobehavioral Deficits in Adult Mice with Neonatal Ischemia. Developmental Neuroscience. PMID 26977597 DOI: 10.1159/000442943 |
0.503 |
|
| 2015 |
Massaro AN, Evangelou I, Brown J, Fatemi A, Vezina G, McCarter R, Glass P, Limperopoulos C. Neonatal neurobehavior after therapeutic hypothermia for hypoxic ischemic encephalopathy. Early Human Development. 91: 593-599. PMID 26246138 DOI: 10.1016/J.Earlhumdev.2015.07.008 |
0.36 |
|
| 2015 |
Nance E, Porambo M, Zhang F, Mishra MK, Buelow M, Getzenberg R, Johnston M, Rangaramanujam K, Fatemi A, Kannan S. Systemic dendrimer-drug treatment of ischemia-induced neonatal white matter injury. Journal of Controlled Release : Official Journal of the Controlled Release Society. PMID 26184052 DOI: 10.1016/J.Jconrel.2015.07.009 |
0.484 |
|
| 2015 |
Lei J, Firdaus W, Rosenzweig JM, Alrebh S, Bakhshwin A, Borbiev T, Fatemi A, Blakemore K, Johnston MV, Burd I. Murine model: maternal administration of stem cells for prevention of prematurity. American Journal of Obstetrics and Gynecology. 212: 639.e1-10. PMID 25555657 DOI: 10.1016/J.Ajog.2014.12.032 |
0.483 |
|
| 2015 |
Porambo M, Phillips AW, Marx J, Ternes K, Arauz E, Pletnikov M, Wilson MA, Rothstein JD, Johnston MV, Fatemi A. Transplanted glial restricted precursor cells improve neurobehavioral and neuropathological outcomes in a mouse model of neonatal white matter injury despite limited cell survival. Glia. 63: 452-65. PMID 25377280 DOI: 10.1002/glia.22764 |
0.44 |
|
| 2015 |
Kadam SD, Chen H, Markowitz GJ, Raja S, George S, Verina T, Shotwell E, Loechelt B, Johnston MV, Kamani N, Fatemi A, Comi AM. Systemic injection of CD34(+)-enriched human cord blood cells modulates poststroke neural and glial response in a sex-dependent manner in CD1 mice. Stem Cells and Development. 24: 51-66. PMID 25121827 DOI: 10.1089/Scd.2014.0135 |
0.473 |
|
| 2015 |
Kadam S, Chen H, Markowitz GJ, Raja S, George S, Verina T, Shotwell E, Loechelt B, Johnston MV, Kamani N, Fatemi A, Comi AM. Correction: Systemic Injection of CD34+ -Enriched Human Cord Blood Cells Modulates Poststroke Neural and Glial Response in a Sex-Dependent Manner in CD1 Mice (Stem Cells and Development (2015) 24, 1 (51-66)) Stem Cells and Development. 24: 916. DOI: 10.1089/Scd.2014.0135.Cxn |
0.446 |
|
| 2014 |
Lee RW, Poretti A, Cohen JS, Levey E, Gwynn H, Johnston MV, Hoon AH, Fatemi A. A diagnostic approach for cerebral palsy in the genomic era. Neuromolecular Medicine. 16: 821-44. PMID 25280894 DOI: 10.1007/S12017-014-8331-9 |
0.519 |
|
| 2014 |
Ghasemi M, Fatemi A. Pathologic role of glial nitric oxide in adult and pediatric neuroinflammatory diseases. Neuroscience and Biobehavioral Reviews. 45: 168-82. PMID 24933692 DOI: 10.1016/J.Neubiorev.2014.06.002 |
0.332 |
|
| 2013 |
Phillips AW, Johnston MV, Fatemi A. The potential for cell-based therapy in perinatal brain injuries. Translational Stroke Research. 4: 137-48. PMID 23814628 DOI: 10.1007/S12975-013-0254-5 |
0.513 |
|
| 2013 |
Verina T, Fatemi A, Johnston MV, Comi AM. Pluripotent possibilities: human umbilical cord blood cell treatment after neonatal brain injury. Pediatric Neurology. 48: 346-54. PMID 23583051 DOI: 10.1016/J.Pediatrneurol.2012.10.010 |
0.506 |
|
| 2013 |
Falahati S, Breu M, Waickman AT, Phillips AW, Arauz EJ, Snyder S, Porambo M, Goeral K, Comi AM, Wilson MA, Johnston MV, Fatemi A. Ischemia-induced neuroinflammation is associated with disrupted development of oligodendrocyte progenitors in a model of periventricular leukomalacia. Developmental Neuroscience. 35: 182-96. PMID 23445614 DOI: 10.1159/000346682 |
0.506 |
|
| 2013 |
Poretti A, Blaser SI, Lequin MH, Fatemi A, Meoded A, Northington FJ, Boltshauser E, Huisman TA. Neonatal neuroimaging findings in inborn errors of metabolism. Journal of Magnetic Resonance Imaging : Jmri. 37: 294-312. PMID 22566357 DOI: 10.1002/Jmri.23693 |
0.331 |
|
| 2013 |
Buelow M, Porambo M, Reisinger D, Phillips AW, Johnston MV, Fatemi A. Combination of neonatal cerebral ischemia and systemic endotoxin modulates expression of oligodendroglial genes Journal of the Neurological Sciences. 333. DOI: 10.1016/J.Jns.2013.07.2325 |
0.459 |
|
| 2013 |
Burd I, Firdaus W, Borbiev T, Dada T, Werner E, Bakshwin A, Fatemi A, Blakemore K, Johnston M. 490: Paradigm shift: cell therapy for preterm birth and prematurity related morbidity American Journal of Obstetrics and Gynecology. 208: S211-S212. DOI: 10.1016/J.Ajog.2012.10.656 |
0.45 |
|
| 2012 |
Phillips AW, Falahati S, DeSilva R, Shats I, Marx J, Arauz E, Kerr DA, Rothstein JD, Johnston MV, Fatemi A. Derivation of glial restricted precursors from E13 mice. Journal of Visualized Experiments : Jove. PMID 22760029 DOI: 10.3791/3462 |
0.454 |
|
| 2011 |
Fatemi A, Wilson MA, Phillips AW, McMahon MT, Zhang J, Smith SA, Arauz EJ, Falahati S, Gummadavelli A, Bodagala H, Mori S, Johnston MV. In vivo magnetization transfer MRI shows dysmyelination in an ischemic mouse model of periventricular leukomalacia. Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism. 31: 2009-18. PMID 21540870 DOI: 10.1038/Jcbfm.2011.68 |
0.497 |
|
| 2011 |
Johnston MV, Fatemi A, Wilson MA, Northington F. Treatment advances in neonatal neuroprotection and neurointensive care. The Lancet. Neurology. 10: 372-82. PMID 21435600 DOI: 10.1016/S1474-4422(11)70016-3 |
0.488 |
|
| 2009 |
Fatemi A, Wilson MA, Johnston MV. Hypoxic-ischemic encephalopathy in the term infant. Clinics in Perinatology. 36: 835-58, vii. PMID 19944838 DOI: 10.1016/J.Clp.2009.07.011 |
0.491 |
|
| 2009 |
Smith SA, Golay X, Fatemi A, Mahmood A, Raymond GV, Moser HW, van Zijl PC, Stanisz GJ. Quantitative magnetization transfer characteristics of the human cervical spinal cord in vivo: application to adrenomyeloneuropathy. Magnetic Resonance in Medicine : Official Journal of the Society of Magnetic Resonance in Medicine / Society of Magnetic Resonance in Medicine. 61: 22-7. PMID 19097204 DOI: 10.1002/Mrm.21827 |
0.504 |
|
| 2005 |
Dubey P, Fatemi A, Huang H, Nagae-Poetscher L, Wakana S, Barker PB, van Zijl P, Moser HW, Mori S, Raymond GV. Diffusion tensor-based imaging reveals occult abnormalities in adrenomyeloneuropathy. Annals of Neurology. 58: 758-66. PMID 16240348 DOI: 10.1002/Ana.20643 |
0.544 |
|
| 2005 |
Smith SA, Golay X, Fatemi A, Jones CK, Raymond GV, Moser HW, van Zijl PC. Magnetization transfer weighted imaging in the upper cervical spinal cord using cerebrospinal fluid as intersubject normalization reference (MTCSF imaging). Magnetic Resonance in Medicine : Official Journal of the Society of Magnetic Resonance in Medicine / Society of Magnetic Resonance in Medicine. 54: 201-6. PMID 15968676 DOI: 10.1002/Mrm.20553 |
0.487 |
|
| 2005 |
Fatemi A, Smith SA, Dubey P, Zackowski KM, Bastian AJ, van Zijl PC, Moser HW, Raymond GV, Golay X. Magnetization transfer MRI demonstrates spinal cord abnormalities in adrenomyeloneuropathy. Neurology. 64: 1739-45. PMID 15911801 DOI: 10.1212/01.Wnl.0000164458.02141.06 |
0.502 |
|
| 2005 |
Dubey P, Fatemi A, Barker PB, Degaonkar M, Troeger M, Zackowski K, Bastian A, Smith SA, Pomper MG, Moser HW, Raymond GV. Spectroscopic evidence of cerebral axonopathy in patients with "pure" adrenomyeloneuropathy. Neurology. 64: 304-10. PMID 15668429 DOI: 10.1212/01.Wnl.0000149514.13580.84 |
0.509 |
|
| 2004 |
Moser H, Dubey P, Fatemi A. Progress in X-linked adrenoleukodystrophy. Current Opinion in Neurology. 17: 263-9. PMID 15167059 DOI: 10.1097/00019052-200406000-00005 |
0.484 |
|
| 2004 |
Moser HW, Fatemi A, Zackowski K, Smith S, Golay X, Muenz L, Raymond G. Evaluation of therapy of X-linked adrenoleukodystrophy. Neurochemical Research. 29: 1003-16. PMID 15139299 DOI: 10.1023/B:Nere.0000021245.12181.90 |
0.482 |
|
| 2004 |
Nagae-Poetscher LM, Bibat G, Philippart M, Rosemberg S, Fatemi A, Lacerda MT, Costa MO, Kok F, Costa Leite C, Horská A, Barker PB, Naidu S. Leukoencephalopathy, cerebral calcifications, and cysts: new observations. Neurology. 62: 1206-9. PMID 15079028 DOI: 10.1212/01.Wnl.0000119341.59445.Cf |
0.326 |
|
| 2003 |
Pizzini F, Fatemi AS, Barker PB, Nagae-Poetscher LM, Horská A, Zimmerman AW, Moser HW, Bibat G, Naidu S. Proton MR spectroscopic imaging in Pelizaeus-Merzbacher disease. Ajnr. American Journal of Neuroradiology. 24: 1683-9. PMID 13679292 |
0.453 |
|
| 2003 |
Loes DJ, Fatemi A, Melhem ER, Gupte N, Bezman L, Moser HW, Raymond GV. Analysis of MRI patterns aids prediction of progression in X-linked adrenoleukodystrophy. Neurology. 61: 369-74. PMID 12913200 DOI: 10.1212/01.Wnl.0000079050.91337.83 |
0.504 |
|
| 2003 |
Fatemi A, Barker PB, UluÄŸ AM, Nagae-Poetscher LM, Beauchamp NJ, Moser AB, Raymond GV, Moser HW, Naidu S. MRI and proton MRSI in women heterozygous for X-linked adrenoleukodystrophy. Neurology. 60: 1301-7. PMID 12707433 DOI: 10.1212/01.Wnl.0000059546.15529.Cb |
0.538 |
|
| 2003 |
Pizzini F, Fatemi A, Barker PB, Moser HW, Naidu S, Beltramello A. Proton MR spectroscopic imaging in Pelizaeus-Merzbacher disease: Correlation with different genotypes Rivista Di Neuroradiologia. 16: 449-450. DOI: 10.1177/197140090301600320 |
0.326 |
|
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