Ali Fatemi, MD - Publications

Affiliations: 
Kennedy Krieger Institute, Baltimore, MD, United States 
Area:
Myelin disorders, neonatal neurology

65 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
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  0.715
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  0.739
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  0.316
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  0.316
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  0.327
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  0.759
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  0.752
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  0.302
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  0.352
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  0.339
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  0.342
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  0.341
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  0.312
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  0.326
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  0.354
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  0.737
2018 Moser AB, Fatemi A. Newborn Screening and Emerging Therapies for X-Linked Adrenoleukodystrophy. Jama Neurology. 75: 1175-1176. PMID 29946687 DOI: 10.1001/Jamaneurol.2018.1585  0.303
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  0.486
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  0.312
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  0.318
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  0.58
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  0.481
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  0.764
2017 Acuna-Hidalgo R, Deriziotis P, Steehouwer M, Gilissen C, Graham SA, van Dam S, Hoover-Fong J, Telegrafi AB, Destree A, Smigiel R, Lambie LA, Kayserili H, Altunoglu U, Lapi E, Uzielli ML, ... ... Fatemi A, et al. Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies. Plos Genetics. 13: e1006683. PMID 28346496 DOI: 10.1371/Journal.Pgen.1006683  0.302
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  0.738
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  0.343
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  0.319
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  0.475
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  0.311
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  0.445
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  0.51
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  0.489
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  0.49
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  0.45
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  0.479
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  0.451
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  0.517
2014 Srivastava S, Cohen J, Pevsner J, Aradhya S, McKnight D, Butler E, Johnston M, Fatemi A. A novel variant in GABRB2 associated with intellectual disability and epilepsy. American Journal of Medical Genetics. Part A. 164: 2914-21. PMID 25124326 DOI: 10.1002/Ajmg.A.36714  0.301
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  0.336
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  0.519
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  0.511
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  0.513
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  0.326
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  0.463
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  0.456
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  0.463
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  0.499
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  0.49
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  0.493
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  0.507
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  0.549
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  0.488
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  0.503
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  0.506
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  0.487
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  0.488
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  0.318
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  0.451
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  0.499
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  0.327
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