Ali Fatemi, MD
Affiliations: | Kennedy Krieger Institute, Baltimore, MD, United States |
Area:
Myelin disorders, neonatal neurologyGoogle:
"Ali Fatemi"Mean distance: 106866
Parents
Sign in to add mentor| Verne S. Caviness, Jr. | post-doc | ||
| Hugo Moser | post-doc | Kennedy Krieger Institute | |
| Katherine Sims | post-doc | Harvard Medical School - Massachusetts General Hospital | |
| Kevin Staley | post-doc | ||
| Michael V. Johnston | research scientist |
Children
Sign in to add trainee| Ryan Lee Okano | post-doc | Kennedy Krieger Institute (Marine Ecology Tree) | |
| Bela Turk | post-doc | 2016- | Kennedy Krieger Institute |
| Christina Nemeth Mertz | research scientist | Kennedy Krieger Institute | |
| Amena W. Smith | research scientist | Kennedy Krieger Institute |
BETA: Related publications
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Publications
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| Yska HAF, Turk BR, Fatemi A, et al. (2024) International validation of meaningfulness of postural sway and gait to assess myeloneuropathy in adults with adrenoleukodystrophy. Journal of Inherited Metabolic Disease |
| Turk BR, Poisson LM, Nemeth CL, et al. (2022) MicroRNA and metabolomics signatures for adrenomyeloneuropathy disease severity. Jimd Reports. 63: 593-603 |
| Engelen M, van Ballegoij WJC, Mallack EJ, et al. (2022) International Recommendations for the Diagnosis and Management of Patients With Adrenoleukodystrophy: A Consensus-Based Approach. Neurology |
| Smith Fine A, Kaufman M, Goodman J, et al. (2022) Wearable sensors detect impaired gait and coordination in LBSL during remote assessments. Annals of Clinical and Translational Neurology. 9: 468-477 |
| Mallack EJ, Turk BR, Yan H, et al. (2020) MRI Surveillance of Boys with X-linked Adrenoleukodystrophy Identified by Newborn Screening: Meta-analysis and Consensus Guidelines. Journal of Inherited Metabolic Disease |
| Sripathy SR, Wang Y, Moses RL, et al. (2020) Generation of 10 patient-specific induced pluripotent stem cells (iPSCs) to model Pitt-Hopkins Syndrome. Stem Cell Research. 48: 102001 |
| Nemeth CL, Tomlinson SN, Sharma R, et al. (2020) Glial restricted precursor delivery of dendrimer N-acetylcysteine promotes migration and differentiation following transplant in mouse white matter injury model. Nanoscale |
| Guillen Sacoto MJ, Tchasovnikarova IA, Torti E, et al. (2020) 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 |
| Turk BR, Theda C, Fatemi A, et al. (2020) 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 |
| Fine AS, Nemeth CL, Kaufman ML, et al. (2019) Mitochondrial aminoacyl-tRNA synthetase disorders: an emerging group of developmental disorders of myelination. Journal of Neurodevelopmental Disorders. 11: 29 |