Articles with public access mandates - Ali FatemiLearn more
Not available anywhere: 3
Deficiency of WARS2, encoding mitochondrial tryptophanyl tRNA synthetase, causes severe infantile onset leukoencephalopathy
BE Theisen, A Rumyantseva, JS Cohen, WA Alcaraz, DN Shinde, S Tang, ...
American Journal of Medical Genetics Part A 173 (9), 2505-2510, 2017
Mandates: US National Institutes of Health, German Research Foundation
Diffusion tensor imaging abnormalities in the cerebral white matter correlate with sex-dependent neurobehavioral deficits in adult mice with neonatal ischemia
M Breu, J Zhang, M Porambo, MV Pletnikov, K Goeral, M Kakara, ...
Developmental Neuroscience 38 (2), 83-95, 2016
Mandates: US National Institutes of Health
Developmental delay can precede neurologic regression in early onset metachromatic leukodystrophy
LA Adang, S Groeschel, C Grzyb, R D'Aiello, F Gavazzi, O Sherbini, ...
Molecular genetics and metabolism 142 (4), 108521, 2024
Mandates: Fonds de recherche du Québec - Santé
Available somewhere: 76
Treatment advances in neonatal neuroprotection and neurointensive care
MV Johnston, A Fatemi, MA Wilson, F Northington
The Lancet Neurology 10 (4), 372-382, 2011
Mandates: US National Institutes of Health
Hypoxic-ischemic encephalopathy in the term infant
A Fatemi, MA Wilson, MV Johnston
Clinics in perinatology 36 (4), 835-858, 2009
Mandates: US National Institutes of Health
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes
P Feliciano, X Zhou, I Astrovskaya, TN Turner, T Wang, L Brueggeman, ...
NPJ genomic medicine 4 (1), 19, 2019
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, Autism …
X‐linked adrenoleukodystrophy: pathology, pathophysiology, diagnostic testing, newborn screening and therapies
BR Turk, C Theda, A Fatemi, AB Moser
International Journal of Developmental Neuroscience 80 (1), 52-72, 2020
Mandates: US National Institutes of Health
Mutations disrupting neuritogenesis genes confer risk for cerebral palsy
SC Jin, SA Lewis, S Bakhtiari, X Zeng, MC Sierant, S Shetty, SM Nordlie, ...
Nature genetics 52 (10), 1046-1056, 2020
Mandates: US National Institutes of Health, American Heart Association, National …
A diagnostic approach for cerebral palsy in the genomic era
RW Lee, A Poretti, JS Cohen, E Levey, H Gwynn, MV Johnston, AH Hoon, ...
Neuromolecular medicine 16, 821-844, 2014
Mandates: US National Institutes of Health
Cognitive impairments induced by necrotizing enterocolitis can be prevented by inhibiting microglial activation in mouse brain
DF Niño, Q Zhou, Y Yamaguchi, LY Martin, S Wang, WB Fulton, H Jia, ...
Science translational medicine 10 (471), eaan0237, 2018
Mandates: US National Institutes of Health
MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathways
AR Paciorkowski, RN Traylor, JA Rosenfeld, JM Hoover, CJ Harris, ...
neurogenetics 14, 99-111, 2013
Mandates: US National Institutes of Health
Systemic dendrimer-drug treatment of ischemia-induced neonatal white matter injury
E Nance, M Porambo, F Zhang, MK Mishra, M Buelow, R Getzenberg, ...
Journal of Controlled Release 214, 112-120, 2015
Mandates: US National Institutes of Health
DNM1 encephalopathy: A new disease of vesicle fission
S Von Spiczak, KL Helbig, DN Shinde, R Huether, M Pendziwiat, ...
Neurology 89 (4), 385-394, 2017
Mandates: US National Institutes of Health, German Research Foundation, National …
X-linked adrenoleukodystrophy
GV Raymond, AB Moser, A Fatemi
Mandates: US National Institutes of Health
Neonatal neuroimaging findings in inborn errors of metabolism
A Poretti, SI Blaser, MH Lequin, A Fatemi, A Meoded, FJ Northington, ...
Journal of Magnetic Resonance Imaging 37 (2), 294-312, 2013
Mandates: US National Institutes of Health
A novel variant in GABRB2 associated with intellectual disability and epilepsy
S Srivastava, J Cohen, J Pevsner, S Aradhya, D McKnight, E Butler, ...
American journal of medical genetics Part A 164 (11), 2914-2921, 2014
Mandates: US National Institutes of Health
Loss of the sphingolipid desaturase DEGS1 causes hypomyelinating leukodystrophy
DC Pant, I Dorboz, A Schluter, S Fourcade, N Launay, J Joya, ...
The Journal of clinical investigation 129 (3), 1240-1256, 2019
Mandates: US Department of Defense, US National Institutes of Health, Howard Hughes …
De novo variants in the ATPase module of MORC2 cause a neurodevelopmental disorder with growth retardation and variable craniofacial dysmorphism
MJG Sacoto, IA Tchasovnikarova, E Torti, C Forster, EH Andrew, I Anselm, ...
The American Journal of Human Genetics 107 (2), 352-363, 2020
Mandates: US National Institutes of Health, Damon Runyon Cancer Research Foundation
White matter tract integrity and developmental outcome in newborn infants with hypoxic‐ischemic encephalopathy treated with hypothermia
AN Massaro, I Evangelou, A Fatemi, G Vezina, R Mccarter, P Glass, ...
Developmental Medicine & Child Neurology 57 (5), 441-448, 2015
Mandates: US National Institutes of Health
Ischemia-induced neuroinflammation is associated with disrupted development of oligodendrocyte progenitors in a model of periventricular leukomalacia
S Falahati, M Breu, AT Waickman, AW Phillips, EJ Arauz, S Snyder, ...
Developmental neuroscience 35 (2-3), 182-196, 2013
Mandates: US National Institutes of Health
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