Segui
Ali Fatemi
Ali Fatemi
Chief Medical Officer, Kennedy Krieger Institute, Professor at Johns Hopkins University
Email verificata su kennedykrieger.org - Home page
Titolo
Citata da
Citata da
Anno
Cerebral plasticity: Windows of opportunity in the developing brain
FY Ismail, A Fatemi, MV Johnston
European journal of paediatric neurology 21 (1), 23-48, 2017
5482017
Treatment advances in neonatal neuroprotection and neurointensive care
MV Johnston, A Fatemi, MA Wilson, F Northington
The Lancet Neurology 10 (4), 372-382, 2011
3692011
Hypoxic-ischemic encephalopathy in the term infant
A Fatemi, MA Wilson, MV Johnston
Clinics in perinatology 36 (4), 835-858, 2009
3572009
Clinical whole exome sequencing in child neurology practice
S Srivastava, JS Cohen, H Vernon, K Barañano, R McClellan, L Jamal, ...
Annals of neurology 76 (4), 473-483, 2014
3062014
Analysis of MRI patterns aids prediction of progression in X-linked adrenoleukodystrophy
DJ Loes, A Fatemi, ER Melhem, N Gupte, L Bezman, HW Moser, ...
Neurology 61 (3), 369-374, 2003
2862003
Swaiman's pediatric neurology: principles and practice
KF Swaiman, S Ashwal, DM Ferriero, NF Schor, RS Finkel, AL Gropman, ...
Elsevier Health Sciences, 2017
2292017
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
1892019
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
1502020
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
1252014
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
1232020
Progress in X-linked adrenoleukodystrophy
H Moser, P Dubey, A Fatemi
Current opinion in neurology 17 (3), 263-269, 2004
1132004
Therapy of X-linked adrenoleukodystrophy
HW Moser
NeuroRx 3, 246-253, 2006
1122006
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
1102013
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
1072018
Pathologic role of glial nitric oxide in adult and pediatric neuroinflammatory diseases
M Ghasemi, A Fatemi
Neuroscience & Biobehavioral Reviews 45, 168-182, 2014
1042014
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
1022015
X-linked adrenoleukodystrophy
GV Raymond, AB Moser, A Fatemi
932018
FOXG1 syndrome: genotype–phenotype association in 83 patients with FOXG1 variants
D Mitter, M Pringsheim, M Kaulisch, KS Plümacher, S Schröder, ...
Genetics in Medicine 20 (1), 98-108, 2018
912018
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
912017
Self-reported organic and nonorganic sleep problems in schoolchildren aged 11 to 15 years in Vienna
OS Ipsiroglu, A Fatemi, I Werner, E Paditz, B Schwarz
Journal of Adolescent Health 31 (5), 436-442, 2002
892002
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
Articoli 1–20