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AHLAM HAMAD
AHLAM HAMAD
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Year
A novel nonsense mutation in DNAJC6 expands the phenotype of autosomal-recessive juvenile-onset Parkinson’s disease
LE Elsayed, V Drouet, T Usenko, IN Mohammed, AA Hamed, MA Elseed, ...
Ann Neurol 79 (2), 335-337, 2016
792016
Expanding the phenome and variome of skeletal dysplasia
S Maddirevula, S Alsahli, L Alhabeeb, N Patel, F Alzahrani, ...
Genetics in Medicine 20 (12), 1609-1616, 2018
572018
Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan
LEO Elsayed, IN Mohammed, AAA Hamed, MA Elseed, A Johnson, ...
European Journal of Human Genetics 25 (1), 100-110, 2017
382017
Fragmentation of 28Si nuclei in nuclear emulsion
M El-Nadi, MS El-Nagdy, N Ali-Mossa, A Abdelsalam, AM Abdalla, ...
Journal of Physics G: Nuclear and Particle Physics 25 (6), 1169, 1999
311999
Effect of pasteurization and storage conditions on the microbiological, chemical and organoleptic properties of Domiati cheese during pickling.
AI Hamed, NA El-Saify, SI Farag, F Orsi
271992
Clinical profile of pediatric neurological disorders: Outpatient department, Khartoum, Sudan
IN Mohamed, MA Elseed, AA Hamed
Child neurology open 3, 2329048X15623548, 2016
242016
Diallel analysis for studying heterosis and combining ability of some economical yield traits in pumpkin
AH Hussien, AA Hamed
Journal of Plant Production 6 (3), 261-270, 2015
222015
Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556
ES Cauley, A Hamed, IN Mohamed, M Elseed, S Martinez, A Yahia, ...
Neurogenetics 20, 91-98, 2019
212019
Impact of PYROXD1 deficiency on cellular respiration and correlations with genetic analyses of limb-girdle muscular dystrophy in Saudi Arabia and Sudan
M Saha, HM Reddy, MA Salih, E Estrella, MD Jones, S Mitsuhashi, ...
Physiological genomics 50 (11), 929-939, 2018
202018
Brain tuberculoma, an unusual cause of stroke in a child with trisomy 21: a case report
AEM Kheir, SA Ibrahim, AA Hamed, BM Yousif, FA Hamid
Journal of medical case reports 11, 1-4, 2017
192017
Prevalence of epilepsy in 74,949 school children in Khartoum State, Sudan
IN Mohamed, MA Elseed, AA Hamed, ME Abdel-Rahman, SM El-Sadig, ...
Paediatrics and international child health 37 (3), 188-192, 2017
172017
The differential effects of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) on seizure frequency in patients with drug-resistant epilepsy—A randomized, double-blind …
FAS Ibrahim, K Ghebremeskel, ME Abdel-Rahman, AAM Ahmed, ...
Epilepsy & Behavior 87, 32-38, 2018
162018
Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family
LEO Elsayed, IN Mohammed, AAA Hamed, MA Elseed, MAM Salih, ...
BMC medical genetics 19, 1-5, 2018
152018
Storm surge generation by winter cyclones at Alexandria, Egypt
AA Hamed, AA El Gindy
The International Hydrographic Review, 1988
141988
Intelligence quotient (IQ) among children with epilepsy: National epidemiological study–Sudan
IN Mohamed, AH Osman, S Mohamed, EK Hamid, AA Hamed, A Alsir, ...
Epilepsy & Behavior 103, 106813, 2020
132020
Effect of Soxhlet method extraction on characterization of pectin of pumpkin peels
AAR Hamed, AEE Elkhedir, SE Mustafa
Journal of Experimental Food Chemistry 3 (1), 1-3, 2017
112017
Novel Homozygous Missense Mutation in the ARG1 Gene in a Large Sudanese Family
LEO Elsayed, IN Mohammed, AAA Hamed, MA Elseed, MAM Salih, ...
Frontiers in neurology 11, 569996, 2020
102020
Novel variants causing megalencephalic leukodystrophy in Sudanese families
M Amin, C Vignal, AAA Hamed, IN Mohammed, MA Elseed, S Drunat, ...
Journal of Human Genetics 67 (3), 127-132, 2022
82022
A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability
M Amin, C Vignal, E Eltaraifee, IN Mohammed, AAA Hamed, MA Elseed, ...
BMC Medical Genomics 15 (1), 236, 2022
72022
Methylation of alpha-synuclein in a Sudanese cohort
Y Bakhit, I Schmitt, A Hamed, EAA Ibrahim, IN Mohamed, SM El-Sadig, ...
Parkinsonism & Related Disorders 101, 6-8, 2022
72022
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