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Inaam  N Mohamed
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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
Traditional and spiritual medicine among Sudanese children with epilepsy
IN Mohammed, HE Babikir
Sudanese journal of paediatrics 13 (1), 31, 2013
512013
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
prevalence of neural tube defects Khartoum, Sudan august 2014–July 2015
IM Omer, OM Abdullah, IN Mohammed, LA Abbasher
BMC research notes 9, 1-4, 2016
352016
The quality of life among Sudanese children with epilepsy and their care givers
Z Abbas, MA Elseed, IN Mohammed
Sudanese journal of paediatrics 14 (1), 51, 2014
252014
Clinical profile of pediatric neurological disorders: Outpatient department, Khartoum, Sudan
IN Mohamed, MA Elseed, AA Hamed
Child neurology open 3, 2329048X15623548, 2016
242016
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
Prevalence of epilepsy in 74,949 school children in Khartoum State, Sudan
ZAKMAS Inaam N. Mohamed, Maha A. Elseed, Ahlam A. Hamed, Manar E ...
Paediatrics and International Child Health, 2017
172017
The profile of childhood epilepsy in Sudan
IN Mohammed, M Abdel Moneim, A A Rahman
Faculty of Medicine, University of Khartoum, 2010
162010
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
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
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
Spectrum of attention deficit hyperactivity disorders (ADHD) among Sudanese children with epilepsy
EE Ahmed, IN Mohamed
Sudanese Journal of Paediatrics 15 (1), 42, 2015
92015
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
Genetic diagnosis in Sudanese and Tunisian families with syndromic intellectual disability through exome sequencing
A Yahia, IB Ayed, AA Hamed, IN Mohammed, MA Elseed, AM Bakhiet, ...
Annals of Human Genetics 86 (4), 181-194, 2022
72022
Pathogenic variants in ABHD16A cause a novel psychomotor developmental disorder with spastic paraplegia.
INM Ashraf Yahia, Liena Elbaghir Omer Elsayed , Remi Valter, Ahlam A. A. Hamed
Frontiers in Neurology 12, 2021
72021
Classification and management of epilepsy and epileptic syndromes in a cohort of 202 school children-a 2 year follow up study-Sudan
IN Mohamed, MA Elseed, S Mohamed, A Alsir, EK Hamid, IM Omer, ...
BMC neurology 19, 1-6, 2019
72019
Congenital brain malformations in Sudanese children: an outpatient-based study
IN Mohammed, SA Suliman, MA Elseed, AA Hamed, MO Babiker, ...
Sudanese Journal of Paediatrics 18 (1), 48, 2018
72018
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