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Ammar Ahmed

Publications (12)

Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degeneration
Article scientifique · 2022
A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability
Article scientifique · 2022
Case Report: A New Family With Pontocerebellar Hypoplasia 10 From Sudan
Article scientifique · 2022
Outcome of Neurocritical Disorders, A Multicenter Study from Sudan
Article scientifique · 2021
Involvement of ADGRV1 Gene in Familial Forms of Genetic Generalized Epilepsy
Article scientifique · 2021
Pathogenic Variants in ABHD16A Cause a Novel Psychomotor Developmental Disorder With Spastic Paraplegia
Article scientifique · 2021
A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report
Article scientifique · 2021
Novel Homozygous Missense Mutation in the ARG1 Gene in a Large Sudanese Family
Article scientifique · 2020
Exome Sequencing Revealed Mutations in ADAT3 and HERC2 Genes in two Sudanese Families with Syndromic Mental Retardation
Article scientifique · 2020
Reference Jitter Values for Concentric Needle Electrode of Orbicularis Oculi and Frontalis Muscles Using Voluntary Activation Method in Sudanese Population
Article scientifique · 2020
Intra-familial phenotypic heterogeneity in a Sudanese family with DARS2-related leukoencephalopathy, brainstem and spinal cord involvement and lactate elevation: a case report
Article scientifique · 2018
Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family
Article scientifique · 2018

Domaines principaux

Sciences de la santé8 Sciences de la vie et biotechnologies4

Statistiques

Consultations45
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