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Ghada M H Abdel-Salam

Showing results (1-10 of 94) with videos related to

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Neuropediatrics|December 3, 2020
Asparagine Synthetase Deficiency with Intracranial Hemorrhage Can Mimic Molybdenum Cofactor DeficiencyGhada M H Abdel-Salam, Mohamed S Abdel-Hamid
Journal of Human Genetics|January 22, 2026
A novel homozygous splicing variant in FRA10AC1: further delineation of the phenotypeMohamed S Abdel-Hamid, Ghada M H Abdel-Salam
Clinical Genetics|May 16, 2023
A founder PPIL1 variant underlies a recognizable form of microlissencephaly with pontocerebellar hypoplasiaGhada M H Abdel-Salam, Mohamed S Abdel-Hamid
Journal of Human Genetics|March 8, 2024
New insights into the clinical and molecular spectrum of the MADD-related neurodevelopmental disorderGhada M H Abdel-Salam, Mohamed S Abdel-Hamid
Brain & Development|March 28, 2006
Isolated Dandy-Walker malformation associated with brain stem dysgenesis in male sibsGhada M H Abdel-Salam, Marwa Shehab, Maha S Zaki
Molecular Syndromology|December 7, 2023
Dandy-Walker Malformation in a Girl with <i>DDX3X-</i>Related Intellectual DisabilityKarima Rafat, Mohamed S Abdel-Hamid, Ghada M H Abdel-Salam
Clinical Genetics|September 25, 2025
A Further Case Supporting BORCS8 as a Cause of an Infantile-Onset Neurodegenerative DisorderMohamed S Abdel-Hamid, Samer H ElKhayat, Ghada M H Abdel-Salam
American Journal of Medical Genetics. Part A|March 30, 2020
KBG syndrome in two patients from EgyptInas S M Sayed, Mohamed S Abdel-Hamid, Ghada M H Abdel-Salam
American Journal of Medical Genetics. Part A|October 18, 2008
Microcephaly, malformation of brain development and intracranial calcification in sibs: pseudo-TORCH or a new syndromeGhada M H Abdel-Salam, Maha S Zaki, Sahar N Saleem, et al.
Neuropediatrics|October 22, 2019
Further Insights into Developmental Brain Malformations and Leukoencephalopathy Associated with 6p25.3 DeletionMaha Eid, Ola Eid, Ibrahim Hegazy, et al.
Pageof 10

Showing results (1-10 of 94) with videos related to

Sort By:
Pageof 10
Neuropediatrics|December 3, 2020
Asparagine Synthetase Deficiency with Intracranial Hemorrhage Can Mimic Molybdenum Cofactor DeficiencyGhada M H Abdel-Salam, Mohamed S Abdel-Hamid
Journal of Human Genetics|January 22, 2026
A novel homozygous splicing variant in FRA10AC1: further delineation of the phenotypeMohamed S Abdel-Hamid, Ghada M H Abdel-Salam
Clinical Genetics|May 16, 2023
A founder PPIL1 variant underlies a recognizable form of microlissencephaly with pontocerebellar hypoplasiaGhada M H Abdel-Salam, Mohamed S Abdel-Hamid
Journal of Human Genetics|March 8, 2024
New insights into the clinical and molecular spectrum of the MADD-related neurodevelopmental disorderGhada M H Abdel-Salam, Mohamed S Abdel-Hamid
Brain & Development|March 28, 2006
Isolated Dandy-Walker malformation associated with brain stem dysgenesis in male sibsGhada M H Abdel-Salam, Marwa Shehab, Maha S Zaki
Molecular Syndromology|December 7, 2023
Dandy-Walker Malformation in a Girl with <i>DDX3X-</i>Related Intellectual DisabilityKarima Rafat, Mohamed S Abdel-Hamid, Ghada M H Abdel-Salam
Clinical Genetics|September 25, 2025
A Further Case Supporting BORCS8 as a Cause of an Infantile-Onset Neurodegenerative DisorderMohamed S Abdel-Hamid, Samer H ElKhayat, Ghada M H Abdel-Salam
American Journal of Medical Genetics. Part A|March 30, 2020
KBG syndrome in two patients from EgyptInas S M Sayed, Mohamed S Abdel-Hamid, Ghada M H Abdel-Salam
American Journal of Medical Genetics. Part A|October 18, 2008
Microcephaly, malformation of brain development and intracranial calcification in sibs: pseudo-TORCH or a new syndromeGhada M H Abdel-Salam, Maha S Zaki, Sahar N Saleem, et al.
Neuropediatrics|October 22, 2019
Further Insights into Developmental Brain Malformations and Leukoencephalopathy Associated with 6p25.3 DeletionMaha Eid, Ola Eid, Ibrahim Hegazy, et al.
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