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Muntaser E Ibrahim

Showing results (51-60 of 55) with videos related to

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Cancers|June 10, 2023
Follicular Helper and Regulatory T Cells Drive the Development of Spontaneous Epstein-Barr Virus Lymphoproliferative DisorderElshafa Hassan Ahmed, Mark Lustberg, Claire Hale, et al.
Frontiers in Neurology|September 7, 2021
Pathogenic Variants in <i>ABHD16A</i> Cause a Novel Psychomotor Developmental Disorder With Spastic ParaplegiaAshraf Yahia, Liena E O Elsayed, Remi Valter, et al.
European Journal of Human Genetics : EJHG|February 5, 2024
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile EpilepsyMahmoud Koko, Maha A Elseed, Inaam N Mohammed, et al.
European Journal of Human Genetics : EJHG|September 8, 2016
Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in SudanLiena E O Elsayed, Inaam N Mohammed, Ahlam A A Hamed, et al.
European Journal of Human Genetics : EJHG|April 3, 2023
Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerationsAshraf Yahia, Ahlam A A Hamed, Inaam N Mohamed, et al.
Pageof 6

Showing results (51-60 of 55) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 55 results.
Cancers|June 10, 2023
Follicular Helper and Regulatory T Cells Drive the Development of Spontaneous Epstein-Barr Virus Lymphoproliferative DisorderElshafa Hassan Ahmed, Mark Lustberg, Claire Hale, et al.
Frontiers in Neurology|September 7, 2021
Pathogenic Variants in <i>ABHD16A</i> Cause a Novel Psychomotor Developmental Disorder With Spastic ParaplegiaAshraf Yahia, Liena E O Elsayed, Remi Valter, et al.
European Journal of Human Genetics : EJHG|February 5, 2024
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile EpilepsyMahmoud Koko, Maha A Elseed, Inaam N Mohammed, et al.
European Journal of Human Genetics : EJHG|September 8, 2016
Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in SudanLiena E O Elsayed, Inaam N Mohammed, Ahlam A A Hamed, et al.
European Journal of Human Genetics : EJHG|April 3, 2023
Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerationsAshraf Yahia, Ahlam A A Hamed, Inaam N Mohamed, et al.
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