Khalid Ibrahim
2PUBLICATIONS
14CO-AUTHORS
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Publications (2)
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|Dec 29, 2025
Rare Presentation of Homozygous SLC20A2 Mutations Causing Intra-Arterial Cerebral Vasculopathy and Stroke in Infancy: Case Report and Review of the Literature.Laila Baker, Faisal Hadid, Sara Salahaldeen Irshaidat
|Aug 29, 2020
A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families.Reem Al-Sulaiman, Amna Othman, Karen El-Akouri
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Frequent Collaborators
1 joint publications
Amna Othman
1 joint publications
Karen El-Akouri
1 joint publications
Shehab Fareed
1 joint publications
Hajer AlMulla
1 joint publications
Aseel Sukik
1 joint publications
Noora Shahbeck
1 joint publications
Rehab Ali
1 joint publications
Fatma Al-Mesaifri
1 joint publications
Sara Musa
1 joint publications
Khalid Mohamed
