Hind Alsharhan
9PUBLICATIONS
16CO-AUTHORS
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Publications (9)
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|Dec 01, 2025
Clinical and Genetic Spectrum of SCN8A-Related Disorders: A Retrospective Study From the Gulf Region.Osama Muthaffar, Mashael Alsubhan, Ali Mir
|Mar 26, 2025
Insights from the Newborn Screening Program for Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency in Kuwait.Hind Alsharhan, Amir A Ahmed, Marwa Abdullah
|May 24, 2024
Tribal Founder EMC1 Variant in 5 Kuwaiti Families Expands Phenotypic Spectrum of EMC1-Related Disorder.Nada T Alzayed, Abdullah H Alzuabi, Reem A Alqusaimi
|Sep 05, 2023
Biotin-thiamine responsive basal ganglia disease: a retrospective review of the clinical, radiological and molecular findings of cases in Kuwait with novel variants.Maryam Aburezq, Ahmad Alahmad, Rasha Alsafi
|Jun 28, 2023
Interstitial Deletion of 3q21 in a Kuwaiti Child with Multiple Congenital Anomalies-Expanding the Phenotype.Noor Almoosawy, Fawaz Albaghli, Haya H Al-Balool
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Frequent Collaborators
1 joint publications
Christina Lam
1 joint publications
Rebecca D Ganetzky
1 joint publications
Nada T Alzayed
1 joint publications
Abdullah H Alzuabi
1 joint publications
Reem A Alqusaimi
1 joint publications
Ehab A El-Anany
1 joint publications
Abdullah Alholle
1 joint publications
Ashraf H Aboelanine
1 joint publications
Amir A Ahmed
1 joint publications
Ahmad Alahmad