Hind Alsharhan

10PUBLICATIONS
21CO-AUTHORS
Medical biochemistry - amino acids and metabolitesHaematologyGene expression (incl. microarray and other genome-wide approaches)NeonatologyMajor global burdens of disease
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Publications (10)

|Jul 21, 2026
A Homozygous Founder ELAC2 Variant in Kuwaiti Infants With Fatal Cardiomyopathy and Refractory Severe Lactic Acidosis: A Retrospective Review of the Clinical, Cardiological and Molecular Findings.

|Jul 01, 2026
Biallelic Variant in HAPLN1 is Associated With Skeletal Dysplasia With or Without Congenital Heart Disease.

|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

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Frequent Collaborators

2 joint publications

Ahmad Alahmad

1 joint publications

Christina Lam

1 joint publications

Rebecca D Ganetzky

1 joint publications

Nada T Alzayed