Khalid Al-Thihli

11PUBLICATIONS
30CO-AUTHORS
Speciation and extinctionHaematologyInfant and child healthPharmacogenomicsImmunogenetics (incl. genetic immunology)
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Publications (11)

|Oct 03, 2024
Periodic Paralysis in a Child With Thermosensitive Mitochondrial Trifunctional Protein Deficiency.

Fatema Al-Amrani, Jos P N Ruiter, Mirjam Doolaard

|Nov 29, 2022
Joint Analysis of Phenotypic and Genomic Diversity Sheds Light on the Evolution of Xenobiotic Metabolism in Humans.

Médéric Mouterde, Youssef Daali, Victoria Rollason

|Feb 25, 2022
Mucolipidosis Type IV in Omani Families with a Novel MCOLN1 Mutation: Search for Evidence of Founder Effect.

Badriya Al-Alawi, Beena Harikrishna, Khalid Al-Thihli

|Nov 12, 2021
Hypoketotic hypoglycemia without neuromuscular complications in patients with SLC25A32 deficiency.

Bushra Al Shamsi, Fathiya Al Murshedi, Asila Al Habsi

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