Khalid Al-Thihli

12PUBLICATIONS
33CO-AUTHORS
Neurology and neuromuscular diseasesSpeciation and extinctionHaematologyInfant and child healthPharmacogenomics
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Journal

Publications (12)

|Sep 26, 2026
Spectrum of Hereditary Ataxia in Omani Children.

|Apr 29, 2026
SLC52A3-related Brown-Vialetto-Van Laere syndrome: a large cohort from the Arabian Peninsula.

|Oct 06, 2025
A Heterozygous Variant in HABP2 Causing Increased Risk of Arterial and Venous Thrombosis in a Young Male: Diagnostic and Therapeutic Challenges.

Salim Al-Busaidi, Nasiba Al-Maqrashi, Khalid Al-Thihli

|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

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Frequent Collaborators

3 joint publications

Almundher Al-Maawali

1 joint publications

J Suleiman

1 joint publications

A W El-Hattab

1 joint publications

Azza Al Shidhani