Fuad Almutairi

7PUBLICATIONS
9CO-AUTHORS
Infant and child healthCell and nuclear divisionEpigenetics (incl. genome methylation and epigenomics)Medical biochemistry - amino acids and metabolitesNeurology and neuromuscular diseases
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Publications (7)

|Jun 11, 2025
Intramuscular Vitamin B12 Treatment in Transcobalamin II Deficiency: Case Series Clinical Outcomes.

Ali M Sawlan, Msaed Alotaibi, Rayan M Alharbi

|Oct 08, 2024
Consanguinity and Occurrence of Monogenic Diseases in a Single Tertiary Centre in Riyadh, Saudi Arabia: A 2 Years Cross-Sectional Study.

Lamia K Alshamlani, Dana S Alsulaim, Raghad S Alabbad

|Jun 07, 2024
Genetic Microcephaly in a Saudi Population: Unique Spectrum of Affected Genes Including a Novel One.

Muhammad Talal Alrifai, Yousof Alrumayyan, Duaa Baarmah

|Oct 26, 2020
Hyperhomocysteinemia: Clinical Insights.

Fuad Al Mutairi

|May 17, 2020
Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: a case report.

Fuad Al Mutairi, Randa Alkhalaf, Abdullah Alkhorayyef

|Sep 09, 2017
Peeling skin syndrome associated with novel variant in FLG2 gene.

Ahmed Alfares, Sultan Al-Khenaizan, Fuad Al Mutairi

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Frequent Collaborators

1 joint publications

Lamia K Alshamlani

1 joint publications

Dana S Alsulaim

1 joint publications

Raghad S Alabbad

1 joint publications

Joud F Alkhoder