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Fuad Almutairi

7PUBLICATIONS

9CO-AUTHORS

Infant and child healthCell and nuclear divisionEpigenetics (incl. genome methylation and epigenomics)Medical biochemistry - amino acids and metabolitesPhotochemistry

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Publications (7)

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|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

|Jun 12, 2020

Peeling of skin as presenting manifestation in congenital disorders of glycosylation.

Meshal Almutairi, Sultan Al-Khenaizan, Fahd Al Sufiani

|May 17, 2020

Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: a case report.

Fuad Al Mutairi, Randa Alkhalaf, Abdullah Alkhorayyef

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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

1 joint publications

Abdulrahman Faiz Alswaid

1 joint publications

Muhammad Umair

1 joint publications

Majid Alfadhel

1 joint publications

Ali M Sawlan

1 joint publications

Muhammad Talal Alrifai

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

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