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Mohammed A Al-Muhaizea

5PUBLICATIONS

23CO-AUTHORS

Dental therapeutics, pharmacology and toxicologyCellular nervous systemNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Medical virology

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Publications (5)

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|Apr 14, 2026

Genetic, Clinical, and Management Characteristics of Duchenne Muscular Dystrophy in Saudi Arabia.

Abdulaziz S AlSaman, Fouad Al Ghamdi, Ahmed K Bamaga

|Jul 17, 2023

SLC4A10 mutation causes a neurological disorder associated with impaired GABAergic transmission.

James Fasham, Antje K Huebner, Lutz Liebmann

|Nov 27, 2021

Phenotypic Variability of <i>MEGF10</i> Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population.

Mohammad AlMuhaizea, Omar Dabbagh, Hanan AlQudairy

|Aug 10, 2021

Expanding the mutational landscape and clinical phenotype of the YIF1B related brain disorder.

Eva Medico Salsench, Reza Maroofian, Ruizhi Deng

|Sep 24, 2017

Molecular and clinical spectra of FBXL4 deficiency.

Ayman W El-Hattab, Hongzheng Dai, Mohammed Almannai

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Frequent Collaborators

2 joint publications

Henry Houlden

2 joint publications

Namik Kaya

1 joint publications

James Fasham

1 joint publications

Reza Maroofian

1 joint publications

Joseph S Leslie

1 joint publications

Grazia M S Mancini

1 joint publications

Fowzan S Alkuraya

1 joint publications

Andrew H Crosby

1 joint publications

Emma L Baple

1 joint publications

Eva Medico Salsench

Frequent Collaborators

2 joint publications

Henry Houlden

2 joint publications

Namik Kaya

1 joint publications

James Fasham

1 joint publications

Reza Maroofian

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