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Brahim Tabarki

8PUBLICATIONS

33CO-AUTHORS

NeurogeneticsMedical infection agents (incl. prions)Other European languagesNeurology and neuromuscular diseasesRespiratory diseases

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Publications (8)

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|Apr 17, 2026

Longitudinal Phenotypic Trajectories in GNAO1-Related Disorders: Defining Disease Progression and Clinical Profiles.

|Oct 07, 2025

Biallelic Variants in TMEM17 Cause Meckel-Gruber Syndrome Within the Ciliopathy Spectrum.

Luba M Pardo, Javier Martini, Emir Zonic

|Jul 09, 2025

SLC25A42-Related Mitochondrial Disorder: New Cases and Literature Review.

Areej Alatawi, Omamah Alshehri, Aminah Alessa

|Jul 23, 2024

Multiplex Consanguineous Family Highlights <i>CLASP1</i> as a Candidate Gene for Lissencephaly.

Rawan Alsafh, Amal Alhashem, Aly Elsyed

|Jan 19, 2024

Bi-allelic variants in HCRT cause autosomal recessive narcolepsy.

Wejdan Hakami, Farah Thabet, Amal Alhashem

|Sep 09, 2020

Problem-solving in clinical practice: breathing difficulty and muscle weakness following allogeneic haematopoietic stem cell transplantation.

Bashaer Albulushi, Farah Thabet, Saad Alshahwan

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Frequent Collaborators

2 joint publications

Fowzan S Alkuraya

2 joint publications

Peter Bauer

2 joint publications

Majid Alfadhel

1 joint publications

Christian Beetz

1 joint publications

Amal Alhashem

1 joint publications

Aly Elsyed

1 joint publications

Farah Thabet

1 joint publications

Javier Martini

1 joint publications

Mohthash Musambil

1 joint publications

Farhan Javed Dar

Frequent Collaborators

2 joint publications

Fowzan S Alkuraya

2 joint publications

Peter Bauer

2 joint publications

Majid Alfadhel

1 joint publications

Christian Beetz

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