Brahim Tabarki
8PUBLICATIONS
33CO-AUTHORS
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Publications (8)
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|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 CLASP1 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
