Brahim Tabarki
Overview
Explore the profile of Brahim Tabarki including associated specialties, affiliations and a list of published articles.
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Articles
86
Citations
1254
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Recent Articles
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Almutair M, Thabet F, Hundallah K, Tabarki B
Mol Genet Metab
. 2024 Sep;
143(1-2):108574.
PMID: 39236564
No abstract available.
3.
Alsafh R, Alhashem A, Elsyed A, Yuksel Z, Graiess-Tlili K, Hundallah K, et al.
Neurol Genet
. 2024 Jul;
10(4):e200172.
PMID: 39040917
Background And Objectives: Noncentrosomal microtubules are essential cytoskeletal filaments that are important for neurite formation, axonal transport, and neuronal migration. They require stabilization by microtubule minus-end-targeting proteins including the CLASP...
4.
Hakami W, Thabet F, Alhashem A, Alghamdi A, Alshahwan S, Alkuraya F, et al.
Neurogenetics
. 2024 Jan;
25(2):79-83.
PMID: 38240911
Narcolepsy with cataplexy is a complex disease with both genetic and environmental risk factors. To gain further insight into the homozygous HCRT-related narcolepsy, we present a case series of five...
5.
Assaleh Y, Tabarki B
Pediatr Neurol
. 2023 Oct;
149:141-144.
PMID: 37879139
Background: Variegate porphyria is caused by mutations in the PPOX gene; it usually presents in adolescents and adults as an autosomal dominant condition, with cutaneous features or acute peripheral and/or...
6.
Himmelreich N, Bertoldi M, Alfadhel M, Alghamdi M, Anikster Y, Bao X, et al.
Mol Genet Metab
. 2023 Jul;
139(4):107647.
PMID: 37453860
No abstract available.
7.
Himmelreich N, Bertoldi M, Alfadhel M, Alghamdi M, Anikster Y, Bao X, et al.
Mol Genet Metab
. 2023 Jun;
139(3):107624.
PMID: 37348148
Aromatic L-amino acid decarboxylase (AADC) deficiency is a rare autosomal recessive genetic disorder affecting the biosynthesis of dopamine, a precursor of both norepinephrine and epinephrine, and serotonin. Diagnosis is based...
8.
Thabet F, Daya A, Zayani S, Chouchane C, Tabarki B, Chouchane S
Pediatr Neurol
. 2023 May;
144:97-98.
PMID: 37201243
The etiology of acute flaccid myelitis (AFM) has yet to be determined. Viral link has been suggested, but severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-associated AFM has not been reported...
9.
de Sainte Agathe J, Pode-Shakked B, Naudion S, Michaud V, Arveiler B, Fergelot P, et al.
J Med Genet
. 2023 May;
60(10):999-1005.
PMID: 37185208
Purpose: was previously implicated in periventricular nodular heterotopia (PVNH) in only five individuals and systematic clinical characterisation was not available. The aim of this study is to provide a comprehensive...
10.
Abukhaled M, Al Muqbil M, Alghamdi M, Hundallah K, Suleiman J, Ben-Omran T, et al.
Eur J Pediatr
. 2023 May;
182(6):2547-2548.
PMID: 37140704
No abstract available.