Publications by authors named "Brahim Tabarki"

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SLC25A42-Related Mitochondrial Disorder: New Cases and Literature Review.
Areej Alatawi, Omamah Alshehri, Aminah Alessa, Fuad Al Mutairi, Norah AlSaleh, Brahim Tabarki

Clin Genet· January 2026

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Clinical and Genetic Spectrum of -Related Disorders: A Retrospective Study From the Gulf Region.
Osama Muthaffar, Mashael Alsubhan, Ali Mir, Hind Alsharhan, Mariam Ayed, Brahim Tabarki

J Child Neurol· December 2025

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Time to reconsider the complex febrile seizure entity.
Hanin Alsini, Brahim Tabarki, Elaine Wirrell, Nicola Specchio

Eur J Paediatr Neurol· December 2025

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Biallelic Variants in TMEM17 Cause Meckel-Gruber Syndrome Within the Ciliopathy Spectrum.
Luba M Pardo, Javier Martini, Emir Zonic, Ligia S Almeida, Maria Iqbal, Brahim Tabarki

Clin Genet· November 2025

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Safety and effectiveness of vagus nerve stimulation in patients with drug-resistant epilepsy: a single center experience.
Ebtehal Alwazna, Jamal Abdullah, Hanin Alsini, Marahib Alshahrani, Wafa Aldhafeeri, Brahim Tabarki

Acta Epileptol· May 2025

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Biotinidase Deficiency: Report of a Tunisian Case With Neuromyelitis Optica-Like Presentation and Review of the Literature.
Abir Zioudi, Hanene Benrhouma, Maha Jamoussi, Thouraya Ben Younes, Zouhour Miladi, Brahim Tabarki

Case Rep Neurol Med· March 2025

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Advancing understanding and treatment of YWHAG-related developmental and epileptic encephalopathy.
Brahim Tabarki

Eur J Paediatr Neurol· November 2024

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CIC variants and folinic acid-responsive seizures.
Meshal Almutair, Farah Thabet, Khalid Hundallah, Brahim Tabarki

Mol Genet Metab· October 2024

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Multiplex Consanguineous Family Highlights as a Candidate Gene for Lissencephaly.
Rawan Alsafh, Amal Alhashem, Aly Elsyed, Zafer Yüksel, Kalthoum Graiess-Tlili, Brahim Tabarki

Neurol Genet· August 2024

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Bi-allelic variants in HCRT cause autosomal recessive narcolepsy.
Wejdan Hakami, Farah Thabet, Amal Alhashem, Abdulaziz Alghamdi, Saad Alshahwan, Brahim Tabarki

Neurogenetics· April 2024

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Further Characterization of the Neuroendocrine Phenotype Associated With the PPOX-Related Variegate Porphyria.
Yousef A Assaleh, Brahim Tabarki

Pediatr Neurol· December 2023

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-related disorder: phenotypic and molecular spectrum.
Jean-Madeleine de Sainte Agathe, Ben Pode-Shakked, Sophie Naudion, Vincent Michaud, Benoit Arveiler, Brahim Tabarki

J Med Genet· October 2023

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Corrigendum to: Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes.
Nastassja Himmelreich, Mariarita Bertoldi, Majid Alfadhel, Malak Ali Alghamdi, Yair Anikster, Brahim Tabarki

Mol Genet Metab· August 2023

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Acute Flaccid Myelitis in a Pediatric Patient With Coronavirus Disease 2019.
Farah Thabet, Abir Daya, Seifeddine Zayani, Chokri Chouchane, Brahim Tabarki

Pediatr Neurol· July 2023

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Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes.
Nastassja Himmelreich, Mariarita Bertoldi, Majid Alfadhel, Malak Ali Alghamdi, Yair Anikster, Brahim Tabarki

Mol Genet Metab· July 2023

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Aromatic L-amino acid decarboxylase deficiency in countries in the Middle East: a case series and literature review.
Musaad Abukhaled, Mohammed Al Muqbil, Malak Ali Alghamdi, Khalid Hundallah, Jehan Suleiman, Brahim Tabarki

Eur J Pediatr· June 2023

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Correction to: Aromatic L-amino acid decarboxylase deficiency in countries in the Middle East: a case series and literature review.
Musaad Abukhaled, Mohammed Al Muqbil, Malak Ali Alghamdi, Khalid Hundallah, Jehan Suleiman, Brahim Tabarki

Eur J Pediatr· June 2023

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Common sleep disorders in children: assessment and treatment.
Farah Thabet, Brahim Tabarki

Neurosciences (Riyadh)· April 2023

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Developmental and/or epileptic encephalopathy with spike-and-wave activation in sleep in Saudi Arabia: Electroclinical, etiologic, genetic, and outcome multicenter study.
Hanin Alsini, Abdulaziz Alghamdi, Shatha Alshafi, Khalid Hundallah, Sameer Almehmadi, Brahim Tabarki

Seizure· April 2023

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CLEC16A interacts with retromer and TRIM27, and its loss impairs endosomal trafficking and neurodevelopment.
Daphne J Smits, Jordy Dekker, Rachel Schot, Brahim Tabarki, Amal Alhashem

Hum Genet· March 2023

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First description of the MEGDEHL syndrome in the Tunisian population via whole-exome sequencing: Novel nonsense mutation in SERAC1 gene.
Rahma Felhi, Kamel Monastiri, Hayet Ben Hamida, Marwa Ammar, Fatma Zohra Chioukh, Brahim Tabarki

Int J Dev Neurosci· December 2022

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Association Between Lysine Reduction Therapies and Cognitive Outcomes in Patients With Pyridoxine-Dependent Epilepsy.
Curtis R Coughlin, Laura A Tseng, Levinus A Bok, Hans Hartmann, Emma Footitt, Brahim M Tabarki

Neurology· December 2022

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Hereditary Hyperekplexia in Saudi Arabia.
Amal Aldhilan, Afnan Alhakeem, Sumayah Al Hajjaj, Musaad Abukhalid, Hisham Aldhalaan, Brahim Tabarki

Pediatr Neurol· September 2022

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