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Page 1
Status dystonicus in childhood.
Touati N, Ben Rhouma H, Kraoua I, Klaa H, Turki I, Gouider-Khouja N. Touati N, et al. Among authors: klaa h. Tunis Med. 2015 Dec;93(12):756-9. Tunis Med. 2015. PMID: 27249384 Free article.
SQSTM1 mutation: Description of the first Tunisian case and literature review.
Akkari M, Kraoua I, Klaa H, Benrhouma H, Ben Younes T, Rouissi A, Chaabouni M, Ben Youssef-Turki I. Akkari M, et al. Among authors: klaa h. Mol Genet Genomic Med. 2020 Dec;8(12):e1543. doi: 10.1002/mgg3.1543. Epub 2020 Nov 2. Mol Genet Genomic Med. 2020. PMID: 33135846 Free PMC article. Review.
Hypomyelination and Congenital Cataract: Clinical, Imaging, and Genetic Findings in Three Tunisian Families and Literature Review.
Kraoua I, Bouyacoub Y, Drissi C, Chargui M, Rebai I, Chebil A, Klaa H, Benrhouma H, Hassen A, Gouider-Khouja N, Abdelhak S, Boespflug-Tanguy O, Youssef-Turki IB, Dorboz I. Kraoua I, et al. Among authors: klaa h. Neuropediatrics. 2021 Aug;52(4):302-309. doi: 10.1055/s-0041-1728654. Epub 2021 Jun 30. Neuropediatrics. 2021. PMID: 34192786 Review.
[Botulinum toxin in the management of spasticity in children].
Benrhouma H, Yacoubi J, Kraoua I, Klaa H, Ben Youssef-Turki I, Gouider-Khouja N. Benrhouma H, et al. Among authors: klaa h. Rev Neurol (Paris). 2014 Aug-Sep;170(8-9):541-7. doi: 10.1016/j.neurol.2014.05.004. Epub 2014 Jun 20. Rev Neurol (Paris). 2014. PMID: 24953170 French.
Pyridoxine-dependent epilepsy: A novel mutation in a Tunisian child.
Ben Younes T, Kraoua I, Benrhouma H, Nasrallah F, Ben Achour N, Klaa H, Hassen-Rouissi A, Drissi C, Benoist JF, Ben Youssef-Turki I. Ben Younes T, et al. Among authors: klaa h. Arch Pediatr. 2017 Mar;24(3):241-243. doi: 10.1016/j.arcped.2016.11.019. Epub 2017 Jan 25. Arch Pediatr. 2017. PMID: 28131559
29 results