Ichraf Kraoua[Author] - Search Results

Year	Number of Results
2009	3
2010	2
2011	2
2012	3
2013	4
2014	4
2015	7
2016	2
2017	3
2018	4
2019	3
2020	2
2021	6
2022	4
2023	5
2024	3

1

MPC2 variants disrupt mitochondrial pyruvate metabolism and cause an early-onset mitochondriopathy.

Pujol C, Lebigot E, Gaignard P, Galai S, Kraoua I, Bault JP, Dard R, Youssef-Turki IB, Omar S, Boutron A, Wai T, Slama A. Pujol C, et al. Among authors: kraoua i. Brain. 2023 Mar 1;146(3):858-864. doi: 10.1093/brain/awac444. Brain. 2023. PMID: 36417180 Free PMC article.

2

Plasma G_M2 ganglioside potential biomarker for diagnosis, prognosis and disease monitoring of GM2-Gangliosidosis.

Blondel A, Kraoua I, Marcelino C, Khrouf W, Schlemmer D, Ganne B, Caillaud C, Fernández-Eulate G, Turki IBY, Dauriat B, Bonnefont-Rousselot D, Nadjar Y, Lamari F. Blondel A, et al. Among authors: kraoua i. Mol Genet Metab. 2023 Feb;138(2):106983. doi: 10.1016/j.ymgme.2022.106983. Epub 2022 Dec 26. Mol Genet Metab. 2023. PMID: 36709536

3

Movement disorders in neuro-metabolic diseases.

Gouider-Khouja N, Kraoua I, Benrhouma H, Fraj N, Rouissi A. Gouider-Khouja N, et al. Among authors: kraoua i. Eur J Paediatr Neurol. 2010 Jul;14(4):304-7. doi: 10.1016/j.ejpn.2009.11.005. Epub 2009 Dec 16. Eur J Paediatr Neurol. 2010. PMID: 20015670 Review.

4

Pediatric Neurotuberculosis: A cases series and review of the literature.

Jamoussi M, Benrhouma H, Miladi Z, Ben Younes T, Klaa H, Rouissi A, Kraoua I, Ben Youssef I. Jamoussi M, et al. Among authors: kraoua i. Eur J Paediatr Neurol. 2023 Mar;43:6-11. doi: 10.1016/j.ejpn.2023.01.012. Epub 2023 Feb 1. Eur J Paediatr Neurol. 2023. PMID: 36739787 Review.

5

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. Neuropediatrics. 2021 Aug;52(4):302-309. doi: 10.1055/s-0041-1728654. Epub 2021 Jun 30. Neuropediatrics. 2021. PMID: 34192786 Review.

6

Acute Movement Disorders in Childhood: A Cohort Study and Review of the Literature.

Benrhouma H, Nasri A, Klaa H, Ben Achour N, Rouissi A, Kraoua I, Turki I. Benrhouma H, et al. Among authors: kraoua i. Pediatr Emerg Care. 2021 Nov 1;37(11):e719-e725. doi: 10.1097/PEC.0000000000002017. Pediatr Emerg Care. 2021. PMID: 34469400 Review.

7

Status dystonicus in childhood.

Touati N, Ben Rhouma H, Kraoua I, Klaa H, Turki I, Gouider-Khouja N. Touati N, et al. Among authors: kraoua i. Tunis Med. 2015 Dec;93(12):756-9. Tunis Med. 2015. PMID: 27249384

8

Muscle-Specific Kinase Autoimmune Myasthenia Gravis: Report of a Pediatric Case and Literature Review.

Ben Younes T, Benrhouma H, Klaa H, Ben Aoun R, Rouissi A, Ben Ahmed M, Kraoua I, Ben Youssef-Turki I. Ben Younes T, et al. Among authors: kraoua i. Neuropediatrics. 2019 Apr;50(2):116-121. doi: 10.1055/s-0038-1676514. Epub 2018 Dec 21. Neuropediatrics. 2019. PMID: 30577044 Review.

9

X-linked Adrenoleukodystrophy, The Tunisian Experience.

Nasrallah F, Kraoua I, Zidi W, Omar S, Sanhaji H, Feki M, Ben Youssef IT, Kaabachi N. Nasrallah F, et al. Among authors: kraoua i. Clin Lab. 2015;61(10):1531-6. doi: 10.7754/clin.lab.2015.150318. Clin Lab. 2015. PMID: 26642716

10

Postencephalitic parkinsonism and selective involvement of substantia nigra in childhood.

Rebai I, Ben Rhouma H, Kraoua I, Klaa H, Rouissi A, Ben Youssef-Turki I, Gouider-Khouja N. Rebai I, et al. Among authors: kraoua i. Brain Dev. 2015 Jan;37(1):153-7. doi: 10.1016/j.braindev.2014.03.009. Epub 2014 Apr 16. Brain Dev. 2015. PMID: 24745788 Review.

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