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Year Number of Results
2008 1
2009 5
2010 2
2011 2
2012 3
2013 6
2014 6
2015 12
2016 5
2017 7
2018 4
2019 3
2020 3
2021 6
2022 4
2023 5
2024 3

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65 results

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Page 1
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.
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.
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 Free article.
Germline homozygous missense DEPDC5 variants cause severe refractory early-onset epilepsy, macrocephaly and bilateral polymicrogyria.
Ververi A, Zagaglia S, Menzies L, Baptista J, Caswell R, Baulac S, Ellard S, Lynch S; Genomics England Research Consortium; Jacques TS, Chawla MS, Heier M, Kulseth MA, Mero IL, Våtevik AK, Kraoua I, Ben Rhouma H, Ben Younes T, Miladi Z, Ben Youssef Turki I, Jones WD, Clement E, Eltze C, Mankad K, Merve A, Parker J, Hoskins B, Pressler R, Sudhakar S, DeVile C, Homfray T, Kaliakatsos M; Ponnudas (Prab) Prabhakar; Robinson R, Keim SMB, Habibi I, Reymond A, Sisodiya SM, Hurst JA. Ververi A, et al. Among authors: kraoua i. Hum Mol Genet. 2023 Jan 27;32(4):580-594. doi: 10.1093/hmg/ddac225. Hum Mol Genet. 2023. PMID: 36067010 Free PMC 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: kraoua i. 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.
65 results