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51 results

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Page 1
Genetic study of Alport syndrome in Tunisia.
Younsi ME, Achour A, Kraoua L, Nesrine M, Sayari T, Abderrahim E, Laabidi J, Zouaghi MK, Kharrat M, Gargah T, Trabelsi M, M'rad R. Younsi ME, et al. Among authors: m rad r. Pediatr Nephrol. 2025 Jan;40(1):103-116. doi: 10.1007/s00467-024-06474-7. Epub 2024 Aug 14. Pediatr Nephrol. 2025. PMID: 39138691
WDR73-related galloway mowat syndrome with collapsing glomerulopathy.
El Younsi M, Kraoua L, Meddeb R, Ferjani M, Trabelsi M, Ouertani I, Maazoul F, Abid N, Gargah T, M'rad R. El Younsi M, et al. Among authors: m rad r. Eur J Med Genet. 2019 Sep;62(9):103550. doi: 10.1016/j.ejmg.2018.10.002. Epub 2018 Oct 10. Eur J Med Genet. 2019. PMID: 30315938
[Myalgia in familial Mediterranean fever].
B'chir Hamzaoui S, Bouslama K, Abdallah M, M'rad R, M'rad S, Ben Dridi M. B'chir Hamzaoui S, et al. Among authors: m rad r. Rev Neurol (Paris). 2007 Jan;163(1):93-5. doi: 10.1016/s0035-3787(07)90360-4. Rev Neurol (Paris). 2007. PMID: 17304178 French.
TOP3B: A Novel Candidate Gene in Juvenile Myoclonic Epilepsy?
Daghsni M, Lahbib S, Fradj M, Sayeb M, Kelmemi W, Kraoua L, Kchaou M, Maazoul F, Echebbi S, Ben Ali N, Abdelhak S, M'rad R. Daghsni M, et al. Among authors: m rad r. Cytogenet Genome Res. 2018;154(1):1-5. doi: 10.1159/000486945. Epub 2018 Feb 28. Cytogenet Genome Res. 2018. PMID: 29490292
Mandibuloacral dysplasia type A in five tunisian patients.
R S, H M, M T, A A, M G, I H, E K, K M, F M, R M. R S, et al. Among authors: r m. Eur J Med Genet. 2021 Feb;64(2):104138. doi: 10.1016/j.ejmg.2021.104138. Epub 2021 Jan 8. Eur J Med Genet. 2021. PMID: 33422685
51 results