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Arginine:glycine amidinotransferase (AGAT) deficiency: Clinical features and long term outcomes in 16 patients diagnosed worldwide.
Stockler-Ipsiroglu S, Apatean D, Battini R, DeBrosse S, Dessoffy K, Edvardson S, Eichler F, Johnston K, Koeller DM, Nouioua S, Tazir M, Verma A, Dowling MD, Wierenga KJ, Wierenga AM, Zhang V, Wong LJ. Stockler-Ipsiroglu S, et al. Among authors: tazir m. Mol Genet Metab. 2015 Dec;116(4):252-9. doi: 10.1016/j.ymgme.2015.10.003. Epub 2015 Oct 17. Mol Genet Metab. 2015. PMID: 26490222 Free article.
Ataxia with oculomotor apraxia type 2: a clinical and genetic study of 19 patients.
Tazir M, Ali-Pacha L, M'Zahem A, Delaunoy JP, Fritsch M, Nouioua S, Benhassine T, Assami S, Grid D, Vallat JM, Hamri A, Koenig M. Tazir M, et al. Among authors: m zahem a. J Neurol Sci. 2009 Mar 15;278(1-2):77-81. doi: 10.1016/j.jns.2008.12.004. Epub 2009 Jan 11. J Neurol Sci. 2009. PMID: 19141356
Phenotypic variability in giant axonal neuropathy.
Tazir M, Nouioua S, Magy L, Huehne K, Assami S, Urtizberea A, Grid D, Hamadouche T, Rautenstrauss B, Vallat JM. Tazir M, et al. Neuromuscul Disord. 2009 Apr;19(4):270-4. doi: 10.1016/j.nmd.2009.01.011. Epub 2009 Feb 23. Neuromuscul Disord. 2009. PMID: 19231187
Multicenter transversal two-phase study to determine a national prevalence of epilepsy in Algeria.
Moualek D, Pacha LA, Abrouk S, Kediha MI, Nouioua S, Aissa LA, Bellatache M, Belarbi S, Slimani S, Khennouf H, Fellahi L, El Amine Hamimed M, Benali N, Chekkour MC, Maamoun R, Dameche R, Assami S, Tazir M. Moualek D, et al. Among authors: tazir m. Neuroepidemiology. 2012;39(2):131-4. doi: 10.1159/000339637. Epub 2012 Aug 9. Neuroepidemiology. 2012. PMID: 22889740
Nerve Biopsy Is Still Useful in Some Inherited Neuropathies.
Duchesne M, Mathis S, Richard L, Magdelaine C, Corcia P, Nouioua S, Tazir M, Magy L, Vallat JM. Duchesne M, et al. Among authors: tazir m. J Neuropathol Exp Neurol. 2018 Feb 1;77(2):88-99. doi: 10.1093/jnen/nlx111. J Neuropathol Exp Neurol. 2018. PMID: 29300988 Review.
112 results