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Focal Dermal Hypoplasia: Case Series.
Mansouri M, Bouzid FZ, Amal S, Hocar O, Aboussair N. Mansouri M, et al. Among authors: aboussair n. Indian J Dermatol. 2023 Jan-Feb;68(1):122. doi: 10.4103/ijd.ijd_508_22. Indian J Dermatol. 2023. PMID: 37151234 Free PMC article.
Phenotype and molecular characterization of Wilson's disease in Morocco.
Abbassi N, Bourrahouat A, Bedoya EC, Pagan C, Qabli ME, Maidoumi S, Belmalih A, Guillaud O, Kissani N, Abkari A, Chahid I, Rafai MA, Mouane N, Kriouile Y, Aidi S, Hida M, Idrissi ML, Belahsen MF, Abkari ME, Rkain M, Ismaili Z, Sedki A, Bost M, Aboussair N, Lachaux A. Abbassi N, et al. Among authors: aboussair n. Clin Res Hepatol Gastroenterol. 2024 May;48(5):102335. doi: 10.1016/j.clinre.2024.102335. Epub 2024 Apr 6. Clin Res Hepatol Gastroenterol. 2024. PMID: 38588792
Clinical, biochemical and molecular characterization of Wilson's disease in Moroccan patients.
Lafhal K, Sabir ES, Hakmaoui A, Hammoud M, Aimrane A, Najeh S, Assiri I, Berrachid A, Imad N, Boujemaa CA, Aziz F, El Hanafi FZ, Lalaoui A, Aamri H, Boyko I, Sánchez-Monteagudo A, Espinós C, Sab IA, Aboussair N, Bourrahouat A, Fdil N. Lafhal K, et al. Among authors: aboussair n. Mol Genet Metab Rep. 2023 Jun 7;36:100984. doi: 10.1016/j.ymgmr.2023.100984. eCollection 2023 Sep. Mol Genet Metab Rep. 2023. PMID: 37323222 Free PMC article.
First characterization of LHON pedigrees in North Africa.
Bouzidi A, Aboussair N, Charif M, Amalou G, Goudenège D, Desquiret-Dumas V, Bris C, Sifeddine N, Nahili H, Elqabli M, Dafir K, Kandil M, Amati-Bonneau P, Procaccio V, Barakat A, Lenaers G. Bouzidi A, et al. Among authors: aboussair n. Eye (Lond). 2020 Nov;34(11):2138-2139. doi: 10.1038/s41433-019-0755-x. Epub 2020 Jan 2. Eye (Lond). 2020. PMID: 31896800 Free PMC article. No abstract available.
Treacher Collins syndrome: a clinical and molecular study based on a large series of patients.
Vincent M, Geneviève D, Ostertag A, Marlin S, Lacombe D, Martin-Coignard D, Coubes C, David A, Lyonnet S, Vilain C, Dieux-Coeslier A, Manouvrier S, Isidor B, Jacquemont ML, Julia S, Layet V, Naudion S, Odent S, Pasquier L, Pelras S, Philip N, Pierquin G, Prieur F, Aboussair N, Attie-Bitach T, Baujat G, Blanchet P, Blanchet C, Dollfus H, Doray B, Schaefer E, Edery P, Giuliano F, Goldenberg A, Goizet C, Guichet A, Herlin C, Lambert L, Leheup B, Martinovic J, Mercier S, Mignot C, Moutard ML, Perez MJ, Pinson L, Puechberty J, Willems M, Randrianaivo H, Szakszon K, Toutain A, Verloes A, Vigneron J, Sanchez E, Sarda P, Laplanche JL, Collet C. Vincent M, et al. Among authors: aboussair n. Genet Med. 2016 Jan;18(1):49-56. doi: 10.1038/gim.2015.29. Epub 2015 Mar 19. Genet Med. 2016. PMID: 25790162 Free article.
Union makes strength: a worldwide collaborative genetic and clinical study to provide a comprehensive survey of RD3 mutations and delineate the associated phenotype.
Perrault I, Estrada-Cuzcano A, Lopez I, Kohl S, Li S, Testa F, Zekveld-Vroon R, Wang X, Pomares E, Andorf J, Aboussair N, Banfi S, Delphin N, den Hollander AI, Edelson C, Florijn R, Jean-Pierre M, Leowski C, Megarbane A, Villanueva C, Flores B, Munnich A, Ren H, Zobor D, Bergen A, Chen R, Cremers FP, Gonzalez-Duarte R, Koenekoop RK, Simonelli F, Stone E, Wissinger B, Zhang Q, Kaplan J, Rozet JM. Perrault I, et al. Among authors: aboussair n. PLoS One. 2013;8(1):e51622. doi: 10.1371/journal.pone.0051622. Epub 2013 Jan 7. PLoS One. 2013. PMID: 23308101 Free PMC article.
15 results