Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Yamina, Sifi"'
Autor:
Assia Boulefkhad, Radja Messikh, Yamina Sifi, Houda Semra, M’zahem Abderrahim, Serradj Fatima, Boubekeur Seddik Fekraoui
Publikováno v:
Revue Neurologique. 179:S131-S132
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::133df8e14dd6545ad8201d83f54e6395
https://doi.org/10.1016/j.neurol.2023.01.628
https://doi.org/10.1016/j.neurol.2023.01.628
Autor:
Nadira, Hamdouche1,2 nadiragene25@gmail.com, Yamina, Sifi1,3, Djahida, Mahdi2,4, Imen, Dalichaouche1,5, Karima, Sifi1,6, Noureddine, Abadi1,6, Abderrahim, M' Zahem3, Dalila, Satta5
Publikováno v:
South Asian Journal of Experimental Biology. 2020, Vol. 10 Issue 3, p176-182. 7p.
Autor:
Assia Boulefkhad, Yamina Sifi, Abderahim Mzahem, Houda Semra, Samia Benhamada, Imene Lemdaoui, Seddik Fekraoui Abubakr
Publikováno v:
Revue Neurologique. 178:S60
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1071a95307758b10337e5ffa732431b8
https://doi.org/10.1016/j.neurol.2022.02.257
https://doi.org/10.1016/j.neurol.2022.02.257
Autor:
Cristina Rusu, Selma Dounia Bensemmane, Mingyan Fang, Magdalena Sandu, Lyudmilla Angelova, Marcella Neri, Veneta Bojinova, Jadranka Sekelj Fureš, Fernanda Fortunato, Ivan Litvinenko, Maria Judith Molnar, Anna Potulska-Chromik, Oussama Dendane, C. Burloiu, Samira Makri-Mokrane, Daniela Vasile, Monica Panzaru, Zhiyuan Lu, Yamina Sifi, Niculina Butoianu, Oana Alexandra Iuhas, Birute Burnyte, Butnariu Lacramioara, Rachele Rossi, Djawed Bouchenak Khelladi, Ivan Lehman, Cecilia Trabanelli, Velina Guergueltcheva, Mariela Militaru, Léna Szabó, Anna Lusakowska, Mihaela Vintan, Sanja Delin, Monica Mager, Anna Kostera-Pruszczyk, Gabriela Visa, Agnes Herczegfalvi, Yurtsever Vildan, Andriy V. Shatillo, Dmitry Vlodavets, Balint Fekete, Adela Chirita Emandi, Rita Selvatici, Ivan S. Ivanov, Francesca Gualandi, Alessandra Ferlini, Alice Margutti, Diana Epure, Theodore Kyriakides
Publikováno v:
Neurology Genetics
Neurology genetics, Philadelphia : Lippincot Williams & Wilkins, 2021, vol. 7, iss. 1, art. no. e536, p. [1-12]
Neurology: Genetics
article-version (Version of Record) 3
Neurology genetics, Philadelphia : Lippincot Williams & Wilkins, 2021, vol. 7, iss. 1, art. no. e536, p. [1-12]
Neurology: Genetics
article-version (Version of Record) 3
ObjectiveGenetic diagnosis and mutation identification are now compulsory for Duchenne (DMD) and Becker muscular dystrophies (BMD), which are due to dystrophin (DMD) gene mutations, either for disease prevention or personalized therapies. To evaluate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26d68b8b9b14e4902793ab448668394d
https://www.bib.irb.hr/1113042
https://www.bib.irb.hr/1113042
Autor:
Abdelmadjid Hamri, Karima Sifi, Isabelle Richard, Yamina Sifi, Imene Dalichaouche, Noureddine Abadi, Carinne Roudaut, Leila Rouabah
Publikováno v:
Muscle & Nerve. 56:129-135
Introduction: We report the genetic analysis of a large series of 76 Algerian patients from 65 unrelated families that presented with early onset severe muscular dystrophy and a clinical phenotype resembling Limb-girdle muscular dystrophy type 2C (LG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed25335c066d0bbcb44122b009b9b07d
https://doi.org/10.1002/mus.25443
https://doi.org/10.1002/mus.25443
Autor:
Abderahim Mzahem, Serradj Fatima, Yamina Sifi, Boubekeur Seddik Fekraoui, A. Hamri, Saddek Khellaf, Assia Boulefkhad
Publikováno v:
Revue Neurologique. 176:S10
Introduction L’epilepsie, troisieme affection neurologique invalidante du sujet âge (SA) est principalement d’origine vasculaire. Les crises epileptiques vasculaires sont separees en crises precoces (CP) et tardives (CT). Objectifs L’objectif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2bc3b90ff46753930ae41a18b4829a9
https://doi.org/10.1016/j.neurol.2020.01.072
https://doi.org/10.1016/j.neurol.2020.01.072
Autor:
Imene Dalichaouche, Karima Sifi, Abdelmadjid Hamri, Yamina Sifi, Djahida Mahdi, Nadira Hamdouche, Nouredine Abadi
Publikováno v:
Revue Neurologique. 176:S23
Introduction La dystrophie musculaire de Duchenne (DMD) et Becker (BMD) sont des troubles alleliques recessifs lies a l’X. Elles sont consecutives a des mutations affectant le gene de la dystrophine DMD. Objectifs Le but de notre etude est de rappo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe45ebcb436dd279ae5f65acf64763ae
https://doi.org/10.1016/j.neurol.2020.01.103
https://doi.org/10.1016/j.neurol.2020.01.103
Autor:
Houda Semra, Samia Benhamada, Assia Boulefkhad, Abdelmadjid Hamri, Yamina Sifi, Amina Meziani
Publikováno v:
Revue Neurologique. 175:S42-S43
Introduction La sclerose laterale amyotrophique (SLA) est une maladie neurodegenerative severe du motoneurone central et peripherique, de diagnostic generalement facile mais dans les formes atypiques et les syndromes apparentes des diagnostics differ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3281a67bd770b09b4c3031ad1ede375d
https://doi.org/10.1016/j.neurol.2019.01.133
https://doi.org/10.1016/j.neurol.2019.01.133
Publikováno v:
Revue Neurologique. 175:S137-S138
Introduction Les manifestations psychiatriques et neurologiques, telles que les crises epileptiques sont frequemment la porte d’entree de plusieurs pathologies, dont le lupus erythemateux systemique (LES) et les tuberculomes cerebraux. Observation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62b4811898ff7d1bf1f86f0cc5d43f52
https://doi.org/10.1016/j.neurol.2019.01.361
https://doi.org/10.1016/j.neurol.2019.01.361
Autor:
N Abadi, N Taghane, S. Semra, Z. Bouderda, K. Sifi, M Medjroubi, H Benmekhebi, A Hamri, R Froissart, S. Lemai, Yamina Sifi, A. Benhabiles
Publikováno v:
Journal of Neurodegenerative Diseases
Pompe’s disease is a metabolic myopathy caused by a deficiency of acid alpha-glucosidase (GAA), also called acid maltase, an enzyme that degrades lysosomal glycogen. The clinical presentation of Pompe’s disease is variable with respect to the age
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b945a99058f73578130f5320e542fc94