Zobrazeno 1 - 10
of 283
pro vyhledávání: '"Tazzite A"'
Publikováno v:
SAGE Open Medical Case Reports, Vol 12 (2024)
ATRX gene (alpha-thalassemia mental retardation X-linked) encodes for a chromatin remodeler and regular transcription protein, part of the SNF2 family of chromatin remodeling proteins. Mutations in this gene have been associated with severe syndromes
Externí odkaz:
https://doaj.org/article/60889a390d2d4cc9b55a7f89a7f5640a
Autor:
Sidibe, Mariam1 (AUTHOR) mariam.sidibe-etu@etu.univh2c.ma, Tazzite, Amal1,2 (AUTHOR), Jouhadi, Hassan1,3 (AUTHOR), Dehbi, Hind1,4 (AUTHOR)
Publikováno v:
Journal of Current Oncology. Dec2023, Vol. 6 Issue 2, p61-67. 7p.
Publikováno v:
SAGE Open Medical Case Reports; 9/14/2024, p1-4, 4p
Publikováno v:
Journal of International Medical Research, Vol 51 (2023)
Variants in SCN8A are associated with several diseases, including developmental and epileptic encephalopathy, intermediate epilepsy or mild-to-moderate developmental and epileptic encephalopathy, self-limited familial infantile epilepsy, neurodevelop
Externí odkaz:
https://doaj.org/article/9d32b47ce7c7469ba22d37623cbca9dd
Autor:
Bouzroud, Wafaa1 (AUTHOR) wafaabouzroud55@gmail.com, Tazzite, Amal2 (AUTHOR), Berrada, Sarah1 (AUTHOR), Gazzaz, Bouchaïb2,3 (AUTHOR), Dehbi, Hind1,2 (AUTHOR)
Publikováno v:
Clinical Pathology. 9/16/2022, Vol. 15, p1-5. 5p.
Publikováno v:
Clinical Pathology, Vol 15 (2022)
Rett syndrome (RTT) is a rare X-linked syndrome that predominantly affects girls. It is characterized by a severe and progressive neurodevelopmental disorder with neurological regression and autism spectrum features. The Rett syndrome is associated w
Externí odkaz:
https://doaj.org/article/a629e2377237432385734e476266821d
Publikováno v:
SAGE Open Medical Case Reports, Vol 10 (2022)
Complement Factor I deficiency is a very rare autosomal recessive disease, with only 38 cases reported in the literature. It is caused by a homozygous mutation in the CFI gene (complement Factor I), which encodes for the Factor I protein, an importan
Externí odkaz:
https://doaj.org/article/fb8af2fc41dc4b85b3f8ab309b3c16ac
Autor:
Samiha Jaddaoui, Hanaa Bencharef, Sara Addakiri, Hind Dehbi, Amal Tazzite, Mouna Lamchahab, Bouchra Oukkache
Publikováno v:
Annales de Biologie Clinique. 81:136-144
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e3d0653436c9c4d1e6afded476ebd7d
https://doi.org/10.1684/abc.2023.1798
https://doi.org/10.1684/abc.2023.1798
Autor:
Fatiha Salmi, Fatima Maachi, Amal Tazzite, Rachid Aboutaib, Jamal Fekkak, Houssine Azeddoug, Hassan Jouhadi
Publikováno v:
PLoS ONE, Vol 16, Iss 7, p e0254101 (2021)
Prostate cancer is the most common male cancer in Morocco. Although sporadic forms account for a large proportion of patients, familial forms of prostate cancer are observed in 20% of cases and about 5% are due to hereditary transmission. Indeed, ger
Externí odkaz:
https://doaj.org/article/f267dd16896d42109772f469e8b5d099
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