Zobrazeno 1 - 10
of 98
pro vyhledávání: '"Hind Dehbi"'
Autor:
Rachid Noureddine, Hanâ Baba, Safaa Aqillouch, Karima Abounouh, Oumaima Laazaazia, Mohcine Elmessaoudi-Idrissi, Fatima Zohra Bahmani, Ikram Allah Tanouti, Ahd Ouladlahsen, M’hammed Sarih, Hind Dehbi, Sayeh Ezzikouri
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-11 (2024)
Abstract The symptoms of SARS-CoV-2 infection vary widely, ranging from asymptomatic cases to severe forms marked by acute respiratory distress syndrome, multi-organ damage, and fatalities. Studies indicate a correlation between specific genes and su
Externí odkaz:
https://doaj.org/article/c53fe762f2ca4dada8256ce9c51ff391
Autor:
Chaimae El Mahdaoui, Nezha Hda, Bouchra Oukkache, Hind Dehbi, Nisrine Khoubila, Abdellah Madani, Siham Cherkaoui
Publikováno v:
Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-5 (2023)
Abstract Background Acute lymphoblastic leukemia is the most common childhood cancer, with an 80% frequency in children between 1 and 10 years old. The outcome and prognosis of acute lymphoblastic leukemia in children depends on various factors, such
Externí odkaz:
https://doaj.org/article/6d064fcb0ba2483e862517959cd005db
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:
Brehima Diakite, Yaya Kassogue, Mamoudou Maiga, Guimogo Dolo, Oumar Kassogue, Jane L. Holl, Brian Joyce, Jun Wang, Kadidiatou Cisse, Fousseyni Diarra, Mamadou L. Keita, Cheick B. Traore, Bakarou Kamate, Sidi B. Sissoko, Bourama Coulibaly, Adama S. Sissoko, Drissa Traore, Fatoumata M. Sidibe, Sekou Bah, Ibrahim Teguete, Madani Ly, Sellama Nadifi, Hind Dehbi, Kyeezu Kim, Robert Murphy, Lifang Hou
Publikováno v:
Genetics Research, Vol 2023 (2023)
Methylenetetrahydrofolate reductase (MTHFR) plays a major role in the metabolism of folates and homocysteine, which in turn can affect gene expression and ultimately promote the development of breast cancer. Thus, mutations in the MTHFR gene could in
Externí odkaz:
https://doaj.org/article/c6e4b6a63bd044518455cbf06f904673
Autor:
Sanaa Nassereddine, Rachida Habbal, Yaya Kassogue, Ait Boujmia Oum Kaltoum, Korchi Farah, Haraka Majda, Abou Elfath Rhizlane, Sellama Nadifi, Hind Dehbi
Publikováno v:
Annals of Human Biology, Vol 48, Iss 7-8, Pp 585-589 (2021)
Background Essential hypertension (EH) results from a complex interaction between environmental factors and an individual’s genetic background. Aim To assess the relationship between polymorphisms in GSTM1 and GSTT1 and the risk of EH. Subjects and
Externí odkaz:
https://doaj.org/article/4b799d203c724600a5aee317ea2bbc0f
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:
Oum Kaltoum Ait Boujmia, Sellama Nadifi, Hind Dehbi, Yaya Kassogue, Mouna Lamchahab, Asma Quessar
Publikováno v:
Middle East Journal of Cancer, Vol 11, Iss 2, Pp 127-139 (2020)
Background: Acute myeloid leukemia (AML) is a complex disease that is linked to genetic and environmental factors. The gluthatione S-transferase (GST) is a family of enzymes that play a crucial role in the detoxification of carcinogens. These compoun
Externí odkaz:
https://doaj.org/article/5f94afa51b42499bb65ac85bc8b3bbee
Publikováno v:
IBRO Reports, Vol 5, Iss , Pp 133-136 (2018)
Glioblastoma is the most aggressive malignant type of central nervous system tumors. The literature review revealed that the most common genetic abnormalities in primary and secondary glioblastomas are IDH1 / 2 mutations, p53 mutations, and overexpre
Externí odkaz:
https://doaj.org/article/4e45c51b12774c83b4672ba3820596f5
Autor:
Fatima Zahra Outtaleb, Ghizlane Jabrane, Rachida Errahli, Nora Imelloul, Nadia Serbati, Hind Dehbi
Publikováno v:
The Pan African Medical Journal, Vol 37, Iss 309 (2020)
La trisomie 18 est une maladie chromosomique, dû à la présence d´un chromosome 18 surnuméraire. Les nourrissons atteints de trisomie 18 ont un taux de mortalité élevé, secondaire aux malformations létales associées à ce syndrome. L´object
Externí odkaz:
https://doaj.org/article/c29b105e6c9f4c71b24bd13d0229758d