Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Houda Benrahma"'
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-6 (2024)
Abstract Background WAGR syndrome is a rare genetic disorder characterized by a de novo deletion of 11p13 and is usually clinically associated with Wilms’ tumor, aniridia, genitourinary anomalies, and mental retardation (W-A-G-R). Although the geno
Externí odkaz:
https://doaj.org/article/3c6bc4dc111d4b6b9b947a50b1ba0088
Autor:
Faiza Chbel, Hicham Charroute, Redouane Boulouiz, Hasna Hamdaoui, Houssein Mossafa, Houda Benrahma, Karim Ouldim
Publikováno v:
Clinical Case Reports, Vol 10, Iss 3, Pp n/a-n/a (2022)
Abstract Myoclonus–dystonia (M‐D) is a pleiotropic neuropsychiatric disorder with autosomal dominant mode of inheritance with variable severity and incomplete penetrance. Pathogenic variants in ξ‐sarcoglycan gene SGCE are the most frequently k
Externí odkaz:
https://doaj.org/article/f486de72d0eb43009a9c5bd19443f981
Autor:
Idrissa Diawara, Houda Benrahma, Nida Meskaouni, Jalila Rahoui, Fatima-Zahra Moujid, Khadija Jaras, Rachid Benmessaoud, Khadija Arouro, Zahra Aadam, Salma Nahir, Zineb Aouzal, Hajar Elguazzar, Leila Jeddan, Hind Rida, Fadoua Ousti, Jalila E. Bakkouri, Imane Smyej, Chakib Nejjari
Publikováno v:
Journal of Public Health in Africa, Vol 12, Iss 2 (2021)
Given the spread of coronavirus disease 2019 (COVID-19) and its impact on human health, laboratory confirmation of diagnosis is essential. This study examined the contribution of laboratory diagnosis to the detection of severe acute respiratory syndr
Externí odkaz:
https://doaj.org/article/21eed883ce3443fea37bb4f25c58b19b
Autor:
Hasna Hamdaoui, Oumaima Benlarroubia, Oum Kaltoum Ait Boujmia, Hossein Mossafa, Karim Ouldim, Aziza Belkhayat, Imane Smyej, Houda Benrahma, Hind Dehbi, Fatima Chegdani
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 9, Pp n/a-n/a (2020)
Abstract Background Multiple myeloma (MM) is a disease characterized by heterogeneous clinical presentations as well as complex genetic and molecular abnormalities. In MM, cytogenetic analysis is a challenge because of the low proliferation of malign
Externí odkaz:
https://doaj.org/article/1f5fda75ed0a41359efd3d2eac8a7bcd
Autor:
Meriem Laamarti, Tarek Alouane, Souad Kartti, M W Chemao-Elfihri, Mohammed Hakmi, Abdelomunim Essabbar, Mohamed Laamarti, Haitam Hlali, Houda Bendani, Nassma Boumajdi, Oussama Benhrif, Loubna Allam, Naima El Hafidi, Rachid El Jaoudi, Imane Allali, Nabila Marchoudi, Jamal Fekkak, Houda Benrahma, Chakib Nejjari, Saaid Amzazi, Lahcen Belyamani, Azeddine Ibrahimi
Publikováno v:
PLoS ONE, Vol 15, Iss 11, p e0240345 (2020)
In late December 2019, an emerging viral infection COVID-19 was identified in Wuhan, China, and became a global pandemic. Characterization of the genetic variants of SARS-CoV-2 is crucial in following and evaluating it spread across countries. In thi
Externí odkaz:
https://doaj.org/article/82192e161f4d4435be04bb6140b0103d
Autor:
Imane Morjane, Hicham Charoute, Sanaa Ouatou, Lamiae Elkhattabi, Houda Benrahma, Rachid Saile, Hassan Rouba, Abdelhamid Barakat
Publikováno v:
Cardiology Research and Practice, Vol 2020 (2020)
Purpose. Coronary artery diseases (CAD) are clinical cardiovascular events associated with dyslipidemia in common. The interaction between environmental and genetic factors can be responsible for CAD. The present paper aimed to examine the associatio
Externí odkaz:
https://doaj.org/article/4ae80b7ce2d74100ad093ab5b8f8a891
Autor:
Tarek Alouane, Meriem Laamarti, Abdelomunim Essabbar, Mohammed Hakmi, El Mehdi Bouricha, M. W. Chemao-Elfihri, Souad Kartti, Nasma Boumajdi, Houda Bendani, Rokia Laamarti, Fatima Ghrifi, Loubna Allam, Tarik Aanniz, Mouna Ouadghiri, Naima El Hafidi, Rachid El Jaoudi, Houda Benrahma, Jalil El Attar, Rachid Mentag, Laila Sbabou, Chakib Nejjari, Saaid Amzazi, Lahcen Belyamani, Azeddine Ibrahimi
Publikováno v:
Pathogens, Vol 9, Iss 10, p 829 (2020)
The COVID-19 pandemic has been ongoing since its onset in late November 2019 in Wuhan, China. Understanding and monitoring the genetic evolution of the virus, its geographical characteristics, and its stability are particularly important for controll
Externí odkaz:
https://doaj.org/article/a948dca00d934aec9d6e8d2c406ab5b8
Autor:
Abdelmajid Eloualid, Omar Abidi, Majida Charif, Brahim El Houate, Houda Benrahma, Noureddine Louanjli, Elbakkay Chadli, Maria Ajjemami, Abdelhamid Barakat, Anu Bashamboo, Ken McElreavey, Houria Rhaissi, Hassan Rouba
Publikováno v:
PLoS ONE, Vol 7, Iss 3, p e34111 (2012)
The methylenetetrahydrofolate reductase (MTHFR) gene is one of the main regulatory enzymes involved in folate metabolism, DNA synthesis and remethylation reactions. The influence of MTHFR variants on male infertility is not completely understood. The
Externí odkaz:
https://doaj.org/article/35d48c0286dd4d50918f69af77266730
Autor:
Youssef Bakri, Chakib Nejjari, Saaïd Amzazi, Malika Allali, Sanae Raoui, Bouchra Chaouni, Sofia Sehli, Najib Al Idrissi, Najwa Benslima, Nihal Habib, Islam El Jaddaoui, Houda Benrahma, Noureddine Hamamouch, Sahar El Kasmi, Kamal El Bissati, Hassan Ghazal, Salsabil Hamdi, Wissal Maher
Publikováno v:
Expert Review of Molecular Diagnostics. 21:141-160
INTRODUCTION: SARS-Cov-2 first appeared in Wuhan, China, in December 2019 and spread all over the world soon after that. Given the infectious nature ofSARS-CoV-2, fast and accurate diagnosis tools are important to detect the virus. In this review, we
Autor:
Nida Meskaouni, Jalila Rahoui, Chakib Nejjari, Imane Smyej, Jalila El Bakkouri, Hind Rida, Khadija Arouro, Idrissa Diawara, Hajar Elguazzar, Rachid Benmessaoud, Houda Benrahma, Fadoua Ousti, Salma Nahir, Khadija Jaras, Zineb Aouzal, Zahra Aadam, Fatima-Zahra Moujid, Leila Jeddan
Publikováno v:
Journal of Public Health in Africa
Journal of Public Health in Africa (2020)
Journal of Public Health in Africa (2020)
Background: Given the spread of coronavirus disease 2019 (COVID-19) and its impact on human health, laboratory confirmation of diagnosis is essential. Objective: This study examined the contribution of laboratory diagnosis to the detection of severe