Zobrazeno 1 - 10
of 82
pro vyhledávání: '"Moez Gribaa"'
Autor:
Yosr Hamdi, Mediha Trabelsi, Kais Ghedira, Maroua Boujemaa, Ikhlas Ben Ayed, Cherine Charfeddine, Amal Souissi, Imen Rejeb, Wafa Kammoun Rebai, Chaima Hkimi, Fadoua Neifar, Nouha Jandoubi, Rahma Mkaouar, Melek Chaouch, Ayda Bennour, Selim Kamoun, Hend Chaker Masmoudi, Nabil Abid, Maha Mezghani Khemakhem, On behalf of the GTCA Consortium, Saber Masmoudi, Ali Saad, Lamia BenJemaa, Alia BenKahla, Samir Boubaker, Ridha Mrad, Hassen Kamoun, Sonia Abdelhak, Moez Gribaa, Neila Belguith, Najla Kharrat, Dorra Hmida, Ahmed Rebai
Publikováno v:
Genome Medicine, Vol 16, Iss 1, Pp 1-19 (2024)
Abstract Background Key discoveries and innovations in the field of human genetics have led to the foundation of molecular and personalized medicine. Here, we present the Genome Tunisia Project, a two-phased initiative (2022–2035) which aims to del
Externí odkaz:
https://doaj.org/article/d62ab665af394533b93e1685ae93dc5f
Autor:
Khouloud Rjiba, Soumaya Mougou-Zerelli, Imen hadj Hamida, Ghada Saad, Bochra Khadija, Afef Jelloul, Wafa Slimani, Yosra Hasni, Sarra Dimassi, Hela Ben khelifa, Amira Sallem, Molka Kammoun, Hamza Hadj Abdallah, Moez Gribaa, Joelle Bignon-Topalovic, Sami Chelly, Hédi Khairi, Mohamed Bibi, Maha Kacem, Ali Saad, Anu Bashamboo, Kenneth McElreavey
Publikováno v:
Reproductive Biology and Endocrinology, Vol 21, Iss 1, Pp 1-13 (2023)
Abstract Background Forty-six ,XY Differences/Disorders of Sex Development (DSD) are characterized by a broad phenotypic spectrum ranging from typical female to male with undervirilized external genitalia, or more rarely testicular regression with a
Externí odkaz:
https://doaj.org/article/886ed788882242ce929a902fe1717027
Autor:
Hamza Elfekih, Asma Ben Abdelkrim, Hajer Marzouk, Ghada Saad, Ayoub Gasmi, Moez Gribaa, Hounaida Zaghouani, Yosra Hasni, Amel Maaroufi
Publikováno v:
Clinical Case Reports, Vol 9, Iss 3, Pp 1655-1662 (2021)
Abstract The presence of prostatic tissue, in addition to uterus and adrenal tumors, is possible in 46XX patients with CAH. Lesions of these organs are usually benign. However, complications including prostate and adrenal cancer were also reported.
Externí odkaz:
https://doaj.org/article/c25181e2326d47d49f044ab4aeff8753
Autor:
Marwa Mahdouani, Slim Ben Ahmed, Fahmi Hmila, Henda Rais, Rihab Ben Sghaier, Hanene Saad, Mariem Ben Said, Saber Masmoudi, Dorra Hmida, Angela Brieger, Stefan Zeuzem, Ali Saad, Moez Gribaa, Guido Plotz
Publikováno v:
PLoS ONE, Vol 17, Iss 12, p e0278283 (2022)
Lynch syndrome is a heritable condition caused by a heterozygous germline inactivating mutation of the DNA mismatch repair (MMR) genes, most commonly the MLH1 gene. However, one third of the identified alterations are missense variants, for which the
Externí odkaz:
https://doaj.org/article/2b67d7a74efa41599d01534fef4f9f3e
Autor:
Hamza Elfekih, Asma Ben Abdelkrim, Hajer Marzouk, Ghada Saad, Moez Gribaa, Yosra Hasni, Amel Maaroufi
Publikováno v:
The Pan African Medical Journal, Vol 36, Iss 226 (2020)
Congenital adrenal hyperplasia refers to a group of rare genetic disorders affecting the adrenal glands. 21-hydroxylase deficiency is the most prevalent and the most studied cause while the remaining enzymatic defects are less common, accounting for
Externí odkaz:
https://doaj.org/article/76ed89c2080940ee8badea3e038e61e4
Autor:
Eliane Chouery, Sandra Corbani, Jaleleddine Dahmen, Leila Zouari, Moez Gribaa, Nadia Leban, Jemni Ben Chibani, Gérard Lefranc, Ali Saad, Amel Haj Khelil, Andoni Urtizberea, André Mégarbané
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 18, Iss 3, Pp 299-303 (2017)
Progressive pseudorheumatoid dysplasia is a rare autosomal recessive spondyloepiphyseal dysplasia characterized by predominant involvement of articular cartilage with progressive joint stiffness and enlargement in the absence of inflammation. Short s
Externí odkaz:
https://doaj.org/article/3e36a88cf41d4bf480912c91ae5e0c6e
Autor:
Imen CHATTI, Jean-Baptiste WOILLARD, Amira MILI, Isabelle CREVEAUX, Ilhem BEN CHARFEDDINE, Jihène FEKI, Sarah LANGLAIS, Leila BEN FATMA, Ali SAAD, Moez GRIBAA, Frédéric LIBERT
Publikováno v:
Iranian Journal of Public Health, Vol 46, Iss 12 (2017)
Background: Pain and its opioid treatments are complex measurable traits. Responses to morphine in terms of pain control is likely to be determined by many factors, including the underlying pain sensitivity of the patient, along with nature and exten
Externí odkaz:
https://doaj.org/article/d33a686ecff44f2fb6bcdb8081c8b973
Autor:
Abdelbasset Amara, Ilhem Ben Charfeddine, Houda Ghédir, Ons Mamaï, Saloua Jemni-Yacoub, Larbi Chaieb, Ali Saad, Molka Chadli-Chaieb, Moez Gribaa
Publikováno v:
Iranian Journal of Public Health, Vol 44, Iss 3 (2015)
Background: HNF4A-p.I463Vvariant, reported previously in two distinct families suspected of MODY-1, is assessed in this report to determine whether it is a mutation or a polymorphism (frequency >1%). Methods: 200 Tunisian healthy people were screene
Externí odkaz:
https://doaj.org/article/90d3fc4e8d3848d3aaf8489fcb1ed9d9
Publikováno v:
Iranian Journal of Public Health, Vol 43, Iss 7 (2014)
Externí odkaz:
https://doaj.org/article/c3d913b0bf914a5c9843e44773f801cc
Autor:
Asma Ben Abdelkrim, Hounaida Zaghouani, Ghada Saad, Ayoub Gasmi, Yosra Hasni, Hamza Elfekih, Moez Gribaa, H. Marzouk, Amel Maaroufi
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 9, Iss 3, Pp 1655-1662 (2021)
Clinical Case Reports, Vol 9, Iss 3, Pp 1655-1662 (2021)
The presence of prostatic tissue, in addition to uterus and adrenal tumors, is possible in 46XX patients with CAH. Lesions of these organs are usually benign. However, complications including prostate and adrenal cancer were also reported.