Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Mariem Ben Rekaya"'
Autor:
Firas Akrout, Ahlem Achour, Carli M. J. Tops, Richard Gallon, Rym Meddeb, Sameh Achoura, Mariem Ben Rekaya, Emna Hamdeni, Soumaya Rammeh, Ridha Chkili, Nada Mansouri, Neila Belguith, Ridha Mrad
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
Constitutional mismatch repair deficiency (CMMRD) syndrome is a rare autosomal recessive genetic disorder caused by biallelic germline mutations in one of the mismatch repair genes. Carriers are at exceptionally high risk for developing, typically in
Externí odkaz:
https://doaj.org/article/5c319bf8d8d8419f96e3348ff672efc1
Autor:
Mariem Ben Rekaya, Feryel Ksontini, Linda Bel Haj Kacem, Farah Sassi, Emna Harigua‐Souiai, Ryma Boujneh, Ahmed H'mayada, Yosra Zaimi, Mouna Ayadi, Mediha Trabelsi, Ridha Mrad, Soumaya Rammeh
Publikováno v:
Clinical Case Reports, Vol 11, Iss 6, Pp n/a-n/a (2023)
Key clinical message We report the first case of pathologic complete response (pCR) to neoadjuvant imatinib in a gastric stromal tumor harboring KIT mutations in both exons 11 and 9. The significance of this co‐occurrence is unknown and might incre
Externí odkaz:
https://doaj.org/article/348465859f9f47bca3a3dbc9997dbcd1
Autor:
Najlaa Khalat, Olfa Messaoud, Mariem Ben Rekaya, Mariem Chargui, Mohamed Zghal, Bashir Zendah, Najat Saqer, Mourad Mokni, Sonia Abdelhak, Othman A. Mohamed
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 6, Pp n/a-n/a (2023)
Abstract Background Xeroderma pigmentosum is an autosomal recessive disease characterized by a high sensitivity to UV radiations. The disease is clinically and genetically heterogeneous, thus making accurate early clinical diagnosis difficult. Althou
Externí odkaz:
https://doaj.org/article/38ec3159672749948c32a81fc0e52b3f
Autor:
Mariem Ben Rekaya, Farah Sassi, Essya Saied, Linda Bel Haj Kacem, Nada Mansouri, Sinda Zarrouk, Saifeddine Azouz, Soumaya Rammeh
Publikováno v:
PLoS ONE, Vol 18, Iss 5, p e0285413 (2023)
BackgroundThe aim of this study was to analyze PIK3CA mutations in exons 9 and 20 in breast cancers (BCs) and their association with clinicopathological characteristics.MethodsMutational analysis of PIK3CA exon 9 and 20 was performed by Sanger sequen
Externí odkaz:
https://doaj.org/article/048ddfc0907f4ea4ad3f373da1548ebd
Autor:
Yosr Hamdi, Najah Mighri, Maroua Boujemaa, Nesrine Mejri, Sonia Ben Nasr, Mariem Ben Rekaya, Olfa Messaoud, Hanen Bouaziz, Yosra Berrazega, Haifa Rachdi, Olfa Jaidane, Nouha Daoud, Aref Zribi, Jihene Ayari, Houda El Benna, Soumaya Labidi, Jamel Ben Hassouna, Abderazzek Haddaoui, Khaled Rahal, Farouk Benna, Ridha Mrad, Slim Ben Ahmed, Hamouda Boussen, Samir Boubaker, Sonia Abdelhak
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
BackgroundBreast cancer is the world’s most common cancer among women. It is becoming an increasingly urgent problem in low- and middle-income countries (LMICs) where a large fraction of women is diagnosed with advanced-stage disease and have no ac
Externí odkaz:
https://doaj.org/article/225f32cd0a4b4ec88e0e601d86e0c31b
Autor:
Yosr Hamdi, Mariem Ben Rekaya, Shan Jingxuan, Majdi Nagara, Olfa Messaoud, Amel Benammar Elgaaied, Ridha Mrad, Lotfi Chouchane, Mohamed Samir Boubaker, Sonia Abdelhak, Hamouda Boussen, Lilia Romdhane
Publikováno v:
BMC Cancer, Vol 18, Iss 1, Pp 1-14 (2018)
Abstract Background Breast cancer is the most common cancer in women worldwide. Around 50% of breast cancer familial risk has been so far explained by known susceptibility alleles with variable levels of risk and prevalence. The vast majority of thes
Externí odkaz:
https://doaj.org/article/0957321ba9cb490d8d06cf0d499519af
Autor:
Najah Mighri, Yosr Hamdi, Maroua Boujemaa, Houcemeddine Othman, Sonia Ben Nasr, Houda El Benna, Nesrine Mejri, Soumaya Labidi, Jihen Ayari, Olfa Jaidene, Hanen Bouaziz, Mariem Ben Rekaya, Ridha M’rad, Abderrazek Haddaoui, Khaled Rahal, Hamouda Boussen, Samir Boubaker, Sonia Abdelhak
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
BackgroundDeleterious mutations on BRCA1/2 genes are known to confer high risk of developing breast and ovarian cancers. The identification of these mutations not only helped in selecting high risk individuals that need appropriate prevention approac
Externí odkaz:
https://doaj.org/article/61eba045787f4423b8153172606745ad
Autor:
Yosr Hamdi, Maroua Boujemaa, Mariem Ben Rekaya, Cherif Ben Hamda, Najah Mighri, Houda El Benna, Nesrine Mejri, Soumaya Labidi, Nouha Daoud, Chokri Naouali, Olfa Messaoud, Mariem Chargui, Kais Ghedira, Mohamed Samir Boubaker, Ridha Mrad, Hamouda Boussen, Sonia Abdelhak, the PEC Consortium
Publikováno v:
Journal of Translational Medicine, Vol 16, Iss 1, Pp 1-13 (2018)
Abstract Background A family history of breast cancer has long been thought to indicate the presence of inherited genetic events that predispose to this disease. In North Africa, many specific epidemio-genetic characteristics have been observed in br
Externí odkaz:
https://doaj.org/article/4aaf76a9dd8f4e0988e7dafd8f4a7f72
Autor:
Mariem Ben rekaya, Yosr Hamdi, Houda El Benna, Nessrine Mejri, Olfa Jaidane, Jihene Ayari, Sonia Ben Nasr, Hamza Dallali, Olfa Messaoud, Rym Meddeb, Najah Mighri, Maroua Boujemaa, Mohamed Samir Boubaker, Abderazek Haddaoui, Ridha Mrad, Hamouda Boussen, Sonia Abdelhak, Soumaya Labidi
Background: Genetic risk factors of breast cancer are very heterogeneous and complex. They vary according to the familial relative risk, the age of cancer diagnosis of the index case and the age of the affected relatives.Objectives: We aimed to inves
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15e760ef9d72f032f61d225a9647584d
https://doi.org/10.21203/rs.3.rs-22989/v2
https://doi.org/10.21203/rs.3.rs-22989/v2
Autor:
Sonia Abdelhak, Yosr Hamdi, Rym Meddeb, Nessrine Mejri, Sonia Ben Nasr, Olfa Messaoud, Mariem Ben Rekaya, Hamza Dallali, Jihene Ayari, Hamouda Boussen, Olfa Jaidane, Ridha Mrad, Abderazek Haddaoui, Soumaya Labidi
Background: Genetic risk factors of breast cancer are very heterogeneous and complex. They vary according to the familial relative risk, the age of cancer diagnosis of the index case and the age of the affected relatives.Objectives: We aimed to inves
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9fcbdb3387e6cc044ace6dfb6a19bee
https://doi.org/10.21203/rs.3.rs-22989/v1
https://doi.org/10.21203/rs.3.rs-22989/v1