Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Maria Kabbage"'
Autor:
Nadia Kheriji, Thouraya Dakhlaoui, Wafa Kamoun Rebai, Sonia Maatoug, Mohamed Taher Thabet, Thouraya Mellah, Mehdi Mrad, Hajer Trabelsi, Manel Soltani, Maria Kabbage, Hichem Ben Hassine, Afef Hadj Salah Bahlous, Faten Mahjoub, Henda Jamoussi, Abdelmajid Abid, Sonia Abdelhak, Rym Kefi
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-10 (2023)
Abstract Diabetes and hypertension are a serious public health problem worldwide. In the last decades, prevalence of these two metabolic diseases has dramatically increased in the Middle East and North Africa region, especially in Tunisia. This study
Externí odkaz:
https://doaj.org/article/69412dadefa24676af55703531bc28f2
Autor:
Azer Farah, Maria Kabbage, Salsabil Atafi, Amira Jaballah Gabteni, Mouadh Barbirou, Mouna Madhioub, Lamine Hamzaoui, Mousadak Azzouz Mohamed, Hassen Touinsi, Asma Ouakaa Kchaou, Emna Chelbi, Samir Boubaker, Rahma Ben Abderrazek, Balkiss Bouhaouala-Zahar
Publikováno v:
BMC Cancer, Vol 20, Iss 1, Pp 1-9 (2020)
Abstract Background Gastric and colorectal cancers are the most common malignant tumours, leading to a significant number of cancer-related deaths worldwide. Recently, increasing evidence has demonstrated that cancer cells exhibit a differential expr
Externí odkaz:
https://doaj.org/article/9eceb0e043cf47dfb58bce4cca623e8a
Autor:
Amira Jaballah-Gabteni, Haifa Tounsi, Maria Kabbage, Yosr Hamdi, Sahar Elouej, Ines Ben Ayed, Mouna Medhioub, Moufida Mahmoudi, Hamza Dallali, Hamza Yaiche, Nadia Ben Jemii, Afifa Maaloul, Najla Mezghani, Sonia Abdelhak, Lamine Hamzaoui, Mousaddak Azzouz, Samir Boubaker
Publikováno v:
Journal of Translational Medicine, Vol 17, Iss 1, Pp 1-13 (2019)
Abstract Background Lynch syndrome (LS) is a highly penetrant inherited cancer predisposition syndrome, characterized by autosomal dominant inheritance and germline mutations in DNA mismatch repair genes. Despite several genetic variations that have
Externí odkaz:
https://doaj.org/article/a09c2b09894543cfad966473641e0ab2
Autor:
benider, Abdellatif, El-hamouchi, Adil, Sonia, AIT YOUNES, Kahla, Alia Ben, Abdelmalik, AMIMER, Zine, AMIR, charif, Jaballah, Amira, Louiza, Amira, GIHBID, Amina, Achouak, BACHIR, Djihad, BELABDI, Said, BELHADEF, Rafika, BELNOUI, Ayed, Belarbi, Nadia, Benchakroune, Nadia, Benchakroun, Meriem, BENINAL, Radja, BENKALI, Asma, BENSIHAMDI, Hichem, BENYOUCEF, Thouraya, BENDIMRED, Nadir, Bensouf, Rafika, BENNOUI, Yosra, Berrazegua, Latefa, Biskri, Saida, BOUAOUNI, Meriem, BOUANIKA, Abderezzak, Bouamra, Hanen, Bouaziz, Zohra, Boudinar Fatma, Sabrina, Bouhara, Nadir, Boussouf, Saber, Boutayeb, Adda, BOUNEDJAR, Omar, Chabati, Cherine, Charfeddine, Dalia, Chilla, Mehemmai, Chiraz, Bouabid, Cyrine, Souad, Dahnane, Soraya, DIAB, Adlane, Dib Hocine, Wider, Dorra, Fawzi, DERRAR, Amina, ELKEBOUB, Hicham, EL ATTAR, Elmostafa, EL FAHIME, Djazia, ELHADEF, Fehri, Emna, Hakkou, Farid, Hadjam, Farida, Mamboisse, Fanny, Widad, GAIS, Merzak, GHARNAOUT, Nidhal, Guessoum Amir, Farida, HADJAM, SAHRAOUI, HADJ, Rachdi, Haifa, Yaiche, Hamza, Leila, HANNACHI, Mahfouf, Hassan, Bouguerra, Hend, Attar, Hicham El, Hassine, Hichem Ben, Filali, Houda, Harmak, Houda, Kanaane, Houda, Benamri, Ichrak, Alami, Imane El, Reda, KASSA, Bendahhou, Karima, Errafii, Khaoula, Bairi, Khalid El, Wafaa, Khaali, Mehdi, KARKOURI, Maria, Kabbage, Wafa, Kammoun, Houda, Kanaane, Reda, Kassa, Narimane, LAOUAR, Biskri, Latefa, Amira, Louiza, Marie, Louise, Chevalier, Charion, Nabila, MALOUM, Monot, Marc, Saadi, Mariem, Campone, Mario, Mrad, Mehdi, KARKOURI, MEHDI, Mohamed, MELIZI, Saadi, Meriem, CHAHER, Meriem, Ardhaoui, Monia, TALEB, Mourad, Jmiaa, Nadia Ben, Benchakroun, Nadia, Hadhri, Najet, SALHI, Nawel, Taoufiq, Nezha, Jandoubi, Nouha, Wahiba, OUAHIOUNE, Salima, OULDSLIMANE, BELNOUI, Rafika, Louiza, Rahman Amira, Benkhalifa, Rym, Boutaib, Saber, Boutayeb, Saber, Menif, Samia, OULDSLIMANE, Salima, Valcke, Samuel, Assia, SLIMANI, Nasr, Sonia Ben, Maatoug, Sonia, Younes, Sonia Ait, BENCHEHIDA, Souad, BEKOUACI, Souad, Sahraoui, Souha, Hassiba, Tali Maamar, Soraya, Talha, Mourad, TALEB, Fella, TERKMANI, Soraya, TALHA, Wassila, TOUISI, Kammoun, Wafa, OUAHIOUNE, Wahiba, Berrazegua, Yosra, Amel, ZEMMOUR, Sarah, ZEROUAL, AMIR, Zine Charif, Zouafi, Zineb, Hamdi, Yosr, Boujemaa, Maroua, Ben Aissa-Haj, Jihenne, Radouani, Fouzia, Khyatti, Meriem, Mighri, Najah, Hannachi, Mariem, Ghedira, Kais, Souiai, Oussema, Hkimi, Chaima, Kammoun, Mohamed Selim, Mejri, Nesrine, Bouaziz, Hanen, Beloufa, Mohamed Amine, Charoute, Hicham, Barakat, Abdelhamid, Najjar, Imène, Taniguchi, Hiroaki, Pietrosemoli, Natalia, Dellagi, Koussay, Abdelhak, Sonia, Boubaker, Mohamed Samir, Chica, Claudia, Rouleau, Etienne
Publikováno v:
In Translational Oncology June 2024 44
Autor:
Afifa Maaloul, M Mahmoudi, Maria Kabbage, Emna Chelbi, Moussadak Azzouz, Lamine Hamzaoui, Haifa Tounsi, Houcemedine Othman, Hassen Touinsi, Amal Khessiba, Houda BelFekih, Jihenne Ben Aissa-Haj, Mouna Medhioub, Sonia Abdelhak, Sarra Laarayedh, Amira Jaballah-Gabteni, Samir Boubaker, Sahar Elouej
Publikováno v:
Genes; Volume 13; Issue 8; Pages: 1355
GENES
GENES, 2022, 13 (8), ⟨10.3390/genes13081355⟩
GENES
GENES, 2022, 13 (8), ⟨10.3390/genes13081355⟩
BACKGROUND Inherited syndromic forms of digestive cancers with age occurrence before 50 seem to be relatively in higher proportions in Tunisia suggesting genetic susceptibility. Several syndromic forms are known to predispose to early onset gastric t
Autor:
Maria, Kabbage, Jihenne, Ben Aissa-Haj, Houcemeddine, Othman, Amira, Jaballah-Gabteni, Sarra, Laarayedh, Sahar, Elouej, Mouna, Medhioub, Haifa Tounsi, Kettiti, Amal, Khsiba, Moufida, Mahmoudi, Houda, BelFekih, Afifa, Maaloul, Hassen, Touinsi, Lamine, Hamzaoui, Emna, Chelbi, Sonia, Abdelhak, Mohamed Samir, Boubaker, Mohamed Mousaddak, Azzouz
Publikováno v:
Genes. 13(8)
Several syndromic forms of digestive cancers are known to predispose to early-onset gastric tumors such as Hereditary Diffuse Gastric Cancer (HDGC) and Lynch Syndrome (LS). LSII is an extracolonic cancer syndrome characterized by a tumor spectrum inc
Autor:
Jihenne Ben Aissa-Haj, Maria Kabbage, Houcemeddine Othmen, Patrick Saulnier, Haifa Tounsi Kettiti, Amira Jaballah-Gabteni, Azer Ferah, Mouna Medhioub, Amal Khsiba, Moufida Mahmoudi, Afifa Maaloul, Sonia Ben Nasr, Emna Chelbi, Sonia Abdelhak, M. Samir Boubaker, Mohamed Mousaddak Azzouz, Etienne Rouleau
Publikováno v:
Genes; Volume 13; Issue 3; Pages: 400
Mutational screening of the CDH1 gene is a standard treatment for patients who fulfill Hereditary Diffuse Gastric Cancer (HDGC) testing criteria. In this framework, the classification of variants found in this gene is a crucial step for the clinical
Autor:
Houda Belfkih, Jihenne Ben Aissa-Haj, Mohamed Samir Boubaker, Amel Khsiba, Lamine Hamzaoui, Emna Chalbi, Amira Jaballah-Gabteni, Patrick Saulnier, Hassen Touinsi, Azer Ferah, Mouna Medhioub, Sonia Abdelhak, Sonia Ben Nasr, Etienne Rouleau, Maria Kabbage, Mousaddak Azzouz, Houcemeddine Othmen, Afifa Maaloul
Background: Mutational screening of the CDH1 gene is a standard treatment for patients who meet the criteria for Hereditary Diffuse Gastric Cancer (HDGC). In this framework, the classification of variants found in this gene is a crucial step for the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79006384a2066a6df59a9a0b56b95527
https://doi.org/10.21203/rs.3.rs-617841/v1
https://doi.org/10.21203/rs.3.rs-617841/v1
Autor:
Mouadh Barbirou, Mousadak Azzouz Mohamed, Mouna Madhioub, Amira Jaballah Gabteni, Balkiss Bouhaouala-Zahar, Salsabil Atafi, Asma Ouakaa Kchaou, Lamine Hamzaoui, Azer Farah, Emna Chelbi, Hassen Touinsi, Maria Kabbage, Rahma Ben Abderrazek, Samir Boubaker
Publikováno v:
BMC Cancer
BMC Cancer, Vol 20, Iss 1, Pp 1-9 (2020)
BMC Cancer, Vol 20, Iss 1, Pp 1-9 (2020)
Background Gastric and colorectal cancers are the most common malignant tumours, leading to a significant number of cancer-related deaths worldwide. Recently, increasing evidence has demonstrated that cancer cells exhibit a differential expression of
Autor:
M Mahmoudi, Samir Boubaker, Amira Jaballah-Gabteni, Haifa Tounsi, Mousaddak Azzouz, Hamza Dallali, Hamza Yaiche, Sahar Elouej, Maria Kabbage, Ines Ben Ayed, Lamine Hamzaoui, Mouna Medhioub, Sonia Abdelhak, Afifa Maaloul, Yosr Hamdi, Nadia Ben Jemii, Najla Mezghani
Publikováno v:
Journal of Translational Medicine, Vol 17, Iss 1, Pp 1-13 (2019)
Journal of Translational Medicine
Journal of Translational Medicine, BioMed Central, 2019, 17 (1), pp.212. ⟨10.1186/s12967-019-1961-9⟩
Journal of Translational Medicine
Journal of Translational Medicine, BioMed Central, 2019, 17 (1), pp.212. ⟨10.1186/s12967-019-1961-9⟩
Background Lynch syndrome (LS) is a highly penetrant inherited cancer predisposition syndrome, characterized by autosomal dominant inheritance and germline mutations in DNA mismatch repair genes. Despite several genetic variations that have been iden