Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Faten Talmoudi"'
Autor:
Abir Ben Haj Ali, Olfa Messaoud, Sahar Elouej, Faten Talmoudi, Wiem Ayed, Fethi Mellouli, Monia Ouederni, Sondes Hadiji, Annachiara De Sandre-Giovannoli, Valérie Delague, Nicolas Lévy, Massimo Bogliolo, Jordi Surrallés, Sonia Abdelhak, Ahlem Amouri
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Populations in North Africa (NA) are characterized by a high rate of consanguinity. Consequently, the proportion of founder mutations might be higher than expected and could be a major cause for the high prevalence of recessive genetic disorders like
Externí odkaz:
https://doaj.org/article/bb022a4210ca418a9084d7233c286fe8
Autor:
Slim Ben Ammar, Neji Tebib, Farah Ouechtati, Khaled Lasram, Marie Françoise Ben Dridi, Faten Talmoudi, Rym Kefi, Houyem Ouragini, Nizar Ben Halim, Insaf Rejeb, Olfa Messaoud, Asma Walha, Yosra Bouyacoub, Sonia Abdelhak, Mourad Mokni, Ahlem Amouri, Habib Messai, Sana Hsouna, Majdi Nagara, Ahlem Sabrine Ben Brick, Wafa Cherif, Leila El Matri, Faten Ben Rhouma, I. Chouchene, Mariem Ben Rekaya
Publikováno v:
American Journal of Human Biology. 28:171-180
Objectives Consanguinity is common in Tunisia. However, little information exists on its impact on recessive disorders. In this study, we evaluate the impact of consanguineous marriages on the occurrence of some specific autosomal recessive disorders
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4de7f5fa3c497e90f4264cfcb27a3572
https://doi.org/10.1002/ajhb.22764
https://doi.org/10.1002/ajhb.22764
Autor:
Olfa Messaoud, Inçaf Mokhtar, Faten Talmoudi, Samir Boubaker, M. Zghal, Sonia Abdelhak, Ahlem Amouri, Mariem Ben Rekaya, Hammouda Boussen, Wafa Cherif
Publikováno v:
International Journal of Dermatology. 49:544-548
BACKGROUND: Xeroderma Pigmentosum (XP) is a rare autosomal recessive disorder characterized by cutaneous and ocular alterations. Eight genes, Xeroderma Pigmentosum group A (XPA) to Xeroderma Pigmentosum group G (XPG) and Xeroderma Pigmentosum group V
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf5763855b2c7b39989074d794c28001
https://doi.org/10.1111/j.1365-4632.2010.04421.x
https://doi.org/10.1111/j.1365-4632.2010.04421.x
Autor:
Sondes H Meseddi, Koussay Dellagi, Dominique Stoppa Lyonnet, Olfa Messaoud, Jean Soulier, Tarek Ben Othmen, Mongia Hachicha, Fethi Mellouli, Sonia Abdelhak, Catherine Dubois d'Enghien, Mohamed Bejaoui, Ahlem Amouri, Faten Talmoudi, Héla Azaiez, Lamia Aissaoui, Tunisian Fanconi, Mariem Ben Rekaya, Rym Kefi, Ines Allegui, Lamia Torjemane, Ahlem Abdelhak, Hela Ben Abid, Monia Ouederni
Publikováno v:
Molecular Genetics and Genomic Medicine
Molecular Genetics and Genomic Medicine, Wiley, 2014, 2 (2), pp.160-5. 〈10.1002/mgg3.55〉
Molecular Genetics and Genomic Medicine, Wiley, 2014, 2 (2), pp.160-5. ⟨10.1002/mgg3.55⟩
Molecular Genetics & Genomic Medicine
Molecular Genetics and Genomic Medicine, Wiley, 2014, 2 (2), pp.160-5. 〈10.1002/mgg3.55〉
Molecular Genetics and Genomic Medicine, Wiley, 2014, 2 (2), pp.160-5. ⟨10.1002/mgg3.55⟩
Molecular Genetics & Genomic Medicine
International audience; Tunisian population is characterized by its heterogeneous ethnic background and high rate of consanguinity. In consequence, there is an increase in the frequency of recessive genetic disorders including Fanconi anemia (FA). Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76bd988f6b3a32d98503ee6dee85a13c
https://hal-riip.archives-ouvertes.fr/pasteur-01098539/document
https://hal-riip.archives-ouvertes.fr/pasteur-01098539/document
Autor:
Faten, Talmoudi, Lobna, Kammoun, Nizar, Benhalim, Lamia, Torjemane, Monia, Ouederni, Lamia, Aissaoui, Amel, Lakhal, Fethi, Mellouli, Tarek B, Othmen, Mohamed, Bejaoui, Sonia, Abdelhak, Mounira, Meddeb, Koussay, Dellagi, Sondes, Hdiji, Ahlem, Amouri, S, Hmida
Publikováno v:
Journal of Pediatric Hematology/Oncology
Journal of Pediatric Hematology/Oncology, Lippincott, Williams & Wilkins, 2013, 35 (7), pp.547-550. ⟨10.1097/MPH.0b013e31827e56cb⟩
Journal of Pediatric Hematology/Oncology, Lippincott, Williams & Wilkins, 2013, 35 (7), pp.547-550. ⟨10.1097/MPH.0b013e31827e56cb⟩
International audience; Background:Chromosome breakage hypersensitivity to alkylating agents is the gold standard test for Fanconi anemia (FA) diagnosis. The aim of the present study was to assess the proportion of FA cases among aplastic anemia (AA)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78ae5a9f6c23b4dbe73c6163bac3598a
https://pubmed.ncbi.nlm.nih.gov/23337544
https://pubmed.ncbi.nlm.nih.gov/23337544
Autor:
Mezni, Faouzi, Mlika, Mona, Boussen, Hamouda, Ghedira, Habib, Fenniche, Soraya, Faten, Talmoudi, Loriot, Marie-Anne
Publikováno v:
Journal of Immunoassay & Immunochemistry; 2018, Vol. 39 Issue 1, p99-107, 9p
Autor:
Helmi Guermani, Imene Chemkhi, Lamia Aissaoui, Lamia Torjmane, Faten Talmoudi, Olfa Kilani, Nabila Abidli, Lobna Kammoun, Neila Ben Romdhane, Tarek Ben Othmane, Nizar Ben Halim, Fethi Mellouli, Wiem Ayed, Moez Elloumi, Sondes Hadiji, Yosra Ben Youssef, Sonia Abdelhak, Ahlem Amouri, Mohamed Bejaoui, Sofiene Hentati
Publikováno v:
Comptes Rendus Biologies
Comptes Rendus Biologies, Elsevier, 2013, 336 (1), pp.29-33. ⟨10.1016/j.crvi.2013.02.001⟩
Comptes Rendus Biologies, Elsevier, 2013, 336 (1), pp.29-33. ⟨10.1016/j.crvi.2013.02.001⟩
International audience; Fanconi anemia (FA) is a recessive chromosomal instability syndrome that is clinically characterized by multiple symptoms. Chromosome breakage hypersensitivity to alkylating agents is the gold standard test for FA diagnosis. I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c32bc0540e464c2477388e3c022d24e6
https://pubmed.ncbi.nlm.nih.gov/23537767
https://pubmed.ncbi.nlm.nih.gov/23537767
Autor:
Mourad Mokni, Imen Arfa, Sonia Abdelhak, Ahlem Amouri, Salem Kachboura, Faten Talmoudi, Neji Tebib, Nissaf Ben Alaya Bouafif, Marie-Françoise Ben Dridi, Wafa Cherif, Leila El Matri, Yosra Bouyacoub, Saida Ben Arab, Sonia Nouira, Welid Ghazouani, Ibtissem Chouchane, Rym Kefi Ben Atig, Lilia Romdhane, Nizar Ben Halim, Abdelmajid Abid, Khaled Lasram, Sana Hsouna, Hela Azaiez, Koussay Dellagi
Publikováno v:
Journal of community genetics. 4(2)
Consanguinity refers to marriages between individuals who share at least one common ancestor. In clinical genetics, a consanguineous marriage is defined as a union between two individuals who are related as second cousins or closer, with the inbreedi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e9215b718b4d1eccfacce5f6a939419
https://pubmed.ncbi.nlm.nih.gov/23208456
https://pubmed.ncbi.nlm.nih.gov/23208456
Autor:
M. Zghal, M. Ben Rekaya, Hammouda Boussen, Sonia Abdelhak, Ahlem Amouri, Samir Boubaker, Sonia Nouira, I Mokthar, Houyem Ouragini, Faten Talmoudi, Olfa Messaoud, Mourad Mokni
Publikováno v:
Journal of human genetics. 54(7)
Xeroderma pigmentosum (XP, OMIM 278700–278780) is a group of autosomal recessive diseases characterized by hypersensitivity to UV rays. There are seven complementation groups of XP (XPA to XPG) and XPV. Among them, the XP group C (XP-C) is the most
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1fc01d6a806eb1c903264060247fd1a
https://pubmed.ncbi.nlm.nih.gov/19478817
https://pubmed.ncbi.nlm.nih.gov/19478817