Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Lobna Kammoun"'
Autor:
Sonia Abdelhak, Ahlem Amouri, Lamia Aissaoui, Koussay Dellagi, Mounir Frikha, Hatem Bellaaj, Hatem Elghezal, H Ben Abid, S Hammemi, Lamia Torjemane, le Groupe d’étude tunisien de l’anémie de Fanconi Getaf, Mohamed Bejaoui, Y Ben Youssef, Mongia Hachicha, S. Hadiji Mseddi, Monia Ouederni, F Telmoudi, T Ben Othmen, Lobna Kammoun, Y. Ben Abdennebi
Publikováno v:
Archives de Pédiatrie. 19:467-475
Resume Introduction L’anemie de Fanconi (AF) est une maladie hereditaire caracterisee par une heterogeneite genetique et phenotypique. De nombreux groupes ont mis en place des registres propres a leur pays. En Tunisie, le groupe tunisien d’etude
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3da2f65142df715c4eaa3fe3c45edc10
https://doi.org/10.1016/j.arcped.2012.02.017
https://doi.org/10.1016/j.arcped.2012.02.017
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:
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