Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Charfeddine, Ilhem Ben"'
Autor:
Khattab, Ahmed, Haider, Shozeb, Kumar, Ameet, Dhawan, Samarth, Alam, Dauood, Romero, Raquel, Burns, James, Li, Di, Estatico, Jessica, Rahi, Simran, Fatima, Saleel, Alzahrani, Ali, Hafez, Mona, Musa, Noha, Azar, Maryam Razzghy, Khaloul, Najoua, Gribaa, Moez, Saad, Ali, Charfeddine, Ilhem Ben, de Mendonça, Berenice Bilharinho, Belgorosky, Alicia, Dumic, Katja, Dumic, Miroslav, Aisenberg, Javier, Kandemir, Nurgun, Alikasifoglu, Ayfer, Ozon, Alev, Gonc, Nazli, Cheng, Tina, Kuhnle-Krahl, Ursula, Cappa, Marco, Holterhus, Paul-Martin, Nour, Munier A., Pacaud, Daniele, Holtzman, Assaf, Li, Sun, Zaidi, Mone, Yuen, Tony, New, Maria I.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2017 Mar 01. 114(10), E1933-E1940.
Externí odkaz:
https://www.jstor.org/stable/26480125
Autor:
AMARA, Abdelbasset, CHARFEDDINE, Ilhem BEN, GHÉDIR, Houda, MAMAÏ, Ons, JEMNI-YACOUB, Saloua, CHAIEB, Larbi, SAAD, Ali, CHADLI-CHAIEB, Molka, GRIBAA, Moez
Publikováno v:
Iranian Journal of Public Health; Mar2015, Vol. 44 Issue 3, p396-403, 8p
Autor:
Mili, Amira, Charfeddine, Ilhem Ben, Mama, Ons, Abdelhak, Sonia, Adala, Labiba, Amara, Abdelbasset, Pagliarani, Serena, Lucchiarri, Sabrina, Ayadi, Abdelkarim, Tebib, Neji, Harbi, Abdelaziz, Bouguila, Jihene, H'Mida, Dorra, Saad, Ali, Limem, Khalifa, Comi, G P, Gribaa, Moez
Publikováno v:
Journal of Human Genetics. Mar2012, Vol. 57 Issue 3, p221-221. 1p.
Autor:
Mamaı, Ons1,2 (AUTHOR), Boussofara, Lobna3 (AUTHOR), Denguezli, Mohamed3 (AUTHOR), Escande-Beillard, Nathalie2 (AUTHOR), Kraeim, Wahiba4 (AUTHOR), Merriman, Barry5 (AUTHOR), Charfeddine, Ilhem Ben1 (AUTHOR), Stevanin, Giovanni6 (AUTHOR), Bouraoui, Sana1 (AUTHOR), Amara, Abdelbasset1 (AUTHOR), Mili, Amira1 (AUTHOR), Nouira, Rafiaa3 (AUTHOR), H’mida, Dorra1 (AUTHOR), Sriha, Badreddine7 (AUTHOR), Gribaa, Moez1 (AUTHOR), Saad, Ali1 (AUTHOR) ali.saad@rns.tn, Reversade, Bruno2,8 (AUTHOR) bruno@reversade.com
Publikováno v:
Journal of Investigative Dermatology. Jul2014, Vol. 134 Issue 7, p304-308. 5p. 2 Color Photographs.
Autor:
Jessica Estatico, Miroslav Dumić, Mona Hafez, Assaf Holtzman, Paul Martin Holterhus, Ali Saad, Marco Cappa, Di Li, Maria I. New, Raquel Romero, James T. Burns, Alicia Belgorosky, Nazli Gonc, Mone Zaidi, Tina Cheng, Noha Musa, Nurgun Kandemir, Berenice B. Mendonca, Saleel Fatima, Dauood Alam, Ahmed Khattab, Javier Aisenberg, Sun Li, Munier Nour, Simran Rahi, Samarth Dhawan, Ali S. Alzahrani, Najoua Khaloul, Danièle Pacaud, Ursula Kuhnle-Krahl, Ilhem Charfeddine, Tony Yuen, Alev Ozon, Ameet Kumar, Katja Dumic, Moez Gribaa, Shozeb Haider, Maryam Razzghy Azar, Ayfer Alikasifoglu
Congenital adrenal hyperplasia (CAH), resulting from mutations in CYP11B1, a gene encoding 11β-hydroxylase, represents a rare autosomal recessive Mendelian disorder of aberrant sex steroid production. Unlike CAH caused by 21-hydroxylase deficiency,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7a2dcd3ac0c6a1cfe7d2094c95e805e
https://europepmc.org/articles/PMC5347606/
https://europepmc.org/articles/PMC5347606/
