Zobrazeno 1 - 10
of 883
pro vyhledávání: '"A., Ladjouze"'
Autor:
Ladjouze, Baya, ben Hamiche, Nadir, Kribeche, Amina, Takka, Melissa, Boulekbache-Makhlouf, Lila, Madani, Khodir
Publikováno v:
In South African Journal of Botany December 2023 163:684-691
Autor:
Bengana, Bilal, Rezig, Aicha Ladjouze, Ayoub, Soraya, Raaf, Nabil Beratmane, Aimeur, Chaffa, Nebab, Abdelkader, Tafiani, Salima Lefkir
Publikováno v:
In Revue du rhumatisme December 2022 89(6):585-589
Publikováno v:
In EMC APARATO LOCOMOTOR August 2022 55(3):1-16
Autor:
Housna Zidoune, Asmahane Ladjouze, Djalila Chellat-Rezgoune, Asma Boukri, Scheher Aman Dib, Nassim Nouri, Meryem Tebibel, Karima Sifi, Noureddine Abadi, Dalila Satta, Yasmina Benelmadani, Joelle Bignon-Topalovic, Maeva El-Zaiat-Munsch, Anu Bashamboo, Ken McElreavey
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
In a majority of individuals with disorders/differences of sex development (DSD) a genetic etiology is often elusive. However, new genes causing DSD are routinely reported and using the unbiased genomic approaches, such as whole exome sequencing (WES
Externí odkaz:
https://doaj.org/article/a30672ccbf724ddaaff9d212a96814dd
Autor:
Asmahane Ladjouze, Malcolm Donaldson, Ingrid Plotton, Nacima Djenane, Kahina Mohammedi, Véronique Tardy-Guidollet, Delphine Mallet, Kamélia Boulesnane, Zair Bouzerar, Yves Morel, Florence Roucher-Boulez
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Background3β-hydroxysteroid dehydrogenase 2 (3βHSD2) deficiency is a rare form of congenital adrenal hyperplasia (CAH), with fewer than 200 cases reported in the world literature and few data on outcomes.Patients and MethodsWe report a mixed longit
Externí odkaz:
https://doaj.org/article/f02b49e95a504f2db237a481c5202d46
Akademický článek
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Autor:
Ladjouze, Asmahane, Donaldson, Malcolm
Publikováno v:
In Best Practice & Research Clinical Endocrinology & Metabolism June 2019 33(3)
Autor:
Asma Deeb, Jean-Pierre Chanoine, Jamal Raza, Amanda Rowlands, Abdulsalam Abu-Libdeh, Asmahane Ladjouze, Rasha T Hamza, Salwa A Musa, Farida Jennane, Bouferoua Fadila, Delileche Hana, Djahlat Larbi, Noumi Mustapha, Haya Alkhayyat, Abdourahman Douksie, Ali Rabbani, Ali Al-Jumaili, Rasha Odeh, Hessa Alkandari, Hala Tfayli, Suleiman Abusrewil, Millad Ghawil, Aisha Al senani, Fawziya Alkhalaf, Abdelhadi Habeb, Noman Ahmad, Omer Elshareef, Mohamed Abdullah, Olivia Al-Hassan, Dima Karah, Mongia Hachicha, Mohammed Alshakka
Publikováno v:
BMJ Global Health, Vol 6, Iss 10 (2021)
Congenital adrenal hyperplasia (CAH), if untreated, carries high morbidity and mortality. A higher incidence of CAH is expected in countries where consanguinity is common, such as in the countries of the WHO Eastern Mediterranean Region (EMRO). CAH i
Externí odkaz:
https://doaj.org/article/56dbc542be5c46a880a38a1bb10953e1
Autor:
Ahlem Saadi, Jie Dang, Shan Shan, Aicha Ladjouze-Rezig, Salima Lefkir-Tafiani, Yaoqin Gong, Qiji Liu, Traki Benhassine
Publikováno v:
Central European Journal of Immunology, Vol 44, Iss 1, Pp 65-74 (2019)
Externí odkaz:
https://doaj.org/article/05508d3d15814a5892a2df7946d565a0
Publikováno v:
Urban Water Journal. :1-15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86b2f6a18868a430083e4afc40a87267
https://doi.org/10.1080/1573062x.2023.2217656
https://doi.org/10.1080/1573062x.2023.2217656