Asmahane Ladjouze

NNT mutations: a cause of primary adrenal insufficiency, oxidative stress and extra-adrenal defects

Florence Roucher‐Boulez, Delphine Mallet-Motak, Dinane Samara‐Boustani et al. · European Journal of Endocrinology · 2016 · 94 citations

Life Sciences, Endocrinology, Genetics +17

Familial Multiplicity of Estrogen Insensitivity Associated with a Loss-of-Function <i>ESR1</i> Mutation

Valérie Bernard, Sakina Kherra, Bruno Francou et al. · The Journal of Clinical Endocrinology & Metabolism · 2016 · 48 citations · Full text

Medicine, Endocrinology, Genetics +17

Genotype, Mortality, Morbidity, and Outcomes of 3β-Hydroxysteroid Dehydrogenase Deficiency in Algeria

Asmahane Ladjouze, Malcolm Donaldson, Ingrid Plotton et al. · Frontiers in Endocrinology · 2022 · 37 citations · Full text

Life Sciences, Endocrinology, Genetics +17

Novel Genomic Variants, Atypical Phenotypes and Evidence of a Digenic/Oligogenic Contribution to Disorders/Differences of Sex Development in a Large North African Cohort

Housna Zidoune, Asmahane Ladjouze, Djalila Chellat-Rezgoune et al. · Frontiers in Genetics · 2022 · 35 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Novel CYP19A1 Mutations Extend the Genotype-Phenotype Correlation and Reveal the Impact on Ovarian Function

Asmahane Ladjouze, Kay‐Sara Sauter, Annie Pulickal et al. · Journal of the Endocrine Society · 2020 · 31 citations · Full text

Medicine, Endocrinology, Genetics +14