| NNT mutations: a cause of primary adrenal insufficiency, oxidative stress and extra-adrenal defects F Roucher-Boulez, D Mallet-Motak, D Samara-Boustani, H Jilani, ... European journal of endocrinology 175 (1), 73-84, 2016 | 73 | 2016 |
| Familial Multiplicity of Estrogen Insensitivity Associated With a Loss-of-Function ESR1 Mutation V Bernard, S Kherra, B Francou, J Fagart, S Viengchareun, J Guéchot, ... The journal of clinical endocrinology & metabolism 102 (1), 93-99, 2017 | 62 | 2017 |
| Novel CYP19A1 Mutations Extend the Genotype-Phenotype Correlation and Reveal the Impact on Ovarian Function VP Praveen, A Ladjouze, KS Sauter, A Pulickal, E Katharopoulos, ... Journal of the Endocrine Society 4 (4), bvaa030, 2020 | 23 | 2020 |
| Expanding DSD phenotypes associated with variants in the DEAH-box RNA helicase DHX37 H Zidoune, L Martinerie, DS Tan, M Askari, D Rezgoune, A Ladjouze, ... Sexual Development 15 (4), 244-252, 2021 | 17 | 2021 |
| Primary gonadal failure A Ladjouze, M Donaldson Best Practice & Research Clinical Endocrinology & Metabolism 33 (3), 101295, 2019 | 17 | 2019 |
| GH deficiency with central precocious puberty: a new rare disorder associated with a developmental defect of the hypothalamic–pituitary area A Ladjouze, S Soskin, C Garel, M Jullien, C Naud-Saudreau, G Pinto, ... European journal of endocrinology 156 (4), 463-469, 2007 | 17 | 2007 |
| Novel genomic variants, atypical phenotypes and evidence of a digenic/oligogenic contribution to disorders/differences of sex development in a large North African cohort H Zidoune, A Ladjouze, D Chellat-Rezgoune, A Boukri, SA Dib, N Nouri, ... Frontiers in genetics 13, 900574, 2022 | 10 | 2022 |
| Genotype, mortality, morbidity, and outcomes of 3β-hydroxysteroid dehydrogenase deficiency in Algeria A Ladjouze, M Donaldson, I Plotton, N Djenane, K Mohammedi, ... Frontiers in endocrinology 13, 867073, 2022 | 8 | 2022 |
| Sex assignment practice in disorders of sexual differentiation: Survey results from paediatric endocrinologists in the Arab region A Deeb, M Khamis, SA Sayed, O Magdy Omar, R Odeh, A Ladjouze, ... Journal of Pediatric Endocrinology and Metabolism 32 (1), 75-82, 2019 | 7 | 2019 |
| Contribution of GHR and IGFALS Mutations to Growth Hormone Resistance-Identification of New Variants and Impact on the Inheritance Pattern M Legendre, F Dastot, N Collot, P Duquesnoy, E Cohen, ML Sobrier, ... HORMONE RESEARCH IN PAEDIATRICS 86, 114-115, 2016 | 5 | 2016 |
| Access to fludrocortisone and to hydrocortisone in children with congenital adrenal hyperplasia in the WHO Eastern Mediterranean Region: it takes a village… A Rowlands, A Deeb, A Ladjouze, RT Hamza, SA Musa, J Raza, ... BMJ Global Health 6 (10), e007195, 2021 | 4 | 2021 |
| Age at Diagnosis and Outcome in Maghreb Patients With 21-Hydroxylase Deficient Congenital Adrenal Hyperplasia; Urgent Need for Newborn Screening A Ladjouze, I Yala, M Yahiaoui, D Zerguini, V Tardy, K Mohammedi, ... SPE Abstracts 89, PP-005, 2018 | 4 | 2018 |
| Résistance aux œstrogènes due à une nouvelle mutation homozygote d’ESR1 V Bernard, S Kherra, B Francou, J Fagart, S Viengchareun, A Ladjouze, ... Annales d'Endocrinologie 76 (4), 336-337, 2015 | 1 | 2015 |
| SFP P-019-Déficit en Hormone de Croissance: à propos de 92 cas. A Ladjouze, Y Ouarezki, A Djermane, L Kedji, A Maoudj, K Berkouk, ... Archives de Pédiatrie 21 (5), 729, 2014 | 1 | 2014 |
| SFP P-158-Facteurs de risque de caries dentaires chez les enfants d’âge préscolaire M Bensmina, K Berkouk, A Ladjouze, L Kedji, A Maoudj, N Bouhafs, ... Archives de Pédiatrie 21 (5), 868, 2014 | 1 | 2014 |
| Development and implementation of a Pediatric Endocrinology Education Program in Francophone Africa (In French: Programme de formation en Endocrinologie et Diabetologie … B Niang, D Boiro, P Bretones, AC Bodieu, C de Beaufort, A Ladjouze, ... HORMONE RESEARCH IN PAEDIATRICS 96, 354-355, 2023 | | 2023 |
| Diagnostic and predictive value of brain magnetic resonance imaging in Algerian children with growth hormone deficiency S Kherra, N Boutaghane, S Bellouti, L Sifour, H Sahli, A Djermane, ... HORMONE RESEARCH IN PAEDIATRICS 96, 550-550, 2023 | | 2023 |
| Congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency: Clinical, Biochemical and Genetic characteristics A Ladjouze, K Mohammedi, M Demdoum, K Boulesnane, R Aboura, ... HORMONE RESEARCH IN PAEDIATRICS 96, 154-154, 2023 | | 2023 |
| 3β-Hydroxysteroid dehydrogenase deficiency F Roucher-Boulez, Y Morel, A Ladjouze, I Plotton, J Simard, M Coll Genetic Steroid Disorders, 81-94, 2023 | | 2023 |
| 66 Optic neuritis in children S Melzi, R Aboura, A Ladjouze, N Bouhafs, K Boulesnane, R Bouadjar, ... Rheumatology 61 (Supplement_2), keac496. 062, 2022 | | 2022 |
