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Dr Adel Djermane
Dr Adel Djermane
Enseignant Chercheur Hospitalo-Universitaire , Université Alger 1 , Département de Médecine
Verified email at univ-alger.dz
Title
Cited by
Cited by
Year
Central diabetes insipidus in infancy with or without hypothalamic adipsic hypernatremia syndrome: early identification and outcome
A Djermane, M Elmaleh, D Simon, A Poidvin, JC Carel, J Léger
The Journal of Clinical Endocrinology & Metabolism 101 (2), 635-643, 2016
352016
Cortisol evaluation during the acute phase of traumatic brain injury—A prospective study
M Bensalah, M Donaldson, Y Aribi, M Iabassen, L Cherfi, M Nebbal, ...
Clinical endocrinology 88 (5), 627-636, 2018
272018
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
12014
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
Cardiovascular risk stratification in Turner syndrome: A study of 173 cases
R Aboura, A Ladjouze, A Djermane, Y Ouarezki, F Bouferoua, A Massif, ...
Archives of Cardiovascular Diseases Supplements 14 (3-4), 245, 2022
2022
Outcome of congenital hypothyroidism in Algeria: the urgent need to implement a national newborn screening program
D Adel, L Asmahane, O Yasmine, TN Ourida, Z Kafia, A Samira, ...
HORMONE RESEARCH IN PAEDIATRICS 91, 275-275, 2019
2019
The Influence of pituitary MRI findings on clinical presentation and growth in GH-Treated Children with Congenital Hypopituitarism
D Adel, L Asmahane, O Yasmine, M Kahina, B Hassina, A Samira, B Zahir, ...
HORMONE RESEARCH IN PAEDIATRICS 91, 435-435, 2019
2019
Severe Hypernatremia Revealing a ROHHAD-NET Syndrome
Ouarezki, Medical Health, F Bouferoua, A Djermane, H Boucenna, ...
HORMONE RESEARCH IN PAEDIATRICS 91, 549-550, 2019
2019
Diazoxide unresponsive Congenital Hyperinsulinism due to a Novel ABCC8 Missense Mutation.
Y Ouarezki, A Ladjouze, A Djermane, J Houghton, H Maouche, ...
HORMONE RESEARCH IN PAEDIATRICS 90, 361-361, 2018
2018
PITUITARY IMAGING IN 189 PATIENTS WITH CONGENITAL GROWTH HORMONE DEFICIENCY
Y Ouarezki, A Ladjouze, A Djermane, K Mohammedi, ON Taleb, A Laraba, ...
HORMONE RESEARCH IN PAEDIATRICS 88, 149-149, 2017
2017
SENSITIVITY AND SPECIFICITY OF BASAL LH LEVELS IN THE DIAGNOSIS OF CENTRAL PRECOCIOUS PUBERTY IN GIRLS
A Djermane, A Ladjouze, H Benlarbi, Y Ouarezki, K Mohamedi, ON Taleb, ...
HORMONE RESEARCH IN PAEDIATRICS 88, 347-347, 2017
2017
Genotype-Phenotype Correlation in Turner Syndrome
A Djermane, A Ladjouze, Y Ouarezki, B Ait-Abdelkader, L Kedji, A Maoudj, ...
European Society for Paediatric Endocrinology, 2014
2014
A Very Rare Case of Rickets: Fanconi-Bickel Syndrome
A Djermane, A Ladjouze, Y Ouarezki, S Vuillaumier-Barrot, BA Khodja, ...
European Society for Paediatric Endocrinology, 2014
2014
The Triptorelin Test Compares Favourably with the GnRH Test in the Diagnosis of Central Precocious Puberty
A Ladjouze, A Djermane, Y Ouarezki, L Kedji, K Berkouk, M Abdeljalil, ...
European Society for Paediatric Endocrinology, 2014
2014
A new mutation of MAMLD1 (CXorf6) associated with NR5A1 (SF1) variant in a patient with 46, XY DSD
A Ladjouzea, P Philibertb, Y Ouarezkic, A Djermaned, L Kedjia, ...
European Society for Paediatric Endocrinology, 2014
2014
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Articles 1–15