Get started
Author

Adel Djermane

Observed names: A Djermane, A. Djermane, A., Djermane, Djermane A
ORCID: 0000-0001-7237-2514
Observed ORCID: 0000-0001-7237-2514
OpenAlex ID: A5061558008
Central Diabetes Insipidus in Infancy With or Without Hypothalamic Adipsic Hypernatremia Syndrome: Early Identification and Outcome
2015 · Adel Djermane, Monique Elmaleh, et al. · The Journal of Clinical Endocrinology & Metabolism · 41
Cortisol evaluation during the acute phase of traumatic brain injury—A prospective study
2018 · Meriem Bensalah, Malcolm Donaldson, et al. · Clinical Endocrinology · 28
Rarity of Congenital Adrenal Hyperplasia in Children Born Very Preterm: Possible Mechanism and Implication for Newborn Screening
2025 · Asmahane Ladjouze, Yasmina Ouarezki, et al. · Hormone Research in Paediatrics · 3
The Burden of Congenital Hypothyroidism Without Newborn Screening: Clinical and Cognitive Findings from a Multicenter Study in Algeria
2025 · Adel Djermane, Yasmine Ouarezki, et al. · International Journal of Neonatal Screening · 2
PDF
Outcome of Congenital Hypothyroidism in Algeria: The Urgent Need to Implement a National Newborn Screening Program
2019 · Adel Djermane, Asmahane Ladjouze, et al. · 58th Annual ESPE Meeting (ESPE 2019) · 1
SFP P-019 - Déficit en Hormone de Croissance: à propos de 92 cas.
2014 · A. Ladjouze, Y. Ouarezki, et al. · Archives de Pédiatrie · 1
The Burden of Congenital Hypothyroidism Without Newborn Screening: Clinical and Cognitive Findings from a Multicenter Study in Algeria
2026 · Djermane A, Ouarezki Y, et al. · Yearbook of pediatric endocrinology
Pediatric Behçet's disease and intracardiac thrombosis
2025 · Yasmine Semar, Yousra Tazerouti, et al. · Archives of cardiovascular diseases
The need for early reassessment in children with growth hormone deficiency
2025 · Adel Djermane, Yasmina Ouarezki, et al. · Endocrine Abstracts
Effects of growth hormone therapy in patients with prader-willi syndrome: the first algerian experience
2025 · Sakina Kherra, Asmahane Ladjouze, et al. · Endocrine Abstracts
Cardiovascular risk stratification in Turner syndrome: A study of 173 cases
2022 · R. Aboura, A. Ladjouze, et al. · Archives of Cardiovascular Diseases Supplements
PDF
The Influence of Pituitary MRI Findings on Clinical Presentation and Growth in GH-Treated Children with Congenital Hypopituitarism
2019 · Adel Djermane, Asmahane Ladjouze, et al. · 58th Annual ESPE Meeting (ESPE 2019)
Severe Hypernatremia Revealing A Rohhad-Net Syndrome
2019 · Fadila Bouferoua, Adel Djermane, et al. · 58th Annual ESPE Meeting (ESPE 2019)
Association maladie de Basedow, diabète de type 1 et myasthénie. À propos d’une observation
2018 · H. Boudina, A. Djermane, et al. · Annales d Endocrinologie
Diazoxide unresponsive Congenital Hyperinsulinism due to a Novel ABCC8 Missense Mutation
2018 · Y Ouarezki, A Ladjouze, et al.
Hypothyroïdie et rhabdomyolyse : à propos d’un cas
2014 · A. Djermane · Annales d Endocrinologie
Genotype-Phenotype Correlation in Turner Syndrome
2014 · Adel Djermane, Asmahane Ladjouze, et al. · 53rd ESPE Meeting
The Triptorelin Test Compares Favourably with the GnRH Test in the Diagnosis of Central Precocious Puberty
2014 · Asmahane Ladjouze, Adel Djermane, et al. · 53rd ESPE Meeting
A Very Rare Case of Rickets: Fanconi-Bickel Syndrome
2014 · Adel Djermane, Asmahane Ladjouze, et al. · ESPE 2014
A New Mutation of MAMLD1 (CXorf6) Associated with NR5A1 (SF1) Variant in a Patient with 46,XY DSD
2014 · Asmahane Ladjouze, Pascal Philibert, et al. · 53rd ESPE Meeting
Works count: 21
Citation count: 76
H-index: 3
I10-index: 2
Year
Topic
Type