Get started
Author

Farida Jennane

Observed names: F Jennane, F. Jennane, Jennane F, Jennane Farida, Jennane, Farida
ORCID: 0000-0001-8281-2114
Observed ORCID: 0000-0001-8281-2114
OpenAlex ID: A5014552154
Glucose Tolerance and Insulin Secretion, Morbidity, and Death in Patients with Cystic Fibrosis
2007 · Elise Bismuth, Kathleen Laborde, et al. · The Journal of Pediatrics · 149
Neuropsychological dysfunction and developmental defects associated with genetic changes in infants with neonatal diabetes mellitus: a prospective cohort study
2013 · Kanetee Busiah, Séverine Drunat, et al. · The Lancet Diabetes & Endocrinology · 116
A positive genotype–phenotype correlation in a large cohort of patients with Pseudohypoparathyroidism Type Ia and Pseudo‐pseudohypoparathyroidism and 33 newly identified mutations in the GNAS gene
2014 · Susanne Thiele, Ralf Werner, et al. · Molecular Genetics & Genomic Medicine · 58
PDF
A Novel Homozygous Missense Mutation in the FU-CRD2 Domain of the R-spondin1 Gene Associated with Familial 46,XX DSD
2017 · Yassine Naasse, Amina Bakhchane, et al. · Sexual Development · 27
Gonadectomy in conditions affecting sex development: a registry-based cohort study
2021 · Angela K Lucas-Herald, Jillian Bryce, et al. · European Journal of Endocrinology · 23
PDF
Two novel mutations in the EIF2AK3 gene in children with Wolcott-Rallison syndrome
2010 · André F Reis, Caroline Kannengiesser, et al. · Pediatric Diabetes · 23
Research of anti-GAD and anti-IA2 autoantibodies by ELISA test in a series of Moroccan pediatric patients with diabetes type 1
2020 · O Belhiba, Z Aadam, et al. · African Health Sciences · 19
PDF
Thyroïdite et intolérance au gluten: maladies auto-immmunes extrapancréatiques associées au diabète de type 1
2006 · S. Faesch, F. Jennane, et al. · Archives de Pédiatrie · 12
Access to fludrocortisone and to hydrocortisone in children with congenital adrenal hyperplasia in the WHO Eastern Mediterranean Region: it takes a village…
2021 · Amanda Rowlands, Asma Deeb, et al. · BMJ Global Health · 10
PDF
Prevalence of celiac disease in Moroccan children with type 1 diabetes mellitus: A 16-year cross-sectional study
2023 · Ouijdane Belhiba, Ahmed Aziz Bousfiha, et al. · Qatar medical journal · 3
A Novel Homozygous Missense Mutation in the FU-CRD2 Domain of the R-spondin1 Gene Associated with Familial 46,XX DSD
2018 · Naasse Y, Bakhchane A, et al. · Yearbook of pediatric endocrinology · 3
P149 - Kyste bronchogénique du nourrisson révélé par une dyspnée sifflante récidivante (À propos de deux cas)
2010 · M. Lahbabi, H. Sadiki, et al. · Archives de Pédiatrie · 2
P507 - L’envenimation scorpionique : à propos de 100 cas
2010 · I. Benhsaien, A. Harrak, et al. · Archives de Pédiatrie · 1
The Clinical and Biological Characterization of Triple A Syndrome (Allgrove Syndrome) in 12 Pediatric Patients
2026 · Ilham Bouarab, Fatimazahra Yakine, et al. · Cureus
PDF
PTPN22 C1858T polymorphism confers risk for familial type 1 diabetes in Moroccan children and adolescents
2026 · Ouijdane Belhiba, Fatima Zahra El Ansari, et al. · Egyptian Journal of Medical Human Genetics
PDF
Monogenic Neonatal Diabetes: Clinical Presentations, Genetic Findings, and Response to Therapy in a Retrospective Case Series
2026 · Fatimazahra Yakine, Ilham Bouarab, et al. · Cureus
PDF
Syndrome de Turner : A propos de 113 cas
2023 · Yakine, Fatima zahra, Chaaybi, Chaymae, et al. · Revue Marocaine des Maladies de l'Enfant
Access to fludrocortisone and to hydrocortisone in children with congenital adrenal hyperplasia in the WHO Eastern Mediterranean region: it takes a village…
2022 · Rowlands A, Deeb A, et al. · Yearbook of pediatric endocrinology
Latest News on Autoantibodies Associated with type 1 Diabetes in Children: -Systematic Review-
2019 · Belhiba Ouijdane, Ahmed Aziz Bousfiha, et al. · Journal of Medical and Surgical Research
Gonadectomy for adults with DSD conditions at risk of hypogonadism in the international disorders of sex development registry
2018 · Angela Lucas Herald, Andreas Kyriakou, et al. · Endocrine Abstracts
Gonadectomy for Adults with DSD Conditions in the International Disorders of Sex Development Registry
2018 · Angela K Lucas‐Herald, Andreas Kyriakou, et al. · Dspace Repository (Marmara Üniversitesi)
Syndrome de triple A ou syndrome d’Allgrove à l’âge adulte : à propos d’un cas
2017 · S. Laidi, S. El Aziz, et al. · Annales d Endocrinologie
Syndrome d’interruption de la tige pituitaire à révélation tardive : à propos de 3 cas
2017 · S. Laidi, S. El Aziz, et al. · Annales d Endocrinologie
Contents Vol. 11, 2017
2017 · Claus H. Gravholt, Ole L. Dollerup, et al. · Sexual Development
PDF
Puberté précoce centrale : les aspects clinique, diagnostique et thérapeutique à travers une cohorte de 16 cas
2016 · R. Moussaid, S. Ouchen, et al. · Annales d Endocrinologie
Works count: 32
Citation count: 446
H-index: 9
I10-index: 9
Year
Topic
Type