Farida Jennane
Overview
Explore the profile of Farida Jennane including associated specialties, affiliations and a list of published articles.
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Articles
7
Citations
108
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0
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Recent Articles
1.
Belhiba O, Bousfiha A, Jennane F
Qatar Med J
. 2024 Jan;
2023(4):37.
PMID: 38187990
Background: There is limited data available regarding the prevalence of celiac disease (CD) among children with type 1 diabetes mellitus (T1DM) in Arab countries and the Middle East. This cross-sectional...
2.
Rowlands A, Deeb A, Ladjouze A, Hamza R, Musa S, Raza J, et al.
BMJ Glob Health
. 2021 Oct;
6(10).
PMID: 34675026
Congenital adrenal hyperplasia (CAH), if untreated, carries high morbidity and mortality. A higher incidence of CAH is expected in countries where consanguinity is common, such as in the countries of...
3.
Lucas-Herald A, Bryce J, Kyriakou A, Ljubicic M, Arlt W, Audi L, et al.
Eur J Endocrinol
. 2021 Mar;
184(6):791-801.
PMID: 33780351
Objectives: To determine trends in clinical practice for individuals with DSD requiring gonadectomy. Design: Retrospective cohort study. Methods: Information regarding age at gonadectomy according to diagnosis; reported sex; time of...
4.
Naasse Y, Bakhchane A, Charoute H, Jennane F, Bignon-Topalovic J, Malki A, et al.
Sex Dev
. 2017 Dec;
11(5-6):269-274.
PMID: 29262419
R-spondin proteins are secreted agonists of canonical WNT/β-catenin signaling. Homozygous RSPO1 mutations cause a syndrome of 46,XX disorder of sexual development (DSD), palmoplantar keratoderma (PPK), and predisposition to squamous cell...
5.
Busiah K, Drunat S, Vaivre-Douret L, Bonnefond A, Simon A, Flechtner I, et al.
Lancet Diabetes Endocrinol
. 2014 Mar;
1(3):199-207.
PMID: 24622368
Background: Neonatal diabetes mellitus is a rare genetic form of pancreatic β-cell dysfunction. We compared phenotypic features and clinical outcomes according to genetic subtypes in a cohort of patients diagnosed...
6.
Reis A, Kannengiesser C, Jennane F, Manna T, Cheurfa N, Oudin C, et al.
Pediatr Diabetes
. 2011 Apr;
12(3 Pt 1):187-91.
PMID: 21518408
Wolcott-Rallison syndrome (WRS, OMIM 226980) is a rare autosomal recessive disorder characterized by permanent neonatal diabetes mellitus, epiphyseal dysplasia, and other multisystemic clinical manifestations. We described two novel mutations in...
7.
Bismuth E, Laborde K, Taupin P, Velho G, Ribault V, Jennane F, et al.
J Pediatr
. 2008 Mar;
152(4):540-5, 545.e1.
PMID: 18346512
Objectives: To describe the history, mechanisms, and consequences of cystic fibrosis (CF)-related diabetes, from childhood to early adulthood. Study Design: Pancreatic beta-cell function was estimated from the plasma insulin/glucose ratios...