A Tunisian Patient with Two Rare Syndromes: Triple A Syndrome and Congenital Hypogonadotropic Hypogonadism-Reference-Cited by-同舟云学术

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A Tunisian Patient with Two Rare Syndromes: Triple A Syndrome and Congenital Hypogonadotropic Hypogonadism

Published:2014 Issue:5 Volume:82 Page:338-343
ISSN:1663-2818
Container-title:Hormone Research in Paediatrics
language:en
Short-container-title:Horm Res Paediatr

Author:

Cherif Ben Abdallah Lamia,Lakhoua Youssef,Nagara Majdi,Khiari Karima,Elouej Sahar,Messaoud Olfa,Bouyacoub Yosra,Romdhane Lilia,Turki Zinet,Abdelhak Sonia,Ben Abdallah Nejib

Publisher

S. Karger AG

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Congenital hypopituitarism in familial Turner syndrome cases caused by a highly prevalent PROP1 gene mutation in Tunisia;Endocrine and Metabolic Science;2024-03

2. Triple-A Syndrome in Morocco: Founder Effect, Age Estimation of the AAAS c.1331+1G>A Variant, and Implications for Genetic Diagnosis;Molecular Syndromology;2023-09-29

3. Growth alterations in rare forms of primary adrenal insufficiency: a neglected issue in paediatric endocrinology;Endocrine;2022-10-30

4. Triple-A Syndrome (TAS): An In-Depth Overview on Genetic and Phenotype Heterogeneity;Protein & Peptide Letters;2020-12-02

5. Understanding the functions of kisspeptin and kisspeptin receptor (Kiss1R) from clinical case studies;Peptides;2019-10

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