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Literature DB >> 20531282

Adult-onset idiopathic hypogonadotropic hypogonadism: possible aetiology, clinical manifestations and management.

Jiang-Feng Mao, Min Nie, Shuang-Yu Lu, Xue-Yan Wu.

Abstract

Entities: Disease

Mesh：

Substances：

Year: 2010 PMID： 20531282 PMCID： PMC3739368 DOI： 10.1038/aja.2010.34

Source DB: PubMed Journal: Asian J Androl ISSN： 1008-682X Impact factor: 3.285

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13 in total

1. Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism.

Authors: Beatriz R Versiani; Ericka Trarbach; Marcel Koenigkam-Santos; Antonio Carlos Dos Santos; Lucila L K Elias; Ayrton C Moreira; Ana Claudia Latronico; Margaret de Castro
Journal: Clin Endocrinol (Oxf) Date: 2007-02 Impact factor: 3.478

2. Adult onset idiopathic hypogonadotrophic hypogonadism may be overdiagnosed.

Authors: R Quinton; G S Conway; H S Jacobs; P M Bouloux; M P Vanderpump
Journal: BMJ Date: 1998-08-29

3. Adult-onset idiopathic hypogonadotropic hypogonadism--a treatable form of male infertility.

Authors: L B Nachtigall; P A Boepple; F P Pralong; W F Crowley
Journal: N Engl J Med Date: 1997-02-06 Impact factor: 91.245

4. A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism.

Authors: Antonio Balsamo; Alessandra Antelli; Lilia Baldazzi; Federico Baronio; Dina Lazareva; Alessandra Cassio; Alessandro Cicognani
Journal: Am J Med Genet A Date: 2005-06-15 Impact factor: 2.802

5. Antipituitary antibodies against gonadotropin-secreting cells in adult male patients with apparently idiopathic hypogonadotropic hypogonadism.

Authors: Annamaria De Bellis; Antonio Agostino Sinisi; Marisa Conte; Concetta Coronella; Giuseppe Bellastella; Dario Esposito; Daniela Pasquali; Giuseppe Ruocco; Antonio Bizzarro; Antonio Bellastella
Journal: J Clin Endocrinol Metab Date: 2006-11-07 Impact factor: 5.958

6. Adult-onset idiopathic hypogonadotropic hypogonadism due to isolated pituitary gonadotropin deficiency.

Authors: Fumika Suzuki; Chikara Shimizu; Masaaki Umetsu; So Nagai; Jun Takeuchi; Mikiko Endo; Hideaki Miyoshi; Narihito Yoshioka; Mitsumasa Kubo; Takao Koike
Journal: Intern Med Date: 2004-07 Impact factor: 1.271

7. X chromosome-linked Kallmann syndrome: clinical heterogeneity in three siblings carrying an intragenic deletion of the KAL-1 gene.

Authors: Nathalie Massin; Christophe Pêcheux; Corinne Eloit; Jean-Louis Bensimon; Julie Galey; Frédérique Kuttenn; Jean-Pierre Hardelin; Catherine Dodé; Philippe Touraine
Journal: J Clin Endocrinol Metab Date: 2003-05 Impact factor: 5.958