Literature DB >> 23207501

Kallmann syndrome.

Neil Smith1, Richard Quinton.   

Abstract

Entities:  

Mesh：

Year:  2012        PMID： 23207501     DOI： 10.1136/bmj.e6971

Source DB:  PubMed          Journal:  BMJ        ISSN： 0959-8138


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  5 in total

1.  Kallmann syndrome with FGFR1 and KAL1 mutations detected during fetal life.

Authors:  Julie Sarfati; Claire Bouvattier; Hélène Bry-Gauillard; Alejandra Cartes; Jérôme Bouligand; Jacques Young
Journal:  Orphanet J Rare Dis       Date:  2015-06-09       Impact factor: 4.123

2.  Psychosexual development in men with congenital hypogonadotropic hypogonadism on long-term treatment: a mixed methods study.

Authors:  Andrew A Dwyer; Richard Quinton; Nelly Pitteloud; Diane Morin
Journal:  Sex Med       Date:  2015-03       Impact factor: 2.491

3.  Safety and tolerability of one-year intramuscular testosterone regime to induce puberty in older men with CHH.

Authors:  Agnieszka Pazderska; Yaasir Mamoojee; Satish Artham; Margaret Miller; Stephen G Ball; Tim Cheetham; Richard Quinton
Journal:  Endocr Connect       Date:  2018-01       Impact factor: 3.335

Review 4.  Congenital Hypogonadotrophic Hypogonadism: Minipuberty and the Case for Neonatal Diagnosis.

Authors:  Du Soon Swee; Richard Quinton
Journal:  Front Endocrinol (Lausanne)       Date:  2019-02-21       Impact factor: 5.555

5.  Identifying the unmet health needs of patients with congenital hypogonadotropic hypogonadism using a web-based needs assessment: implications for online interventions and peer-to-peer support.

Authors:  Andrew A Dwyer; Richard Quinton; Diane Morin; Nelly Pitteloud
Journal:  Orphanet J Rare Dis       Date:  2014-06-11       Impact factor: 4.123
  5 in total

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