Kallmann's syndrome: Clues to clinical diagnosis

International Journal of Impotence Research

Volumn 12, Issue 5, 2000, Pages 269-271

  John, H ^a   Schmid, C ^a  

^a UNIVERSITY HOSPITAL ZURICH   (Switzerland)

Author keywords

Anosmia; Cryptorchidism; Gonadotropin releasing hormone; Hypogonadism

Indexed keywords

GONADORELIN; TESTOSTERONE;

ADOLESCENT; ADULT; ANOSMIA; ARTICLE; CLINICAL ARTICLE; CRYPTORCHISM; HORMONE SUBSTITUTION; HUMAN; HYPOGONADOTROPIC HYPOGONADISM; KALLMANN SYNDROME; MALE; ORCHIDOPEXY; OUTPATIENT; PRIORITY JOURNAL; PUBERTY;

EID: 0034534717     PISSN: 09559930     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ijir.3900568     Document Type: Article

References (7)

1. The genetic aspects of primary eunuchoidism
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3. A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
4. Testosterone supplementation for hypogonadal impotence: Assessment of biochemical measures and therapeutic outcomes
5. Transdermal androgen treatment in the impotent hypogonadal aging male
6. Gonadotropin-releasing hormone deficiency in man: Diagnosis and treatment with exogenous gonadotropin-releasing hormone
7. Comparison of gonadotropin-releasing hormone and gonadotropin therapy in male patients with idiopathic hypothalamic hypogonadism