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Der Hautarzt, 2011
The Kallmann syndrome is a very rare congenital association of gonadotropin-releasing hormone deficiency and hyposmia or anosmia. Clinically it is characterized by low serum concentrations of testosterone and inadequate low levels of luteinizing hormone and follicle-stimulating hormone as well as incomplete sexual maturation, lack of secondary sexual ...
N.J. Neumann+3 more
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The Kallmann syndrome is a very rare congenital association of gonadotropin-releasing hormone deficiency and hyposmia or anosmia. Clinically it is characterized by low serum concentrations of testosterone and inadequate low levels of luteinizing hormone and follicle-stimulating hormone as well as incomplete sexual maturation, lack of secondary sexual ...
N.J. Neumann+3 more
openaire +3 more sources
The Indian Journal of Pediatrics, 2007
Kallmann's syndrome is a rare genetic disorder due to abnormal migration of olfactory axons and gonadotropin releasing hormone producing neurons, characterized by hypogonadism and anosmia. The prevalence of Kallmann's syndrome is 1:10,000 to 1:60,000 with a male to female ratio of 5:1.
Akhil M. Kulkarni+4 more
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Kallmann's syndrome is a rare genetic disorder due to abnormal migration of olfactory axons and gonadotropin releasing hormone producing neurons, characterized by hypogonadism and anosmia. The prevalence of Kallmann's syndrome is 1:10,000 to 1:60,000 with a male to female ratio of 5:1.
Akhil M. Kulkarni+4 more
openaire +3 more sources
Kallmann's Syndrome and Transsexualism
Archives of Sexual Behavior, 2001Until the present, in the world literature only one patient with Kallmann's syndrome has been reported who became transsexual. This patient was seen almost 50 years ago. In this report, a second case is presented to encourage studies of the sexual and gender identity development in these patients.
Bernd Meyenburg, Volkmar Sigusch
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