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2010, Frontiers of hormone research, ISBN 9783805586177, Volume 39
Web Resource
Case Report - MRI findings in Kallmann syndrome, 10/2004
Kallmann syndrome (KS) is a neuronal migration disorder characterised by hypogonadotrophic hypogonadism and anosmia or hyposmia. Five patients with clinical... 
Neurology | Kallmann syndrome, Hypogonadotrophic hypogonadism, Anosmia, Magnetic Resonance Imaging, Olfactory system. ni04168
Journal
Clinical Neurophysiology, ISSN 1388-2457, 03/2018, Volume 129, Issue 3, pp. 707 - 708
Journal Article
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, ISSN 1008-8830, 11/2018, Volume 20, Issue 11, pp. 925 - 929
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 08/2013, Volume 93, Issue 2, pp. 249 - 263
Journal Article
Medicine (United States), ISSN 0025-7974, 07/2018, Volume 97, Issue 27
Journal Article
JAMA Otolaryngology–Head & Neck Surgery, ISSN 2168-6181, 01/2016, Volume 142, Issue 1, pp. 97 - 98
Journal Article
2010, Frontiers of hormone research, ISBN 3805586175, Volume 39., x, 174
Over the past decade, the understanding of the processes involved in the regulation of gonadotropin-releasing hormone and its dysfunction has greatly... 
Kallmann Syndrome | Hypogonadism | genetics
Book
Annales d'Endocrinologie, ISSN 0003-4266, 10/2017, Volume 78, Issue 5, pp. 455 - 461
Objective The aim of this retrospective study was to perform magnetic resonance imaging assessment of olfactory pathway and skull base abnormalities in... 
Olfaction Disorder | Magnetic resonance imaging | Olfactory bulb | Kallmann syndrome | Hypogonadism
Journal Article
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, ISSN 0027-8424, 08/2017, Volume 114, Issue 31, pp. 8132 - 8134
Journal Article
Frontiers in cellular neuroscience, ISSN 1662-5102, 2019, Volume 13, pp. 146 - 146
[This corrects the article DOI: 10.3389/fncel.2019.00070.]. 
olfactory bulbs | hypogonadotropic hypogonadism | Robo | GnRH-1 | Kallmann syndrome | neuronal migration
Journal Article
Ear, Nose & Throat Journal, ISSN 0145-5613, 3/2019, Volume 98, Issue 3, pp. 129 - 130
Journal Article
Journal fur Gynakologische Endokrinologie, ISSN 1997-6690, 12/2018, Volume 28, Issue 4, pp. 137 - 147
Journal Article
European Journal of Endocrinology, ISSN 0804-4643, 06/2016, Volume 174, Issue 6, pp. R267 - R274
Congenital hypogonadotropic hypogonadism (CHH) is characterized by lack of puberty and infertility. Traditionally, it has been considered a life-long condition... 
DELAYED PUBERTY | GONADOTROPIN-RELEASING-HORMONE | ENDOCRINOLOGY & METABOLISM | FERTILE EUNUCH | LINKED KALLMANN-SYNDROME | RECEPTOR GENE | HOMOZYGOUS R262Q MUTATION | CANDIDATE GENE | INDUCTION | DEFICIENCY | PULSATILE
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 05/2005, Volume 90, Issue 5, pp. 3122 - 3127
A common cause of micropenis is congenital hypogonadotropic hypogonadism, whether isolated or associated with multiple pituitary hormone deficiencies. The... 
GERM-CELLS | ANGELMAN-SYNDROMES | ENDOCRINOLOGY & METABOLISM | ADRENAL HYPOPLASIA CONGENITA | IDIOPATHIC HYPOGONADOTROPIC HYPOGONADISM | OPTIC-NERVE HYPOPLASIA | KALLMANN-SYNDROME | SERTOLI-CELLS | GROWTH-HORMONE DEFICIENCY | PRADER-WILLI-SYNDROME | LUTEINIZING-HORMONE
Journal Article
Gynakologische Endokrinologie, ISSN 1610-2894, 05/2018, Volume 16, Issue 2, pp. 103 - 114
Journal Article
HUMAN REPRODUCTION, ISSN 0268-1161, 03/2017, Volume 32, Issue 3, pp. 704 - 711
STUDY QUESTION: What is the prevalence and functional consequence of ANOS1 (KAL1) mutations in a group of men with congenital hypogonadotropic hypogonadism... 
NLGN4 | VCX-A | hypogonadotropic hypogonadism | Kallmann syndrome | DEFICIENCY | MOLECULES | OBSTETRICS & GYNECOLOGY | mutation | ADHESION | REPRODUCTIVE BIOLOGY | ANOS1 | KAL1 | LINKED KALLMANN-SYNDROME | GNRH | DELETIONS
Journal Article
CLINICAL AND EXPERIMENTAL OBSTETRICS & GYNECOLOGY, ISSN 0390-6663, 2019, Volume 46, Issue 2, pp. 331 - 332
Kallmann syndrome (KS) is a genetic disorder characterized by hypogonadotropic hypogonadism, anosmia, and infertility, occurring in approximately one in 50,000... 
Balanced reciprocal translocation | Kallmann syndrome | Anti-Mullerian hormone | OBSTETRICS & GYNECOLOGY
Journal Article
Annals of Pediatric Endocrinology and Metabolism, ISSN 2287-1012, 06/2018, Volume 23, Issue 2, pp. 57 - 61
Constitutional delay of growth and puberty (CDGP) is the most common cause of delayed puberty (DP), is mainly found in males, and is characterized by short... 
Puberty | Turner syndrome | Kallmann syndrome | Delayed puberty | Hypogonadism | Review
Journal Article
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