Results 11 to 20 of about 30,173 (242)
Metabolic Disorders and Male Hypogonadotropic Hypogonadism [PDF]
Frontiers in Endocrinology, 2019 Several studies highlight that testosterone deficiency is associated with, and predicts, an increased risk of developing metabolic disorders, and, on the other hand, is highly prevalent in obesity, metabolic syndrome and type-2 diabetes mellitus.
Rosario Pivonello +6 more
doaj +6 more sources
Psychological Aspects of Congenital Hypogonadotropic Hypogonadism [PDF]
Frontiers in Endocrinology, 2019 Congenital hypogonadotropic hypogonadism/Kallmann syndrome (CHH/KS) is a rare, treatable form of infertility. Like other rare disease patients, individuals with CHH/KS frequently experience feelings of isolation, shame, and alienation.
Andrew A. Dwyer +3 more
doaj +5 more sources
Genetics of hypogonadotropic hypogonadism [PDF]
Translational Andrology and Urology, 2020 Male congenital hypogonadotropic hypogonadism (CHH) is a heterogenous group of genetic disorders that cause impairment in the production or action of gonadotropin releasing hormone (GnRH). These defects result in dysfunction of the hypothalamic-pituitary-
Adam C. Millar, H. Faghfoury, J. Bieniek
semanticscholar +4 more sources
Hypogonadotropic Hypogonadism in Men With Diabesity [PDF]
Diabetes Care, 2018 One-third of men with obesity or type 2 diabetes have subnormal free testosterone concentrations. The lower free testosterone concentrations are observed in obese men at all ages, including adolescents at completion of puberty.
S. Dhindsa +3 more
semanticscholar +3 more sources
Hypogonadotropic Hypogonadism Revisited [PDF]
Clinics, 2013 Impaired testicular function, i.e., hypogonadism, can result from a primary testicular disorder (hypergonadotropic) or occur secondary to hypothalamic-pituitary dysfunction (hypogonadotropic).
Renato Fraietta +2 more
doaj +6 more sources
JCRPE, 2021 Objective:Carboxypeptidase E (CPE) plays a critical role in the biosynthesis of peptide hormones and neuropeptides in the endocrine system and central nervous system.
Asude Durmaz +9 more
doaj +2 more sources
Update on the Genetics of Idiopathic Hypogonadotropic Hypogonadism [PDF]
Journal of Clinical Research in Pediatric Endocrinology, 2017 Traditionally, idiopathic hypogonadotropic hypogonadism (IHH) is divided into two major categories: Kallmann syndrome (KS) and normosmic IHH (nIHH). To date, inactivating variants in more than 50 genes have been reported to cause IHH. These mutations are
A. Topaloğlu
semanticscholar +5 more sources
HYPOGONADOTROPIC HYPOGONADISM (REVIEW)
Педиатрическая фармакология, 2008 The review is dedicated to the problem of hypogonadotropic hypogonadism. Modern ideas of the stages of normal sexual development of girls, etiology and pathogenesis of constitutional arrest of sexual development and hypogonadotropic hypogonadism are ...
E.V. Uvarova, E.V. Trifonova
doaj +3 more sources
Gonadotropin-Releasing Hormone Receptor (GnRHR) and Hypogonadotropic Hypogonadism. [PDF]
Int J Mol Sci, 2023 Human sexual and reproductive development is regulated by the hypothalamic-pituitary-gonadal (HPG) axis, which is primarily controlled by the gonadotropin-releasing hormone (GnRH) acting on its receptor (GnRHR).
Fanis P +4 more
europepmc +2 more sources
New perspectives in functional hypogonadotropic hypogonadism: beyond late onset hypogonadism
Frontiers in Endocrinology, 2023 Functional hypogonadotropic hypogonadism (FHH) is an increasingly frequent condition, whose pathological mechanisms are not yet fully clarified. The concept of FHH has now completely replaced that of late onset hypogonadism, that only concerned the ...
M. Spaziani +5 more
semanticscholar +1 more source