Results 11 to 20 of about 41,302 (312)
Metabolic Disorders and Male Hypogonadotropic Hypogonadism
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 +2 more sources
New findings in oligogenic inheritance of congenital hypogonadotropic hypogonadism
Introduction Congenital hypogonadotropic hypogonadism results from a dysfunction of the hypothalamic-pituitary-gonadal axis, which is essential for the development and function of the reproductive system. It may be associated with anosmia, referred to as
Agnieszka Gach +13 more
doaj +2 more sources
Normosmic idiopathic hypogonadotropic hypogonadism due to a novel GNRH1 variant in two siblings
Hypogonadotropic hypogonadism is characterised by insufficient secretion of pituitary gonadotropins resulting in delayed puberty, anovulation and azoospermia. When hypogonadotropic hypogonadism occurs in the absence of structural or functional lesions of
Satyanarayana V Sagi +9 more
doaj +2 more sources
New perspectives in functional hypogonadotropic hypogonadism: beyond late onset hypogonadism [PDF]
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 ...
Matteo Spaziani +5 more
openalex +2 more sources
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
Psychological Aspects of Congenital Hypogonadotropic Hypogonadism
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 +2 more sources
Gonadotropin-Releasing Hormone Receptor (GnRHR) and Hypogonadotropic Hypogonadism
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).
P. Fanis +4 more
semanticscholar +1 more source
Objective Hypogonadotropic hypogonadism is characterized by inadequate secretion of pituitary gonadotropins, leading to absent, partial, or arrested puberty.
E. Alexander +7 more
semanticscholar +1 more source
Genetic architecture of self-limited delayed puberty and congenital hypogonadotropic hypogonadism
Distinguishing between self limited delayed puberty (SLDP) and congenital hypogonadotropic hypogonadism (CHH) may be tricky as they share clinical and biochemical characteristics. and appear to lie within the same clinical spectrum.
V. Vezzoli +7 more
semanticscholar +1 more source
The nitric oxide (NO) signaling pathway in hypothalamic neurons plays a key role in the regulation of the secretion of gonadotropin-releasing hormone (GnRH), which is crucial for reproduction.
Konstantina Chachlaki +34 more
semanticscholar +1 more source

