Results 21 to 30 of about 1,468 (202)
Successful fertility treatment with gonadotrophin therapy for male hypogonadotrophic hypogonadism. [PDF]
Endocrinol Diabetes Metab Case Rep, 2016 Rajkanna J, Tariq S, Oyibo SO.
europepmc +3 more sources
The first Australian evidence-based guidelines on male infertility. [PDF]
Med J AustAbstract Introduction Infertility affects about one in six couples and a male factor may contribute to 50% of cases. Until recently, no Australian‐based clinical guidelines for the management of male infertility had been published. A panel of experts was assembled to formulate the first Australian evidence‐based guidelines on male infertility.
Katz DJ +6 more
europepmc +2 more sources
Use of genetic models of idiopathic hypogonadotrophic hypogonadism in mice and men to understand the mechanisms of disease. [PDF]
Exp Physiol, 2013 Lippincott MF, True C, Seminara SB.
europepmc +3 more sources
Adult onset idiopathic hypogonadotrophic hypogonadism may be overdiagnosed. [PDF]
BMJ, 1998 Quinton R +4 more
europepmc +3 more sources
Adipocyte insulin action in hypogonadotrophic hypogonadism [PDF]
Human Reproduction, 2000 In-vitro studies of adipose tissue have shown that patients with polycystic ovarian syndrome (PCOS) have marked insulin resistance, the abnormalities being more pronounced during amenorrhoea compared to following an ovulatory cycle. If the insulin resistance in PCOS is a reflection of anovulation then patients with hypogonadotrophic hypogonadism (HH ...
Marsden PJ, Murdoch AP, Taylor R
openaire +3 more sources
Pitfalls of using sequence databases for heterologous expression studies – a technical review
The Journal of Physiology, Volume 601, Issue 9, Page 1611-1623, 1 May 2023., 2023 Abstract figure legend Projects involving heterologous gene expression are often characterised by similar steps. Initially, database research (A) is necessary to retrieve information of full or partial sequences of a gene of interest. A multitude of genome assemblies are annotated and deposited in public databases or are available for refined search ...
Stephan Maxeiner +2 more
wiley +1 more source
Kallmann syndrome: MRI findings
Indian Journal of Endocrinology and Metabolism, 2013 Kallmann syndrome (KS) is a disease clinically characterized by the association of hypogonadotrophic hypogonadism and anosmia or hyposmia. It is a neuronal migration disorder.
Houneida Zaghouani +5 more
doaj +1 more source
Clinical Genetics, Volume 103, Issue 1, Page 45-52, January 2023., 2023 We describe the first patient with biallelic loss‐of‐function variants in the SLC13A1 gene, encoding a renal and intestinal sulfate transporter. The consequential loss of renal sulfate reabsorption leads to hypersulfaturia and hyposulfatemia which is associated with a mild Spondylo‐Epi‐Metaphyseal skeletal Dysplasia. Abstract Sulfate is the fourth most
Jiddeke M. van de Kamp +13 more
wiley +1 more source
EBioMedicine, 2018 Background: Nerve growth factor (NGF) plays essential roles in regulating the development and maintenance of central sympathetic and sensory neurons. However, the effects of NGF on hypogonadism remain unexplored.
Jiao Luo +11 more
doaj +1 more source
Constitutional delay of growth and puberty in boys: review
Mìžnarodnij Endokrinologìčnij Žurnal, 2019 The review focuses on the diagnosis, clinical and general therapeutic approach to constitutional growth and delayed puberty and hypogonadotrophic hypogonadism in men, which are difficult to distinguish. Clinical history and physical examination should be
A.B. Grossman +4 more
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