Effects of gonadotropin and testosterone treatments on Lipoprotein(a), high density lipoprotein particles, and other lipoprotein levels in male hypogonadism. [PDF]
, 1996 Metin Özata +6 more
openalex +1 more source
Journal of Neuroendocrinology, EarlyView.Abstract Patients with gastroenteropancreatic–neuroendocrine tumors (GEP‐NETs) may present skeletal fragility that might be related to multiple factors, including bone metastases, vitamin D deficiency, hormone secretion, and disease treatments. This study examines the prevalence and determinants of fragility fractures in low grading (G1‐G2) GEP‐NETs ...
Alessandro Brunetti +15 more
wiley +1 more source
New mutations of DAX-1 genes in two Japanese patients with X-linked congenital adrenal hypoplasia and hypogonadotropic hypogonadism. [PDF]
, 1996 Toshihiko Yanase +5 more
openalex +1 more source
Germ cell and other tumors in individuals with differences in sex development
CA: A Cancer Journal for Clinicians, EarlyView.Abstract Approximately one in 3500 to one in 5100 live‐born infants have atypical external genital development, known as differences in sex development (DSD). In 2005, an expert consensus conference thoroughly reviewed aspects of health care for individuals with DSD.
Selma Feldman Witchel +1 more
wiley +1 more source
Profound Hypogonadism Has Significant Negative Effects on Calcium Balance in Males: A Calcium Kinetic Study [PDF]
, 1999 Nelly Mauras +4 more
openalex +1 more source
Medical Journal of Australia, EarlyView.Abstract Introduction Monogenic diabetes accounts for 2–5% of diabetes. Although its identification has substantial therapeutic implications, more than 80% of affected individuals are undiagnosed or misdiagnosed as having type 1 or 2 diabetes. This consensus statement reviews genetic testing for monogenic diabetes in adults and provides evidence‐based ...
Sunita MC De Sousa +10 more
wiley +1 more source
Prolonged post-androgen abuse hypogonadism: potential mechanisms and a proposed standardized diagnosis. [PDF]
Front Endocrinol (Lausanne)van Os J, Smit DL, Bond P, de Ronde W.
europepmc +1 more source
American Journal of Medical Genetics Part A, Volume 197, Issue 8, August 2025.ABSTRACT Prader‐Willi syndrome (PWS) is a neurodevelopmental disorder typically caused by large deletions or imprinting defects on chromosome 15q11.2, encompassing multiple genes. While the contribution of individual genes to the PWS phenotype remains unclear, previous studies suggested that isolated deletions of MAGEL2, NDN, and MKRN3, excluding the ...
Jannis Buecking +6 more
wiley +1 more source
Certain Metabolic Syndrome Component Combinations are Linked to Increased Risk of Hypogonadism in Taiwanese Men. [PDF]
Diabetes Metab Syndr ObesHong YH +6 more
europepmc +1 more source
Successful Treatment of Dwarfism and Hypogonadism after Total Removal of Craniopharyngioma
, 1985 Tatsuya Kobayashi +4 more
openalex +2 more sources