Results 101 to 110 of about 30,173 (242)

Neuroradiological findings in hypogonadotropic hypogonadism.

Minerva endocrinologica, 2016
Hypogonadotropic hypogonadism (HH) is a clinical hallmark of a heterogeneous group of acquired and inherited diseases. Patients with HH undergo brain imaging in order to investigate morphological or signal abnormalities at the level of the hypothalamic-pituitary structures.
Salvalaggio A., Elefante A., Manara R
openaire   +3 more sources

MRI of ectopic posterior pituitary gland with dysgenesis of pituitary stalk in a patient with hypogonadotropic hypogonadism

Radiology Case Reports, 2018
The ectopic posterior pituitary is a rare condition which is characterized by the ectopic location of posterior lobe of pituitary, pituitary stalk abnormalities, and associated clinical manifestations of anterior lobe related growth hormone dysfunction ...
Ashim Kumar Lahiri, Ramanivas Sundareyan, David Jenkins, Anjumara Nilak   +3 more
doaj  

INFERTILITY IN MEN WITH PRIMARY HYPOGONADOTROPIC HYPOGONADISM

Андрология и генитальная хирургия, 2017
In this study, an analysis data on the etiology, pathogenesis, diagnosis and treatment of male sterility with hypogonadotropic hypogonadism. Examination of the patients requires attention of urologist, andrologist, endocrinologist, neurosurgeon, medical ...
O. B. Zhukov, L. I. Astafieva, S. V. Blinova   +2 more
doaj   +1 more source

Delayed-onset adrenal hypoplasia congenita and hypogonadotropic hypogonadism caused by a novel mutation in

Journal of International Medical Research, 2020
In this study, we described a male who presented with delayed-onset adrenal hypoplasia congenita (AHC) and mild hypogonadotropic hypogonadism (HHG) without a relevant family history. A novel mutation in the DAX1 (dosage-sensitive sex reversal, congenital
Siyue Liu, Libin Yan, Xinrong Zhou, Chen Chen, Daowen Wang, Gang Yuan   +5 more
doaj   +1 more source

Targeted Gene Panel Sequencing for Molecular Diagnosis of Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism.

Experimental and clinical endocrinology & diabetes, 2018
BACKGROUND Isolated gonadotropin-releasing hormone (GnRH) deficiency (IGD) is classified either as Kallmann syndrome (KS) with anosmia or normosmic idiopathic hypogonadotropic hypogonadism (nIHH) and caused by mutations in more than 30 different genes ...
Ja Hye Kim, G. Seo, Gu-Hwan Kim, Juyoung Huh, I. Hwang, J. Jang, H. Yoo, Jin-Ho Choi   +7 more
semanticscholar   +1 more source

Hypogonadotropic Hypogonadism in a Patient with Morbid Obesity

Obesity Surgery, 2007
Obesity has recently become one of the most important public health problems. It is associated with a high rate of mortality, mainly because of cardiovascular disease, and can cause hormonal abnormalities such as hypogonadotropic hypogonadism. Weight loss is very beneficial for obese patients, because it results in improvement or even normalization of ...
Mollar-Puchades, Miguel Ángel, Cámara-Gómez, Rosa, del Olmo-García, María Isabel, Ponce-Marco, José Luis, Segovia-Portolés, Raquel, Abellán-Galiana, Pablo, Piñón-Sellés, Francisco   +6 more
openaire   +4 more sources

PROKR2 mutations in idiopathic hypogonadotropic hypogonadism: selective disruption of the binding to a Gα‐protein leads to biased signaling

The FASEB Journal, 2018
Idiopathic hypogonadotropic hypogonadism (IHH) is a rare disorder caused by the deficient production, secretion, or action of gonadotropin‐releasing hormone. Prokineticin (PROK) receptor 2 (PROKR2), a causative gene for IHH, encodes a GPCR PROKR2.
Yaguang Zhao, Jiayu Wu, Hong Jia, Xinying Wang, R. Zheng, Fang Jiang, Dan-Na Chen, Zhiheng Chen, Jia-Da Li   +8 more
semanticscholar   +1 more source

The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome

Case Reports in Genetics, 2015
Two consanguineous Qatari siblings presented for evaluation: a 17-4/12-year-old male with hypogonadotropic hypogonadism, alopecia, intellectual disability, and microcephaly and his 19-year-old sister with primary amenorrhea, alopecia, and normal ...
Molly B. Sheridan, Elizabeth Wohler, Denise A. S. Batista, Carolyn Applegate, Julie Hoover-Fong   +4 more
doaj   +1 more source

Functional State of Pituitary-Gonadal System in Men with Non-functional Pituitary Adenomas and Growth Hormone Deficiency in Adults

Mìžnarodnij Endokrinologìčnij Žurnal, 2014
We examined 71 adult patients with growth hormone deficiency caused by non-functional masses of chiasmosellar area. Patients were divided into two groups: the first one — men aged 18 to 49 years and the second one — 49 years and above.
Yu.M. Urmanova, M.Yu. Shakirova, D.A. Aliyeva   +2 more
doaj   +1 more source

Studies of the pituitary-Leydig cell axis in young men with hypogonadotropic hypogonadism and hyposmia: comparison with normal men, prepuberal boys, and hypopituitary patients [PDF]

, 1969
C. Wayne Bardin, Griff T. Ross, Arleen B. Rifkind, Charles M. Cargille, Mortimer B. Lipsett   +4 more
openalex   +1 more source