Results 31 to 40 of about 25,285 (271)

Growth hormone deficiency during young adulthood and the benefits of growth hormone replacement [PDF]

open access: yes, 2016
Until quite recently, the management of children with growth hormone deficiency (GHD) had focussed on the use of recombinant human GH (rhGH) therapy to normalise final adult height.
Ahmed, S.F.   +3 more
core   +2 more sources

Hypopituitarism in the tropics

open access: yesIndian Journal of Endocrinology and Metabolism, 2011
Pituitary disorders, including hypopituitarism and hypothalamic pituitary insufficiency (HPI), are common conditions seen by endocrinologists in tertiary/referral centers. The important causes of hypopituitarism are pituitary tumors (including craniopharyngioma), postoperative and postradiotherapy states, vascular conditions, autoimmune diseases such ...
Vaman Khadilkar   +2 more
openaire   +4 more sources

Hypopituitarism: A Sequela of Severe Hypoxic Encephalopathy

open access: yesJournal of the Formosan Medical Association, 2006
Central diabetes insipidus (DI) is an established phenomenon after hypoxic encephalopathy or brain death, but hypopituitarism is seldom described. This study investigated the characteristics of 11 patients with DI and hypopituitarism which developed ...
Deng-Huang Su
doaj   +1 more source

Evidence That the Etiology of Congenital Hypopituitarism Has a Major Genetic Component but Is Infrequently Monogenic

open access: yesFrontiers in Genetics, 2021
PurposeCongenital hypopituitarism usually occurs sporadically. In most patients, the etiology remains unknown.MethodsWe studied 13 children with sporadic congenital hypopituitarism. Children with non-endocrine, non-familial idiopathic short stature (NFSS)
Youn Hee Jee   +14 more
doaj   +1 more source

Non-functioning pituitary adenoma underwent surgery: a multicenter retrospective study over the last four decades (1977–2015) [PDF]

open access: yes, 2017
[Abstract] Objective. To assess clinical features, diagnostic procedures, therapies and outcomes in patients with clinically non-functioning pituitary adenomas (NFPAs) surgically treated over the last four decades. Design and methods.
Arcano, Karina   +6 more
core   +2 more sources

Hypothalamic hypopituitarism secondary to suprasellar metastases from small cell lung cancer: a case report and review of the literature

open access: yesJournal of Medical Case Reports, 2018
Background Metastasis to the pituitary gland is an infrequent clinical problem, and the symptoms caused by metastases have been reported in only 2.5–18.2% of the cases.
Ryohei Ono   +5 more
doaj   +1 more source

Effects of human recombinant growth hormone on exercise capacity, cardiac structure, and cardiac function in patients with adult-onset growth hormone deficiency [PDF]

open access: yes, 2017
Objective Epidemiological studies suggest that adult-onset growth hormone deficiency (AGHD) might increase the risk of death from cardiovascular causes. Methods This was a 6-month double-blind, placebo-controlled, randomised, cross-over trial followed by
Atkin, S. L.   +11 more
core   +1 more source

Development and validation of a new questionnaire assessing quality of life in adults with hypopituitarism: Adult Hypopituitarism Questionnaire (AHQ). [PDF]

open access: yesPLoS ONE, 2012
OBJECTIVE: To develop and validate the Adult Hypopituitarism Questionnaire (AHQ) as a disease-specific, self-administered questionnaire for evaluation of quality of life (QOL) in adult patients with hypopituitarism.
Hitoshi Ishii   +10 more
doaj   +1 more source

Sheehan's syndrome (postpartum hypopituitarism), report of a case [PDF]

open access: yes, 1962
A case of postpartum necrosis of the anterior lobe of the pituitary, known as Sheehan's syndrome, is presented. The patient has done well on a combined replacement therapy with cortisone and thyroid.
Kibata, Masayoshi, Miyoshi, Isao
core   +1 more source

Homozygous CDH2 variant may be associated with hypopituitarism without neurological disorders

open access: yesEndocrine Connections, 2023
Context: Congenital hypopituitarism is a genetically heterogeneous cond ition. Whole exome sequencing (WES) is a promising approach for molecular di agnosis of patients with this condition.
Nathalia G B P Ferreira   +19 more
doaj   +1 more source

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