Results 191 to 200 of about 14,409 (206)
Some of the next articles are maybe not open access.

Gigantism with hypopituitarism

The American Journal of Medicine, 1963
Abstract A case is reported in which there is definite evidence of diminished production of thyrotropin, adrenocorticotropin and gonadotropin, with presumptive evidence of production of somatotropin, and a normal sella turcica. A review of the literature is included and fails to reveal a similar previous case documented by clinical and laboratory ...
George F. Cahill   +2 more
openaire   +3 more sources

HYPOPARATHYROIDISM AND HYPOPITUITARISM

Australasian Annals of Medicine, 1962
SUMMARYAn instance of hypoparathyroidism and hypopituitarism is reported as it occurred in a man, aged 27 years. The clinical features and the methods of establishing the diagnosis are discussed. Some dental features unusual in humans are also described.
R. F. Thew, Stanley Goulston
openaire   +3 more sources

Subclinical hypopituitarism

Best Practice & Research Clinical Endocrinology & Metabolism, 2012
The presence of subclinical or minor pituitary hormone deficiencies could be recognised in clinical practice and might represent intermediate situations among normal pituitary hormone secretion and clinical hypopituitarism. However, this entity has not been correctly identified and associated clinical impairment and even more, long-term consequences ...
Eva, Fernandez-Rodriguez   +3 more
openaire   +2 more sources

Transient Hypopituitarism

Endocrine Practice, 1995
Spontaneous recovery of pituitary function in patients with hypopituitarism is rare. We report the case of a 30-year-old man in whom hypopituitarism and sudden onset of bilateral hearing loss developed after a viral infection. No evidence of a mass lesion was detected on computed tomography or magnetic resonance imaging of the pituitary gland.
G H, Tan, W F, Young
openaire   +2 more sources

THE INVESTIGATION OF HYPOPITUITARISM

Australasian Annals of Medicine, 1967
SummaryA dynamic scheme is described for the investigation of patients suspected of having hypopituitarism. The hypothalamus and pituitary are investigated as a single functional unit by the use of basal studies of each trophic hormone and the subsequent hormonal response to stimuli.
openaire   +3 more sources

Congenital Hypopituitarism

Clinics in Perinatology, 2018
Mutations of growth hormone genes and pituitary transcription factors account for a small proportion of cases of severe congenital hypopituitarism. Most cases show characteristic MRI findings of pituitary stalk interruption syndrome. Clinical suspicion should prompt assessment of cortisol, free T4, thyroid-stimulating hormone, and growth hormone levels
openaire   +2 more sources

Fertility and hypopituitarism.

Journal of endocrinological investigation, 2008
Fertility outcomes in hypopituitaric women are about half of those reported in isolated hypogonadotropic hypogonadism; GH deficiency (GHD) is a major contributor to poor pregnancy rate. GH seems to play a physiological role in the control of male sexual maturation and adult reproductive functions.
Milardi, Domenico   +4 more
openaire   +2 more sources

Mortality and hypopituitarism

Growth Hormone & IGF Research, 1999
Michael C. Sheppard, Paul M. Stewart
openaire   +3 more sources

Hypopituitarism

New England Journal of Medicine, 1994
openaire   +2 more sources

Hypopituitarism

1984
Publisher Summary This chapter discusses the causes of hypopituitarism. Hypopituitarism can result from metastatic spread either to the pituitary itself or it may be secondary to failure of release of hypothalamic factors. The hormonal abnormality reflects the exact anatomical site of tumor spread.
openaire   +2 more sources

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