Results 171 to 180 of about 15,927 (211)
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Southern Medical Journal, 1977
Hypopituitarism is a rarely reported accompaniment of diabetes mellitus. Autopsy studies suggest, however, that pituitary lesions are ten times more common in diabetics than in nondiabetics. Three cases of diabetes with hypopituitarism are reported.
L D, Olson, W W, Winternitz
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Hypopituitarism is a rarely reported accompaniment of diabetes mellitus. Autopsy studies suggest, however, that pituitary lesions are ten times more common in diabetics than in nondiabetics. Three cases of diabetes with hypopituitarism are reported.
L D, Olson, W W, Winternitz
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The Lancet
Partial or complete deficiency of anterior or posterior pituitary hormone production leads to central hypoadrenalism, central hypothyroidism, hypogonadotropic hypogonadism, growth hormone deficiency, or arginine vasopressin deficiency depending on the hormones affected. Hypopituitarism is rare and likely to be underdiagnosed, with an unknown but rising
Maria, Fleseriu +4 more
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Partial or complete deficiency of anterior or posterior pituitary hormone production leads to central hypoadrenalism, central hypothyroidism, hypogonadotropic hypogonadism, growth hormone deficiency, or arginine vasopressin deficiency depending on the hormones affected. Hypopituitarism is rare and likely to be underdiagnosed, with an unknown but rising
Maria, Fleseriu +4 more
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Gigantism with hypopituitarism
The American Journal of Medicine, 1963Abstract 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 ...
J K, GOLDMAN, G F, CAHILL, G W, THORN
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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
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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
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Hypopituitarism in the elderly
Maturitas, 2012Pituitary dysfunction in elderly can represent a true diagnostic and therapeutic challenge to clinicians caring for these patients. Symptoms associated with partial or total hypopituitarism, such as fatigue, lower muscle strength and decreased libido, are nonspecific and can be often attributed to normal aging.
Marianna, Antonopoulou +4 more
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Hyponatremia in Hypopituitarism
New England Journal of Medicine, 1965IN recent years several patients with panhypopituitarism and serum sodium concentrations as low as 106 milliequiv. per liter have been seen by us. These patients have usually had associated stressful situations and unrecognized panhypopituitarism. Present physiologic concepts suggest that the pituitary gland is of definite secondary importance in the ...
J E, BETHUNE, D H, NELSON
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Gigantism with hypopituitarism
The American Journal of Medicine, 1972Abstract A forty-one year old man described in 1963 as having hypo-pituitarism with gigantism due to normal or excessive growth hormone secretion associated with a deficiency of other pituitary hormones was reevaluated with specific tests of growth hormone reserve.
G, Baumann, J P, Cain, J F, Dingman
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HYPOPARATHYROIDISM AND HYPOPITUITARISM
Australasian Annals of Medicine, 1962SUMMARYAn 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, S, GOULSTON
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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
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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
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[Posttraumatic hypopituitarism].
Nederlands tijdschrift voor geneeskunde, 2004A 39-year-old woman was admitted with complaints of weight gain, a decreased sense of well-being and amenorrhoea. One and a half year prior to admission she had been involved in a serious road accident and had spent several days in coma due to an epidural haematoma. She was found to have hypopituitarism with deficient somatotropic and gonadotropic axes,
Alwani, RA +2 more
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