Results 231 to 240 of about 28,437 (272)
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Keratitis with Hypoparathyroidism
American Journal of Ophthalmology, 1977Chronic kiratitis developed in two children with nonsurgical hypoparathyroidism, as part of an autosomal recessive syndrome that included adrenal insufficiency and moniliasis in what was postulated to be an autoimmune disease. The corneal changes may also have been caused by autoimmune mechanism.
L N, Stieglitz +4 more
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Treatment of hypoparathyroidism
Best Practice & Research Clinical Endocrinology & Metabolism, 2018The goal of the clinical management of hypoparathyroidism is to correct acute and chronic hypocalcemia. Treatment of acute hypoparathyroidism via intravenous infusion of Ca++ salts, is necessary only in symptomatic patients, or in asymptomatic patients in the setting of a rapid decrease in ionized Ca++ levels.
Tecilazich, Francesco +4 more
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Pediatrics, 1956
IDIOPATHIC hypoparathyroidism is one of the rarer abnormalities of endocrine function in childhood. For that reason it may be missed on occasion because it is not considered among the diagnostic possibilities. There have been 6 cases of idiopathic hypoparathyroidism seen at the Harriet Lane during the past 10 years and the youngest child of this series
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IDIOPATHIC hypoparathyroidism is one of the rarer abnormalities of endocrine function in childhood. For that reason it may be missed on occasion because it is not considered among the diagnostic possibilities. There have been 6 cases of idiopathic hypoparathyroidism seen at the Harriet Lane during the past 10 years and the youngest child of this series
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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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Current Opinion in Rheumatology, 2019
Purpose of review Hypoparathyroidism is a rare endocrine disorder characterized by low or insufficient parathyroid hormone (PTH) concentrations leading to hypocalcemia, hyperphosphatemia, and markedly reduced bone turnover. Despite being a rare disease, hypoparathyroidism has a profound impact on affected patients.
Natalie E, Cusano, John P, Bilezikian
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Purpose of review Hypoparathyroidism is a rare endocrine disorder characterized by low or insufficient parathyroid hormone (PTH) concentrations leading to hypocalcemia, hyperphosphatemia, and markedly reduced bone turnover. Despite being a rare disease, hypoparathyroidism has a profound impact on affected patients.
Natalie E, Cusano, John P, Bilezikian
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Endocrinology and Metabolism Clinics of North America, 2018
Surgical hypoparathyroidism is the most common cause of hypoparathyroidism and the result of intentional or inadvertent extirpation, trauma, or devascularization of the parathyroid glands. Surgical hypoparathyroidism may present as a medical emergency.
Hadiza S, Kazaure, Julie Ann, Sosa
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Surgical hypoparathyroidism is the most common cause of hypoparathyroidism and the result of intentional or inadvertent extirpation, trauma, or devascularization of the parathyroid glands. Surgical hypoparathyroidism may present as a medical emergency.
Hadiza S, Kazaure, Julie Ann, Sosa
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Hypoparathyroidism in pregnancy
American Journal of Obstetrics and Gynecology, 1973H Y P 0 P AR AT H Y R 0 I D I S M iS KiI-dy SUXl ZiS a complication of pregnancy. It is of special interest to the obstetrician because of the role of calcium metabolism during gestation and lactation. By far the most common cause of hypoparathyroidism is damage or removal of the glands during thyroid surgery.
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Hypoparathyroidism and the Kidney
Endocrinology and Metabolism Clinics of North America, 2018Hypocalcemia and hyperphosphatemia are the pathognomonic biochemical features of hypoparathyroidism, and result directly from lack of parathyroid hormone (PTH) action on the kidney. In the absence of PTH action, the renal mechanisms transporting calcium and phosphate reabsorption deregulate, resulting in hypocalcemia and hyperphosphatemia.
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