Results 221 to 230 of about 28,678 (267)
Some of the next articles are maybe not open access.
Best Practice & Research Clinical Endocrinology & Metabolism, 2012
Hypoparathyroidism is characterized by hypocalcemia, hyperphosphatemia and low or inappropriately normal levels of parathyroid hormone (PTH). Pseudohypoparathyroidism is characterized by similar findings however PTH is elevated due to PTH resistance. PTH is a key calcium regulating hormone essential for calcium homeostasis, vitamin D-dependant calcium ...
Hafsah, Al-Azem, Aliya A, Khan
openaire +3 more sources
Hypoparathyroidism is characterized by hypocalcemia, hyperphosphatemia and low or inappropriately normal levels of parathyroid hormone (PTH). Pseudohypoparathyroidism is characterized by similar findings however PTH is elevated due to PTH resistance. PTH is a key calcium regulating hormone essential for calcium homeostasis, vitamin D-dependant calcium ...
Hafsah, Al-Azem, Aliya A, Khan
openaire +3 more sources
Metabolism, 1979
Recent advances in our understanding of the physiologic actions of PTH and vitamin D have clarified certain aspects of the pathogenesis, classification, and management of hypoparathyroidism. Central to pathogenesis and categorization is the recognition that hypoparathyroidism may result from PTH deficiency, ineffectiveness, or resistance, with a ...
N A, Breslau, C Y, Pak
openaire +2 more sources
Recent advances in our understanding of the physiologic actions of PTH and vitamin D have clarified certain aspects of the pathogenesis, classification, and management of hypoparathyroidism. Central to pathogenesis and categorization is the recognition that hypoparathyroidism may result from PTH deficiency, ineffectiveness, or resistance, with a ...
N A, Breslau, C Y, Pak
openaire +2 more sources
Acta Paediatrica, 1954
SummaryA case of idiopathic hypoparathyroidism with elevated intracranial pressure and epileptiform attacks is described. It concerns the case of a boy, six years old, that diagnostically answers to the criteria stipulated by DRAKE and others. The symptoms of the disease were brought under satisfactory control, and the pressure of the cerebrospinal ...
L, STROM, J, WINBERG
openaire +2 more sources
SummaryA case of idiopathic hypoparathyroidism with elevated intracranial pressure and epileptiform attacks is described. It concerns the case of a boy, six years old, that diagnostically answers to the criteria stipulated by DRAKE and others. The symptoms of the disease were brought under satisfactory control, and the pressure of the cerebrospinal ...
L, STROM, J, WINBERG
openaire +2 more sources
Acta Endocrinologica, 1964
ABSTRACT Three patients with atypical, intermittent tetany of recent origin, hypocalcaemia, hypocalciuria and normal serum inorganic phosphorus concentration are described. Two patients were postoperative from thyroidectomy by more than 20 years and one had recently experienced metastatic malignant invasion of the thyroid area.
L R, KING, R E, GOLDSMITH
openaire +2 more sources
ABSTRACT Three patients with atypical, intermittent tetany of recent origin, hypocalcaemia, hypocalciuria and normal serum inorganic phosphorus concentration are described. Two patients were postoperative from thyroidectomy by more than 20 years and one had recently experienced metastatic malignant invasion of the thyroid area.
L R, KING, R E, GOLDSMITH
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
Endocrinology and Metabolism Clinics of North America, 2018
Hypoparathyroidism is a metabolic disorder characterized by hypocalcemia, hyperphosphatemia, and inadequate levels of or function of parathyroid hormone (PTH). The authors review the nonsurgical or medical causes of hypoparathyroidism. The most common of the nonsurgical causes is autoimmune destruction of the parathyroid. Magnesium deficiency or excess
Namrah, Siraj +2 more
openaire +2 more sources
Hypoparathyroidism is a metabolic disorder characterized by hypocalcemia, hyperphosphatemia, and inadequate levels of or function of parathyroid hormone (PTH). The authors review the nonsurgical or medical causes of hypoparathyroidism. The most common of the nonsurgical causes is autoimmune destruction of the parathyroid. Magnesium deficiency or excess
Namrah, Siraj +2 more
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
American Journal of Diseases of Children, 1991
We encountered three children who had neonatal hypocalcemia followed by a period of normocalcemia and recurrence of hypocalcemia later in childhood. They were full-term infants with normal birth weights who developed hypocalcemia within the first 48 hours after birth.
S W, Kooh, A, Binet
openaire +2 more sources
We encountered three children who had neonatal hypocalcemia followed by a period of normocalcemia and recurrence of hypocalcemia later in childhood. They were full-term infants with normal birth weights who developed hypocalcemia within the first 48 hours after birth.
S W, Kooh, A, Binet
openaire +2 more sources