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10 in total

1. Neonatal severe hyperparathyroidism: further clinical and molecular delineation.

Authors: Fawziya A Al-Khalaf; Adel Ismail; Ashraf T Soliman; David E C Cole; Tawfeg Ben-Omran
Journal: Eur J Pediatr Date: 2010-10-23 Impact factor: 3.183

2. In vivo and in vitro characterization of neonatal hyperparathyroidism resulting from a de novo, heterozygous mutation in the Ca2+-sensing receptor gene: normal maternal calcium homeostasis as a cause of secondary hyperparathyroidism in familial benign hypocalciuric hypercalcemia.

Authors: M Bai; S H Pearce; O Kifor; S Trivedi; U G Stauffer; R V Thakker; E M Brown; B Steinmann
Journal: J Clin Invest Date: 1997-01-01 Impact factor: 14.808

3. Neonatal Severe Hyperparathyroidism: Novel Insights From Calcium, PTH, and the CASR Gene.

Authors: Stephen J Marx; Ninet Sinaii
Journal: J Clin Endocrinol Metab Date: 2020-04-01 Impact factor: 5.958

4. Markedly reduced activity of mutant calcium-sensing receptor with an inserted Alu element from a kindred with familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism.

Authors: M Bai; N Janicic; S Trivedi; S J Quinn; D E Cole; E M Brown; G N Hendy
Journal: J Clin Invest Date: 1997-04-15 Impact factor: 14.808

Hereditary parathyroid hyperplasia: a surgical emergency of early infancy.

1. Neonatal severe hyperparathyroidism: further clinical and molecular delineation.

2. In vivo and in vitro characterization of neonatal hyperparathyroidism resulting from a de novo, heterozygous mutation in the Ca2+-sensing receptor gene: normal maternal calcium homeostasis as a cause of secondary hyperparathyroidism in familial benign hypocalciuric hypercalcemia.

3. Neonatal Severe Hyperparathyroidism: Novel Insights From Calcium, PTH, and the CASR Gene.

4. Markedly reduced activity of mutant calcium-sensing receptor with an inserted Alu element from a kindred with familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism.

Review 5. The pathophysiology and clinical aspects of hypercalcemic disorders.

Review 6. Endocrine control and disturbances of calcium and phosphate metabolism in children.

Review 7. "Asymptomatic" and symptomatic primary hyperparathyroidism.

8. A novel mutation in Ca2+-sensing receptor gene in familial hypocalciuric hypercalcemia.

9. Primary infantile hyperparathyroidism: clinical, laboratory, and radiographic features in 21 cases.

Review 10. Hyperplasia in glands with hormone excess.