Association of polymorphic alleles of the calcium-sensing receptor gene with the clinical severity of primary hyperparathyroidism (Q43758664)

26 November 2017

title

Association of polymorphic alleles of the calcium-sensing receptor gene with the clinical severity of primary hyperparathyroidism (English)

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26 November 2017

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Yamauchi M

1

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Sugimoto T

2

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Yamaguchi T

3

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Yano S

4

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26 November 2017

Kanzawa M

5

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Kobayashi A

6

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Chihara K

7

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publication date

1 September 2001

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26 November 2017

published in

Clinical Endocrinology

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26 November 2017

volume

55

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issue

3

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26 November 2017

page(s)

373-379

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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 [...]

26 November 2017

cites work

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Cloning and characterization of an extracellular Ca(2 )-sensing receptor from bovine parathyroid

21 January 2018

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Vitamin D receptor genotypes in primary hyperparathyroidism

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The calcium-sensing receptor: a window into the physiology and pathophysiology of mineral ion metabolism

21 January 2018

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A986S polymorphism of the calcium-sensing receptor and circulating calcium concentrations

21 January 2018

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Estrogen replacement may be an alternative to parathyroid surgery for the treatment of osteoporosis in elderly postmenopausal women presenting with primary hyperparathyroidism: a preliminary report

21 January 2018

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Immunoradiometric assay for intact human parathyroid hormone: characteristics, clinical application and comparison with a radio-immunoassay

21 January 2018

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Mutations of the calcium-sensing receptor (CASR) in familial hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia

21 January 2018

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Vitamin D Receptor Genotype Is Associated with Cortical Bone Loss in Japanese Patients with Primary Hyperparathyroidism

21 January 2018

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Interpretation of serum calcium in patients with abnormal serum proteins.

21 January 2018

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Mutations in the human Ca(2 )-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

21 January 2018

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Autosomal dominant hypocalcaemia caused by a Ca(2 )-sensing receptor gene mutation

21 January 2018

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Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype

21 January 2018

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A 10-year prospective study of primary hyperparathyroidism with or without parathyroid surgery

21 January 2018

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21 January 2018

Identifiers

DOI

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26 November 2017

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