(Q41933787)

14 October 2017

title

Imparied calcitonin secretion in patients with Williams syndrome (English)

1 reference

14 October 2017

Culler FL

1

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14 October 2017

Jones KL

series ordinal

2

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14 October 2017

Deftos LJ

series ordinal

3

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14 October 2017

language of work or name

English

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publication date

1 November 1985

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The Journal of Pediatrics

14 October 2017

published in

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14 October 2017

volume

107

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14 October 2017

issue

5

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14 October 2017

page(s)

720-723

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The Williams elfin facies syndrome. A new perspective

14 October 2017

cites work

1 reference

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7 January 2021

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Etiology of the severe form of idiopathic hypercalcemia of infancy; a defect in vitamin D metabolism

7 January 2021

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Abnormal regulation of circulating 25-hydroxyvitamin D in the Williams syndrome

7 January 2021

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Oral calcium-loading test in infancy, with particular reference to idiopathic hypercalcaemia.

7 January 2021

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Abnormal muscle cylinder ratio in idiopathic infantile hypercalcemia: a new roentgen sign

7 January 2021

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Impaired calcium homeostasis in the infantile hypercalcemic syndrome

7 January 2021

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Calcitonin secretion in congenital nongoitrous cretinism

7 January 2021

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Modulation of plasma 1,25-dihydroxyvitamin D in man by stimulation and suppression tests

7 January 2021

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The cytoreceptor assay for 1,25-dihydroxyvitamin D and its application to clinical studies

7 January 2021

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Supravalvular aortic stenosis with parafollicular cell (C-cell) hyperplasia

7 January 2021

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Altered expression of the calcitonin gene associated with RNA polymorphism.

7 January 2021

1 reference

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Production of a novel neuropeptide encoded by the calcitonin gene via tissue-specific RNA processing

7 January 2021

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Calcitonin gene-related peptide in the human thyroid, pituitary and brain.

7 January 2021

1 reference

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10.1016/S0022-3476(85)80399-1

7 January 2021

Identifiers

DOI

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14 October 2017

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