Disorders of phosphorus homeostasis. - Wikidata - awgldk - TriplyDB

Disorders of phosphorus homeostasis.

Disorders of phosphorus homeostasis.

http://www.wikidata.org/entity/Q37801814

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Disorders of phosphorus homeostasis.

http://www.wikidata.org/entity/Q37801814

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on December 2010

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Disorders of phosphorus homeostasis.

@en

Disorders of phosphorus homeostasis.

@nl

type

label

Disorders of phosphorus homeostasis.

@en

Disorders of phosphorus homeostasis.

@nl

prefLabel

Disorders of phosphorus homeostasis.

@en

Disorders of phosphorus homeostasis.

@nl

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MED.0B013E32834041D4

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Current Opinion in Endocrinology, Diabetes and Obesity

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Disorders of phosphorus homeostasis.

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Richard Lee

http://www.w3.org/2001/XMLSchema#string

Thomas J Weber

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P2860

Mutation of the mouse klotho gene leads to a syndrome resembling ageing

Treatment of X-linked hypophosphatemia with calcitriol and phosphate increases circulating fibroblast growth factor 23 concentrations

FGF23 fails to inhibit uremic parathyroid glands

Parathyroid cell resistance to fibroblast growth factor 23 in secondary hyperparathyroidism of chronic kidney disease

Targeted ablation of Fgf23 demonstrates an essential physiological role of FGF23 in phosphate and vitamin D metabolism

Effects of cinacalcet and concurrent low-dose vitamin D on FGF23 levels in ESRD.

In vivo genetic evidence for suppressing vascular and soft-tissue calcification through the reduction of serum phosphate levels, even in the presence of high serum calcium and 1,25-dihydroxyvitamin d levels

Nuclear isoforms of fibroblast growth factor 2 are novel inducers of hypophosphatemia via modulation of FGF23 and KLOTHO

Loss-of-function ENPP1 mutations cause both generalized arterial calcification of infancy and autosomal-recessive hypophosphatemic rickets

Autosomal-recessive hypophosphatemic rickets is associated with an inactivation mutation in the ENPP1 gene.

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561-567

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scholarly article

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10.1097/MED.0B013E32834041D4

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6

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17

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2010-12-01T00:00:00Z

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20962635

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3740176

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