Treatment of Hypophosphatemic Rickets with Phosphate and Active Vitamin D in Japan: A Questionnaire-based Survey. - Wikidata - wikimedia - TriplyDB

Treatment of Hypophosphatemic Rickets with Phosphate and Active Vitamin D in Japan: A Questionnaire-based Survey.

Treatment of Hypophosphatemic Rickets with Phosphate and Active Vitamin D in Japan: A Questionnaire-based Survey.

http://www.wikidata.org/entity/Q37107383

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Magnetic Resonance Imaging Features as Surrogate Markers of X-Linked Hypophosphatemic Rickets Activity

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Treatment of Hypophosphatemic Rickets with Phosphate and Active Vitamin D in Japan: A Questionnaire-based Survey.

http://www.wikidata.org/entity/Q37107383

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on January 2013

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Treatment of Hypophosphatemic ...... A Questionnaire-based Survey.

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Treatment of Hypophosphatemic ...... A Questionnaire-based Survey.

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type

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Treatment of Hypophosphatemic ...... A Questionnaire-based Survey.

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Treatment of Hypophosphatemic ...... A Questionnaire-based Survey.

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Treatment of Hypophosphatemic ...... A Questionnaire-based Survey.

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Treatment of Hypophosphatemic ...... A Questionnaire-based Survey.

@nl

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Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology

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Treatment of Hypophosphatemic ...... A Questionnaire-based Survey.

@en

P2093

Committee on Drugs, Japanese Society for Pediatric Endocrinology*

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Keiichi Ozono

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Makoto Fujiwara

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Noriyuki Namba

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Osamu Arisaka

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Susumu Yokoya

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P2860

Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23

Growth-related renal type II Na/Pi cotransporter

SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasis

A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP Consortium

Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3.

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

Cloning and characterization of FGF23 as a causative factor of tumor-induced osteomalacia

Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23

Familial hypophosphatemic rickets caused by a large deletion in PHEX gene

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

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9-14

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scholarly article

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10.1297/CPE.22.9

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23966755

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