VITAMIN D-RESISTANT RICKETS. ANALYSIS OF TWENTY-FOUR PEDIGREES WITH HEREDITARY AND SPORADIC CASES.
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FGF23, PHEX, and MEPE regulation of phosphate homeostasis and skeletal mineralizationX-linked hypophosphatemia: the mutant gene is expressed in teeth as well as in kidneyBridging markers defining the map position of X linked hypophosphataemic rickets.X chromosome inactivation pattern in female carriers of X linked hypophosphataemic rickets.Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant gene.New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice.Defective binding of macrophages to bone in rodent osteomalacia and vitamin D deficiency. In vitro evidence for a cellular defect and altered saccharides in the bone matrix.Metabolism of vitamin D3-3H in vitamin D-resistant rickets and familial hypophosphatemia.Effect of paricalcitol on circulating parathyroid hormone in X-linked hypophosphatemia: a randomized, double-blind, placebo-controlled studyNormal regulation of calcitriol production in Gy mice. Evidence for biochemical heterogeneity in the X-linked hypophosphatemic diseases.HYPERCALCURIC RICKETS ASSOCIATED WITH RENAL TUBULAR DAMAGE.Pharmacokinetics and pharmacodynamics of a human monoclonal anti-FGF23 antibody (KRN23) in the first multiple ascending-dose trial treating adults with X-linked hypophosphatemia.Genetic factors in determining bone mass.Recessive hypophosphataemic rickets, and possible aetiology of the 'vitamin D-resistant' syndrome.Rickets (and osteomalacia), nutritional and metabolic (1919-69)Prolonged Correction of Serum Phosphorus in Adults With X-Linked Hypophosphatemia Using Monthly Doses of KRN23.New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis.Hereditary hypophosphatemia in Norway: a retrospective population-based study of genotypes, phenotypes, and treatment complications.Evaluation of a role for 1,25-dihydroxyvitamin D3 in the pathogenesis and treatment of X-linked hypophosphatemic rickets and osteomalacia.Deformity correction in children with hereditary hypophosphatemic rickets.Disorders of phosphate homeostasis and tissue mineralisation.FGF23 and syndromes of abnormal renal phosphate handlingThe skeleton as an endocrine organ.X-linked hypophosphatemia and growth.Population pharmacokinetic and pharmacodynamic analyses from a 4-month intradose escalation and its subsequent 12-month dose titration studies for a human monoclonal anti-FGF23 antibody (KRN23) in adults with X-linked hypophosphatemia.Isocyanates in industry: environmental control.Genetic linkage studies of X-linked hypophosphataemic rickets in a Saudi Arabian family.The relation between attained adult height and the metaphyseal lesions in hypophosphataemic vitamin-D resistant rickets.
P2860
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P2860
VITAMIN D-RESISTANT RICKETS. ANALYSIS OF TWENTY-FOUR PEDIGREES WITH HEREDITARY AND SPORADIC CASES.
description
1964 nî lūn-bûn
@nan
1964年の論文
@ja
1964年学术文章
@wuu
1964年学术文章
@zh-cn
1964年学术文章
@zh-hans
1964年学术文章
@zh-my
1964年学术文章
@zh-sg
1964年學術文章
@yue
1964年學術文章
@zh
1964年學術文章
@zh-hant
name
VITAMIN D-RESISTANT RICKETS. A ...... HEREDITARY AND SPORADIC CASES.
@en
VITAMIN D-RESISTANT RICKETS. A ...... HEREDITARY AND SPORADIC CASES.
@nl
type
label
VITAMIN D-RESISTANT RICKETS. A ...... HEREDITARY AND SPORADIC CASES.
@en
VITAMIN D-RESISTANT RICKETS. A ...... HEREDITARY AND SPORADIC CASES.
@nl
prefLabel
VITAMIN D-RESISTANT RICKETS. A ...... HEREDITARY AND SPORADIC CASES.
@en
VITAMIN D-RESISTANT RICKETS. A ...... HEREDITARY AND SPORADIC CASES.
@nl
P2093
P1476
VITAMIN D-RESISTANT RICKETS. A ...... HEREDITARY AND SPORADIC CASES.
@en
P2093
P304
P356
10.1016/0002-9343(64)90085-3
P407
P577
1964-02-01T00:00:00Z