X-linked hypophosphatemia: a clinical, biochemical, and histopathologic assessment of morbidity in adults.

X-linked hypophosphatemia: a clinical, biochemical, and histopathologic assessment of morbidity in adults.

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http://www.wikidata.org/entity/Q51618480
X chromosome inactivation pattern in female carriers of X linked hypophosphataemic rickets.Survey of the enthesopathy of X-linked hypophosphatemia and its characterization in Hyp micePharmacokinetics and pharmacodynamics of a human monoclonal anti-FGF23 antibody (KRN23) in the first multiple ascending-dose trial treating adults with X-linked hypophosphatemia.Approach to the hypophosphatemic patientHereditary hypophosphatemia in Norway: a retrospective population-based study of genotypes, phenotypes, and treatment complications.Mineralizing enthesopathy is a common feature of renal phosphate-wasting disorders attributed to FGF23 and is exacerbated by standard therapy in hyp miceHypophosphatemic rickets is associated with disruption of mineral orientation at the nanoscale in the flat scapula bones of rachitic mice with developmentSclerostin antibody (Scl-Ab) improves osteomalacia phenotype in dentin matrix protein 1(Dmp1) knockout mice with little impact on serum levels of phosphorus and FGF23.Effect of four monthly doses of a human monoclonal anti-FGF23 antibody (KRN23) on quality of life in X-linked hypophosphatemiaDosage effect of a Phex mutation in a murine model of X-linked hypophosphatemia.Dmp1 Null Mice Develop a Unique Osteoarthritis-like Phenotype.Randomized trial of the anti-FGF23 antibody KRN23 in X-linked hypophosphatemia.Patients with Hypophosphatemic Osteomalacia Need Continuous Treatment during Adulthood.Three-year successful cinacalcet treatment of secondary hyperparathyroidism in a patient with x-linked dominant hypophosphatemic rickets: a case report.Chiari malformation, syringomyelia and bulbar palsy in X linked hypophosphataemia.FGF2 High Molecular Weight Isoforms Contribute to Osteoarthropathy in Male Mice.Outcome of adult patients with X-linked hypophosphatemia caused by PHEX gene mutations.
P2860

X-linked hypophosphatemia: a clinical, biochemical, and histopathologic assessment of morbidity in adults.

Item
http://www.wikidata.org/entity/Q51618480
description
1989 nî lūn-bûn
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1989年の論文
@ja
1989年学术文章
@wuu
1989年学术文章
@zh
1989年学术文章
@zh-cn
1989年学术文章
@zh-hans
1989年学术文章
@zh-my
1989年学术文章
@zh-sg
1989年學術文章
@yue
1989年學術文章
@zh-hant
name
X-linked hypophosphatemia: a c ...... ssment of morbidity in adults.
@en
X-linked hypophosphatemia: a c ...... ssment of morbidity in adults.
@nl
type
label
X-linked hypophosphatemia: a c ...... ssment of morbidity in adults.
@en
X-linked hypophosphatemia: a c ...... ssment of morbidity in adults.
@nl
prefLabel
X-linked hypophosphatemia: a c ...... ssment of morbidity in adults.
@en
X-linked hypophosphatemia: a c ...... ssment of morbidity in adults.
@nl
P1433
P1476
P2093
P304
P31
P407
P433
P478
P50
P577
P698
P1433
P1476
X-linked hypophosphatemia: a c ...... ssment of morbidity in adults.
@en
P2093
P304
P31
P407
P433
P478
P50
P577
P698