Asfotase Alfa Treatment Improves Survival for Perinatal and Infantile Hypophosphatasia - Wikidata - awgldk - TriplyDB

Asfotase Alfa Treatment Improves Survival for Perinatal and Infantile Hypophosphatasia

Asfotase Alfa Treatment Improves Survival for Perinatal and Infantile Hypophosphatasia

http://www.wikidata.org/entity/Q36431644

about

Asfotase alfa therapy for children with hypophosphatasia.Alkaline phosphatase: a novel treatment target for cardiovascular disease in CKD.Ultrastructural and biochemical aspects of matrix vesicle-mediated mineralization Alkaline Phosphatase and Hypophosphatasia.Skeletal Dysplasias: Growing Therapy for Growing Bones.Skeletal Dysplasias: What Every Bone Health Clinician Needs to Know.Hypophosphatasia - aetiology, nosology, pathogenesis, diagnosis and treatment.Clinical, radiographic and biochemical characteristics of adult hypophosphatasia.Safety and efficacy of treatment with asfotase alfa in patients with hypophosphatasia: Results from a Japanese clinical trial.Recurrent Metatarsal Fractures in Postmenopausal Woman With Low Serum Alkaline Phosphatase: A Rare Diagnosis Not to Miss.Alkaline Phosphatase, an Unconventional Immune Protein.Efficacy of anti-sclerostin monoclonal antibody BPS804 in adult patients with hypophosphatasia.Transformative therapy in hypophosphatasia.Gene therapy improves dental manifestations in hypophosphatasia model mice.Enzyme replacement therapy in perinatal hypophosphatasia: Case report of a negative outcome and lessons for clinical practice.Hypophosphatasia: clinical manifestation and burden of disease in adult patients.Adult-onset hypophosphatasia diagnosed following bilateral atypical femoral fractures in a 55-year-old woman.Developments in rare bone diseases and mineral disorders.Asfotase alfa treatment for 1 year in a 16 year-old male with severe childhood hypophosphatasia.Successful Use of Enzyme Replacement Therapy in Infantile Hypophosphatasia.Hypophosphatasia: Enzyme Replacement Therapy Brings New Opportunities and New Challenges.Successful Asfotase Alfa Treatment in an Adult Dialysis Patient With Childhood-Onset Hypophosphatasia.Brief Clinical Report: Hypophosphatasia-Diagnostic Considerations and Treatment Outcomes in an Infant.Hypophosphatasie Profile of asfotase alfa in the treatment of hypophosphatasia: design, development, and place in therapy Fracture Healing in Two Adult Patients With Hypophosphatasia After Asfotase Alfa Therapy Bone health in patients with inborn errors of metabolism

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Asfotase Alfa Treatment Improves Survival for Perinatal and Infantile Hypophosphatasia

http://www.wikidata.org/entity/Q36431644

description

2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

@wuu

2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

@zh-sg

2015年學術文章

@yue

2015年學術文章

@zh

2015年學術文章

@zh-hant

name

Asfotase Alfa Treatment Improves Survival for Perinatal and Infantile Hypophosphatasia

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Asfotase Alfa Treatment Improves Survival for Perinatal and Infantile Hypophosphatasia

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type

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Asfotase Alfa Treatment Improves Survival for Perinatal and Infantile Hypophosphatasia

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Asfotase Alfa Treatment Improves Survival for Perinatal and Infantile Hypophosphatasia

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prefLabel

Asfotase Alfa Treatment Improves Survival for Perinatal and Infantile Hypophosphatasia

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Asfotase Alfa Treatment Improves Survival for Perinatal and Infantile Hypophosphatasia

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The Journal of Clinical Endocrinology and Metabolism

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Asfotase Alfa Treatment Improves Survival for Perinatal and Infantile Hypophosphatasia

@en

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Agustin Melian

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

Christine Hofmann

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David D Thompson

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Keiichi Ozono

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Michael P Whyte

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Nicholas Bishop

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Richard Riese

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Scott Moseley

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P2860

A missense mutation in the human liver/bone/kidney alkaline phosphatase gene causing a lethal form of hypophosphatasia

Infantile hypophosphatasia: disappointing results of treatment

Hypophosphatasia

A homoallelic Gly317-->Asp mutation in ALPL causes the perinatal (lethal) form of hypophosphatasia in Canadian mennonites

Neurosurgical aspects of childhood hypophosphatasia

Pyridoxine-responsive seizures as the first symptom of infantile hypophosphatasia caused by two novel missense mutations (c.677T>C, p.M226T; c.1112C>T, p.T371I) of the tissue-nonspecific alkaline phosphatase gene

Identification of novel missense mutations (Phe310Leu and Gly439Arg) in a neonatal case of hypophosphatasia

Chronic multifocal non-bacterial osteomyelitis in hypophosphatasia mimicking malignancy.

Unexpected high intrafamilial phenotypic variability observed in hypophosphatasia.

Hypophosphatasia: nonlethal disease despite skeletal presentation in utero (17 new cases and literature review).

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334-342

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scholarly article

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10.1210/JC.2015-3462

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1

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101

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Cheryl Rockman-Greenberg

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2015-11-03T00:00:00Z

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26529632

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hypophosphatasia

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4701846

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