asfotase alfa

Known as: Asfotase alpha 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2012-2017
051020122017

Papers overview

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2017
2017
OBJECTIVE Hypophosphatasia (HPP) is a rare skeletal disease characterized by hypomineralization and low alkaline phosphatase… (More)
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Review
2017
Review
2017
Hypophosphatasia (HPP) is a rare, inherited, systemic, metabolic disorder caused by autosomal recessive mutations or a single… (More)
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2017
2017
Hypophosphatasia is an inherited disease characterized by reduced alkaline phosphatase activity, extracellular accumulation of… (More)
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2017
2017
We describe the clinical outcome of asfotase alfa therapy in a 16-year-old boy with severe childhood hypophosphatasia (HPP), who… (More)
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2016
2016
CONTEXT Hypophosphatasia (HPP) is an inborn error of metabolism that, in its most severe perinatal and infantile forms, results… (More)
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2016
2016
Background. Hypophosphatasia (HPP) is caused by loss-of-function mutation(s) of the gene that encodes the tissue-nonspecific… (More)
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Review
2016
Review
2016
  • Hideo Orimo
  • Therapeutics and clinical risk management
  • 2016
Hypophosphatasia (HPP) is an inherited systemic bone disease that is characterized by bone hypomineralization. HPP is classified… (More)
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Review
2016
Review
2016
Hypophosphatasia (HPP) is a rare inheritable disease that results from loss-of-function mutations in the ALPL gene encoding… (More)
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Review
2016
Review
2016
Hypophosphatasia (HPP) is a rare disease caused by loss-of-function mutations in the tissue-nonspecific alkaline phosphatase… (More)
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2012
2012
Hypophosphatasia (HPP) is the inborn-error-of-metabolism caused by loss-of-function mutation(s) in the gene that encodes the… (More)
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