Characterization of early disease status in treatment-naive male paediatric patients with Fabry disease enrolled in a randomized clinical trial.
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Enzyme replacement therapy for Anderson-Fabry diseaseSkin globotriaosylceramide 3 deposits are specific to Fabry disease with classical mutations and associated with small fibre neuropathy.Skin Globotriaosylceramide 3 Load Is Increased in Men with Advanced Fabry Disease.Hearing loss in children with Fabry disease.Characterization of Classical and Nonclassical Fabry Disease: A Multicenter Study.Retrospective study of long-term outcomes of enzyme replacement therapy in Fabry disease: Analysis of prognostic factorsPathomechanisms of renal Fabry disease.
P2860
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P2860
Characterization of early disease status in treatment-naive male paediatric patients with Fabry disease enrolled in a randomized clinical trial.
description
2015 nî lūn-bûn
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2015年の論文
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2015年論文
@yue
2015年論文
@zh-hant
2015年論文
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2015年論文
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2015年論文
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2015年论文
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2015年论文
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2015年论文
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name
Characterization of early dise ...... n a randomized clinical trial.
@ast
Characterization of early dise ...... n a randomized clinical trial.
@en
type
label
Characterization of early dise ...... n a randomized clinical trial.
@ast
Characterization of early dise ...... n a randomized clinical trial.
@en
prefLabel
Characterization of early dise ...... n a randomized clinical trial.
@ast
Characterization of early dise ...... n a randomized clinical trial.
@en
P2093
P2860
P50
P1433
P1476
Characterization of early dise ...... n a randomized clinical trial.
@en
P2093
Alejandro Fainboim
Andreas Fellgiebel
Behzad Najafian
Bernard Bénichou
Beth L Thurberg
C Ronald Scott
Camilla Tøndel
Cassiano Forcelini
Frits A Wijburg
Gabriela Dostalova
P2860
P304
P356
10.1371/JOURNAL.PONE.0124987
P407
P577
2015-05-08T00:00:00Z