Orthopedic Pathology in Children with Mucopolysaccharidosis Type I
Author(s) -
Nato D. Vashakmadze,
Leyla S. Namazova-Baranova,
А. К. Геворкян,
Л. М. Кузенкова,
Tatyana V. Podkletnova,
Marina А. Babaykina,
A. B. Anikin,
Галина Кузнецова,
Л. А. Осипова,
K. V. Jerdev
Publication year - 2016
Publication title -
вопросы современной педиатрии
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.12
H-Index - 5
eISSN - 1682-5535
pISSN - 1682-5527
DOI - 10.15690/vsp.v15i6.1652
Subject(s) - enzyme replacement therapy , mucopolysaccharidosis type i , hurler syndrome , mucopolysaccharidosis i , dermatan sulfate , glycosaminoglycan , orthopedic surgery , medicine , mucopolysaccharidosis , heparan sulfate , lysosomal storage disease , bone marrow transplantation , disease , mucopolysaccharidosis type ii , pathology , phenotype , bone marrow , biology , surgery , genetics , anatomy , gene
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