Open AccessOrthopedic Pathology in Children with Mucopolysaccharidosis Type I
Author(s) -
Вашакмадзе Нато Джумберовна,
Л.С. Намазова-Баранова,
А. К. Геворкян,
Л. М. Кузенкова,
Tatyana V. Podkletnova,
М. А. Бабайкина,
А В Аникин,
Galina V. Kuznetsova,
Liliya A. Osipova,
К. В. Жердев
Publication year - 2016
Publication title -
voprosy sovremennoj pediatrii
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) - mucopolysaccharidosis type i , enzyme replacement therapy , hurler syndrome , mucopolysaccharidosis i , dermatan sulfate , glycosaminoglycan , heparan sulfate , mucopolysaccharidosis , medicine , orthopedic surgery , bone marrow transplantation , mucopolysaccharidosis type ii , phenotype , lysosomal storage disease , disease , pathology , bone marrow , endocrinology , biology , genetics , surgery , anatomy , gene