MODERN APPROACHES TO THERAPY FOR CHILDREN WITH MUCOPOLYSACCHARIDOSIS
Mucopolysaccharidosis is the group of hereditary metabolic disorders; it is characterized by accumulation of glycosaminoglycans owing to storage of specific lysosomal enzymes. Background: Research objective was to study the influence of enzyme replacement therapy on a somatic state and psychomotor d...
Saved in:
Main Authors: | N. V. Buchinskaya (Author), I. А. Chikova (Author), E. А. Isupova (Author), О. V. Kalashnikova (Author), М. М. Kostik (Author), V. G. Chasnyk (Author) |
---|---|
Format: | Book |
Published: |
"Paediatrician" Publishers LLC,
2014-05-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
FARBER DISEASE - DISEASE DESCRIPTION WITH CASE REPORTS
by: I. A. Chikova, et al.
Published: (2014) -
Use of Implantable Venous Port Systems in the Treatment of Children with Orphan Diseases (Mucopolysaccharidosis and Pompe Disease): Case Series
by: M. Yu. Rykov, et al.
Published: (2015) -
Modern Approaches to the Management of Children with Mucopolysaccharidosis Type I
by: Galina V. Baidakova, et al.
Published: (2022) -
How Not to Miss the Mild Forms of Mucopolysaccharidosis Type I in Patients With Articular Manifestations of the Disease?
by: Natalia V. Buchinskaya, et al.
Published: (2019) -
DIFFERENTIATED APPROACH TO NON-BACTERIAL OSTEOMYELITIS TREATMENT IN CHILDREN: THE RETROSPECTIVE STUDY RESULTS
by: Mikhail M. Kostik, et al.
Published: (2016)