Bone marrow transplantation in metabolic diseases.
1988
S O Lie, and
A Glomstein, and
S H Slørdahl, and
I Storm-Mathisen, and
D Albrechtsen, and
E P Young, and
A Patrick
Department of Pediatrics, Rikshospitalet, National Hospital, Oslo 1, Norway.
UI
MeSH Term
Description
Entries
D009083
Mucopolysaccharidoses
Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency.
Mucopolysaccharidosis
D002675
Child, Preschool
A child between the ages of 2 and 5.
Children, Preschool,Preschool Child,Preschool Children
D005260
Female
Females
D006025
Glycosaminoglycans
Heteropolysaccharides which contain an N-acetylated hexosamine in a characteristic repeating disaccharide unit. The repeating structure of each disaccharide involves alternate 1,4- and 1,3-linkages consisting of either N-acetylglucosamine (see ACETYLGLUCOSAMINE) or N-acetylgalactosamine (see ACETYLGALACTOSAMINE).
Glycosaminoglycan,Mucopolysaccharides
D006801
Humans
Members of the species Homo sapiens.
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D016026
Bone Marrow Transplantation
The transference of BONE MARROW from one human or animal to another for a variety of purposes including HEMATOPOIETIC STEM CELL TRANSPLANTATION or MESENCHYMAL STEM CELL TRANSPLANTATION.
Bone Marrow Cell Transplantation,Grafting, Bone Marrow,Transplantation, Bone Marrow,Transplantation, Bone Marrow Cell,Bone Marrow Grafting
Related Publications
S O Lie, and
A Glomstein, and
S H Slørdahl, and
I Storm-Mathisen, and
D Albrechtsen, and
E P Young, and
A Patrick