The Hurler syndrome, an autosomal recessive storage disease of childhood, leads to death within the first decade of life from progressive deposition of glycosaminoglycans within the myointima of the coronary arteries and airways. Cardiac ultrasound findings of patients with this syndrome >10 years after successful bone marrow transplantation are described.Elizabeth A. Braunlin, Nanci R. Stauffer, Charles H. Peters, John L. Bass, James M. Berry, John J. Hopwood and William Krivi
The article describes the transplantation of hematopoietic stem cells (HSC) in children with severe ...
Hurler syndrome type 1 (MPS-1) is an autosomal recessive lysosomal disorder due to the deficiency of...
Children affected by mucopolysaccharidosis (MPS) type IH (Hurler Syndrome), an autosomal recessive m...
ence progressive neurologic deterioration and early death. Allogeneic bone marrow transplantation (B...
Mucopolysaccharidosis type I-Hurler syndrome (MPS-IH) is a lysosomal storage disease characterized b...
Mucopolysaccharidosis type I-Hurler syndrome (MPS-IH) is a lysosomal storage disease characterized b...
The most severe form of Mucopolysaccharosidosis type I (MPS-I), Hurler syndrome, presents with progr...
Hurler syndrome is a severe inherited metabolic disorder caused by a deficiency of the lysosomal enz...
Mucopolysaccharidosis type I-Hurler syndrome (MPS-IH) is a lysosomal storage disease characterized b...
Mucopolysaccharidosis type I (MPS I; Hurler syndrome) is a lysosomal storage disease caused by a def...
BackgroundHurler's syndrome (the most severe form of mucopolysaccharidosis type I) causes progressiv...
Mucopolysaccharidosis type I (MPS I) is the hereditary disease characterized with alpha-L-iduronidas...
We report the long-term follow-up of successful treatment of mucopolysaccharidosis type I H (MPS IH,...
BACKGROUND Hurler's syndrome (the most severe form ofmucopolysaccharidosis type I) causes progressiv...
AbstractAllogeneic stem cell transplantation (SCT) is considered effective in preventing disease pro...
The article describes the transplantation of hematopoietic stem cells (HSC) in children with severe ...
Hurler syndrome type 1 (MPS-1) is an autosomal recessive lysosomal disorder due to the deficiency of...
Children affected by mucopolysaccharidosis (MPS) type IH (Hurler Syndrome), an autosomal recessive m...
ence progressive neurologic deterioration and early death. Allogeneic bone marrow transplantation (B...
Mucopolysaccharidosis type I-Hurler syndrome (MPS-IH) is a lysosomal storage disease characterized b...
Mucopolysaccharidosis type I-Hurler syndrome (MPS-IH) is a lysosomal storage disease characterized b...
The most severe form of Mucopolysaccharosidosis type I (MPS-I), Hurler syndrome, presents with progr...
Hurler syndrome is a severe inherited metabolic disorder caused by a deficiency of the lysosomal enz...
Mucopolysaccharidosis type I-Hurler syndrome (MPS-IH) is a lysosomal storage disease characterized b...
Mucopolysaccharidosis type I (MPS I; Hurler syndrome) is a lysosomal storage disease caused by a def...
BackgroundHurler's syndrome (the most severe form of mucopolysaccharidosis type I) causes progressiv...
Mucopolysaccharidosis type I (MPS I) is the hereditary disease characterized with alpha-L-iduronidas...
We report the long-term follow-up of successful treatment of mucopolysaccharidosis type I H (MPS IH,...
BACKGROUND Hurler's syndrome (the most severe form ofmucopolysaccharidosis type I) causes progressiv...
AbstractAllogeneic stem cell transplantation (SCT) is considered effective in preventing disease pro...
The article describes the transplantation of hematopoietic stem cells (HSC) in children with severe ...
Hurler syndrome type 1 (MPS-1) is an autosomal recessive lysosomal disorder due to the deficiency of...
Children affected by mucopolysaccharidosis (MPS) type IH (Hurler Syndrome), an autosomal recessive m...