Bone marrow transplant in a case of mucopolysaccharidosis I Scheie phenotype: skin ultrastructure before and after transplantation

[1]  J. Kersey,et al.  Bone marrow transplantation for Hurler syndrome: assessment of metabolic correction. , 1986, Birth defects original article series.

[2]  R. Desnick,et al.  Bone marrow transplantation in Maroteaux-Lamy syndrome (MPS type 6): status 40 months after BMT. , 1986, Birth defects original article series.

[3]  P. Gasper,et al.  Bone marrow transplantation in the feline model of arylsulfatase B deficiency. , 1986, Birth defects original article series.

[4]  J. Opitz,et al.  The clinical spectrum of a-L-iduronidase deficiency , 1985 .

[5]  J. Spranger,et al.  The clinical spectrum of alpha-L-iduronidase deficiency. , 1985, American journal of medical genetics.

[6]  D. Snover,et al.  Bone-marrow transplantation in the Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI). Biochemical and clinical status 24 months after transplantation. , 1984, The New England journal of medicine.

[7]  K. Henry,et al.  BONE MARROW TRANSPLANTATION IN MUCOPOLYSACCHARIDOSES , 1984 .

[8]  P. Gasper,et al.  Correction of feline arylsulphatase B deficiency (mucopolysaccharidosis VI) by bone marrow transplantation , 1984, Nature.

[9]  J. Martín,et al.  Prenatal pathology in mucopolysaccharidoses: a comparison with postnatal cases. , 1983, Clinical neuropathology.

[10]  Jerry R. Hobbs,et al.  REVERSAL OF CLINICAL FEATURES OF HURLER'S DISEASE AND BIOCHEMICAL IMPROVEMENT AFTER TREATMENT BY BONE-MARROW TRANSPLANTATION , 1981, The Lancet.

[11]  E. Neufeld.  The uptake of enzymes into lysosomes: an overview. , 1980, Birth defects original article series.

[12]  J. Hopwood,et al.  A fluorometric assay using 4-methylumbelliferyl α-l-iduronide for the estimation of α-l-iduronidase activity and the detection of Hurler and Scheie syndromes , 1979 .

[13]  J. Hopwood,et al.  A fluorometric assay using 4-methylumbelliferyl alpha-L-iduronide for the estimation of alpha-L-iduronidase activity and the detection of Hurler and Scheie syndromes. , 1979, Clinica chimica acta; international journal of clinical chemistry.

[14]  J.-J. Martin,et al.  Contribution de la biopsie cutanée au diagnostic des encéphalopathies métaboliques , 1976 .

[15]  D. Fontan,et al.  The Diagnosis of Mucopolysaccharidoses by Electron Microscopy of Skin Biopsies , 1975, Journal of cutaneous pathology.

[16]  Belcher Rw.  Ultrastructure of the skin in the genetic mucopolysaccharidoses. , 1972 .

[17]  R. Belcher.  Ultrastructure of the skin in the genetic mucopolysaccharidoses. , 1972, Archives of pathology.

[18]  R. Giugliani,et al.  The mucopolysaccharidoses. , 1976, Journal of medical genetics.

[19]  O. H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.