INHERITED DISORDERS OF LYSOSOMAL METABOLISM

[1] NOVEL METHOD FOR IMMOBILIZATION OF CHICKEN BRAIN ARYLSULFATASE A USING CONCANAVALIN A [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1973, 53 (03) : 730 - 736

[2] DEFECT IN HUNTER SYNDROME - DEFICIENCY OF SULFOIDURONATE SULFATASE [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1973, 70 (07) : 2134 - 2138

[3] DEFECT IN HURLER AND SCHEIE SYNDROMES - DEFICIENCY OF ALPHA-IDURONIDASE [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1972, 69 (08) : 2048 - &

[4] IMMUNOCHEMICAL CHARACTERIZATION OF HUMAN BETA-D-N-ACETYL HEXOSAMINIDASE FROM NORMAL INDIVIDUALS AND PATIENTS WITH TAY-SACHS DISEASE .1. ANTIGENIC DIFFERENCES BETWEEN HEXOSAMINIDASE-A AND HEXOSAMINIDASE-B [J]. INTERNATIONAL ARCHIVES OF ALLERGY AND APPLIED IMMUNOLOGY, 1974, 46 (04): : 512 - 524

[5] BARTON RW, 1971, J BIOL CHEM, V246, P7773

[6] DISTINCT BIOCHEMICAL DEFICIT IN MAROTEAUX-LAMY SYNDROME (MUCOPOLYSACCHARIDOSIS VI) [J]. JOURNAL OF PEDIATRICS, 1972, 80 (01) : 114 - +

[7] BAUDHUIN P, 1964, LAB INVEST, V13, P1139

[8] BEAUDET AL, IN PRESS

[9] CONGENITAL CORNEAL CLOUDING WITH ABNORMAL SYSTEMIC STORAGE BODIES - NEW VARIANT OF MUCOLIPIDOSIS [J]. JOURNAL OF PEDIATRICS, 1974, 84 (04) : 519 - 526

[10] BERMAN ER, 1974, CLIN CHIM ACTA, V52, P115

[1] NOVEL METHOD FOR IMMOBILIZATION OF CHICKEN BRAIN ARYLSULFATASE A USING CONCANAVALIN A [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1973, 53 (03) : 730 - 736

[2] DEFECT IN HUNTER SYNDROME - DEFICIENCY OF SULFOIDURONATE SULFATASE [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1973, 70 (07) : 2134 - 2138

[3] DEFECT IN HURLER AND SCHEIE SYNDROMES - DEFICIENCY OF ALPHA-IDURONIDASE [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1972, 69 (08) : 2048 - &

[4] IMMUNOCHEMICAL CHARACTERIZATION OF HUMAN BETA-D-N-ACETYL HEXOSAMINIDASE FROM NORMAL INDIVIDUALS AND PATIENTS WITH TAY-SACHS DISEASE .1. ANTIGENIC DIFFERENCES BETWEEN HEXOSAMINIDASE-A AND HEXOSAMINIDASE-B [J]. INTERNATIONAL ARCHIVES OF ALLERGY AND APPLIED IMMUNOLOGY, 1974, 46 (04): : 512 - 524

[5] BARTON RW, 1971, J BIOL CHEM, V246, P7773

[6] DISTINCT BIOCHEMICAL DEFICIT IN MAROTEAUX-LAMY SYNDROME (MUCOPOLYSACCHARIDOSIS VI) [J]. JOURNAL OF PEDIATRICS, 1972, 80 (01) : 114 - +

[7] BAUDHUIN P, 1964, LAB INVEST, V13, P1139

[8] BEAUDET AL, IN PRESS

[9] CONGENITAL CORNEAL CLOUDING WITH ABNORMAL SYSTEMIC STORAGE BODIES - NEW VARIANT OF MUCOLIPIDOSIS [J]. JOURNAL OF PEDIATRICS, 1974, 84 (04) : 519 - 526

[10] BERMAN ER, 1974, CLIN CHIM ACTA, V52, P115