MACULAR CHERRY-RED SPOT, CORNEAL CLOUDING, AND BETA-GALACTOSIDASE DEFICIENCY

[11] CALLAHAN WP, 1966, AM J PATHOL, V48, P277

[12] CERAMIDE TRIHEXOSIDOSIS (FABRYS DISEASE) WITHOUT SKIN LESIONS [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1971, 284 (05) : 233 - &

[13] CHEMICAL AND ENZYMIC STUDIES OF A FAMILY WITH SKELETAL ABNORMALITIES ASSOCIATED WITH MENTAL RETARDATION [J]. CLINICA CHIMICA ACTA, 1970, 29 (02) : 197 - &

[14] MUCOPOLYSACCHARIDOSIS - PAPER ELECTROPHORETIC AND INFRA-RED ANALYSIS OF URINE IN GARGOYLISM AND MORQUIO-ULLRICHS DISEASE [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1963, 38 (200) : 364 - +

[15] COGAN DG, 1968, ARCH OPHTHALMOL-CHIC, V79, P437

[16] METACHROMATIC LEUCODYSTROPHY [J]. OPHTHALMOLOGICA, 1970, 160 (1-2) : 2 - &

[17] LACTOSYL CERAMIDOSIS - CATABOLIC ENZYME DEFECT OF GLYCOSPHINGOLIPID METABOLISM [J]. SCIENCE, 1970, 170 (3957) : 556 - &

[18] DIFERRANTE N, 1971, P NATL ACAD SCI USA, V68, P303

[19] MORQUIO-ULLRICHS DISEASE - AN INBORN ERROR OF METABOLISM [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1962, 37 (195) : 525 - &

[20] GM1-GANGLIOSIDOSIS - OCULAR AND PATHOLOGICAL MANIFESTATIONS [J]. ARCHIVES OF OPHTHALMOLOGY, 1971, 85 (02) : 177 - &

[11] CALLAHAN WP, 1966, AM J PATHOL, V48, P277

[12] CERAMIDE TRIHEXOSIDOSIS (FABRYS DISEASE) WITHOUT SKIN LESIONS [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1971, 284 (05) : 233 - &

[13] CHEMICAL AND ENZYMIC STUDIES OF A FAMILY WITH SKELETAL ABNORMALITIES ASSOCIATED WITH MENTAL RETARDATION [J]. CLINICA CHIMICA ACTA, 1970, 29 (02) : 197 - &

[14] MUCOPOLYSACCHARIDOSIS - PAPER ELECTROPHORETIC AND INFRA-RED ANALYSIS OF URINE IN GARGOYLISM AND MORQUIO-ULLRICHS DISEASE [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1963, 38 (200) : 364 - +

[15] COGAN DG, 1968, ARCH OPHTHALMOL-CHIC, V79, P437

[16] METACHROMATIC LEUCODYSTROPHY [J]. OPHTHALMOLOGICA, 1970, 160 (1-2) : 2 - &

[17] LACTOSYL CERAMIDOSIS - CATABOLIC ENZYME DEFECT OF GLYCOSPHINGOLIPID METABOLISM [J]. SCIENCE, 1970, 170 (3957) : 556 - &

[18] DIFERRANTE N, 1971, P NATL ACAD SCI USA, V68, P303

[19] MORQUIO-ULLRICHS DISEASE - AN INBORN ERROR OF METABOLISM [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1962, 37 (195) : 525 - &

[20] GM1-GANGLIOSIDOSIS - OCULAR AND PATHOLOGICAL MANIFESTATIONS [J]. ARCHIVES OF OPHTHALMOLOGY, 1971, 85 (02) : 177 - &