POMPES DISEASE ( DIFFUSE GLYCOGENOSIS ) WITH NEURONAL STORAGE

[1] AGNESE PAD, 1959, ANN NY ACAD SCI, V72, P439

[2] BODANSKY M, 1952, BIOCHEMISTRY DISEASE

[3] CADDELL JL, 1962, PEDIATRICS, V29, P743

[4] CANTAROW A, 1962, CLINICAL BIOCHEMISTR

[5] CHILDS AW, 1952, PEDIATRICS, V10, P208

[6] GLYCOGEN DISEASE RESEMBLING MONGOLISM, CRETINISM, AND AMYTONIA CONGENITA - CASE REPORT AND REVIEW OF LITERATURE [J]. JOURNAL OF PEDIATRICS, 1950, 36 (01) : 11 - 30

[7] CROME J, 1963, PSYCHIATRY, V26, P422

[8] LATE-ONSET TYPE OF SKELETAL-MUSCLE PHOSPHORYLASE DEFICIENCY - A NEW FAMILIAL VARIETY WITH COMPLETELY AND PARTIALLY AFFECTED SUBJECTS [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1963, 268 (03) : 135 - &

[9] ESSER M, 1937, SCHWEIZ MED WCHNSCHR, V67, P970

[10] FIELD RA, 1960, METABOLIC BASIS INHE, pCH6

[1] AGNESE PAD, 1959, ANN NY ACAD SCI, V72, P439

[2] BODANSKY M, 1952, BIOCHEMISTRY DISEASE

[3] CADDELL JL, 1962, PEDIATRICS, V29, P743

[4] CANTAROW A, 1962, CLINICAL BIOCHEMISTR

[5] CHILDS AW, 1952, PEDIATRICS, V10, P208

[6] GLYCOGEN DISEASE RESEMBLING MONGOLISM, CRETINISM, AND AMYTONIA CONGENITA - CASE REPORT AND REVIEW OF LITERATURE [J]. JOURNAL OF PEDIATRICS, 1950, 36 (01) : 11 - 30

[7] CROME J, 1963, PSYCHIATRY, V26, P422

[8] LATE-ONSET TYPE OF SKELETAL-MUSCLE PHOSPHORYLASE DEFICIENCY - A NEW FAMILIAL VARIETY WITH COMPLETELY AND PARTIALLY AFFECTED SUBJECTS [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1963, 268 (03) : 135 - &

[9] ESSER M, 1937, SCHWEIZ MED WCHNSCHR, V67, P970

[10] FIELD RA, 1960, METABOLIC BASIS INHE, pCH6