Thomas GH - Search Results

1

Mucolipidosis III (pseudo-Hurler polydystrophy): Clinical and laboratory studies in a series of 12 patients.

Kelly TE, Thomas GH, Taylor HA Jr, McKusick VA, Sly WS, Glaser JH, Robinow M, Luzzatti L, Espiritu C, Feingold M, Bull MJ, Ashenhurst EM, Ives EJ. Kelly TE, et al. Among authors: thomas gh. Johns Hopkins Med J. 1975 Oct;137(4):156-75. Johns Hopkins Med J. 1975. PMID: 810612

2

Mucolipidosis III: clinical and laboratory findings.

Kelly TE, Thomas GH, Taylor HA, McKusick VA. Kelly TE, et al. Among authors: thomas gh. Birth Defects Orig Artic Ser. 1975;11(6):295-9. Birth Defects Orig Artic Ser. 1975. PMID: 811281 No abstract available.

3

Letter: Screening for mucolipidosis.

Kelly TE, Thomas GH, Taylor HA Jr. Kelly TE, et al. Among authors: thomas gh. Lancet. 1973 Nov 10;2(7837):1089. doi: 10.1016/s0140-6736(73)92698-6. Lancet. 1973. PMID: 4127346 No abstract available.

4

Mucolipidosis 3 (Pseudo-Hurler polydystrophy): multiple lysosomal enzyme abnormalities in serum and cultured fibroblast cells.

Thomas GH, Taylor HA, Reynolds LW, Miller CS. Thomas GH, et al. Pediatr Res. 1973 Sep;7(9):751-6. doi: 10.1203/00006450-197309000-00004. Pediatr Res. 1973. PMID: 4200718 No abstract available.

5

Mucolipidosis 3 (pseudo-Hurler polydystrophy): cytological and ultrastructural observations of cultured fibroblast cells.

Taylor HA, Thomas GH, Miller CS, Kelly TE, Siggers D. Taylor HA, et al. Among authors: thomas gh. Clin Genet. 1973;4(5):388-97. doi: 10.1111/j.1399-0004.1973.tb01165.x. Clin Genet. 1973. PMID: 4201594 No abstract available.

6

Analysis of N-acetyl- -D-glucosaminidase in mucolipidosis II (I-cell disease).

Lie KK, Thomas GH, Taylor HA, Sensenbrenner JA. Lie KK, et al. Among authors: thomas gh. Clin Chim Acta. 1973 May 18;45(3):243-8. doi: 10.1016/0009-8981(73)90433-6. Clin Chim Acta. 1973. PMID: 4708053 No abstract available.

7

Pseudodeficiency of alpha-iduronidase.

Taylor HA, Thomas GH. Taylor HA, et al. Among authors: thomas gh. J Inherit Metab Dis. 1993;16(6):1058-9. doi: 10.1007/BF00711533. J Inherit Metab Dis. 1993. PMID: 8127064 No abstract available.

8

Mannosidosis: deficiency of a specific alpha-mannosidase component in cultured fibroblasts.

Taylor HA, Thomas GH, Aylsworth A, Stevenson RE, Reynolds LW. Taylor HA, et al. Among authors: thomas gh. Clin Chim Acta. 1975 Feb 22;59(1):93-9. doi: 10.1016/0009-8981(75)90223-5. Clin Chim Acta. 1975. PMID: 235386

9

Mannosidosis: phenotype of a severely affected child and characterization of alpha-mannosidase activity in cultured fibroblasts from the patient and his parents.

Aylsworth AS, Taylor HA, Stuart CM, Thomas GH. Aylsworth AS, et al. Among authors: thomas gh. J Pediatr. 1976 May;88(5):814-8. doi: 10.1016/s0022-3476(76)81120-1. J Pediatr. 1976. PMID: 5584

10

Partial trisomy 4q resulting from a familial 4/3 translocation.

Kelly TE, Haslam RH, Thomas GH. Kelly TE, et al. Among authors: thomas gh. South Med J. 1979 Nov;72(11):1459-61. doi: 10.1097/00007611-197911000-00032. South Med J. 1979. PMID: 505083

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