Valentine WN - Search Results

1

Unique phenotypic expression of glucosephosphate isomerase deficiency.

Paglia DE, Paredes R, Valentine WN, Dorantes S, Konrad PN. Paglia DE, et al. Among authors: valentine wn. Am J Hum Genet. 1975 Jan;27(1):62-70. Am J Hum Genet. 1975. PMID: 1155451 Free PMC article.

2

Hereditary glucosephosphate isomerase deficiency. A review.

Paglia DE, Valentine WN. Paglia DE, et al. Among authors: valentine wn. Am J Clin Pathol. 1974 Dec;62(6):740-51. doi: 10.1093/ajcp/62.6.740. Am J Clin Pathol. 1974. PMID: 4611197 Review. No abstract available.

3

Hereditary hemolytic anemia associated with glucosephosphate isomerase (GPI) deficiency--a new enzyme defect of human erythrocytes.

Baughan MA, Valentine WN, Paglia DE, Ways PO, Simons ER, DeMarsh QB. Baughan MA, et al. Among authors: valentine wn. Blood. 1968 Aug;32(2):236-49. Blood. 1968. PMID: 5672849 Free article. No abstract available.

4

An isozyme of erythrocyte pyruvate kinase (PK-Los Angeles) with impaired kinetics corrected by fructose-1, 6-diphosphate.

Paglia DE, Valentine WN, Williams KO, Konrad PN. Paglia DE, et al. Among authors: valentine wn. Am J Clin Pathol. 1977 Aug;68(2):229-34. doi: 10.1093/ajcp/68.2.229. Am J Clin Pathol. 1977. PMID: 18004

5

Nonrecessively transmitted nonspherocytic hereditary haemolytic anaemia associated with increased red cell glutathione.

Valentine WN, Paglia DE. Valentine WN, et al. Br J Haematol. 1979 Jun;42(2):231-7. doi: 10.1111/j.1365-2141.1979.tb01128.x. Br J Haematol. 1979. PMID: 465369

6

Congenital hemolytic anemia due to hexokinase deficiency.

Gilsanz F, Meyer E, Paglia DE, Valentine WN. Gilsanz F, et al. Among authors: valentine wn. Am J Dis Child. 1978 Jun;132(6):636-7. doi: 10.1001/archpedi.1978.02120310100023. Am J Dis Child. 1978. PMID: 655151 No abstract available.

7

Biphasic reaction kinetics in an anomalous isozyme of erythrocyte pyruvate kinase.

Paglia DE, Konrad PN, Wolff JA, Valentine WN. Paglia DE, et al. Among authors: valentine wn. Clin Chim Acta. 1976 Dec;73(3):395-405. doi: 10.1016/0009-8981(76)90140-6. Clin Chim Acta. 1976. PMID: 1000857

8

Hereditary hemolytic anemia with human erythrocyte pyrimidine 5'-nucleotidase deficiency.

Valentine WN, Fink K, Paglia DE, Harris SR, Adams WS. Valentine WN, et al. J Clin Invest. 1974 Oct;54(4):866-79. doi: 10.1172/JCI107826. J Clin Invest. 1974. PMID: 4372252 Free PMC article.

9

Erythrocyte and leukocyte phosphoglycerate kinase deficiency with neurologic disease.

Konrad PN, McCarthy DJ, Mauer AM, Valentine WN, Paglia DE. Konrad PN, et al. Among authors: valentine wn. J Pediatr. 1973 Mar;82(3):456-60. doi: 10.1016/s0022-3476(73)80120-9. J Pediatr. 1973. PMID: 4698932 No abstract available.

10

Studies on human erythrocyte nucleotide metabolism. II. Nonspherocytic hemolytic anemia, high red cell ATP, and ribosephosphate pyrophosphokinase (RPK, E.C.2.7.6.1) deficiency.

Valentine WN, Anderson HM, Paglia DE, Jaffé ER, Konrad PN, Harris SR. Valentine WN, et al. Blood. 1972 May;39(5):674-84. Blood. 1972. PMID: 5022715 Free article. No abstract available.

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