Baughan MA - Search Results

1

Hereditary hemolytic anemia with hexokinase deficiency. Role of hexokinase in erythrocyte aging.

Valentine WN, Oski FA, Paglia DE, Baughan MA, Schneider AS, Naiman JL. Valentine WN, et al. Among authors: baughan ma. N Engl J Med. 1967 Jan 5;276(1):1-11. doi: 10.1056/NEJM196701052760101. N Engl J Med. 1967. PMID: 6015552 No abstract available.

2

Hereditary hemolytic anemia associated with phosphoglycerate kinase deficiency in erythrocytes and leukocytes. A probable X-chromosome-linked syndrome.

Valentine WN, Hsieh HS, Paglia DE, Anderson HM, Baughan MA, Jaffé ER, Garson OM. Valentine WN, et al. Among authors: baughan ma. N Engl J Med. 1969 Mar 6;280(10):528-34. doi: 10.1056/NEJM196903062801003. N Engl J Med. 1969. PMID: 5764452 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. Blood. 1968 Aug;32(2):236-49. Blood. 1968. PMID: 5672849 Free article. No abstract available.

4

Hereditary hemolytic anemia: association with phosphoglycerate kinase deficiency in erythrocytes and leukocytes.

Valentine WN, Hsieh HS, Paglia DE, Anderson HM, Baughan MA, Jaffé ER, Garson OM. Valentine WN, et al. Among authors: baughan ma. Trans Assoc Am Physicians. 1968;81:49-65. Trans Assoc Am Physicians. 1968. PMID: 5721411 No abstract available.

5

Occurrence of defective hexosephosphate isomerization in human erythrocytes and leukocytes.

Paglia DE, Holland P, Baughan MA, Valentine WN. Paglia DE, et al. Among authors: baughan ma. N Engl J Med. 1969 Jan 9;280(2):66-71. doi: 10.1056/NEJM196901092800203. N Engl J Med. 1969. PMID: 5782480 No abstract available.

6

An inherited molecular lesion of erythrocyte pyruvate kinase. Identification of a kinetically aberrant isozyme associated with premature hemolysis.

Paglia DE, Valentine WN, Baughan MA, Miller DR, Reed CF, McIntyre OR. Paglia DE, et al. Among authors: baughan ma. J Clin Invest. 1968 Aug;47(8):1929-46. doi: 10.1172/JCI105883. J Clin Invest. 1968. PMID: 5666119 Free PMC article.

7

An unusual hematological syndrome with pyruvate-kinase deficiency and thalassemia minor in the kindreds.

Baughan MA, Paglia DE, Schneider AS, Valentine WN. Baughan MA, et al. Acta Haematol. 1968;39(6):345-58. doi: 10.1159/000208980. Acta Haematol. 1968. PMID: 4972369 No abstract available.

8

Blood cell enzymes in trisomy E (18) syndrome.

Baughan MA, Sparkes RS, Paglia DE, Wilson MG. Baughan MA, et al. J Med Genet. 1969 Mar;6(1):42-7. doi: 10.1136/jmg.6.1.42. J Med Genet. 1969. PMID: 4239000 Free PMC article. No abstract available.

9

Inherited variations in human phosphohexose isomerase.

Detter JC, Ways PO, Giblett ER, Baughan MA, Hopkinson DA, Povey S, Harris H. Detter JC, et al. Among authors: baughan ma. Ann Hum Genet. 1968 May;31(4):329-38. doi: 10.1111/j.1469-1809.1968.tb00565.x. Ann Hum Genet. 1968. PMID: 5673159 No abstract available.

10

Blood cell pyruvate kinase activity in translocation Down's syndrome.

Sparkes RS, Baughan MA. Sparkes RS, et al. Among authors: baughan ma. Humangenetik. 1969;7(3):253-4. doi: 10.1007/BF00273176. Humangenetik. 1969. PMID: 4241255 No abstract available.

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