These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
159 related items for PubMed ID: 1129019
21. Prenatal diagnosis of a red-cell enzymopathy: triose phosphate isomerase deficiency. Bellingham AJ, Lestas AN, Williams LH, Nicolaides KH. Lancet; 1989 Aug 19; 2(8660):419-21. PubMed ID: 2569601 [Abstract] [Full Text] [Related]
23. Prenatal diagnosis of triose phosphate isomerase deficiency. Bellingham AJ, Lestas AN. Lancet; 1990 Jan 27; 335(8683):230. PubMed ID: 1967698 [No Abstract] [Full Text] [Related]
24. [Congenital hemolytic anemia associated with phosphoglycerate kinase deficiency in erythrocytes, polynuclear cells and lymphocytes]. Cartier P, Habibi B, Leroux JP, Marchand JC. Nouv Rev Fr Hematol; 1971 Jan 27; 11(4):565-78. PubMed ID: 4257431 [No Abstract] [Full Text] [Related]
25. Occurrence of defective hexosephosphate isomerization in human erythrocytes and leukocytes. Paglia DE, Holland P, Baughan MA, Valentine WN. N Engl J Med; 1969 Jan 09; 280(2):66-71. PubMed ID: 5782480 [No Abstract] [Full Text] [Related]
29. Myopathy with altered mitochondria due to a triosephosphate isomerase (TPI) deficiency. Bardosi A, Eber SW, Hendrys M, Pekrun A. Acta Neuropathol; 1990 Jan 09; 79(4):387-94. PubMed ID: 2339591 [Abstract] [Full Text] [Related]
31. Congenital non-spherocytic haemolytic anaemias. Zanella A, Colombo MB, Rossi F, Merati G, Sirchia G. Haematologica; 1989 Jan 09; 74(4):387-96. PubMed ID: 2551797 [Abstract] [Full Text] [Related]
32. [Erythrocyte enzyme defects and their clinical significance (author's transl)]. Schröter W. Monatsschr Kinderheilkd; 1981 Aug 09; 129(8):432-43. PubMed ID: 6116182 [No Abstract] [Full Text] [Related]
33. Diminished blood levels of reduced glutathione and alpha-tocopherol in two triosephosphate isomerase-deficient brothers. Karg E, Németh I, Horányi M, Pintér S, Vécsei L, Hollán S. Blood Cells Mol Dis; 2000 Feb 09; 26(1):91-100. PubMed ID: 10772880 [Abstract] [Full Text] [Related]
34. Prevalence of partial deficiency of red cell triosephosphate isomerase in Germany--a study of 3000 people. Eber SW, Dünnwald M, Heinemann G, Hofstätter T, Weinmann HM, Belohradsky BH. Hum Genet; 1984 Feb 09; 67(3):336-9. PubMed ID: 6381286 [Abstract] [Full Text] [Related]
37. [Deficiency of red cell glucose-6-phosphate-dehydrogenase due to a slow variant in a French family. Relationship with the Gd (-) Seattle variant (author's transl)]. Kahn A, Boivin P, Lagneau J, Cruveiller J. Nouv Rev Fr Hematol; 1973 Feb 09; 13(2):163-71. PubMed ID: 4270706 [No Abstract] [Full Text] [Related]
38. [Glucosephosphate dehydrogenase deficiency in erythrocytes and leukocytes of patients with congenital nonspherocytic hemolytic anemia and favism]. Jabłońska-Skwiecińska E, Staniszewska K. Pol Tyg Lek; 1988 Feb 15; 43(7):207-9. PubMed ID: 3405890 [No Abstract] [Full Text] [Related]
39. [Red cell enzyme deficiencies - clinical manifestation and pathophysiology (author's transl)]. Gahr M. Monatsschr Kinderheilkd; 1981 Aug 15; 129(8):444-53. PubMed ID: 6116183 [No Abstract] [Full Text] [Related]
40. Hereditary triosephosphate isomerase (TPI) deficiency: two severely affected brothers one with and one without neurological symptoms. Hollán S, Fujii H, Hirono A, Hirono K, Karro H, Miwa S, Harsányi V, Gyódi E, Inselt-Kovács M. Hum Genet; 1993 Nov 15; 92(5):486-90. PubMed ID: 8244340 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]