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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

138 related articles for article (PubMed ID: 7411886)

  • 21. Glucosephosphate-isomerase type Kaiserslautern. A new variant causing congenital nonspherocytic hemolytic anemia.
    Arnold H; Hasslinger K; Witt I
    Blut; 1983 May; 46(5):271-7. PubMed ID: 6839028
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Clinical trial of mannose treatment of hemolytic anemia caused by congenital deficiency of erythrocyte glucosephosphate isomerase].
    Jabłońska-Skwiecińska E; Giro E; Rokicka-Milewska R
    Acta Haematol Pol; 1992; 23(2):123-8. PubMed ID: 1488862
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Glucosephosphate isomerase (GPI) deficiency hereditary nonspherocytic hemolytic anemia. Report of the second case found in Japanese.
    Miwa S; Nakashima K; Oda S; Matsumoto N; Ogawa H
    Nihon Ketsueki Gakkai Zasshi; 1973 Feb; 36(1):70-3. PubMed ID: 4738993
    [No Abstract]   [Full Text] [Related]  

  • 24. [Congenital erythrocytic pyrimidine 5'-nucleotidase deficiency. A new type of haemolytic erythro-enzymopathy (author's transl)].
    Vives-Corrons JL; Montserrat-Costa E; Pujades A; Woessner S; Rozman C
    Sangre (Barc); 1976; 21(4):827-35. PubMed ID: 1006499
    [No Abstract]   [Full Text] [Related]  

  • 25. [Glucose phosphate isomerase type Recklinghausen: a new enzyme variant with haemolytic anaemia (author's transl)].
    Arnold H; Engelhardt R; Löhr GW; Jacobi H; Liebold I
    Klin Wochenschr; 1973 Dec; 51(24):1198-204. PubMed ID: 4789327
    [No Abstract]   [Full Text] [Related]  

  • 26. Genetic and molecular mechanisms of the congenital defects in glucose phosphate isomerase activity: studies of four families.
    Kahn A; Van Biervliet JP; Vives-Corrons JL; Cottreau D; Stall GE
    Pediatr Res; 1977 Nov; 11(11):1123-9. PubMed ID: 411100
    [No Abstract]   [Full Text] [Related]  

  • 27. [A case of new G 6 PD variant associated with chronic nonspherocytic anemia: G 6 PD Sapporo (author's transl)].
    Konno M; Sato T; Nishina T; Fujii H; Takegawa S; Miwa S
    Rinsho Ketsueki; 1981 May; 22(5):701-6. PubMed ID: 7277713
    [No Abstract]   [Full Text] [Related]  

  • 28. Combination of congenital nonspherocytic haemolytic anaemia and impairment of granulocyte function in severe glucosephosphate isomerase deficiency. A new variant enzyme designated GPI Calden.
    Neubauer BA; Eber SW; Lakomek M; Gahr M; Schröter W
    Acta Haematol; 1990; 83(4):206-10. PubMed ID: 2115718
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Formal genetics of phosphoglucose isomerase (EC:5.3.1.9). Studies of a family with PGI-deficiency].
    Tariverdian G; Arnold H; Blume KG; Lenkeit U; Löhr GW
    Humangenetik; 1970; 10(3):218-23. PubMed ID: 5475506
    [No Abstract]   [Full Text] [Related]  

  • 30. Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study.
    Manco L; Bento C; Victor BL; Pereira J; Relvas L; Brito RM; Seabra C; Maia TM; Ribeiro ML
    Blood Cells Mol Dis; 2016 Sep; 60():18-23. PubMed ID: 27519939
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Characterization of two new variants of glucose-phosphate-isomerase deficiency with hereditary nonspherocytic hemolytic anemia.
    Blume KG; Hryniuk W; Powars D; Trinidad F; West C; Beutler E
    J Lab Clin Med; 1972 Jun; 79(6):942-9. PubMed ID: 5025461
    [No Abstract]   [Full Text] [Related]  

  • 32. Glucose phosphate isomerase deficiency demasked by whole-genome sequencing: a case report.
    Holme S; van Wijk R; Rasmussen AØ; Petersen J; Glenthøj A
    J Med Case Rep; 2024 Mar; 18(1):130. PubMed ID: 38539245
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Glucose phosphate isomerase deficiency with hereditary nonspherocytic hemolytic anemia.
    Hutton JJ; Chilcote RR
    J Pediatr; 1974 Oct; 85(4):494-7. PubMed ID: 4443856
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Glucose phosphate isomerase deficiency: enzymatic and familial characterization of Arg346His mutation.
    Repiso A; Oliva B; Vives Corrons JL; Carreras J; Climent F
    Biochim Biophys Acta; 2005 Jun; 1740(3):467-71. PubMed ID: 15949716
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Glucose phosphate isomerase deficiency as a cause of hydrops fetalis.
    Ravindranath Y; Paglia DE; Warrier I; Valentine W; Nakatani M; Brockway RA
    N Engl J Med; 1987 Jan; 316(5):258-61. PubMed ID: 3796702
    [No Abstract]   [Full Text] [Related]  

  • 36. Fine structure of the spleen and liver in glucosephosphate isomerase (GPI) deficiency hereditary nonspherocytic hemolytic anemia. Selective reticulocyte destruction as a mechanism of hemolysis.
    Matsumoto N; Ishihara T; Oda E; Miwa S; Nakashima K
    Nihon Ketsueki Gakkai Zasshi; 1973 Feb; 36(1):46-54. PubMed ID: 4738991
    [No Abstract]   [Full Text] [Related]  

  • 37. A new variant of glucosephosphate isomerase deficiency.
    Van Biervliet JP; Vlug A; Bartstra H; Rotteveel JJ; de Vaan GA; Staal GE
    Humangenetik; 1975 Oct; 30(1):35-40. PubMed ID: 1339
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A novel missense mutation in glucose-6-phosphate dehydrogenase gene causing chronic nonspherocytic hemolytic anemia in an Indian family.
    Edison ES; Melinkeri SR; Chandy M
    Ann Hematol; 2006 Dec; 85(12):879-80. PubMed ID: 16944148
    [No Abstract]   [Full Text] [Related]  

  • 39. Clinical, laboratory, and mutational profile of children with glucose phosphate isomerase deficiency: a single centre report.
    Sampagar A; Gosavi M; Kedar P; Patel T; Dongerdiye R; Mahantashetti N
    Int J Hematol; 2022 Feb; 115(2):255-262. PubMed ID: 34704234
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Two novel mutations (p.(Ser160Pro) and p.(Arg472Cys)) causing glucose-6-phosphate isomerase deficiency are associated with erythroid dysplasia and inappropriately suppressed hepcidin.
    Mojzikova R; Koralkova P; Holub D; Saxova Z; Pospisilova D; Prochazkova D; Dzubak P; Horvathova M; Divoky V
    Blood Cells Mol Dis; 2018 Mar; 69():23-29. PubMed ID: 28803808
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.