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31. Red cell glucose phosphate isomerase (GPI): a molecular study of three novel mutations associated with hereditary nonspherocytic hemolytic anemia. Repiso A; Oliva B; Vives-Corrons JL; Beutler E; Carreras J; Climent F Hum Mutat; 2006 Nov; 27(11):1159. PubMed ID: 17041899 [TBL] [Abstract][Full Text] [Related]
32. Molecular diagnosis of unexplained haemolytic anaemia using targeted next-generation sequencing panel revealed (p.Ala337Thr) novel mutation in GPI gene in two Indian patients. Kedar PS; Gupta V; Dongerdiye R; Chiddarwar A; Warang P; Madkaikar MR J Clin Pathol; 2019 Jan; 72(1):81-85. PubMed ID: 30337328 [TBL] [Abstract][Full Text] [Related]
33. Laparoscopic cholecystectomy and postoperative pain control in a patient with chronic non-spherocytic hemolytic anemia from glucose-6-phosphate dehydrogenase deficiency. Watanabe M; Kashiwadate T; Hagiwara M; Hashizume E J Clin Anesth; 2019 May; 54():128-129. PubMed ID: 30476701 [No Abstract] [Full Text] [Related]
34. [From gene to disease; hereditary non-spherocytic hemolytic anemia caused by pyruvate kinase deficiency]. de Vooght KM; van Wijk R; Nieuwenhuis HK; Ploos van Amstel JK; Rijksen G; van Solinge WW Ned Tijdschr Geneeskd; 2002 Sep; 146(39):1828-31. PubMed ID: 12382367 [TBL] [Abstract][Full Text] [Related]
35. [Hereditary non-spherocytic hemolytic anemia caused by glucosephosphate isomerase deficiency: 1. case observed in Switzerland]. Müller E; Marti HR; Bach J; Micheli JL; Gasser C Schweiz Med Wochenschr; 1974 Sep; 104(39):1379-81. PubMed ID: 4419288 [No Abstract] [Full Text] [Related]
37. Severe Presentation of Congenital Hemolytic Anemias in the Neonatal Age: Diagnostic and Therapeutic Issues. Cortesi V; Manzoni F; Raffaeli G; Cavallaro G; Fattizzo B; Amelio GS; Gulden S; Amodeo I; Giannotta JA; Mosca F; Ghirardello S Diagnostics (Basel); 2021 Aug; 11(9):. PubMed ID: 34573891 [TBL] [Abstract][Full Text] [Related]
38. [NON-SPHEROCYTIC CONGENITAL HEMOLYTIC ANEMIA CAUSED BY PYRUVATE-KINASE DEFICIENCY]. MALLARME J; BOIVIN P; GERBEAUX J Bull Mem Soc Med Hop Paris; 1964 Mar 6-13; 115():483-91. PubMed ID: 14156103 [No Abstract] [Full Text] [Related]
39. Study of pathophysiology and molecular characterization of congenital anemia in India using targeted next-generation sequencing approach. Kedar PS; Harigae H; Ito E; Muramatsu H; Kojima S; Okuno Y; Fujiwara T; Dongerdiye R; Warang PP; Madkaikar MR Int J Hematol; 2019 Nov; 110(5):618-626. PubMed ID: 31401766 [TBL] [Abstract][Full Text] [Related]
40. A Family Affected by a Life-Threatening Erythrocyte Defect Caused by Pyruvate Kinase Deficiency With Normal Iron Status: A Case Report. Maciak K; Adamowicz-Salach A; Poznanski J; Gora M; Fronk J; Burzynska B Front Genet; 2020; 11():560248. PubMed ID: 33193643 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]