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.
225 related articles for article (PubMed ID: 10702808)
101. [Erythrocyte membrane proteins in patients with hereditary spherocytosis]. Zakharov SF; Gromov PS; Shcheglova MV; Al'-Radi LS; Shishkin SS Gematol Transfuziol; 1992; 37(11-12):23-6. PubMed ID: 1295777 [TBL] [Abstract][Full Text] [Related]
102. Increased adsorption of cytoplasmic proteins to the erythrocyte membrane in ATP-depleted normal and pyruvate kinase-deficient mature cells and reticulocytes. Allen DW; Groat JD; Finkel B; Rank BH; Wood PA; Eaton JW Am J Hematol; 1983 Feb; 14(1):11-25. PubMed ID: 6837565 [TBL] [Abstract][Full Text] [Related]
103. Profound spherocytosis in adulthood: Acquired, hereditary or both? Langeveld TJC; van Rossum AP; van der Zwaag B; van Wijk R; Vlasveld LT Int J Lab Hematol; 2017 Oct; 39(5):e117-e120. PubMed ID: 28488802 [No Abstract] [Full Text] [Related]
104. Pyruvate kinase deficiency in sub-Saharan Africa: identification of a highly frequent missense mutation (G829A;Glu277Lys) and association with malaria. Machado P; Manco L; Gomes C; Mendes C; Fernandes N; Salomé G; Sitoe L; Chibute S; Langa J; Ribeiro L; Miranda J; Cano J; Pinto J; Amorim A; do Rosário VE; Arez AP PLoS One; 2012; 7(10):e47071. PubMed ID: 23082140 [TBL] [Abstract][Full Text] [Related]
105. Siblings with severe pyruvate kinase deficiency and a complex genotype. Christensen RD; Yaish HM; Nussenzveig RH; Agarwal AM Am J Med Genet A; 2016 Sep; 170(9):2449-52. PubMed ID: 27354418 [TBL] [Abstract][Full Text] [Related]
106. Next generation sequencing (NGS) interest in deciphering erythrocyte molecular defects' association in red cell disorders: Clinical and erythrocyte phenotypes of patients with mutations inheritance in PIEZO1, Spectrin ß1, RhAG and SLC4A1. Allegrini B; NGuyen LD; Mignotet M; Etchebest C; Fenneteau O; Platon J; Lambilliotte A; Guizouarn H; Da Costa L Blood Cells Mol Dis; 2023 Nov; 103():102780. PubMed ID: 37516005 [TBL] [Abstract][Full Text] [Related]
107. Atypical pyruvate kinase in a family with spherocytic haemolytic anaemia. Hanel HK; Pedersen JT Scand J Haematol; 1972; 9(6):557-61. PubMed ID: 4644419 [No Abstract] [Full Text] [Related]
108. [Gene analysis and genetic diagnosis of hereditary erythrocyte abnormalities. Pyruvate kinase deficiency]. Noguchi T; Tanaka T Nihon Rinsho; 1987 Dec; 45(12):2899-904. PubMed ID: 3446877 [No Abstract] [Full Text] [Related]
109. Band 4.2 Shiga: 317 CGC-->TGC in compound heterozygotes with 142 GCT-->ACT results in band 4.2 deficiency and microspherocytosis. Kanzaki A; Yasunaga M; Okamoto N; Inoue T; Yawata A; Wada H; Andoh A; Hodohara K; Fujiyama Y; Bamba T Br J Haematol; 1995 Oct; 91(2):333-40. PubMed ID: 8547071 [TBL] [Abstract][Full Text] [Related]
110. Defective membrane phosphorylation in red cells of a patient with hereditary spherocytosis. Yawata Y; Koresawa S; Yamada O; Shibata S Nihon Ketsueki Gakkai Zasshi; 1975 Jun; 38(3):311-4. PubMed ID: 1243224 [No Abstract] [Full Text] [Related]
111. Whole-exome sequencing for the genetic diagnosis of congenital red blood cell membrane disorders in Taiwan. Lin PC; Chiou SS; Lin CY; Wang SC; Huang HY; Chang YS; Tseng YH; Kan TM; Liao YM; Tsai SP; Peng CT; Chang JG Clin Chim Acta; 2018 Dec; 487():311-317. PubMed ID: 30317022 [TBL] [Abstract][Full Text] [Related]
112. Iron overload associated with congenital pyruvate kinase deficiency and high dose ascorbic acid ingestion. Rowbotham B; Roeser HP Aust N Z J Med; 1984 Oct; 14(5):667-9. PubMed ID: 6597712 [TBL] [Abstract][Full Text] [Related]
113. Mitapivat reprograms the RBC metabolome and improves anemia in a mouse model of hereditary spherocytosis. Matte A; Wilson AB; Gevi F; Federti E; Recchiuti A; Ferri G; Brunati AM; Pagano MA; Russo R; Leboeuf C; Janin A; Timperio AM; Iolascon A; Gremese E; Dang L; Mohandas N; Brugnara C; De Franceschi L JCI Insight; 2023 Oct; 8(20):. PubMed ID: 37676741 [TBL] [Abstract][Full Text] [Related]
114. DNA methylation in promoter regions of red cell membrane protein genes in healthy individuals and patients with hereditary membrane disorders. Remus R; Kanzaki A; Yawata A; Nakanishi H; Wada H; Sugihara T; Zeschnigk M; Zuther I; Schmitz B; Naumann F; Doerfler W; Yawata Y Int J Hematol; 2005 Jun; 81(5):385-95. PubMed ID: 16158818 [TBL] [Abstract][Full Text] [Related]
115. A new pyruvate kinase variant (PK Osaka) demonstrated by partial purification and condensation. Shinohara K; Miwa S; Nakashima K; Oda E; Kageoka T Am J Hum Genet; 1976 Sep; 28(5):474-81. PubMed ID: 984043 [TBL] [Abstract][Full Text] [Related]
116. Hereditary spherocytosis with band 3 deficiency. Association with a nonsense mutation of the band 3 gene (allele Lyon), and aggravation by a low-expression allele occurring in trans (allele Genas). Alloisio N; Maillet P; Carré G; Texier P; Vallier A; Baklouti F; Philippe N; Delaunay J Blood; 1996 Aug; 88(3):1062-9. PubMed ID: 8704215 [TBL] [Abstract][Full Text] [Related]
117. Hereditary erythrocyte pyruvate kinase deficiency: molecular and functional studies of four mutant PK variants detected in Spain. Marie J; Vives-Corrons JL; Kahn A; Kernemp B Clin Chim Acta; 1977 Dec; 81(2):153-62. PubMed ID: 589795 [No Abstract] [Full Text] [Related]
118. Hereditary spherocytosis: a review of the clinical and molecular aspects of the disease. Hassoun H; Palek J Blood Rev; 1996 Sep; 10(3):129-47. PubMed ID: 8932827 [TBL] [Abstract][Full Text] [Related]
119. Four new pyruvate kinase (PK) variants and a classical PK deficiency. Miwa S; Nakashima K; Ariyoshi K; Shinohara K; Oda E Br J Haematol; 1975 Jan; 29(1):157-69. PubMed ID: 1201198 [TBL] [Abstract][Full Text] [Related]
120. Hereditary spherocytosis associated with a variant of band 3 protein in the erythrocyte membrane. Imamura T; Matsuo T; Yanase T; Kagiyama S Jpn J Med; 1984 Aug; 23(3):216-9. PubMed ID: 6492485 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]