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28. Characterization of hereditary red blood cell membranopathies using combined targeted next-generation sequencing and osmotic gradient ektacytometry. Vives-Corrons JL; Krishnevskaya E; Rodriguez IH; Ancochea A Int J Hematol; 2021 Feb; 113(2):163-174. PubMed ID: 33074480 [TBL] [Abstract][Full Text] [Related]
29. A family affair-Severe fetal and neonatal hemolytic anemia due to novel alpha-spectrin mutations in two siblings. Donepudi R; Westerfield L; Stonecipher A; A Nassr A; Cortes MS; Espinoza J; Belfort M; Shamshirsaz A Am J Med Genet A; 2020 Mar; 182(3):561-564. PubMed ID: 31854503 [TBL] [Abstract][Full Text] [Related]
30. Inherited erythrocyte metabolic and membrane disorders. Brewer GJ Med Clin North Am; 1980 Jul; 64(4):579-96. PubMed ID: 6995724 [TBL] [Abstract][Full Text] [Related]
31. Hereditary high phosphatidylcholine hemolytic anemia: report of a new family and review of the literature. Shojania AM; Godin DV; Frohlich J Clin Invest Med; 1990 Dec; 13(6):313-21. PubMed ID: 1964113 [TBL] [Abstract][Full Text] [Related]
32. Gene disruption of dematin causes precipitous loss of erythrocyte membrane stability and severe hemolytic anemia. Lu Y; Hanada T; Fujiwara Y; Nwankwo JO; Wieschhaus AJ; Hartwig J; Huang S; Han J; Chishti AH Blood; 2016 Jul; 128(1):93-103. PubMed ID: 27073223 [TBL] [Abstract][Full Text] [Related]
33. Red blood cell aquaporin-1 expression is decreased in hereditary spherocytosis. Crisp RL; Maltaneri RE; Vittori DC; Solari L; Gammella D; Schvartzman G; GarcĂa E; Rapetti MC; Donato H; Nesse A Ann Hematol; 2016 Oct; 95(10):1595-601. PubMed ID: 27465156 [TBL] [Abstract][Full Text] [Related]
35. [Surface architechtonics of the erythrocytes and their functional importance under normal conditions and in various anemias (scanning electron microscopic study). Review of the literature and the authors' data]. Riapolova IV; Shishkanova ZG Probl Gematol Pereliv Krovi; 1978 Dec; (12):42-5. PubMed ID: 746035 [No Abstract] [Full Text] [Related]
36. Stomatin: a putative cation transport regulator in the red cell membrane. Stewart GW; Argent AC; Dash BC Biochim Biophys Acta; 1993 Nov; 1225(1):15-25. PubMed ID: 7694657 [No Abstract] [Full Text] [Related]
37. The molecular basis of disorders of the red cell membrane. McMullin MF J Clin Pathol; 1999 Apr; 52(4):245-8. PubMed ID: 10474512 [No Abstract] [Full Text] [Related]
38. Inherited haemolytic anaemia created by insertional inactivation of the alpha-spectrin gene. Grimber G; Galand C; Garbarz M; Mattei MG; Cavard C; Zider A; Blanchet P; Boivin P; Briand P; Dhermy D Transgenic Res; 1992 Nov; 1(6):268-74. PubMed ID: 1338695 [TBL] [Abstract][Full Text] [Related]
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40. Elevated levels of redox regulators, membrane-bound globin chains, and cytoskeletal protein fragments in hereditary spherocytosis erythrocyte proteome. Saha S; Ramanathan R; Basu A; Banerjee D; Chakrabarti A Eur J Haematol; 2011 Sep; 87(3):259-66. PubMed ID: 21575061 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]