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.
5. Novel exon 2 α spectrin mutation and intragenic crossover: three morphological phenotypes associated with four distinct α spectrin defects. Swierczek S; Agarwal AM; Naidoo K; Lorenzo FR; Whisenant J; Nussenzveig RH; Agarwal N; Coetzer TL; Prchal JT Haematologica; 2013 Dec; 98(12):1972-9. PubMed ID: 24077844 [TBL] [Abstract][Full Text] [Related]
6. Red cell ektacytometry in two patients with chronic hemolytic anemia and three new α-spectrin variants. Vives-Corrons JL; Krishnevskaya E; Hernández-Rodriguez I; Payán-Pernia S; Sevilla ÁFR; Badell I Ann Hematol; 2022 Mar; 101(3):549-555. PubMed ID: 34845540 [TBL] [Abstract][Full Text] [Related]
7. Expression of spectrin alphaI/50 hereditary elliptocytosis and its association with the alphaLELY allele. Bassères DS; Pranke PH; Vicentim D; Costa FF; Saad ST Acta Haematol; 1998; 100(1):32-8. PubMed ID: 9691144 [TBL] [Abstract][Full Text] [Related]
13. Unravelling the genetic and phenotypic heterogeneity of SPTA1 gene variants in Hereditary Elliptocytosis and Hereditary Pyropoikilocytosis patients using next-generation sequencing. Anil More T; Kedar P Gene; 2022 Nov; 843():146796. PubMed ID: 35961434 [TBL] [Abstract][Full Text] [Related]
14. Dizygotic twins with prolonged jaundice and microcytic, hypochromic, hemolytic anemia with pyropoikilocytosis. Bahr TM; Lozano-Chinga M; Agarwal AM; Meznarich JA; Gerday E; Smoot JL; Taylor A; Christensen RD Blood Cells Mol Dis; 2020 Nov; 85():102462. PubMed ID: 32623341 [TBL] [Abstract][Full Text] [Related]
17. Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain. Garbarz M; Lecomte MC; Féo C; Devaux I; Picat C; Lefebvre C; Galibert F; Gautero H; Bournier O; Galand C Blood; 1990 Apr; 75(8):1691-8. PubMed ID: 2328319 [TBL] [Abstract][Full Text] [Related]
19. A novel splicing mutation of the alpha-spectrin gene in the original hereditary pyropoikilocytosis kindred. Costa DB; Lozovatsky L; Gallagher PG; Forget BG Blood; 2005 Dec; 106(13):4367-9. PubMed ID: 16150946 [TBL] [Abstract][Full Text] [Related]
20. Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin alpha I/74-kilodalton tryptic peptide. Floyd PB; Gallagher PG; Valentino LA; Davis M; Marchesi SL; Forget BG Blood; 1991 Sep; 78(5):1364-72. PubMed ID: 1878597 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]