231 related articles for article (PubMed ID: 34845540)
1. 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]
2. Alteration of the erythrocyte membrane skeletal ultrastructure in hereditary spherocytosis, hereditary elliptocytosis, and pyropoikilocytosis.
Liu SC; Derick LH; Agre P; Palek J
Blood; 1990 Jul; 76(1):198-205. PubMed ID: 2364170
[TBL] [Abstract][Full Text] [Related]
3. Spectrin mutations in hereditary elliptocytosis and hereditary spherocytosis.
Maillet P; Alloisio N; Morlé L; Delaunay J
Hum Mutat; 1996; 8(2):97-107. PubMed ID: 8844207
[TBL] [Abstract][Full Text] [Related]
4. Genotype-phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis.
Niss O; Chonat S; Dagaonkar N; Almansoori MO; Kerr K; Rogers ZR; McGann PT; Quarmyne MO; Risinger M; Zhang K; Kalfa TA
Blood Cells Mol Dis; 2016 Oct; 61():4-9. PubMed ID: 27667160
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Red cell membrane disorders.
Narla J; Mohandas N
Int J Lab Hematol; 2017 May; 39 Suppl 1():47-52. PubMed ID: 28447420
[TBL] [Abstract][Full Text] [Related]
7. Clinical utility of targeted next-generation sequencing panel in routine diagnosis of hereditary hemolytic anemia: A national reference laboratory experience.
Agarwal AM; McMurty V; Clayton AL; Bolia A; Reading NS; Mani C; Patel JL; Rets A
Eur J Haematol; 2023 Jun; 110(6):688-695. PubMed ID: 36825813
[TBL] [Abstract][Full Text] [Related]
8. Use of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) in the Diagnosis of RBC Membrane Disorders, Enzyme Defects, and Congenital Dyserythropoietic Anemias: A Monocentric Study on 202 Patients.
Zaninoni A; Fermo E; Vercellati C; Consonni D; Marcello AP; Zanella A; Cortelezzi A; Barcellini W; Bianchi P
Front Physiol; 2018; 9():451. PubMed ID: 29755372
[TBL] [Abstract][Full Text] [Related]
9. Effects of
Herrera-Tirado IM; Espinoza-Mata LL; Rizo-delaTorre LDC; Becerra-Solano LE; Ibarra-Cortés B; Perea-Díaz FJ
Genet Test Mol Biomarkers; 2022 May; 26(5):270-276. PubMed ID: 35638908
[No Abstract] [Full Text] [Related]
10. Concomitant Hereditary Spherocytosis and Pyruvate Kinase Deficiency in a Spanish Family with Chronic Hemolytic Anemia: Contribution of Laser Ektacytometry to Clinical Diagnosis.
Vives Corrons JL; Krishnevskaya E; Montllor L; Leguizamon V; Garcia Bernal M
Cells; 2022 Mar; 11(7):. PubMed ID: 35406697
[TBL] [Abstract][Full Text] [Related]
11. Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis.
King MJ; Telfer P; MacKinnon H; Langabeer L; McMahon C; Darbyshire P; Dhermy D
Cytometry B Clin Cytom; 2008 Jul; 74(4):244-50. PubMed ID: 18454487
[TBL] [Abstract][Full Text] [Related]
12. Hereditary poikilocytic anemia associated with the co-inheritance of two alpha spectrin abnormalities.
Iarocci TA; Wagner GM; Mohandas N; Lane PA; Mentzer WC
Blood; 1988 May; 71(5):1390-6. PubMed ID: 3359047
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Molecular insights into hereditary elliptocytosis and pyropoikilocytosis: NGS uncovers multiple potential candidate genes.
Shome DK; Das P; Akbar GA; Taha S; Radhi A; Al-Saad K; Helmy R
Ann Hematol; 2023 Sep; 102(9):2343-2351. PubMed ID: 37400730
[TBL] [Abstract][Full Text] [Related]
15. Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family. Transmission of the same molecular defect in spectrin through three generations with different clinical expression.
Lecomte MC; Dhermy D; Garbarz M; Feo C; Gautero H; Bournier O; Picat C; Chaveroche I; Galand C; Boivin P
Hum Genet; 1987 Dec; 77(4):329-34. PubMed ID: 3692477
[TBL] [Abstract][Full Text] [Related]
16. Mechanics of diseased red blood cells in human spleen and consequences for hereditary blood disorders.
Li H; Lu L; Li X; Buffet PA; Dao M; Karniadakis GE; Suresh S
Proc Natl Acad Sci U S A; 2018 Sep; 115(38):9574-9579. PubMed ID: 30190436
[TBL] [Abstract][Full Text] [Related]
17. Structural and functional heterogeneity of alpha spectrin mutations involving the spectrin heterodimer self-association site: relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosis.
Coetzer T; Palek J; Lawler J; Liu SC; Jarolim P; Lahav M; Prchal JT; Wang W; Alter BP; Schewitz G
Blood; 1990 Jun; 75(11):2235-44. PubMed ID: 2346784
[TBL] [Abstract][Full Text] [Related]
18. Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosis.
Gallagher PG; Kotula L; Wang Y; Marchesi SL; Curtis PJ; Speicher DW; Forget BG
Am J Hum Genet; 1996 Aug; 59(2):351-9. PubMed ID: 8755921
[TBL] [Abstract][Full Text] [Related]
19. Clinical and laboratory study of two Caucasian families with hereditary pyropoikilocytosis and hereditary elliptocytosis.
Peterson LC; Dampier C; Coetzer T; Lawler J; White J; Palek J
Am J Clin Pathol; 1987 Jul; 88(1):58-65. PubMed ID: 3604989
[TBL] [Abstract][Full Text] [Related]
20. [Disorders of the membrane skeleton of erythrocytes in hereditary spherocytosis and elliptocytosis: significance of the molecular defect for pathogenesis and clinical severity].
Eber SW
Klin Padiatr; 1991; 203(4):284-95. PubMed ID: 1942935
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]