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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

232 related articles for article (PubMed ID: 34201899)

  • 1. Complex Modes of Inheritance in Hereditary Red Blood Cell Disorders: A Case Series Study of 155 Patients.
    Andolfo I; Martone S; Rosato BE; Marra R; Gambale A; Forni GL; Pinto V; Göransson M; Papadopoulou V; Gavillet M; Elalfy M; Panarelli A; Tomaiuolo G; Iolascon A; Russo R
    Genes (Basel); 2021 Jun; 12(7):. PubMed ID: 34201899
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary red blood cell membrane defects. Detection of
    Fortugno C; Galea E; Cantaffa R; Gigliotti F; Fabiano RL; Talarico V; Raiola G; Galati MC
    Pediatr Hematol Oncol; 2021 Mar; 38(2):184-190. PubMed ID: 33136529
    [No Abstract]   [Full Text] [Related]  

  • 3. Mild erythrocytosis as a presenting manifestation of
    Knight T; Zaidi AU; Wu S; Gadgeel M; Buck S; Ravindranath Y
    Pediatr Hematol Oncol; 2019 Aug; 36(5):317-326. PubMed ID: 31298594
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mechanosensitive Piezo1 ion channel protein (PIEZO1 gene): update and extended mutation analysis of hereditary xerocytosis in India.
    More TA; Dongerdiye R; Devendra R; Warang PP; Kedar PS
    Ann Hematol; 2020 Apr; 99(4):715-727. PubMed ID: 32112123
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hereditary dehydrated stomatocytosis with splicing site mutation of PIEZO1 mimicking myelodysplastic syndrome diagnosed by targeted next-generation sequencing.
    Park J; Jang W; Han E; Chae H; Yoo J; Kim Y; Kim YJ; Kim M
    Pediatr Blood Cancer; 2018 Jul; 65(7):e27053. PubMed ID: 29603612
    [No Abstract]   [Full Text] [Related]  

  • 6. Hereditary xerocytosis - spectrum and clinical manifestations of variants in the PIEZO1 gene, including co-occurrence with a novel β-globin mutation.
    Maciak K; Adamowicz-Salach A; Siwicka A; Poznanski J; Urasinski T; Plochocka D; Gora M; Burzynska B
    Blood Cells Mol Dis; 2020 Feb; 80():102378. PubMed ID: 31670187
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel PIEZO1 mutation in a patient with dehydrated hereditary stomatocytosis: a case report and a brief review of literature.
    Zama D; Giulietti G; Muratore E; Andolfo I; Russo R; Iolascon A; Pession A
    Ital J Pediatr; 2020 Jul; 46(1):102. PubMed ID: 32703298
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hemoglobin C trait accentuates erythrocyte dehydration in hereditary xerocytosis.
    Yang E; Voelkel EB; Lezon-Geyda K; Schulz VP; Gallagher PG
    Pediatr Blood Cancer; 2017 Aug; 64(8):. PubMed ID: 28121068
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels.
    Albuisson J; Murthy SE; Bandell M; Coste B; Louis-Dit-Picard H; Mathur J; Fénéant-Thibault M; Tertian G; de Jaureguiberry JP; Syfuss PY; Cahalan S; Garçon L; Toutain F; Simon Rohrlich P; Delaunay J; Picard V; Jeunemaitre X; Patapoutian A
    Nat Commun; 2013; 4():1884. PubMed ID: 23695678
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Advances in understanding the pathogenesis of red cell membrane disorders.
    Iolascon A; Andolfo I; Russo R
    Br J Haematol; 2019 Oct; 187(1):13-24. PubMed ID: 31364155
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hereditary xerocytosis and familial haemolysis due to mutation in the PIEZO1 gene: a simple diagnostic approach.
    Sandberg MB; Nybo M; Birgens H; Frederiksen H
    Int J Lab Hematol; 2014 Aug; 36(4):e62-5. PubMed ID: 24314002
    [No Abstract]   [Full Text] [Related]  

  • 13. Inherited hemolytic anemia: a possessive beginner's guide.
    Mohandas N
    Hematology Am Soc Hematol Educ Program; 2018 Nov; 2018(1):377-381. PubMed ID: 30504335
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Erythrocyte ion content and dehydration modulate maximal Gardos channel activity in KCNN4 V282M/+ hereditary xerocytosis red cells.
    Rivera A; Vandorpe DH; Shmukler BE; Andolfo I; Iolascon A; Archer NM; Shabani E; Auerbach M; Hamerschlak N; Morton J; Wohlgemuth JG; Brugnara C; Snyder LM; Alper SL
    Am J Physiol Cell Physiol; 2019 Aug; 317(2):C287-C302. PubMed ID: 31091145
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. [Hereditary xerocytosis. Presentation of two pediatric cases].
    Eandi Eberle S; Pepe C; Aguirre F; Milanesio B; Fernández D; Ávalos Gómez V; Kinen A; Feliu Torres A
    Arch Argent Pediatr; 2019 Dec; 117(6):e684-e687. PubMed ID: 31758911
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Polycythemia revealing PIEZO1 hereditary xerocytosis.
    Cordeil S; Jallades L
    Blood; 2024 Jul; 144(1):123. PubMed ID: 38963666
    [No Abstract]   [Full Text] [Related]  

  • 18. Hereditary dehydrated and overhydrated stomatocytosis: recent advances.
    Delaunay J; Stewart G; Iolascon A
    Curr Opin Hematol; 1999 Mar; 6(2):110-4. PubMed ID: 10088641
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. RBCs prevent rapid PIEZO1 inactivation and expose slow deactivation as a mechanism of dehydrated hereditary stomatocytosis.
    Evans EL; Povstyan OV; De Vecchis D; Macrae F; Lichtenstein L; Futers TS; Parsonage G; Humphreys NE; Adamson A; Kalli AC; Ludlow MJ; Beech DJ
    Blood; 2020 Jul; 136(1):140-144. PubMed ID: 32305040
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.