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 *

133 related articles for article (PubMed ID: 24797868)

  • 1. Dehydrated red blood cells in a peripheral blood film: a case of hereditary xerocytosis.
    Velasco-Rodríguez D; Alonso-Domínguez JM; Ruiz E; Acedo N; González-Fernández FA; Villarrubia J
    Br J Haematol; 2014 Aug; 166(3):309. PubMed ID: 24797868
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. Dehydrated stomatocytic anemia due to the heterozygous mutation R2456H in the mechanosensitive cation channel PIEZO1: a case report.
    Shmukler BE; Vandorpe DH; Rivera A; Auerbach M; Brugnara C; Alper SL
    Blood Cells Mol Dis; 2014 Jan; 52(1):53-4. PubMed ID: 23973043
    [No Abstract]   [Full Text] [Related]  

  • 4. Hereditary xerocytosis revisited.
    Archer NM; Shmukler BE; Andolfo I; Vandorpe DH; Gnanasambandam R; Higgins JM; Rivera A; Fleming MD; Sachs F; Gottlieb PA; Iolascon A; Brugnara C; Alper SL; Nathan DG
    Am J Hematol; 2014 Dec; 89(12):1142-6. PubMed ID: 25044010
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. Dehydrated hereditary stomatocytosis masquerading as MDS.
    Paessler M; Hartung H
    Blood; 2015 Mar; 125(11):1841. PubMed ID: 25927085
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. Nonimmune hydrops fetalis due to congenital xerocytosis.
    Vicente-Gutiérrez MP; Castelló-Almazán I; Salvía-Roiges MD; Rodríguez-Miguélez JM; Vives-Corrons JL; Figueras-Aloy J; Carbonell-Estrany X
    J Perinatol; 2005 Jan; 25(1):63-5. PubMed ID: 15608620
    [TBL] [Abstract][Full Text] [Related]  

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

  • 10. Hereditary xerocytosis, a misleading anemia.
    Del Orbe Barreto R; Arrizabalaga B; De la Hoz Rastrollo AB; García-Orad A; Gonzalez Vallejo I; Bento C; Villegas A; García-Ruiz JC
    Ann Hematol; 2016 Sep; 95(9):1545-6. PubMed ID: 27250707
    [No Abstract]   [Full Text] [Related]  

  • 11. Dehydrated hereditary stomatocytosis and recurrent prenatal ascites.
    Poret H; Simon EG; Hervé P; Perrotin F
    J Obstet Gynaecol; 2013 Jul; 33(5):527. PubMed ID: 23815216
    [No Abstract]   [Full Text] [Related]  

  • 12. Recurrent mutation in the PIEZO1 gene in two families of hereditary xerocytosis with fetal hydrops.
    Beneteau C; Thierry G; Blesson S; Le Vaillant C; Picard V; Béné MC; Eveillard M; Le Caignec C
    Clin Genet; 2014 Mar; 85(3):293-5. PubMed ID: 23581886
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Dehydrated hereditary stomatocytosis.
    Layton DM; Bain BJ
    Am J Hematol; 2016 Feb; 91(2):266. PubMed ID: 26440377
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Red blood cell Gardos channel (KCNN4): the essential determinant of erythrocyte dehydration in hereditary xerocytosis.
    Rapetti-Mauss R; Picard V; Guitton C; Ghazal K; Proulle V; Badens C; Soriani O; Garçon L; Guizouarn H
    Haematologica; 2017 Oct; 102(10):e415-e418. PubMed ID: 28619848
    [No Abstract]   [Full Text] [Related]  

  • 19. Diagnosis and clinical management of red cell membrane disorders.
    Kalfa TA
    Hematology Am Soc Hematol Educ Program; 2021 Dec; 2021(1):331-340. PubMed ID: 34889366
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Iron overload in a teenager with xerocytosis: the importance of nuclear magnetic resonance imaging.
    Assis RA; Kassab C; Seguro FS; Costa FF; Silveira PA; Wood J; Hamerschlak N
    Einstein (Sao Paulo); 2013 Dec; 11(4):528-32. PubMed ID: 24488397
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.