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 *

173 related articles for article (PubMed ID: 28847351)

  • 1. Hereditary Spherocytosis in the Neonatal Period: A Case Report.
    Will A; Henderson CA; Jnah AJ; Newberry D
    Neonatal Netw; 2017 Sep; 36(5):280-288. PubMed ID: 28847351
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Neonatal hereditary spherocytosis caused by a de novo frameshift mutation of the SPTB gene characterized by hydrops fetalis: A case report.
    Zhang Y; Shao S; Liu J; Zeng C; Han Y; Zhang X
    Medicine (Baltimore); 2021 Mar; 100(12):e24804. PubMed ID: 33761640
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Use of capillary blood to diagnose hereditary spherocytosis.
    Crisp RL; Solari L; Gammella D; Schvartzman GA; Rapetti MC; Donato H
    Pediatr Blood Cancer; 2012 Dec; 59(7):1299-301. PubMed ID: 22488885
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A prospective study to assess the predictive value for hereditary spherocytosis using five laboratory tests (cryohemolysis test, eosin-5'-maleimide flow cytometry, osmotic fragility test, autohemolysis test, and SDS-PAGE) on 50 hereditary spherocytosis families in Argentina.
    Crisp RL; Solari L; Vota D; García E; Miguez G; Chamorro ME; Schvartzman GA; Alfonso G; Gammella D; Caldarola S; Riccheri C; Vittori D; Venegas B; Nesse A; Donato H
    Ann Hematol; 2011 Jun; 90(6):625-34. PubMed ID: 21080168
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Early postnatal diagnosis of hereditary spherocytosis by combining light microscopy, acidified glycerol lysis test and eosin-5'-maleimide binding assay.
    Andres O; Eber S; Speer CP
    Ann Hematol; 2015 Dec; 94(12):1959-64. PubMed ID: 26336967
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A pediatrician's practical guide to diagnosing and treating hereditary spherocytosis in neonates.
    Christensen RD; Yaish HM; Gallagher PG
    Pediatrics; 2015 Jun; 135(6):1107-14. PubMed ID: 26009624
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hereditary Spherocytosis - Diagnosis, Surgical Treatment and Outcomes. A Literature Review.
    Manciu S; Matei E; Trandafir B
    Chirurgia (Bucur); 2017; 112(2):110-116. PubMed ID: 28463670
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hereditary spherocytosis: Retrospective evaluation of 65 children.
    Güngör A; Yaralı N; Fettah A; Ok-Bozkaya İ; Özbek N; Kara A
    Turk J Pediatr; 2018; 60(3):264-269. PubMed ID: 30511538
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Recombinant Human Erythropoietin (r-HuEPO) therapy in a newborn with hereditary spherocytosis].
    Schiff M; Haÿs S; Sann L; Putet G
    Arch Pediatr; 2003 Apr; 10(4):333-6. PubMed ID: 12818755
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinico-hematological profile of hereditary spherocytosis: experience from a tertiary care center in North India.
    Kar R; Rao S; Srinivas UM; Mishra P; Pati HP
    Hematology; 2009 Jun; 14(3):164-7. PubMed ID: 19490762
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Natural history of hereditary spherocytosis during the first year of life.
    Delhommeau F; Cynober T; Schischmanoff PO; Rohrlich P; Delaunay J; Mohandas N; Tchernia G
    Blood; 2000 Jan; 95(2):393-7. PubMed ID: 10627440
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Hereditary spherocytosis in the experience of two pediatric clinics from Targu Mures].
    Papp ZE; Chincesan M; Horváth AM; Kelemen I
    Orv Hetil; 2019 Nov; 160(45):1798-1803. PubMed ID: 31680538
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Hereditary spherocytosis: guidelines for the diagnosis and management in children].
    Guitton C; Garçon L; Cynober T; Gauthier F; Tchernia G; Delaunay J; Leblanc T; Thuret I; Bader-Meunier B
    Arch Pediatr; 2008 Sep; 15(9):1464-73. PubMed ID: 18556182
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hereditary spherocytosis in a 27-year-old woman: case report.
    Hassan A; Babadoko AA; Isa AH; Abunimye P
    Ann Afr Med; 2009; 8(1):61-3. PubMed ID: 19763011
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hereditary Spherocytosis in a Middle-aged Man Complicated with Common Bile Duct Stones.
    Sawahara H; Iwamuro M; Harada R; Yoshioka M; Niguma T; Mimura T; Yamamoto K
    Intern Med; 2015; 54(12):1509-12. PubMed ID: 26073240
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A 6-Day-Old Male Infant with Severe Hyperbilirubinemia Diagnosed with Hereditary Spherocytosis at a Tertiary Hospital in East Java, Indonesia: A Diagnostic and Management Challenge in a Developing Country.
    Corebima BIRV; Monica C; Sulistijono E; Nugroho S; Wicaksono S; Hartiastuti SM
    Am J Case Rep; 2022 Nov; 23():e937416. PubMed ID: 36399434
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Flow cytometric osmotic fragility test: Increased assay sensitivity for clinical application in pediatric hematology.
    Ciepiela O; Adamowicz-Salach A; Zgodzińska A; Łazowska M; Kotuła I
    Cytometry B Clin Cytom; 2018 Jan; 94(1):189-195. PubMed ID: 28103644
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary spherocytosis in neonates with hyperbilirubinemia.
    Christensen RD; Henry E
    Pediatrics; 2010 Jan; 125(1):120-5. PubMed ID: 19948573
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel compound heterozygous mutations in the SPTA1 gene, causing hereditary spherocytosis in a neonate with Coombs‑negative hemolytic jaundice.
    Wang X; Liu A; Lu Y; Hu Q
    Mol Med Rep; 2019 Apr; 19(4):2801-2807. PubMed ID: 30816434
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Previously undiagnosed hereditary spherocytosis in a patient with jaundice and pyelonephritis: a case report.
    Tateno Y; Suzuki R; Kitamura Y
    J Med Case Rep; 2016 Dec; 10(1):337. PubMed ID: 27906107
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.