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 *

174 related articles for article (PubMed ID: 3141191)

  • 21. Efficacy of low dose intravenous immunoglobulins for post-splenectomy treatment of autoimmune haemolytic anaemia in a patient with hereditary spherocytosis.
    Ames PR; Nardiello S; Tommasino C
    Clin Lab Haematol; 2000 Aug; 22(4):225-8. PubMed ID: 11012635
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Effect of splenectomy of hepatic bilirubin clearance in patients with hereditary spherocytosis. Implications for the diagnosis of Gilbert's syndrome.
    Berk PD; Berman MD; Blitzer BL; Chretien P; Martin JF; Scharschmidt BF; Vierling JM; Wolkoff AW; Vergalla J; Waggoner JG
    J Lab Clin Med; 1981 Jul; 98(1):37-45. PubMed ID: 7252326
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [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]  

  • 24. Hereditary spherocytosis coexisting with Gilbert's syndrome: a diagnostic dilemma.
    Garg PK; Kumar A; Teckchandani N; Hadke NS
    Singapore Med J; 2008 Nov; 49(11):e308-9. PubMed ID: 19037536
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [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]  

  • 26. Splenectomy in anaemia.
    Nightingale D; Prankerd TA; Richards JD; Thompson D
    Q J Med; 1972 Jul; 41(163):261-7. PubMed ID: 5072053
    [No Abstract]   [Full Text] [Related]  

  • 27. Prophylactic splenectomy and cholecystectomy in mild hereditary spherocytosis: analyzing the decision in different clinical scenarios.
    Marchetti M; Quaglini S; Barosi G
    J Intern Med; 1998 Sep; 244(3):217-26. PubMed ID: 9747744
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Hereditary spherocytosis].
    Esselborn H; Löhr GW
    Blut; 1970; 20(3):185-92. PubMed ID: 4245218
    [No Abstract]   [Full Text] [Related]  

  • 29. The hereditary haemolytic anaemias.
    Dacie JV
    J R Coll Physicians Lond; 1974 Apr; 8(3):206-19. PubMed ID: 4824998
    [No Abstract]   [Full Text] [Related]  

  • 30. Red cell membrane disorders.
    Gallagher PG
    Hematology Am Soc Hematol Educ Program; 2005; ():13-8. PubMed ID: 16304353
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Hereditary spherocytosis.
    Bajracharya BL; Giri A; Baral MR
    Kathmandu Univ Med J (KUMJ); 2004; 2(2):145-8. PubMed ID: 15821383
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genetic diagnosis and pathogenic analysis of an atypical hereditary spherocytosis combined with UGT1A1 partial deficiency: A case report.
    Yi Y; Dang X; Li Y; Zhao C; Tang H; Shi X
    Mol Med Rep; 2018 Jan; 17(1):382-387. PubMed ID: 29115431
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Extreme hyperbilirubinemia associated with spherocytosis and choledocholithiasis].
    Peralta-Zagal JA; Hernández-Estrada M
    Bol Med Hosp Infant Mex; 1990 Jan; 47(1):43-7. PubMed ID: 2337461
    [TBL] [Abstract][Full Text] [Related]  

  • 34. First experience with single incision laparoscopic surgery in Slovakia: concomitant cholecystectomy and splenectomy in an 11-year-old girl with hereditary spherocytosis.
    Cingel V; Zabojnikova L; Kurucova P; Varga I
    Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub; 2014 Sep; 158(3):479-85. PubMed ID: 24026144
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Acute non-immune haemolytic anaemia during infectious mononucleosis unmasking spherocytosis.
    Lambert M; Smellie S; Chatelain C; Ferrant A; De Meyer R
    Acta Clin Belg; 1989; 44(3):192-5. PubMed ID: 2816226
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Efficacy of cytochemical tests in gene analysis of hereditary spherocytosis: a case study of six patients with different disease subtypes.
    Shibuya A; Kawashima H; Tanaka M
    Hematology; 2021 Dec; 26(1):827-834. PubMed ID: 34672909
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Kernicterus associated with hereditary spherocytosis and UGT1A1 promoter polymorphism.
    Berardi A; Lugli L; Ferrari F; Gargano G; D'Apolito M; Marrone A; Iolascon A
    Biol Neonate; 2006; 90(4):243-6. PubMed ID: 16735790
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Hereditary spherocytosis. Recent experience and current concepts of pathophysiology.
    Croom RD; McMillan CW; Orringer EP; Sheldon GF
    Ann Surg; 1986 Jan; 203(1):34-9. PubMed ID: 3942420
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Hereditary spherocytosis and related disorders.
    Becker PS; Lux SE
    Clin Haematol; 1985 Feb; 14(1):15-43. PubMed ID: 3886234
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.