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 *

105 related articles for article (PubMed ID: 3237424)

  • 21. A case report of spherocytosis presenting with choledocholithiasis in early childhood and a review of the literature.
    el-Halabi IM
    Ann Trop Paediatr; 1999 Dec; 19(4):401-3. PubMed ID: 10716037
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Hereditary spherocytosis and wandering spleen.
    Polat A; Ozgurler F; Balcı YI; Kocyigit A; Tan M
    Pediatr Hematol Oncol; 2014 Feb; 31(1):101-3. PubMed ID: 24088174
    [No Abstract]   [Full Text] [Related]  

  • 23. 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]  

  • 24. An inadvertent in vivo osmotic fragility test.
    Antonucci RA; Walker RI
    N C Med J; 1986 Apr; 47(4):185-6. PubMed ID: 3459025
    [No Abstract]   [Full Text] [Related]  

  • 25. [Simple method for measurement of erythrocyte osmotic fragility].
    Ideguchi H; Shinohara K; Ishikawa A; Futata Y; Sugisaki S; Hamasaki N
    Rinsho Byori; 1992 May; 40(5):552-6. PubMed ID: 1507483
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Interaction of hereditary spherocytosis and alpha thalassaemia: a family study.
    Li CK; Ng MH; Cheung KL; Lam TK; Shing MM
    Acta Haematol; 1994; 91(4):201-5. PubMed ID: 7976119
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Juvenile polyposis coli associated with hereditary spherocytosis].
    Agnifili A; Carducci G; Gola P; Mancini E; Marino M; Verzaro R; Ibi I
    Minerva Chir; 1998 Oct; 53(10):811-7. PubMed ID: 9882972
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Acquired hemolytic anemia with features simulating hereditary spherocytosis and paroxysmal nocturnal hemoglobinuria in the same patient.
    Mohler DN
    Trans Am Clin Climatol Assoc; 1972; 83():177-85. PubMed ID: 5040114
    [No Abstract]   [Full Text] [Related]  

  • 29. Management in rare association of Moyamoya syndrome and hereditary spherocytosis.
    Yadegari S; Aminian A
    Minerva Pediatr; 2017 Aug; 69(4):368-369. PubMed ID: 28612582
    [No Abstract]   [Full Text] [Related]  

  • 30. [Hereditary spherocytosis: clinical characteristics and treatment with splenectomy].
    Jonte F; Ramírez A; Medina J; García Gala J; Rosón C; Corte JR; Vargas M; Pérez Lozana L
    Sangre (Barc); 1995 Feb; 40(1):45-8. PubMed ID: 7716671
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect.
    Mariani M; Barcellini W; Vercellati C; Marcello AP; Fermo E; Pedotti P; Boschetti C; Zanella A
    Haematologica; 2008 Sep; 93(9):1310-7. PubMed ID: 18641031
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Hereditary spherocytosis in a newborn with carrier state parents--a family study.
    Tsai YM; Wang SY; Lee PP
    Zhonghua Yi Xue Za Zhi (Taipei); 1989 Aug; 44(2):129-34. PubMed ID: 2819575
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Clinical profile of hereditary spherocytosis in North India.
    Panigrahi I; Phadke SR; Agarwal A; Gambhir S; Agarwal SS
    J Assoc Physicians India; 2002 Nov; 50():1360-7. PubMed ID: 12583462
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Failure of ouabain to influence the osmotic fragility in hereditary spherocytosis.
    Godal HC; Gjønnes G; Ruyter R
    Scand J Haematol; 1982 Mar; 28(3):251-3. PubMed ID: 7089484
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Near-total splenectomy for hereditary spherocytosis: clinical prospects in relation to disease severity.
    Stoehr GA; Sobh JN; Luecken J; Heidemann K; Mittler U; Hilgers R; Eber SW
    Br J Haematol; 2006 Mar; 132(6):791-3. PubMed ID: 16487182
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Neonatal diagnosis and the course of congenital spherocytosis].
    Sansone G
    Pediatria (Napoli); 1971; 79(1):68-72. PubMed ID: 5097729
    [No Abstract]   [Full Text] [Related]  

  • 37. Open heart operation in a patient with hereditary spherocytosis: a case report.
    Aoyagi S; Kawano H; Tomoeda H; Hiratsuka R; Kawara T
    Ann Thorac Cardiovasc Surg; 2001 Dec; 7(6):375-7. PubMed ID: 11888479
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Splenic infarction due to concomitant hereditary spherocytosis and sickle cell trait.
    Dulman RY; Buchanan GR; Ginsburg H; Fefferman NR; Greco MA; Borys D; Blei F
    J Pediatr Surg; 2007 Dec; 42(12):2129-31. PubMed ID: 18082724
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 'Pink test' and osmotic fragility test for the diagnosis of hereditary spherocytosis: another view.
    Judkiewicz L; Bugala I; Bartosz G
    Eur J Haematol; 1989 Feb; 42(2):217. PubMed ID: 2917640
    [No Abstract]   [Full Text] [Related]  

  • 40. [Current data on the pathogenesis of hereditary spherocytosis (Minkowski-Shauffard's anemia) (review of the literature and personal study)].
    Kovalev IuR; Shabalov NP; Iuzhanina TA; Borisova TZ
    Probl Gematol Pereliv Krovi; 1970 Oct; 15(10):34-9. PubMed ID: 4255204
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.