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 *

162 related articles for article (PubMed ID: 7070421)

  • 1. Spectrin and spherocytosis.
    Shohet SB
    N Engl J Med; 1982 May; 306(19):1170-1. PubMed ID: 7070421
    [No Abstract]   [Full Text] [Related]  

  • 2. Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosis.
    Coetzer TL; Lawler J; Liu SC; Prchal JT; Gualtieri RJ; Brain MC; Dacie JV; Palek J
    N Engl J Med; 1988 Jan; 318(4):230-4. PubMed ID: 2961992
    [No Abstract]   [Full Text] [Related]  

  • 3. Deficient red-cell spectrin in severe, recessively inherited spherocytosis.
    Agre P; Orringer EP; Bennett V
    N Engl J Med; 1982 May; 306(19):1155-61. PubMed ID: 7070419
    [No Abstract]   [Full Text] [Related]  

  • 4. Hemolytic anemias due to abnormalities in red cell spectrin: a brief review.
    Lux SE; Wolfe LC; Pease B; Tomaselli MB; John KM; Bernstein SE
    Prog Clin Biol Res; 1981; 45():159-68. PubMed ID: 7017750
    [No Abstract]   [Full Text] [Related]  

  • 5. Lipid loss in spectrin deficient mouse erythrocytes.
    Shohet SB
    Prog Clin Biol Res; 1979; 30():471-4. PubMed ID: 531038
    [No Abstract]   [Full Text] [Related]  

  • 6. [Erythrocyte membrane protein abnormalities and membrane disease].
    Yawata Y
    Nihon Rinsho; 1979 Dec; 37(12):3885-99. PubMed ID: 395337
    [No Abstract]   [Full Text] [Related]  

  • 7. Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosis.
    Agre P; Asimos A; Casella JF; McMillan C
    N Engl J Med; 1986 Dec; 315(25):1579-83. PubMed ID: 3785322
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Inherited hemolytic disease in mice: a review and update.
    Bernstein SE
    Lab Anim Sci; 1980 Apr; 30(2 Pt 1):197-205. PubMed ID: 6763106
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Marked reduction of spectrinin hereditary spherocytosis in the common house mouse.
    Greenquist AC; Shohet SB; Bernstein SE
    Blood; 1978 Jun; 51(6):1149-55. PubMed ID: 647119
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Erythrocyte membrane protein abnormalities in hereditary hemolytic anemias].
    Boivin P; Galand C
    Nouv Rev Fr Hematol Blood Cells; 1977; 18(1):95-116. PubMed ID: 197487
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The erythrocyte membrane skeleton: pathophysiology.
    Shohet SB; Lux SE
    Hosp Pract (Off Ed); 1984 Nov; 19(11):89-95, 99, 103 passim. PubMed ID: 6436279
    [No Abstract]   [Full Text] [Related]  

  • 12. Spectrin oligomers of the red cell membrane extracts in hereditary spherocytosis.
    Marík T; Kodícek M; Brabec V
    Biomed Biochim Acta; 1983; 42(11-12):S32-7. PubMed ID: 6675711
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The genetic disorders of the red cell skeleton.
    Delaunay J; Alloisio N; Morle L; Baklouti F
    Nouv Rev Fr Hematol (1978); 1991; 33(2):63-70. PubMed ID: 1766857
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Application of 2 electrophoresis techniques to the analysis of erythrocyte membrane proteins in hereditary spherocytosis].
    Ferrándiz F; Ródenas S; Villegas A
    Sangre (Barc); 1993 Oct; 38(5):393-7. PubMed ID: 8140503
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Reductions of erythrocyte membrane viscoelastic coefficients reflect spectrin deficiencies in hereditary spherocytosis.
    Waugh RE; Agre P
    J Clin Invest; 1988 Jan; 81(1):133-41. PubMed ID: 3335631
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hemolytic anemias associated with deficient or dysfunctional spectrin.
    Lux SE; Pease B; Tomaselli MB; John KM; Bernstein SE
    Prog Clin Biol Res; 1979; 30():463-9. PubMed ID: 531037
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Hereditary diseases of the human erythrocyte membrane skeleton (author's transl)].
    Boivin P
    Nouv Presse Med; 1982 Jul; 11(31):2347-51. PubMed ID: 7111000
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Relation between types of erythrocyte membrane defects and the clinical picture in hereditary spherocytosis].
    Brabec V; Palek J; Petrtýlová K; Cermák J; Jarolím P
    Vnitr Lek; 1997 Feb; 43(2):91-4. PubMed ID: 9245075
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Hereditary spherocytosis: one year study of erythrocyte membrane proteins].
    Tshilolo L; Kagambega F; Sztern B; Vertongen F; Gulbis B
    Rev Med Brux; 1998 Oct; 19(5 Pt 1):417-23. PubMed ID: 9844481
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Erythrocyte membrane and hereditary spherocytosis].
    Ideguchi H
    Rinsho Byori; 1990 Apr; 38(4):360-4. PubMed ID: 2195190
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.