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 *

180 related articles for article (PubMed ID: 3671334)

  • 1. Prenatal diagnosis of hereditary elliptocytosis with molecular defect of spectrin.
    Dhermy D; Feo C; Garbarz M; Lecomte MC; Bournier O; Chaveroche I; Gautero H; Boivin P; Daffos F; Forestier F
    Prenat Diagn; 1987 Sep; 7(7):471-83. PubMed ID: 3671334
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Abnormal electrophoretic mobility of spectrin tetramers in hereditary elliptocytosis.
    Dhermy D; Garbarz M; Lecomte MC; Chaveroche I; Bournier O; Gautero H; Blot I; Boivin P
    Hum Genet; 1986 Dec; 74(4):363-7. PubMed ID: 3793099
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary elliptocytosis: clinical, morphological and biochemical studies of 38 cases.
    Dhermy D; Garbarz M; Lecomte MC; Féo C; Bournier O; Chaveroche I; Gautero H; Galand C; Boivin P
    Nouv Rev Fr Hematol (1978); 1986; 28(3):129-40. PubMed ID: 3748797
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular basis of clinical and morphological heterogeneity in hereditary elliptocytosis (HE) with spectrin alpha I variants.
    Lecomte MC; Garbarz M; Gautero H; Bournier O; Galand C; Boivin P; Dhermy D
    Br J Haematol; 1993 Nov; 85(3):584-95. PubMed ID: 8136282
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular defect of spectrin in the family of a child with congenital hemolytic poikilocytic anemia.
    Dhermy D; Lecomte MC; Garbarz M; Feo C; Gautero H; Bournier O; Galand C; Herrera A; Gretillat F; Boivin P
    Pediatr Res; 1984 Oct; 18(10):1005-12. PubMed ID: 6493844
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis.
    Garbarz M; Lecomte MC; Dhermy D; Feo C; Chaveroche I; Gautero H; Bournier O; Picat C; Goepp A; Boivin P
    Blood; 1986 Jun; 67(6):1661-7. PubMed ID: 3708157
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Defective spectrin dimer-dimer association in a family with transfusion dependent homozygous hereditary elliptocytosis.
    Evans JP; Baines AJ; Hann IM; Al-Hakim I; Knowles SM; Hoffbrand AV
    Br J Haematol; 1983 Jun; 54(2):163-72. PubMed ID: 6849840
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain.
    Garbarz M; Lecomte MC; Féo C; Devaux I; Picat C; Lefebvre C; Galibert F; Gautero H; Bournier O; Galand C
    Blood; 1990 Apr; 75(8):1691-8. PubMed ID: 2328319
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis of hereditary red cell membrane defect.
    Morris SA; Ohanian V; Lewis ML; Chahwala SB; Rodeck CH; Mibashan RS; Gratzer WB
    Br J Haematol; 1986 Apr; 62(4):763-72. PubMed ID: 3964564
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A new abnormal variant of spectrin in black patients with hereditary elliptocytosis.
    Lecomte MC; Dhermy D; Solis C; Ester A; Féo C; Gautero H; Bournier O; Boivin P
    Blood; 1985 May; 65(5):1208-17. PubMed ID: 3922449
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sp alpha I/65 hereditary elliptocytosis in North Africa.
    Alloisio N; Guetarni D; Morlé L; Pothier B; Ducluzeau MT; Soun A; Colonna P; Clerc M; Philippe N; Delaunay J
    Am J Hematol; 1986 Oct; 23(2):113-22. PubMed ID: 3752066
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family. Transmission of the same molecular defect in spectrin through three generations with different clinical expression.
    Lecomte MC; Dhermy D; Garbarz M; Feo C; Gautero H; Bournier O; Picat C; Chaveroche I; Galand C; Boivin P
    Hum Genet; 1987 Dec; 77(4):329-34. PubMed ID: 3692477
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Elliptical erythrocyte membrane skeletons and heat-sensitive spectrin in hereditary elliptocytosis.
    Tomaselli MB; John KM; Lux SE
    Proc Natl Acad Sci U S A; 1981 Mar; 78(3):1911-5. PubMed ID: 6940197
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Defective binding of spectrin to ankyrin in a kindred with recessively inherited hereditary elliptocytosis.
    Zail SS; Coetzer TL
    J Clin Invest; 1984 Sep; 74(3):753-62. PubMed ID: 6236232
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pathologic and nonpathologic variants of the spectrin molecule in two black families with hereditary elliptocytosis.
    Lecomte MC; Dhermy D; Garbarz M; Feo C; Gautero H; Bournier O; Picat C; Chaveroche I; Ester A; Galand C
    Hum Genet; 1985; 71(4):351-7. PubMed ID: 4077050
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Interactions of spectrin in hereditary elliptocytes containing truncated spectrin beta-chains.
    Eber SW; Morris SA; Schröter W; Gratzer WB
    J Clin Invest; 1988 Feb; 81(2):523-30. PubMed ID: 3276733
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Altered spectrin association and membrane fragility without abnormal spectrin heat sensitivity in a case of congenital hemolytic anemia.
    Ravindranath Y; Johnson RM
    Am J Hematol; 1985 Sep; 20(1):53-65. PubMed ID: 4025321
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Structural and functional heterogeneity of alpha spectrin mutations involving the spectrin heterodimer self-association site: relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosis.
    Coetzer T; Palek J; Lawler J; Liu SC; Jarolim P; Lahav M; Prchal JT; Wang W; Alter BP; Schewitz G
    Blood; 1990 Jun; 75(11):2235-44. PubMed ID: 2346784
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical and laboratory study of two Caucasian families with hereditary pyropoikilocytosis and hereditary elliptocytosis.
    Peterson LC; Dampier C; Coetzer T; Lawler J; White J; Palek J
    Am J Clin Pathol; 1987 Jul; 88(1):58-65. PubMed ID: 3604989
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.