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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

207 related items for PubMed ID: 10447256

  • 21. Absence of linkage between type III protein S deficiency and the PROS1 and C4BP genes in families carrying the protein S Heerlen allele.
    Espinosa-Parrilla Y, Morell M, Souto JC, Borrell M, Heine-Suñer D, Tirado I, Volpini V, Estivill X, Sala N.
    Blood; 1997 Apr 15; 89(8):2799-806. PubMed ID: 9108398
    [Abstract] [Full Text] [Related]

  • 22. The prevalence of, and molecular defects underlying, inherited protein S deficiency in the general population.
    Beauchamp NJ, Dykes AC, Parikh N, Campbell Tait R, Daly ME.
    Br J Haematol; 2004 Jun 15; 125(5):647-54. PubMed ID: 15147381
    [Abstract] [Full Text] [Related]

  • 23. Association of protein S p.Pro667Pro dimorphism with plasma protein S levels in normal individuals and patients with inherited protein S deficiency.
    Castaman G, Biguzzi E, Razzari C, Tosetto A, Fontana G, Asti D, Brancaccio V, Castori D, Lane DA, Faioni EM, ProSIT (Protein S Italian Team).
    Thromb Res; 2007 Jun 15; 120(3):421-6. PubMed ID: 17157360
    [Abstract] [Full Text] [Related]

  • 24. Influence of PROS1 gene mutations affecting protein S amino-acid 275 on plasma free protein S measurement.
    Alhenc Gelas M, Juin F, de Raucourt E, Gandrille S, Borgel D, Aiach M.
    Thromb Haemost; 2007 Apr 15; 97(4):678-80. PubMed ID: 17393035
    [No Abstract] [Full Text] [Related]

  • 25. Three novel mutations in five unrelated subjects with hereditary protein S deficiency type I.
    Reitsma PH, Ploos van Amstel HK, Bertina RM.
    J Clin Invest; 1994 Feb 15; 93(2):486-92. PubMed ID: 8113388
    [Abstract] [Full Text] [Related]

  • 26. Low cut-off values increase diagnostic performance of protein S assays.
    Mulder R, Ten Kate MK, Kluin-Nelemans HC, Mulder AB.
    Thromb Haemost; 2010 Sep 15; 104(3):618-25. PubMed ID: 20539904
    [Abstract] [Full Text] [Related]

  • 27. [Protein S deficiency in three patients with thrombosis].
    Minami R, Urata M, Kurihara M, Hara K, Abe Y, Muta K, Nawata H.
    Rinsho Ketsueki; 2001 Aug 15; 42(8):610-5. PubMed ID: 11579499
    [Abstract] [Full Text] [Related]

  • 28. Biochemical activity and gene analysis of inherited protein C and antithrombin deficiency in two Chinese pedigrees.
    Zhou RF, Fu QH, Wang WB, Xie S, Hu YQ, Wang XF, Wang ZY, Wang HL.
    Chin Med J (Engl); 2004 Jun 15; 117(6):813-7. PubMed ID: 15198878
    [Abstract] [Full Text] [Related]

  • 29. First frameshift mutation in the active protein S gene associated with a quantitative hereditary deficiency.
    Borgel D, Gandrille S, Gouault-Heilmann M, Aiach M.
    Blood Coagul Fibrinolysis; 1994 Aug 15; 5(4):593-600. PubMed ID: 7841316
    [Abstract] [Full Text] [Related]

  • 30. [Hereditary protein S deficiency and familial thrombosis. A review with description of a Danish family with protein S deficiency].
    Ingerslev J, Ingerslev J, Thelle T.
    Ugeskr Laeger; 1993 May 31; 155(22):1703-7. PubMed ID: 8317013
    [Abstract] [Full Text] [Related]

  • 31. Similar hypercoagulable state and thrombosis risk in type I and type III protein S-deficient individuals from mixed type I/III families.
    Castoldi E, Maurissen LF, Tormene D, Spiezia L, Gavasso S, Radu C, Hackeng TM, Rosing J, Simioni P.
    Haematologica; 2010 Apr 07. PubMed ID: 20378562
    [Abstract] [Full Text] [Related]

  • 32. Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency.
    Pintao MC, Garcia AA, Borgel D, Alhenc-Gelas M, Spek CA, de Visser MC, Gandrille S, Reitsma PH.
    Hum Genet; 2009 Sep 07; 126(3):449-56. PubMed ID: 19466456
    [Abstract] [Full Text] [Related]

  • 33. Small and large PROS1 deletions but no other types of rearrangements detected in patients with protein S deficiency.
    Lind-Halldén C, Dahlen A, Hillarp A, Zöller B, Dahlbäck B, Halldén C.
    Thromb Haemost; 2012 Jul 07; 108(1):94-100. PubMed ID: 22627709
    [Abstract] [Full Text] [Related]

  • 34. Homozygous protein S deficiency due to a one base pair deletion that leads to a stop codon in exon III of the protein S gene.
    Gómez E, Ledford MR, Pegelow CH, Reitsma PH, Bertina RM.
    Thromb Haemost; 1994 Jun 07; 71(6):723-6. PubMed ID: 7974339
    [Abstract] [Full Text] [Related]

  • 35. Large deletions of the PROS1 gene in a large fraction of mutation-negative patients with protein S deficiency.
    Johansson AM, Hillarp A, Säll T, Zöller B, Dahlbäck B, Halldén C.
    Thromb Haemost; 2005 Nov 07; 94(5):951-7. PubMed ID: 16363235
    [Abstract] [Full Text] [Related]

  • 36. Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study.
    Biguzzi E, Razzari C, Lane DA, Castaman G, Cappellari A, Bucciarelli P, Fontana G, Margaglione M, D'Andrea G, Simmonds RE, Rezende SM, Preston R, Prisco D, Faioni EM, Protein S Italian Team.
    Hum Mutat; 2005 Mar 07; 25(3):259-69. PubMed ID: 15712227
    [Abstract] [Full Text] [Related]

  • 37. A mutation in the protein S pseudogene is linked to protein S deficiency in a thrombophilic family.
    Ploos van Amstel HK, Reitsma PH, Hamulyák K, de Die-Smulders CE, Mannucci PM, Bertina RM.
    Thromb Haemost; 1989 Nov 24; 62(3):897-901. PubMed ID: 2531940
    [Abstract] [Full Text] [Related]

  • 38. Confirmation of inherited protein S deficiency by PROS1 mutational screening: Identification of three novel PROS1 mutations and haplotype analysis of p.Q279X recurrence.
    Hurtado B, Abasolo N, Domènech-Santasusana P, Fuentes-Prior P, García de Frutos P, Sala N.
    Thromb Haemost; 2008 Oct 24; 100(4):721-4. PubMed ID: 18841302
    [No Abstract] [Full Text] [Related]

  • 39. Severe arterial thrombosis in a family with type III protein S deficiency caused by a frameshift mutation in the PROS1 gene.
    Larsen TB, Brusgaard K, Nybo M.
    Thromb Res; 2010 Aug 24; 126(2):e159-61. PubMed ID: 20398916
    [No Abstract] [Full Text] [Related]

  • 40. Familial thrombophilia is an oligogenetic disease: involvement of the prothrombin G20210A, PROC and PROS gene mutations.
    Boinot C, Borgel D, Kitzis A, Guicheteau M, Aiach M, Alhenc-Gelas M.
    Blood Coagul Fibrinolysis; 2003 Feb 24; 14(2):191-6. PubMed ID: 12632031
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 11.