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Journal Abstract Search

192 related items for PubMed ID: 12753286

  • 21. A novel homozygous missense ADAMTS13 mutation Y658C in a patient with recurrent thrombotic thrombocytopenic purpura.
    Lee SH, Park JH, Park SK, Lee EH, Choi JI, Visentin GP, Park TS, Oh SH, Kim SR.
    Ann Clin Lab Sci; 2011; 41(3):273-6. PubMed ID: 22075512
    [Abstract] [Full Text] [Related]

  • 22. Thrombocytopenia and severe hyperbilirubinemia in the neonatal period secondary to congenital thrombotic thrombocytopenic purpura and ADAMTS13 deficiency.
    Schiff DE, Roberts WD, Willert J, Tsai HM.
    J Pediatr Hematol Oncol; 2004 Aug; 26(8):535-8. PubMed ID: 15284596
    [Abstract] [Full Text] [Related]

  • 23. Deficient activity of von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura.
    Furlan M.
    Expert Rev Cardiovasc Ther; 2003 Jul; 1(2):243-55. PubMed ID: 15030284
    [Abstract] [Full Text] [Related]

  • 24. ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura.
    Lotta LA, Garagiola I, Palla R, Cairo A, Peyvandi F.
    Hum Mutat; 2010 Jan; 31(1):11-9. PubMed ID: 19847791
    [Abstract] [Full Text] [Related]

  • 25. Identification of novel mutations in ADAMTS13 in an adult patient with congenital thrombotic thrombocytopenic purpura.
    Uchida T, Wada H, Mizutani M, Iwashita M, Ishihara H, Shibano T, Suzuki M, Matsubara Y, Soejima K, Matsumoto M, Fujimura Y, Ikeda Y, Murata M, Research Project on Genetics of Thrombosis.
    Blood; 2004 Oct 01; 104(7):2081-3. PubMed ID: 15126318
    [Abstract] [Full Text] [Related]

  • 26. Thrombotic thrombocytopenic purpura in humans and mice.
    Desch KC, Motto DG.
    Arterioscler Thromb Vasc Biol; 2007 Sep 01; 27(9):1901-8. PubMed ID: 17525362
    [Abstract] [Full Text] [Related]

  • 27. Thrombotic microangiopathy in malignant hypertension and hemolytic uremic syndrome (HUS)/ thrombotic thrombocytopenic purpura (TTP): can we differentiate one from the other?
    Shibagaki Y, Fujita T.
    Hypertens Res; 2005 Jan 01; 28(1):89-95. PubMed ID: 15969259
    [Abstract] [Full Text] [Related]

  • 28. A novel homozygous frameshift mutation in Exon 7 of the ADAMTS13 gene in a patient with congenital thrombotic thrombocytopenic purpura from India: a case report.
    Yadav S, Shetty S, Kulkarni B.
    Transfusion; 2017 Nov 01; 57(11):2712-2714. PubMed ID: 28833243
    [Abstract] [Full Text] [Related]

  • 29. Remission of thrombotic thrombocytopenic purpura in a patient with compound heterozygous deficiency of von Willebrand factor-cleaving protease by infusion of solvent/detergent plasma.
    Kentouche K, Budde U, Furlan M, Scharfe V, Schneppenheim R, Zintl F.
    Acta Paediatr; 2002 Nov 01; 91(10):1056-9. PubMed ID: 12434890
    [Abstract] [Full Text] [Related]

  • 30. Thrombotic thrombocytopenic purpura.
    Lämmle B, Kremer Hovinga JA, Alberio L.
    J Thromb Haemost; 2005 Aug 01; 3(8):1663-75. PubMed ID: 16102032
    [Abstract] [Full Text] [Related]

  • 31. Adult-onset congenital thrombotic thrombocytopenic purpura caused by a novel compound heterozygous mutation of the ADAMTS13 gene.
    Krabbe JG, Kemna EW, Strunk AL, Jobse PA, Kramer PA, Dikkeschei LD, van den Heuvel LP, Fijnheer R, Verdonck LF.
    Int J Hematol; 2015 Oct 01; 102(4):477-81. PubMed ID: 26267233
    [Abstract] [Full Text] [Related]

  • 32. Congenital thrombotic thrombocytopenic purpura in association with a mutation in the second CUB domain of ADAMTS13.
    Pimanda JE, Maekawa A, Wind T, Paxton J, Chesterman CN, Hogg PJ.
    Blood; 2004 Jan 15; 103(2):627-9. PubMed ID: 14512317
    [Abstract] [Full Text] [Related]

  • 33. Two novel heterozygote missense mutations of the ADAMTS13 gene in a child with recurrent thrombotic thrombocytopenic purpura.
    Rossio R, Ferrari B, Cairo A, Mancini I, Pisapia G, Palazzo G, Peyvandi F.
    Blood Transfus; 2013 Apr 15; 11(2):241-4. PubMed ID: 23058857
    [Abstract] [Full Text] [Related]

  • 34. Molecular mechanisms in thrombotic thrombocytopenic purpura.
    Tsai HM.
    Semin Thromb Hemost; 2004 Oct 15; 30(5):549-57. PubMed ID: 15497097
    [Abstract] [Full Text] [Related]

  • 35. Assay of von Willebrand factor (vWF)-cleaving protease based on decreased collagen binding affinity of degraded vWF: a tool for the diagnosis of thrombotic thrombocytopenic purpura (TTP).
    Gerritsen HE, Turecek PL, Schwarz HP, Lämmle B, Furlan M.
    Thromb Haemost; 1999 Nov 15; 82(5):1386-9. PubMed ID: 10595623
    [Abstract] [Full Text] [Related]

  • 36. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura.
    Levy GG, Nichols WC, Lian EC, Foroud T, McClintick JN, McGee BM, Yang AY, Siemieniak DR, Stark KR, Gruppo R, Sarode R, Shurin SB, Chandrasekaran V, Stabler SP, Sabio H, Bouhassira EE, Upshaw JD, Ginsburg D, Tsai HM.
    Nature; 2001 Oct 04; 413(6855):488-94. PubMed ID: 11586351
    [Abstract] [Full Text] [Related]

  • 37. Assays of von Willebrand factor-cleaving protease: a test for diagnosis of familial and acquired thrombotic thrombocytopenic purpura.
    Furlan M, Lämmle B.
    Semin Thromb Hemost; 2002 Apr 04; 28(2):167-72. PubMed ID: 11992240
    [Abstract] [Full Text] [Related]

  • 38. Thrombotic thrombocytopenic purpura in a newborn.
    Jubinsky PT, Moraille R, Tsai HM.
    J Perinatol; 2003 Jan 04; 23(1):85-7. PubMed ID: 12556937
    [Abstract] [Full Text] [Related]

  • 39. Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity.
    Kokame K, Matsumoto M, Soejima K, Yagi H, Ishizashi H, Funato M, Tamai H, Konno M, Kamide K, Kawano Y, Miyata T, Fujimura Y.
    Proc Natl Acad Sci U S A; 2002 Sep 03; 99(18):11902-7. PubMed ID: 12181489
    [Abstract] [Full Text] [Related]

  • 40. [Hereditary form of thrombotic thrombocytopenic purpura].
    Hrachovinová I, Rittich S, Salaj P, Suttnar J, Dyr JE, Suláková T, Pták J, Dulícek P, Seeman T.
    Cas Lek Cesk; 2006 Sep 03; 145(5):390-2. PubMed ID: 16755777
    [Abstract] [Full Text] [Related]

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