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Journal Abstract Search

126 related items for PubMed ID: 26352112

  • 1. Congenital late onset thrombotic thrombocytopenic purpura: a diagnostic challenge.
    Enjeti AK, Chapman K, Taylor PJ, Meldrum C.
    Pathology; 2015 Oct; 47(6):585-6. PubMed ID: 26352112
    [No Abstract] [Full Text] [Related]

  • 2. 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; 102(4):477-81. PubMed ID: 26267233
    [Abstract] [Full Text] [Related]

  • 3. Drop of residual plasmatic activity of ADAMTS13 to undetectable levels during acute disease in a patient with adult-onset congenital thrombotic thrombocytopenic purpura.
    Lotta LA, Wu HM, Cairo A, Bentivoglio G, Peyvandi F.
    Blood Cells Mol Dis; 2013 Jan; 50(1):59-60. PubMed ID: 22981442
    [No Abstract] [Full Text] [Related]

  • 4. Congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) caused by novel ADAMTS13 mutations.
    Kim HY, Lee KO, Yoo KH, Kim SH, Oh D, Kim HJ.
    Br J Haematol; 2016 Apr; 173(1):156-9. PubMed ID: 26085195
    [No Abstract] [Full Text] [Related]

  • 5. A new ADAMTS13 missense mutation (D1362V) in thrombotic thrombocytopenic purpura diagnosed during pregnancy.
    Calderazzo JC, Kempfer A, Powazniak Y, López IR, Sánchez-Luceros A, Woods AI, Lazzari MA.
    Thromb Haemost; 2012 Aug; 108(2):401-3. PubMed ID: 22627385
    [No Abstract] [Full Text] [Related]

  • 6. A novel mutation in ADAMTS13 of a child with Upshaw-Schulman Syndrome.
    Pérez-Rodríguez A, Batlle-López A, Blanco R, Varela I, León J, Delgado MD, Lourés E, Rodríguez-Trillo A, García-Rivero A, Costa-Pinto J, Batlle J, López-Fernández MF.
    Thromb Haemost; 2014 Nov; 112(5):1065-8. PubMed ID: 25057114
    [No Abstract] [Full Text] [Related]

  • 7. Late onset and pregnancy-induced congenital thrombotic thrombocytopenic purpura.
    Falter T, Kremer Hovinga JA, Lackner K, Füllemann HG, Lämmle B, Scharrer I.
    Hamostaseologie; 2014 Nov; 34(3):244-8. PubMed ID: 24994604
    [Abstract] [Full Text] [Related]

  • 8. A first bout of thrombotic thrombocytopenic purpura triggered by herpes simplex infection in a 45-year-old nulliparous female with Upshaw-Schulman syndrome.
    Morioka M, Matsumoto M, Saito M, Kokame K, Miyata T, Fujimura Y.
    Blood Transfus; 2014 Jan; 12 Suppl 1(Suppl 1):s153-5. PubMed ID: 24120584
    [No Abstract] [Full Text] [Related]

  • 9. Single-nucleotide variations defining previously unreported ADAMTS13 haplotypes are associated with differential expression and activity of the VWF-cleaving protease in a Salvadoran congenital thrombotic thrombocytopenic purpura family.
    Kim B, Hing ZA, Wu A, Schiller T, Struble EB, Liuwantara D, Kempert PH, Broxham EJ, Edwards NC, Marder VJ, Simhadri VL, Sauna ZE, Howard TE, Kimchi-Sarfaty C.
    Br J Haematol; 2014 Apr; 165(1):154-8. PubMed ID: 24433405
    [No Abstract] [Full Text] [Related]

  • 10. Congenital thrombotic thrombocytopenic purpura caused by new compound heterozygous mutations of the ADAMTS13 gene.
    Rank CU, Kremer Hovinga J, Taleghani MM, Lämmle B, Gøtze JP, Nielsen OJ.
    Eur J Haematol; 2014 Feb; 92(2):168-71. PubMed ID: 24033710
    [Abstract] [Full Text] [Related]

  • 11. [Pathophysiology of thrombotic thrombocytopenic purpura].
    Fujimura Y, Isonishi A.
    Nihon Jinzo Gakkai Shi; 2014 Feb; 56(7):1043-51. PubMed ID: 25420404
    [No Abstract] [Full Text] [Related]

  • 12. The impact of congenital thrombotic thrombocytopenic purpura on pregnancy complications.
    von Krogh AS, Kremer Hovinga JA, Tjønnfjord GE, Ringen IM, Lämmle B, Waage A, Quist-Paulsen P.
    Thromb Haemost; 2014 Jun; 111(6):1180-3. PubMed ID: 24499950
    [No Abstract] [Full Text] [Related]

  • 13. Low incidence of ADAMTS13 missense mutation R1060W in adult Egyptian patients with thrombotic thrombocytopenic purpura.
    El Sissy MH, El Hafez AA, El Sissy AH.
    Acta Haematol; 2014 Jun; 132(1):30-5. PubMed ID: 24401653
    [Abstract] [Full Text] [Related]

  • 14. The novel ADAMTS13-p.D187H mutation impairs ADAMTS13 activity and secretion and contributes to thrombotic thrombocytopenic purpura in mice.
    De Cock E, Hermans C, De Raeymaecker J, De Ceunynck K, De Maeyer B, Vandeputte N, Vandenbulcke A, Deckmyn H, Rottensteiner H, De Maeyer M, De Meyer SF, Vanhoorelbeke K.
    J Thromb Haemost; 2015 Feb; 13(2):283-92. PubMed ID: 25442981
    [Abstract] [Full Text] [Related]

  • 15. 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 Feb; 41(3):273-6. PubMed ID: 22075512
    [Abstract] [Full Text] [Related]

  • 16. Difficulties in diagnosing congenital thrombotic thrombocytopenic purpura.
    Klukowska A, Niewiadomska E, Budde U, Oyen F, Schneppenheim R.
    J Pediatr Hematol Oncol; 2010 Mar; 32(2):103-7. PubMed ID: 20118810
    [Abstract] [Full Text] [Related]

  • 17. Thrombotic thrombocytopenic purpura: a thrombotic disorder caused by ADAMTS13 deficiency.
    Tsai HM.
    Hematol Oncol Clin North Am; 2007 Aug; 21(4):609-32, v. PubMed ID: 17666281
    [Abstract] [Full Text] [Related]

  • 18. Congenital thrombotic thrombocytopenic purpura: Lessons for recognition and management of rare syndromes.
    George JN.
    Pediatr Blood Cancer; 2008 May; 50(5):947-8. PubMed ID: 18360884
    [No Abstract] [Full Text] [Related]

  • 19. The homozygous p.C1024R- ADAMTS13 gene mutation links to a late-onset phenotype of Upshaw-Schulman syndrome in Japan.
    Taguchi F, Yagi H, Matsumoto M, Sadamura S, Isonishi A, Soejima K, Fujimura Y.
    Thromb Haemost; 2012 May; 107(5):1003-5. PubMed ID: 22398507
    [No Abstract] [Full Text] [Related]

  • 20. Congenital thrombotic thrombocytopenic purpura (cTTP) with two novel mutations.
    Prestidge TD, Rurali E, Wadsworth L, Wu JK, Moore JC, Bresin E.
    Pediatr Blood Cancer; 2012 Dec 15; 59(7):1296-8. PubMed ID: 22488907
    [Abstract] [Full Text] [Related]

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