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 *

172 related articles for article (PubMed ID: 29554699)

  • 21. Paradigm shift of childhood thrombotic thrombocytopenic purpura with severe ADAMTS13 deficiency.
    Yagi H; Matsumoto M; Fujimura Y
    Presse Med; 2012 Mar; 41(3 Pt 2):e137-55. PubMed ID: 22264931
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Two newborn-onset patients of Upshaw-Schulman syndrome with distinct subsequent clinical courses.
    Tanabe S; Yagi H; Kimura T; Isonishi A; Kato S; Yoshida Y; Hayakawa M; Matsumoto M; Ohtaki S; Takahashi Y; Fujimura Y
    Int J Hematol; 2012 Dec; 96(6):789-97. PubMed ID: 23188471
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Complement activation associated with ADAMTS13 deficiency may contribute to the characteristic glomerular manifestations in Upshaw-Schulman syndrome.
    Itami H; Hara S; Matsumoto M; Imamura S; Kanai R; Nishiyama K; Ishimura M; Ohga S; Yoshida M; Tanaka R; Ogawa Y; Asada Y; Sekita-Hatakeyama Y; Hatakeyama K; Ohbayashi C
    Thromb Res; 2018 Oct; 170():148-155. PubMed ID: 30195146
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Genetic polymorphism of von Willebrand factor (VWF)-cleaving protease, ADAMTS13].
    Kokame K
    Brain Nerve; 2008 Nov; 60(11):1325-32. PubMed ID: 19069166
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Novel ADAMTS13 mutations in an obstetric patient with Upshaw-Schulman syndrome.
    Deal T; Kremer Hovinga JA; Marques MB; Adamski J
    J Clin Apher; 2013 Aug; 28(4):311-6. PubMed ID: 23208954
    [TBL] [Abstract][Full Text] [Related]  

  • 26. ADAMTS13 kinetics after therapeutic plasma exchange and plasma infusion in patients with Upshaw-Schulman syndrome.
    Kovarova P; Hrdlickova R; Blahutova S; Cermakova Z
    J Clin Apher; 2019 Feb; 34(1):13-20. PubMed ID: 30394580
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Experiences in a family with the Upshaw-Schulman syndrome over a 44-year period.
    Bennett M; Chubar Y; Gavish I; Aviv A; Stemer G; Chap-Marshak D
    Clin Appl Thromb Hemost; 2014 Apr; 20(3):296-303. PubMed ID: 23872162
    [TBL] [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; 57(11):2712-2714. PubMed ID: 28833243
    [TBL] [Abstract][Full Text] [Related]  

  • 29. From the Discovery of ADAMTS13 to Current Understanding of Its Role in Health and Disease.
    Woods AI; Paiva J; Dos Santos C; Alberto MF; Sánchez-Luceros A
    Semin Thromb Hemost; 2023 Apr; 49(3):284-294. PubMed ID: 36368692
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Natural history of Upshaw-Schulman syndrome based on ADAMTS13 gene analysis in Japan.
    Fujimura Y; Matsumoto M; Isonishi A; Yagi H; Kokame K; Soejima K; Murata M; Miyata T
    J Thromb Haemost; 2011 Jul; 9 Suppl 1():283-301. PubMed ID: 21781265
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The D173G mutation in ADAMTS-13 causes a severe form of congenital thrombotic thrombocytopenic purpura. A clinical, biochemical and in silico study.
    Lancellotti S; Peyvandi F; Pagliari MT; Cairo A; Abdel-Azeim S; Chermak E; Lazzareschi I; Mastrangelo S; Cavallo L; Oliva R; De Cristofaro R
    Thromb Haemost; 2016 Jan; 115(1):51-62. PubMed ID: 26272487
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Rare Variants in the ADAMTS13 Von Willebrand Factor-Binding Domain Contribute to Pediatric Stroke.
    Stoll M; Rühle F; Witten A; Barysenka A; Arning A; Strauss C; Nowak-Göttl U
    Circ Cardiovasc Genet; 2016 Aug; 9(4):357-67. PubMed ID: 27412500
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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; 99(18):11902-7. PubMed ID: 12181489
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Case of maternal and fetal deaths due to severe congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) during pregnancy.
    Tanaka H; Tenkumo C; Mori N; Kokame K; Fujimura Y; Hata T
    J Obstet Gynaecol Res; 2014 Jan; 40(1):247-9. PubMed ID: 23937165
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Inherited thrombotic thrombocytopenic purpura in pregnancy.
    Drews K; Seremak-Mrozikiewicz A; Sobieszczyk S; Barlik M
    Neuro Endocrinol Lett; 2013; 34(6):508-13. PubMed ID: 24378452
    [TBL] [Abstract][Full Text] [Related]  

  • 37. ADAMTS13 gene defects in two brothers with constitutional thrombotic thrombocytopenic purpura and normalization of von Willebrand factor-cleaving protease activity by recombinant human ADAMTS13.
    Antoine G; Zimmermann K; Plaimauer B; Grillowitzer M; Studt JD; Lämmle B; Scheiflinger F
    Br J Haematol; 2003 Mar; 120(5):821-4. PubMed ID: 12614216
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A phenotype-genotype correlation of ADAMTS13 mutations in congenital thrombotic thrombocytopenic purpura patients treated in the United Kingdom.
    Camilleri RS; Scully M; Thomas M; Mackie IJ; Liesner R; Chen WJ; Manns K; Machin SJ
    J Thromb Haemost; 2012 Sep; 10(9):1792-801. PubMed ID: 22783805
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Congenital thrombotic thrombocytopenic purpura in a large cohort of patients carrying a novel mutation in ADAMTS13 gene.
    Pikovsky O; Arafat M; Ovadia H; Sharoni Y; Al-Athamen K; Kanengisser-Pines B; Keren-Politansky A; Levi I; Erez O; Parvari R; Rabinovich A
    Thromb Res; 2020 Jan; 185():167-170. PubMed ID: 31837614
    [No Abstract]   [Full Text] [Related]  

  • 40. Molecular characterization of ADAMTS13 gene mutations in Japanese patients with Upshaw-Schulman syndrome.
    Matsumoto M; Kokame K; Soejima K; Miura M; Hayashi S; Fujii Y; Iwai A; Ito E; Tsuji Y; Takeda-Shitaka M; Iwadate M; Umeyama H; Yagi H; Ishizashi H; Banno F; Nakagaki T; Miyata T; Fujimura Y
    Blood; 2004 Feb; 103(4):1305-10. PubMed ID: 14563640
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.