Two newborn-onset patients of Upshaw-Schulman syndrome with distinct subsequent clinical courses (Q33404583)

26 July 2017

Two newborn-onset patients of Upshaw-Schulman syndrome with distinct subsequent clinical courses (English)

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26 July 2017

Saori Tanabe

1

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26 July 2017

Hideo Yagi

2

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26 July 2017

Toshiyuki Kimura

3

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26 July 2017

Ayami Isonishi

4

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26 July 2017

Seiji Kato

5

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26 July 2017

Yoko Yoshida

6

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26 July 2017

Masaki Hayakawa

7

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26 July 2017

Masanori Matsumoto

8

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26 July 2017

Shinsuke Ohtaki

9

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26 July 2017

Yukihiro Takahashi

10

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26 July 2017

Yoshihiro Fujimura

11

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26 July 2017

language of work or name

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28 November 2012

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International Journal of Hematology

26 July 2017

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26 July 2017

96

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26 July 2017

6

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26 July 2017

789-797

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https://scigraph.springernature.com/pub.10.1007/s12185-012-1221-8

26 July 2017

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cites work

Congenital deficiency of a factor in normal plasma that reverses microangiopathic hemolysis and thrombocytopenia

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1221-8

Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1221-8

Natural history of Upshaw-Schulman syndrome based on ADAMTS13 gene analysis in Japan

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12185-012-1221-8

ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura

21 January 2018

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Von Willebrand factor-cleaving protease and Upshaw-Schulman syndrome

21 January 2018

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Aetiology and pathogenesis of thrombotic thrombocytopenic purpura and haemolytic uraemic syndrome: the role of von Willebrand factor-cleaving protease

21 January 2018

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Platelets treated with ticlopidine are less reactive to unusually large von Willebrand factor multimers than are those treated with aspirin under high shear stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12185-012-1221-8

Variant von Willebrand's disease: characterization of two subtypes by analysis of multimeric composition of factor VIII/von Willebrand factor in plasma and platelets

21 January 2018

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Novel monoclonal antibody-based enzyme immunoassay for determining plasma levels of ADAMTS13 activity

21 January 2018

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Brain nerve symptoms due to thrombotic microangiopathy

21 January 2018

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Quantitative Western blot analysis of plasma ADAMTS13 antigen in patients with Upshaw-Schulman syndrome

21 January 2018

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Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity

21 January 2018

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Molecular characterization of ADAMTS13 gene mutations in Japanese patients with Upshaw-Schulman syndrome

21 January 2018

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Hypoxia-induced exocytosis of endothelial cell Weibel-Palade bodies. A mechanism for rapid neutrophil recruitment after cardiac preservation

21 January 2018

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Upshaw-Schulman syndrome revisited: a concept of congenital thrombotic thrombocytopenic purpura

21 January 2018

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Placental ecto-ATP diphosphohydrolase: its structural feature distinct from CD39, localization and inhibition on shear-induced platelet aggregation

21 January 2018

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The cDNA cloning of human placental ecto-ATP diphosphohydrolases I and II.

21 January 2018

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Luminographic detection of von Willebrand factor multimers in agarose gels and on nitrocellulose membranes

21 January 2018

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12 December 2020

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12 December 2020

The homozygous p.C1024R- ADAMTS13 gene mutation links to a late-onset phenotype of Upshaw-Schulman syndrome in Japan

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12 December 2020

Studies on thrombopoiesis. I. A factor in normal human plasma required for platelet production; chronic thrombocytopenia due to its deficiency

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12 December 2020

von Willebrand factor-to-ADAMTS13 ratio increases with age in a Japanese population

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12 December 2020

Prevalence of the ADAMTS-13 missense mutation R1060W in late onset adult thrombotic thrombocytopenic purpura

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12 December 2020

Polymorphisms and mutations of ADAMTS13 in the Japanese population and estimation of the number of patients with Upshaw-Schulman syndrome

1 reference

12 December 2020

Hypoxia-induced von Willebrand factor release is blocked by verapamil

1 reference

12 December 2020

10.1007/S12185-012-1221-8

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26 July 2017

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