Literature DB >> 28083987

VWF collagen (types III and VI)-binding defects in a cohort of type 2M VWD patients - a strategy for improvement of a challenging diagnosis.

T Fidalgo1, A Oliveira1, C Silva Pinto1, P Martinho1, G Ferreira1, R Salvado1, T Sevivas1, C Catarino2, M L Ribeiro1.   

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Year:  2017        PMID： 28083987     DOI： 10.1111/hae.13156

Source DB:  PubMed          Journal:  Haemophilia        ISSN： 1351-8216            Impact factor:   4.287


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  4 in total

1.  Identification of a missense mutation (p.Leu1733Pro) in the A3 domain of von Willebrand factor in a family with type 2M von Willebrand disease.

Authors:  Toshio Shigekiyo; Hikaru Yagi; Etsuko Sekimoto; Hironobu Shibata; Shuji Ozaki; Masanori Matsumoto
Journal:  Int J Hematol       Date:  2019-10-11       Impact factor: 2.490

2.  Phenotypic and genetic characterizations of the Milan cohort of von Willebrand disease type 2.

Authors:  Omid Seidizadeh; Luciano Baronciani; Maria Teresa Pagliari; Giovanna Cozzi; Paola Colpani; Andrea Cairo; Simona Maria Siboni; Eugenia Biguzzi; Flora Peyvandi
Journal:  Blood Adv       Date:  2022-07-12

Review 3.  VWF, Platelets and the Antiphospholipid Syndrome.

Authors:  Shengshi Huang; Marisa Ninivaggi; Walid Chayoua; Bas de Laat
Journal:  Int J Mol Sci       Date:  2021-04-18       Impact factor: 5.923

4.  Combined effects of two mutations in von Willebrand disease 2M phenotype.

Authors:  Adriana I Woods; Juvenal Paiva; Ana C Kempfer; Debora M Primrose; Alicia N Blanco; Analía Sanchez-Luceros; María A Lazzari
Journal:  Res Pract Thromb Haemost       Date:  2017-12-20
  4 in total

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