Literature DB >> 20694274

Intriguing outcome of JAK2V617F mutation seen in a patient with MYH9-related hereditary macrothrombocytopenia.

Fabrizio Fabris, Raffaella Scandellari, Silvia Vettore, Margherita Scapin, Nicola Bizzaro, Maria L Randi.   

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Year:  2010        PMID： 20694274     DOI： 10.1160/TH10-01-0041

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN： 0340-6245            Impact factor:   5.249


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  2 in total

1.  Transient hemiparesis in a 14-year-old boy with MYH9 disorders.

Authors:  Katsumasa Kitamura; Shinji Kunishima; Mayu Tahara; Shigetoshi Ogiwara; Nana Dobata; Tomoyuki Dobata; Akemi Sugihara; Taiji Nakashima; Yasushi Sasaki; Kiyoshi Nagumo; Mitsuru Kubota; Yoshikazu Kinugawa; Masahiro Ieko; Satoru Kumaki
Journal:  Int J Hematol       Date:  2012-07-22       Impact factor: 2.490

2.  Thrombotic events in MYH9 gene-related autosomal macrothrombocytopenias (old May-Hegglin, Sebastian, Fechtner and Epstein syndromes).

Authors:  Antonio Girolami; Girolami Antonio; Silvia Vettore; Vettore Silvia; Emanuela Bonamigo; Bonamigo Emanuela; Fabrizio Fabris; Fabris Fabrizio
Journal:  J Thromb Thrombolysis       Date:  2011-11       Impact factor: 2.300
  2 in total

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