Nefropatía asociada a mutación del gen MYH9

Author:

Furlano Mónica,Arlandis Rosa,Venegas María del Prado,Novelli Silvana,Crespi Jaume,Bullich Gemma,Ayasreh Nadia,Remacha Ángel,Ruiz Patricia,Lorente Laura,Ballarín José,Matamala Anna,Ars Elisabet,Torra Roser

Publisher

Elsevier BV

Subject

Nephrology

Reference48 articles.

1. Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes;Arrondel;J Am Soc Nephrol,2002

2. Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related disease;Pecci;Hum Mutat,2008

3. Thrombotic events in MYH9 gene-related autosomal macrothrombocytopenias (old May-Hegglin, Sebastian Fechtner and Epstein syndromes);Girolami;J Thromb Thrombolysis,2011

4. Heavy chain myosin 9-related disease (MYH9 -RD): neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder;Savoia;Thromb Haemost,2010

5. MYH9 gene mutations associated with bleeding;Savoia;Platelets,2017

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