Literature DB >> 18503011

Renin-angiotensin system blockade is effective in reducing proteinuria of patients with progressive nephropathy caused by MYH9 mutations (Fechtner-Epstein syndrome).

Alessandro Pecci1, Antonio Granata, Carmelo E Fiore, Carlo L Balduini.   

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Year:  2008        PMID: 18503011     DOI: 10.1093/ndt/gfn277

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


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  17 in total

1.  Macrothrombocytopenia With Döhle Body-Like Granulocyte Inclusions: A Case Report of May-Hegglin Anomaly in a 33-Year-Old White Woman With an Update on the Molecular Findings of MYH9-Related Disease.

Authors:  Steven M Ruhoy; Amanda Yates
Journal:  Lab Med       Date:  2016-06-28

2.  Inherited thrombocytopenias in the era of personalized medicine.

Authors:  Patrizia Noris; Carlo L Balduini
Journal:  Haematologica       Date:  2015-02       Impact factor: 9.941

Review 3.  Hereditary thrombocytopenias: a growing list of disorders.

Authors:  Patrizia Noris; Alessandro Pecci
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2017-12-08

Review 4.  MYH9: Structure, functions and role of non-muscle myosin IIA in human disease.

Authors:  Alessandro Pecci; Xuefei Ma; Anna Savoia; Robert S Adelstein
Journal:  Gene       Date:  2018-04-19       Impact factor: 3.688

5.  MYH-9 Related Platelet Disorders: Strategies for Management and Diagnosis.

Authors:  Karina Althaus; Andreas Greinacher
Journal:  Transfus Med Hemother       Date:  2010-09-15       Impact factor: 3.747

6.  Macrothrombocytopenia, renal dysfunction and nephrotic syndrome in a young male patient: a case report of MYH9-related disease.

Authors:  Gabriela Sevignani; Giovana Memari Pavanelli; Sibele Sauzem Milano; Bianca Ramos Ferronato; Maria Aparecida Pachaly; Hae Ii Cheong; Mauricio de Carvalho; Fellype Carvalho Barreto
Journal:  J Bras Nefrol       Date:  2018-05-17

7.  MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations.

Authors:  Alessandro Pecci; Catherine Klersy; Paolo Gresele; Kieran J D Lee; Daniela De Rocco; Valeria Bozzi; Giovanna Russo; Paula G Heller; Giuseppe Loffredo; Matthias Ballmaier; Fabrizio Fabris; Eloise Beggiato; Walter H A Kahr; Nuria Pujol-Moix; Helen Platokouki; Christel Van Geet; Patrizia Noris; Preethi Yerram; Cedric Hermans; Bernhard Gerber; Marina Economou; Marco De Groot; Barbara Zieger; Erica De Candia; Vincenzo Fraticelli; Rogier Kersseboom; Giorgina B Piccoli; Stefanie Zimmermann; Tiziana Fierro; Ana C Glembotsky; Fabrizio Vianello; Carlo Zaninetti; Elena Nicchia; Christiane Güthner; Carlo Baronci; Marco Seri; Peter J Knight; Carlo L Balduini; Anna Savoia
Journal:  Hum Mutat       Date:  2013-12-12       Impact factor: 4.878

8.  Alteration of liver enzymes is a feature of the MYH9-related disease syndrome.

Authors:  Alessandro Pecci; Ginevra Biino; Tiziana Fierro; Valeria Bozzi; Annamaria Mezzasoma; Patrizia Noris; Ugo Ramenghi; Giuseppe Loffredo; Fabrizio Fabris; Stefania Momi; Umberto Magrini; Mario Pirastu; Anna Savoia; Carlo Balduini; Paolo Gresele
Journal:  PLoS One       Date:  2012-04-25       Impact factor: 3.240

9.  Myosin heavy chain-9-related disorders (MYH9-RD): a case report.

Authors:  Diana Vassallo; Ibi Erekosima; Durga Kanigicherla; Edmond O'Riordan; Puchimada Uthappa; Constantina Chrysochou
Journal:  Clin Kidney J       Date:  2013-09-01

10.  MYH9-related disease: five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations.

Authors:  Daniela De Rocco; Barbara Zieger; Helen Platokouki; Paula G Heller; Annalisa Pastore; Roberta Bottega; Patrizia Noris; Serena Barozzi; Ana C Glembotsky; Helen Pergantou; Carlo L Balduini; Anna Savoia; Alessandro Pecci
Journal:  Eur J Med Genet       Date:  2012-10-30       Impact factor: 2.708

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