Inherited thrombocytopenias frequently diagnosed in adults-Reference-Cited by-同舟云学术

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Inherited thrombocytopenias frequently diagnosed in adults

Published:2013-06 Issue:6 Volume:11 Page:1006-1019
ISSN:1538-7933
Container-title:Journal of Thrombosis and Haemostasis
language:en
Short-container-title:J Thromb Haemost

Author:

Balduini C. L.¹,Savoia A.²,Seri M.³

Affiliation:

1. Department of Internal Medicine; University of Pavia-IRCCS Policlinico San Matteo Foundation; Pavia Italy

2. Institute of Maternal and Child Health - IRCCS ‘Burlo Garofolo’; University of Trieste; Trieste Italy

3. Medical Genetics Unit; Policlinico S. Orsola-Malpighi; University of Bologna; Bologna Italy

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jth.12196/fullpdf

Reference77 articles.

1. Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families;Noris;Blood,2011

2. Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIb{alpha} (Bolzano mutation);Noris;Haematologica,2012

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

4. Automated platelet-sizing parameters on a normal population;Graham;Am J Clin Pathol,1987

5. A sex difference in the platelet count;Stevens;Br J Haematol,1977

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