Suppr
超能文献

Inherited thrombocytopenias.

作者信息

Nurden Alan T, Nurden Paquita

出版信息

Haematologica. 2007 Sep;92(9):1158-64. doi: 10.3324/haematol.11256.

DOI:10.3324/haematol.11256

PMID:17768118

Abstract

摘要

相似文献

Inherited thrombocytopenias.

Haematologica. 2007 Sep;92(9):1158-64. doi: 10.3324/haematol.11256.

Mediterranean macrothrombocytopenia and phytosterolaemia/sitosterolaemia.

Haematologica. 2008 Feb;93(2):e29. doi: 10.3324/haematol.12311.

Diagnosis and management of inherited thrombocytopenias.

Semin Thromb Hemost. 2013 Mar;39(2):161-71. doi: 10.1055/s-0032-1333540. Epub 2013 Feb 8.

[Inherited thrombocytopenias].

Duodecim. 1992;108(15):1339-43.

[Hereditary thrombocytopenia. Differential diagnosis of a case].

Cas Lek Cesk. 2003;142(11):683-6.

Inherited thrombocytopenias in the era of personalized medicine.

Haematologica. 2015 Feb;100(2):145-8. doi: 10.3324/haematol.2014.122549.

Innovation in the field of thrombocytopenias: achievements since the beginning of the century and promises for the future.

Haematologica. 2016 Jan;101(1):2-4. doi: 10.3324/haematol.2015.138149.

[Diagnosis of inherited thrombocytopenia].

Rev Med Interne. 2016 Feb;37(2):117-26. doi: 10.1016/j.revmed.2015.10.346. Epub 2015 Nov 23.

Inherited thrombocytopenias: an approach to diagnosis and management.

Int J Lab Hematol. 2013 Feb;35(1):14-25. doi: 10.1111/j.1751-553X.2012.01454.x. Epub 2012 Jul 30.

Prognostic impact of germline mutations in inherited cancer syndromes.

Future Oncol. 2017 Oct;13(24):2125-2127. doi: 10.2217/fon-2017-0296. Epub 2017 Oct 6.

引用本文的文献

Busy signal: platelet-derived growth factor activation in myelofibrosis.

Haematologica. 2020 Aug;105(8):1988-1990. doi: 10.3324/haematol.2020.253708.

Application of High-Throughput Sequencing in the Diagnosis of Inherited Thrombocytopenia.

Clin Appl Thromb Hemost. 2018 Dec;24(9_suppl):94S-103S. doi: 10.1177/1076029618790696. Epub 2018 Aug 13.

Mutation in is associated with severe congenital thrombocytopenia.

Blood. 2018 Oct 25;132(17):1855-1858. doi: 10.1182/blood-2018-04-847798. Epub 2018 Jun 25.

Role of the novel endoribonuclease SLFN14 and its disease-causing mutations in ribosomal degradation.

RNA. 2018 Jul;24(7):939-949. doi: 10.1261/rna.066415.118. Epub 2018 Apr 20.

Evaluation of the immature platelet fraction contribute to the differential diagnosis of hereditary, immune and other acquired thrombocytopenias.

Sci Rep. 2017 Jun 13;7(1):3355. doi: 10.1038/s41598-017-03668-y.

SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects.

J Clin Invest. 2015 Sep;125(9):3600-5. doi: 10.1172/JCI80347. Epub 2015 Aug 17.

Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2.

Am J Hum Genet. 2011 Jan 7;88(1):115-20. doi: 10.1016/j.ajhg.2010.12.006.

[Differential diagnosis and treatment of thrombocytopenia].

Internist (Berl). 2010 Nov;51(11):1397-410. doi: 10.1007/s00108-010-2731-1.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验

相似文献

Inherited thrombocytopenias.

Haematologica. 2007 Sep;92(9):1158-64. doi: 10.3324/haematol.11256.

Mediterranean macrothrombocytopenia and phytosterolaemia/sitosterolaemia.

Haematologica. 2008 Feb;93(2):e29. doi: 10.3324/haematol.12311.

Diagnosis and management of inherited thrombocytopenias.

Semin Thromb Hemost. 2013 Mar;39(2):161-71. doi: 10.1055/s-0032-1333540. Epub 2013 Feb 8.

[Inherited thrombocytopenias].

Duodecim. 1992;108(15):1339-43.

[Hereditary thrombocytopenia. Differential diagnosis of a case].

Cas Lek Cesk. 2003;142(11):683-6.

Inherited thrombocytopenias in the era of personalized medicine.

Haematologica. 2015 Feb;100(2):145-8. doi: 10.3324/haematol.2014.122549.

Innovation in the field of thrombocytopenias: achievements since the beginning of the century and promises for the future.

Haematologica. 2016 Jan;101(1):2-4. doi: 10.3324/haematol.2015.138149.

[Diagnosis of inherited thrombocytopenia].

Rev Med Interne. 2016 Feb;37(2):117-26. doi: 10.1016/j.revmed.2015.10.346. Epub 2015 Nov 23.

Inherited thrombocytopenias: an approach to diagnosis and management.

Int J Lab Hematol. 2013 Feb;35(1):14-25. doi: 10.1111/j.1751-553X.2012.01454.x. Epub 2012 Jul 30.

Prognostic impact of germline mutations in inherited cancer syndromes.

Future Oncol. 2017 Oct;13(24):2125-2127. doi: 10.2217/fon-2017-0296. Epub 2017 Oct 6.

引用本文的文献

Busy signal: platelet-derived growth factor activation in myelofibrosis.

Haematologica. 2020 Aug;105(8):1988-1990. doi: 10.3324/haematol.2020.253708.

Application of High-Throughput Sequencing in the Diagnosis of Inherited Thrombocytopenia.

Clin Appl Thromb Hemost. 2018 Dec;24(9_suppl):94S-103S. doi: 10.1177/1076029618790696. Epub 2018 Aug 13.

Mutation in is associated with severe congenital thrombocytopenia.

Blood. 2018 Oct 25;132(17):1855-1858. doi: 10.1182/blood-2018-04-847798. Epub 2018 Jun 25.

Role of the novel endoribonuclease SLFN14 and its disease-causing mutations in ribosomal degradation.

RNA. 2018 Jul;24(7):939-949. doi: 10.1261/rna.066415.118. Epub 2018 Apr 20.

Evaluation of the immature platelet fraction contribute to the differential diagnosis of hereditary, immune and other acquired thrombocytopenias.

Sci Rep. 2017 Jun 13;7(1):3355. doi: 10.1038/s41598-017-03668-y.

SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects.

J Clin Invest. 2015 Sep;125(9):3600-5. doi: 10.1172/JCI80347. Epub 2015 Aug 17.

Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2.

Am J Hum Genet. 2011 Jan 7;88(1):115-20. doi: 10.1016/j.ajhg.2010.12.006.

[Differential diagnosis and treatment of thrombocytopenia].

Internist (Berl). 2010 Nov;51(11):1397-410. doi: 10.1007/s00108-010-2731-1.

Suppr超能文献

Inherited thrombocytopenias.

作者信息

出版信息

相似文献

引用本文的文献

文献AI研究员

用中文搜PubMed

文档翻译