Aspirin responsive erythromelalgia in JAK2-thrombocythemia and incurable inherited erythrothermalgia in neuropathic Nav1.7 sodium channelopathy: from Mitchell 1878 to Michiels 2017-Reference-Cited by-同舟云学术

Aspirin responsive erythromelalgia in JAK2-thrombocythemia and incurable inherited erythrothermalgia in neuropathic Nav1.7 sodium channelopathy: from Mitchell 1878 to Michiels 2017

Published:2016-12-26 Issue:2 Volume:5 Page:111-129
ISSN:2167-8707
Container-title:Expert Opinion on Orphan Drugs
language:en
Short-container-title:Expert Opinion on Orphan Drugs

Author:

Michiels Jan Jacques¹²³

Affiliation:

1. Department of Hematology & Coagulation, Academic Hospital Dijkzigt and Erasmus University, Rotterdam, The Netherlands

2. Department of Blood and Coagulation Disorders, University Hospital Antwerp, Edegem, Belgium

3. Blood, Coagulation and Vascular Medicine Research Center, Goodheart Institute & Foundation in Nature Medicine & Health, Freedom of Science and Education, European Free University, Erasmus Tower, Rotterdam

Publisher

Informa UK Limited

Subject

Pharmacology (medical),Health Policy,Pharmacology, Toxicology and Pharmaceutics (miscellaneous)

Link

https://www.tandfonline.com/doi/pdf/10.1080/21678707.2017.1270822

Reference128 articles.

1. Erythromelalgia and Vascular Complications in Polycythemia Vera

2. A CASE OF ERYTHEOMELALGIA, WITH MICROSCOPICAL EXAMINATION OF THE TISSUE FROM AN AMPUTATED TOE

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2. Novel European Asiatic Clinical, Laboratory, Molecular and Pathobiological (2015-2020 CLMP) criteria for JAK2V617F trilinear polycythemia vera (PV), JAK2exon12 PV and JAK2V617F, CALR and MPL515 thrombocythemias: From Dameshek to Constantinescu-Vainchenker, Kralovics and Michiels;International Journal of Bone Marrow Research;2020-04-03

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4. Corrigendum;Expert Opinion on Orphan Drugs;2017-01-12