Aims and Scope
Journal of Rare Cardiovascular Diseases (JRCD) is an international, quarterly issued, peer-reviewed, open access, online journal that keeps cardiologists and non-cardiologists up-to-date with rare disorders of the heart and vessels.
The Journal publishes fine quality review articles, original, basic and clinical sciences research papers, either positive or negative, case reports and articles on public health issues in the field of rare cardiovascular diseases and orphan cardiovascular drugs.
Topics of interest include, but are not limited to the following areas:
(1) rare diseases of systemic circulation
(2) rare diseases of pulmonary circulation
(3) rare diseases of the heart (cardiomyopathies)
(4) rare congenital cardiovascular diseases
(5) rare arrhythmias
(6) cardiac tumors and cardiovascular diseases in malignancy
(7) cardiovascular diseases in pregnancy
(8) basic science
Journal of Rare Cardiovascular Diseases follows the International Committee of Medical Journal Editors (ICMJE) Recommendations for the Conduct, Reporting, Editing and Publication of Scholarly Work in Medical Journals. JRCD respects publication ethics as set out by the Committee on Publication Ethics (COPE).
Submission of a manuscript to the Journal of Rare Cardiovascular Diseases implies that all authors have read and agreed to its content and that the manuscript conforms to the journal’s policies.
JRCD accepts submissions from all international regions.
Forthcoming Issue: JRCD vol. 2 no. 7
|We invite You to read the forthcoming issue table of contents.|
Thanks to reviewers: Thanks to reviewers: 2015
Let me thank, on behalf of the Editorial Board and Editorial Office Members, each and all of the following colleagues for their significant contribution to the development of the Journal by reviewing articles submitted to the Journal in 2015.
Vol 2, No 7 (2016)
Table of Contents
|For one mistake made for not knowing, ten mista kes are made for not looking|
Diseases of the Heart
|The role of biomarkers as an alternative and completion of the diagnostic and therapeutic pathway in patients with aortic stenosis|
|Podolec J, Baran J, , Guzik B, Żmudka K||209-214|
Cardiovascular diseases in pregnancy
|Pregnancy in pulmonary arterial hypertension|
|Kaźnica-Wiatr M, Leśniak-Sobelga A, Kopeć G, Błaszczak P, Frynas K, Olszowska M, Rytlewski K, Kasprzak J, Podolec P||215-219|
|A 33-year-old man after sudden cardiac arrest as a first manifestation of Brugada syndrome|
|Holcman K, Rubiś P, Wiśniowska-Śmiałek S, Biernacka-Fiałkowska B, Hlawaty M, Leśniak-Sobelga A, Karkowski G, Bednarek J, Lelakowski J, Kostkiewicz M, Podolec P||220-224|
|Spontaneous implantation of a left atrial myxoma into the left ventricle|
|Stettner-Leonkiewicz D, Tomaszewski A, Wysokiński A, Stążka J, Czajkowski M, Tomaszewski M||225-227|
|31-year old man with Short QT syndrome||PDF PDF|
|Wiśniowska-Śmiałek S, Rubiś P, Holcman K, Biernacka-Fijałkowska B, Leśniak-Sobelga A, Kostkiewicz M, Podolec P, Kopeć G||228-230|
Rare diseases of the heart
|Eosinophilic myocarditis: Gardia lamblia infestation and Garcinia cambogia. Coincidence or causality?|
|Dzierwa K, Rudnicka-Sosin L, Rubiś P, Tekieli L, Pieniążek P||231-235|
|Report from the 65th American College of Cardiology Congress 2016 in Chicago, USA|