Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Maria Kharlap"'
Autor:
Karapet Davtyan, Svetlana Serdyuk, Arpi Topchyan, Georgiy Simonyan, Maria Kharlap, Sergey Burd
Publikováno v:
BMC Cardiovascular Disorders, Vol 24, Iss 1, Pp 1-5 (2024)
Abstract Background The muscle artifacts, caused by prominent muscle contractions, mimicking cardiac arrhythmias, might compromise the ECG signal quality and the implantable loop recorder memory capacity in patients with epilepsy. We developed an epi
Externí odkaz:
https://doaj.org/article/e40768f0e5b5481ebfc82f4ed3463eb2
Autor:
Roman Myasnikov, Anna Bukaeva, Olga Kulikova, Alexey Meshkov, Anna Kiseleva, Alexandra Ershova, Anna Petukhova, Mikhail Divashuk, Evgenia Zotova, Evgeniia Sotnikova, Maria Kharlap, Anastasia Zharikova, Yuri Vyatkin, Vasily Ramensky, Alexandra Abisheva, Alisa Muraveva, Sergey Koretskiy, Maria Kudryavtseva, Sergey Popov, Marina Utkina, Elena Mershina, Valentin Sinitsyn, Evgeniya Kogan, Olga Blagova, Oxana Drapkina
Publikováno v:
Genes. 13:309
Left ventricular noncompaction (LVNC) is a highly heterogeneous primary disorder of the myocardium. Its clinical features and genetic spectrum strongly overlap with other types of primary cardiomyopathies, in particular, hypertrophic cardiomyopathy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf85c683ed939aaf40f65314aae121c8
https://doi.org/10.3390/genes13020309
https://doi.org/10.3390/genes13020309
Autor:
Gaetano M. De Ferrari, Peter J. Schwartz, Antoine Leenhardt, Maria Shkolnikova, Attilio Odero, Lia Crotti, Veronica Dusi, Michael Eldar, Maria Kharlap, J. Martijn Bos, Asaad Khoury, Carla Spazzolini, Jan Till, Ferran Rosés I. Noguer, Andrew D. Krahn, Dominic Abrams, Thomas Paul, Louise R.A. Olde Nordkamp, Andrew M. Davis, Charles I. Berul, Michael J. Ackerman, Christopher R. Moir, Arthur A.M. Wilde
Publikováno v:
Circulation, 131(25), 2185-2193. Lippincott Williams and Wilkins
Circulation 131, 2185-2193 (2015)
Circulation 131, 2185-2193 (2015)
Background— Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a genetic disorder causing life-threatening arrhythmias whenever sympathetic activity increases. β-Βlockers are the mainstay of therapy; when they fail, implantable cardi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::761e6f8ffdc0afb13a746510aa015c0d
https://doi.org/10.1161/circulationaha.115.015731
https://doi.org/10.1161/circulationaha.115.015731
Autor:
Peter J. Schwartz, Attilio Odero, Arthur A.M. Wilde, Gaetano M. De Ferrari, Christopher R. Moir, Thomas Paul, Dominic Abrams, Michael J. Ackerman, Louise R.A. Olde Nordkamp, Maria Kharlap, Ferran Rosés I. Noguer, Charles I. Berul, Asaad Khoury, Lia Crotti, Veronica Dusi, Jan Till, Andrew D. Krahn, Maria Shkolnikova, Carla Spazzolini, Michael Eldar, J. Martijn Bos, Antoine Leenhardt
Publikováno v:
Circulation, 133(4), e366-e367. Lippincott Williams and Wilkins
We are glad to have the opportunity to respond to the points kindly raised by Drs Patane and Gow in reference to our recent article on catecholaminergic polymorphic ventricular tachycardia (CPVT).1 We are obviously aware of the article by Faggioni et
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7c760a9f447a6c4435dd67fe197f17a
https://pure.amc.nl/en/publications/response-to-letters-regarding-article-clinical-management-of-catecholaminergic-polymorphic-ventricular-tachycardia-the-role-of-left-cardiac-sympathetic-denervation(ae49feee-9d57-4749-9de7-e2a520374943).html
https://pure.amc.nl/en/publications/response-to-letters-regarding-article-clinical-management-of-catecholaminergic-polymorphic-ventricular-tachycardia-the-role-of-left-cardiac-sympathetic-denervation(ae49feee-9d57-4749-9de7-e2a520374943).html
Autor:
Barry J. Maron, Richard N. Mitchell, Jonathan G. Seidman, Andrey G. Zenovich, Christine E. Seidman, Lei Song, Allison L. Cirino, Carolyn Y. Ho, Maria Kharlap, Barbara McDonough, Steven R. DePalma
Publikováno v:
Circulation. 113(18)
Background— Genetic mutations are the most common cause of hypertrophic cardiomyopathy (HCM) and an increasingly recognized cause of dilated cardiomyopathy. Autosomal dominant HCM is caused by mutations in sarcomere proteins; such mutations are not
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::162cdaac14e1dd6eceafa58b097b3475
https://pubmed.ncbi.nlm.nih.gov/16651466
https://pubmed.ncbi.nlm.nih.gov/16651466
Autor:
Belikov, E. A., Davtyan, K. V., Tkacheva, O. N., Boytsov, S. A., Mazygula, E. P., Shabanova, T. N., Molodtsov, M. S., Maria Kharlap, Serdyuk, S. E.
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0f2b4a76c7d25f502c53e629c5df43ab
http://www.scopus.com/inward/record.url?eid=2-s2.0-84934282696&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-84934282696&partnerID=MN8TOARS