Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Sholeh, Bazrafshan"'
Autor:
Sholeh Bazrafshan, Robert Sibilia, Saavia Girgla, Shiv Kumar Viswanathan, Megan J. Puckelwartz, Kiranpal S. Sangha, Rohit R. Singh, Mashhood Kakroo, Roman Jandarov, David M. Harris, Jack Rubinstein, Richard C. Becker, Elizabeth M. McNally, Sakthivel Sadayappan
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
Background: A 25-base pair (25bp) intronic deletion in the MYBPC3 gene enriched in South Asians (SAs) is a risk allele for late-onset left ventricular (LV) dysfunction, hypertrophy, and heart failure (HF) with several forms of cardiomyopathy. However
Externí odkaz:
https://doaj.org/article/4d34f9ba9f1248d4abac472353c3f6cf
Autor:
Marilia Silva Paulo, Balazs Adam, Cyril Akagwu, Issaka Akparibo, Rami H. Al-Rifai, Sholeh Bazrafshan, Fabriziomaria Gobba, Adele C. Green, Ivan Ivanov, Sanja Kezic, Nancy Leppink, Tom Loney, Alberto Modenese, Frank Pega, Cheryl E. Peters, Annette M. Prüss-Üstün, Thomas Tenkate, Yuka Ujita, Marc Wittlich, Swen M. John
Publikováno v:
Environment International, Vol 126, Iss , Pp 804-815 (2019)
Background: The World Health Organization (WHO) and the International Labour Organization (ILO) are developing a joint methodology for estimating the national and global work-related burden of disease and injury (WHO/ILO joint methodology), with cont
Externí odkaz:
https://doaj.org/article/36fd09357b6146f391fb692e0ef62886
Autor:
Sholeh Bazrafshan, Hani Kushlaf, Mashhood Kakroo, John Quinlan, Richard C. Becker, Sakthivel Sadayappan
Publikováno v:
Cells, Vol 10, Iss 2, p 349 (2021)
Novel genetic variants exist in patients with hereditary neuromuscular disorders (NMD), including muscular dystrophy. These patients also develop cardiac manifestations. However, the association between these gene variants and cardiac abnormalities i
Externí odkaz:
https://doaj.org/article/7ab3130989b74c3ab83d8da0c43627a7
Autor:
Rohit Singh, Pooneh Nabavizadeh, Darshini Desai, Sholeh Bazrafshan, Evangelia G. Kranias, Yigang Wang, Sakthivel Sadayappan, Richard C. Becker, Perundurai S. Dhandapany, Mohammed Arif, Mohit Kumar, Richard J. Gilbert, Taejeong Song
Publikováno v:
Biophysical Reviews. 12:1065-1084
Hypertrophic cardiomyopathy (HCM) is a cardiac genetic disease characterized by ventricular enlargement, diastolic dysfunction, and increased risk for sudden cardiac death. Sarcomeric genetic defects are the predominant known cause of HCM. In particu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52fa94823619136e1e19b246cd9200d0
https://doi.org/10.1007/s12551-020-00725-1
https://doi.org/10.1007/s12551-020-00725-1
Autor:
Ralph Knoell, Evangelia G. Kranias, Mohit Kumar, Kobra Haghighi, Sholeh Bazrafshan, Perundurai S. Dhandapany, Sakthivel Sadayappan, Rohit R. Singh
Publikováno v:
Circulation Research. 129
Rationale: Hypertrophic cardiomyopathy (HCM) is common inheritable heart disease. HCM is highly associated with arrhythmias and/or sudden death. Studies show that molecular defects in calcium handling impairing the cardiomyocyte contractility is a pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6524c39284f820d9c6c918c201b49ce6
https://doi.org/10.1161/res.129.suppl_1.p348
https://doi.org/10.1161/res.129.suppl_1.p348
Autor:
Mathieu, Boniol, Bayan, Hosseini, Ivan, Ivanov, Bálint, Náfrádi, Maria, Neira, Ann, Olsson, Felix, Onyije, Frank, Pega, Joaquim Pintado Nunes, Annette, Prüss-Üstün, Mary, Schubauer-Berigan, Joachim, Schüz, Yuka, Ujita, Maria Leon-Roux, Emilie van Deventer., Natalie, Momen, Balázs, Ádám, Ojochide, Akagwu, Issaka, Akparibo, Rami Al Rifai, Sholeh, Bazrafshan, Bravo, Giulia, Gobba, Fabriziomaria, Adele, Green, Sanja, Kezic, Tom, Loney, Modenese, Alberto, Marilia, Paulo, Cheryl, Peters, Thomas, Tenkate, David, Whiteman, Marc, Wittlich, Swen, John
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3674::f34d4d15d2a969428aa6acfd82751bab
https://hdl.handle.net/11380/1257118
https://hdl.handle.net/11380/1257118
Autor:
Mohammed, Arif, Pooneh, Nabavizadeh, Taejeong, Song, Darshini, Desai, Rohit, Singh, Sholeh, Bazrafshan, Mohit, Kumar, Yigang, Wang, Richard J, Gilbert, Perundurai S, Dhandapany, Richard C, Becker, Evangelia G, Kranias, Sakthivel, Sadayappan
Publikováno v:
Biophys Rev
Hypertrophic cardiomyopathy (HCM) is a cardiac genetic disease characterized by ventricular enlargement, diastolic dysfunction, and increased risk for sudden cardiac death. Sarcomeric genetic defects are the predominant known cause of HCM. In particu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4bda69546e91553cc3f5919bf155263f
https://pubmed.ncbi.nlm.nih.gov/32656747
https://pubmed.ncbi.nlm.nih.gov/32656747
Autor:
Sakthivel Sadayappan, Hani Kushlaf, Mashhood Kakroo, John G. Quinlan, Sholeh Bazrafshan, Richard C. Becker
Publikováno v:
Cells
Cells, Vol 10, Iss 349, p 349 (2021)
Volume 10
Issue 2
Cells, Vol 10, Iss 349, p 349 (2021)
Volume 10
Issue 2
Novel genetic variants exist in patients with hereditary neuromuscular disorders (NMD), including muscular dystrophy. These patients also develop cardiac manifestations. However, the association between these gene variants and cardiac abnormalities i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e372ae51e97d319d659d89e70077aec
https://doi.org/10.3390/cells10020349
https://doi.org/10.3390/cells10020349
Autor:
Ghamartaj, Khanbabaee, Mehrnoosh, Hassas Yeganeh, Seyed Ahmad, Tabatabaei, Alireza, Khatami, Sholeh, Bazrafshan, Nima, Rezaei
Publikováno v:
The Turkish journal of pediatrics. 52(6)
Langerhans cell histiocytosis (LCH) is a rare disorder of Langerhans cell with unknown etiology, which can uncommonly be associated with pneumothorax. A 14-month-old female is presented here who was referred to our center due to acute respiratory dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::42254594a69a6596aee5b066c8a0ad54
https://pubmed.ncbi.nlm.nih.gov/21428197
https://pubmed.ncbi.nlm.nih.gov/21428197
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