Zobrazeno 1 - 10
of 93
pro vyhledávání: '"WILLIAM J. GROH"'
Autor:
Elizabeth M. McNally, Douglas L. Mann, Yigal Pinto, Deepak Bhakta, Gordon Tomaselli, Saman Nazarian, William J. Groh, Takuhisa Tamura, Denis Duboc, Hideki Itoh, Leah Hellerstein, Pradeep P. A. Mammen
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 9, Iss 4 (2020)
Abstract Myotonic dystrophy is an inherited systemic disorder affecting skeletal muscle and the heart. Genetic testing for myotonic dystrophy is diagnostic and identifies those at risk for cardiac complications. The 2 major genetic forms of myotonic
Externí odkaz:
https://doaj.org/article/d0d42e502cd741a8a36287c7ec5cd3e7
Autor:
Patrícia B S Celestino-Soper, Anisiia Doytchinova, Hillel A Steiner, Andrea Uradu, Ty C Lynnes, William J Groh, John M Miller, Hai Lin, Hongyu Gao, Zhiping Wang, Yunlong Liu, Peng-Sheng Chen, Matteo Vatta
Publikováno v:
PLoS ONE, Vol 11, Iss 1, p e0147455 (2016)
Externí odkaz:
https://doaj.org/article/da04ac1d6e57448db5b41ba7666a648d
Autor:
Patrícia B S Celestino-Soper, Anisiia Doytchinova, Hillel A Steiner, Andrea Uradu, Ty C Lynnes, William J Groh, John M Miller, Hai Lin, Hongyu Gao, Zhiping Wang, Yunlong Liu, Peng-Sheng Chen, Matteo Vatta
Publikováno v:
PLoS ONE, Vol 10, Iss 12, p e0143588 (2015)
BACKGROUND:The etiology of conduction disturbances necessitating permanent pacemaker (PPM) implantation is often unknown, although familial aggregation of PPM (faPPM) suggests a possible genetic basis. We developed a pan-cardiovascular next generatio
Externí odkaz:
https://doaj.org/article/671e576e314343f9af53efa7ab3c57d5
Autor:
Yigal M. Pinto, Hideki Itoh, Gordon F. Tomaselli, Pradeep P.A. Mammen, Douglas L. Mann, Saman Nazarian, Denis Duboc, Leah Hellerstein, Deepak Bhakta, Elizabeth M. McNally, Takuhisa Tamura, William J. Groh
Publikováno v:
Journal of the American Heart Association, 9(4):e014006. Wiley-Blackwell
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Abstract Myotonic dystrophy is an inherited systemic disorder affecting skeletal muscle and the heart. Genetic testing for myotonic dystrophy is diagnostic and identifies those at risk for cardiac complications. The 2 major genetic forms of myotonic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfcfd8431cb3de580ab91ccda3247897
https://pure.amc.nl/en/publications/clinical-care-recommendations-for-cardiologists-treating-adults-with-myotonic-dystrophy(7578cccb-db89-4f28-aadc-e53c975ffdee).html
https://pure.amc.nl/en/publications/clinical-care-recommendations-for-cardiologists-treating-adults-with-myotonic-dystrophy(7578cccb-db89-4f28-aadc-e53c975ffdee).html
Autor:
William J. Groh, Deepak Bhakta
Publikováno v:
JACC: Clinical Electrophysiology. 7:1624
Autor:
Valeria A. Sansone, Marla B. Ferschl, Elisa De Mattia, John W. Day, Anne-Berit Ekström, Gordon F. Tomaselli, James E. Hilbert, Todd Goodglick, Tetsuo Ashizawa, Laurie Gutmann, Ericka Simpson, Nicholas E. Johnson, Linda Nguyen, S. H. Subramony, Laurie Sterling, Nathalie Angeard, Marie Kierkegaard, Belen Esparis, Careniña Trujillo, Baziel G.M. van Engelen, Benedikt Schoser, William J. Groh, Tina Duong, Edith H. C. Cup, Elisabetta Roma, Wilma J. Koopman, Shannon L. Venance, Venessa Holland, Kiera Berggren, Janice L.B. Byrne, Ann Broderick, Guillaume Bassez, Daphne Maas, Saman Nazarian, Kari Lane, Chad Heatwole, Peg Nopoulos, Giovanni Meola, Jacinda B. Sampson, Cuixia Tian, Aparajitha Verma, Louis Richer, Marco Bozzali, Subha Raman, Richard T. Moxley, Jack Puymirat, Shahinaz M. Gadalla, Cynthia Gagnon, Katherine D. Mathews, Stefan Winblad, Katy Eichinger, Craig Campbell, Benjamin Gallais, Jeffrey Statland, Richard E. Petty, David J. Moser, Deepak Bhakta, Shree Pandya, Denis Duboc, Chris Turner, Ami Mankodi, Janel Phetteplace, Darren G. Monckton, Molly White, Bruno Eymard, Mark T. Rogers
Publikováno v:
Paediatrics Publications
Neurology. Clinical Practice, 8, 6, pp. 507-520
Neurology: Clinical Practice
Neurology: Clinical Practice, 2018, 8 (6), pp.507-520. ⟨10.1212/CPJ.0000000000000531⟩
Neurology. Clinical Practice, 8, 507-520
Neurology. Clinical Practice, 8, 6, pp. 507-520
Neurology: Clinical Practice
Neurology: Clinical Practice, 2018, 8 (6), pp.507-520. ⟨10.1212/CPJ.0000000000000531⟩
Neurology. Clinical Practice, 8, 507-520
Purpose of review: Myotonic dystrophy type 1 (DM1) is a severe, progressive genetic disease that affects between 1 in 3,000 and 8,000 individuals globally. No evidence-based guideline exists to inform the care of these patients, and most do not have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aee3d1ad9bb57439767406ba7ad93787
https://ir.lib.uwo.ca/paedpub/202
https://ir.lib.uwo.ca/paedpub/202
Autor:
William J. Groh, Archana Rajdev
Publikováno v:
Cardiac Electrophysiology Clinics. 7:303-308
In patients with muscular dystrophies, cardiac involvement leading to cardiomyopathy and arrhythmias occur with variable prevalence mirroring the phenotypic variability seen among and within the various hereditary myopathies. These patients are at ri
Autor:
William J. Groh
Publikováno v:
Heart Rhythm. 15:969-970
Autor:
Hicham El Masry, Melvin M. Scheinman, Anil V. Yadav, William J. Groh, Nassir F. Marrouche, John M. Miller, Yanfei Yang, Nitish Badhwar, Barbara J. Drew, Babak Nazer, Andrea Natale
Publikováno v:
JACC. Clinical electrophysiology. 3(7)
Objectives This study sought to determine the ability of conventional electrocardiographic (ECG) criteria to correctly differentiate idiopathic ventricular tachycardia (VT) from supraventricular tachycardia (SVT) with aberrancy. Background Previously
Autor:
William J. Groh
Publikováno v:
Heart Rhythm. 9:1890-1895
The muscular dystrophies are a group of inherited diseases affecting skeletal muscle that also affect cardiac muscle. Cardiac involvement occurs as a degenerative process with fibrosis and fatty replacement of the myocardium. Electrophysiologists are