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Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel function. [electronic resource] by
- Lehnart, Stephan E
- Ackerman, Michael J
- Benson, D Woodrow
- Brugada, Ramon
- Clancy, Colleen E
- Donahue, J Kevin
- George, Alfred L
- Grant, Augustus O
- Groft, Stephen C
- January, Craig T
- Lathrop, David A
- Lederer, W Jonathan
- Makielski, Jonathan C
- Mohler, Peter J
- Moss, Arthur
- Nerbonne, Jeanne M
- Olson, Timothy M
- Przywara, Dennis A
- Towbin, Jeffrey A
- Wang, Lan-Hsiang
- Marks, Andrew R
Producer: 20071218
In:
Circulation vol. 116
Availability: No items available.
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Multidisciplinary study of a new ClC-1 mutation causing myotonia congenita: a paradigm to understand and treat ion channelopathies. [electronic resource] by
- Imbrici, Paola
- Altamura, Concetta
- Camerino, Giulia Maria
- Mangiatordi, Giuseppe Felice
- Conte, Elena
- Maggi, Lorenzo
- Brugnoni, Raffaella
- Musaraj, Kejla
- Caloiero, Roberta
- Alberga, Domenico
- Marsano, Renè Massimiliano
- Ricci, Giulia
- Siciliano, Gabriele
- Nicolotti, Orazio
- Mora, Marina
- Bernasconi, Pia
- Desaphy, Jean-Francois
- Mantegazza, Renato
- Camerino, Diana Conte
Producer: 20170908
In:
FASEB journal : official publication of the Federation of American Societies for Experimental Biology vol. 30
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318.
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Low clinical penetrance in causal mutation carriers for cardiac channelopathies. [electronic resource] by
- Jiménez-Jáimez, Juan
- Álvarez, Miguel
- Algarra, María
- Macías Ruíz, Rosa
- Peñas, Rocío
- Valverde, Francisca
- Tortajada, Gustavo
- Lorente, Jose Antonio
- Melgares, Rafael
- Tercedor, Luis
Producer: 20150706
In:
Revista espanola de cardiologia (English ed.) vol. 66
Availability: No items available.
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