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'Gardos Channelopathy': a variant of hereditary Stomatocytosis with complex molecular regulation. [electronic resource] by
- Fermo, Elisa
- Bogdanova, Anna
- Petkova-Kirova, Polina
- Zaninoni, Anna
- Marcello, Anna Paola
- Makhro, Asya
- Hänggi, Pascal
- Hertz, Laura
- Danielczok, Jens
- Vercellati, Cristina
- Mirra, Nadia
- Zanella, Alberto
- Cortelezzi, Agostino
- Barcellini, Wilma
- Kaestner, Lars
- Bianchi, Paola
Producer: 20181211
In:
Scientific reports vol. 7
Availability: No items available.
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586.
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587.
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A common co-morbidity modulates disease expression and treatment efficacy in inherited cardiac sodium channelopathy. [electronic resource] by
- Rivaud, Mathilde R
- Jansen, John A
- Postema, Pieter G
- Nannenberg, Eline A
- Mizusawa, Yuka
- van der Nagel, Roel
- Wolswinkel, Rianne
- van der Made, Ingeborg
- Marchal, Gerard A
- Rajamani, Sridharan
- Belardinelli, Luiz
- van Tintelen, J Peter
- Tanck, Michael W T
- van der Wal, Allard C
- de Bakker, Jacques M T
- van Rijen, Harold V
- Creemers, Esther E
- Wilde, Arthur A M
- van den Berg, Maarten P
- van Veen, Toon A B
- Bezzina, Connie R
- Remme, Carol Ann
Producer: 20191125
In:
European heart journal vol. 39
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588.
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589.
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590.
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Genetically determined differences in sodium current characteristics modulate conduction disease severity in mice with cardiac sodium channelopathy. [electronic resource] by
- Remme, Carol Ann
- Scicluna, Brendon P
- Verkerk, Arie O
- Amin, Ahmad S
- van Brunschot, Sandra
- Beekman, Leander
- Deneer, Vera H M
- Chevalier, Catherine
- Oyama, Fumitaka
- Miyazaki, Haruko
- Nukina, Nobuyuki
- Wilders, Ronald
- Escande, Denis
- Houlgatte, Rémi
- Wilde, Arthur A M
- Tan, Hanno L
- Veldkamp, Marieke W
- de Bakker, Jacques M T
- Bezzina, Connie R
Producer: 20090708
In:
Circulation research vol. 104
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591.
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592.
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A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies. [electronic resource] by
- Coutelier, Marie
- Coarelli, Giulia
- Monin, Marie-Lorraine
- Konop, Juliette
- Davoine, Claire-Sophie
- Tesson, Christelle
- Valter, Rémi
- Anheim, Mathieu
- Behin, Anthony
- Castelnovo, Giovanni
- Charles, Perrine
- David, Albert
- Ewenczyk, Claire
- Fradin, Mélanie
- Goizet, Cyril
- Hannequin, Didier
- Labauge, Pierre
- Riant, Florence
- Sarda, Pierre
- Sznajer, Yves
- Tison, François
- Ullmann, Urielle
- Van Maldergem, Lionel
- Mochel, Fanny
- Brice, Alexis
- Stevanin, Giovanni
- Durr, Alexandra
Producer: 20170719
In:
Brain : a journal of neurology vol. 140
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593.
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594.
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A channelopathy contributes to cerebellar dysfunction in a model of multiple sclerosis. [electronic resource] by
- Shields, Shannon D
- Cheng, Xiaoyang
- Gasser, Andreas
- Saab, Carl Y
- Tyrrell, Lynda
- Eastman, Emmanuella M
- Iwata, Masashi
- Zwinger, Pamela J
- Black, Joel A
- Dib-Hajj, Sulayman D
- Waxman, Stephen G
Producer: 20120426
In:
Annals of neurology vol. 71
Availability: No items available.
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595.
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Plan of Action for Inherited Cardiovascular Diseases: Synthesis of Recommendations and Action Algorithms. [electronic resource] by
- Barriales-Villa, Roberto
- Gimeno-Blanes, Juan Ramón
- Zorio-Grima, Esther
- Ripoll-Vera, Tomás
- Evangelista-Masip, Artur
- Moya-Mitjans, Angel
- Serratosa-Fernández, Luis
- Albert-Brotons, Dimpna C
- García-Pinilla, José Manuel
- García-Pavía, Pablo
Producer: 20170117
In:
Revista espanola de cardiologia (English ed.) vol. 69
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596.
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597.
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Prevalence and mutation spectrum of skeletal muscle channelopathies in the Netherlands. [electronic resource] by
- Stunnenberg, B C
- Raaphorst, J
- Deenen, J C W
- Links, T P
- Wilde, A A
- Verbove, D J
- Kamsteeg, E J
- van den Wijngaard, A
- Faber, C G
- van der Wilt, G J
- van Engelen, B G M
- Drost, G
- Ginjaar, H B
Producer: 20191024
In:
Neuromuscular disorders : NMD vol. 28
Availability: No items available.
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598.
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600.
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