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	261.	Three family members with elevated plasma cobalamin, transcobalamin and soluble transcobalamin receptor (sCD320). [electronic resource] by Hoffmann-Lücke, Elke Arendt, Johan F B Nissen, Peter H Mikkelsen, Gustav Aasly, Jan O Nexo, Ebba Producer: 20130905 In: Clinical chemistry and laboratory medicine vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	262.	Reduced muscle-fiber conduction but normal slowing after cold exposure in paramyotonia congenita. [electronic resource] by Blijham, Paul J Drost, Gea Stegeman, Dick F Zwarts, Machiel J Producer: 20080225 In: Muscle & nerve vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	263.	The frequency and severity of cardiac involvement in myotonic dystrophy type 2 (DM2): long-term outcomes. [electronic resource] by Sansone, V A Brigonzi, E Schoser, B Villani, S Gaeta, M De Ambroggi, G Bandera, F De Ambroggi, L Meola, G Producer: 20140530 In: International journal of cardiology vol. 168 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	264.	Predictors of atrio-ventricular conduction disease, long-term outcomes in patients with myotonic dystrophy types I and II. [electronic resource] by Ha, Andrew H Tarnopolsky, Mark A Bergstra, T Graham Nair, Girish M Al-Qubbany, Atif Healey, Jeff S Producer: 20130401 In: Pacing and clinical electrophysiology : PACE vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	265.	Cold-induced defects of sodium channel gating in atypical periodic paralysis plus myotonia. [electronic resource] by Webb, Jadon Cannon, Stephen C Producer: 20080403 In: Neurology vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	266.	Splicing biomarkers of disease severity in myotonic dystrophy. [electronic resource] by Nakamori, Masayuki Sobczak, Krzysztof Puwanant, Araya Welle, Steve Eichinger, Katy Pandya, Shree Dekdebrun, Jeannne Heatwole, Chad R McDermott, Michael P Chen, Tian Cline, Melissa Tawil, Rabi Osborne, Robert J Wheeler, Thurman M Swanson, Maurice S Moxley, Richard T Thornton, Charles A Producer: 20140318 In: Annals of neurology vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	267.	Efficacy of propafenone in paramyotonia congenita. [electronic resource] by Alfonsi, E Merlo, I M Tonini, M Ravaglia, S Brugnoni, R Gozzini, A Moglia, A Producer: 20070425 In: Neurology vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	268.	Muscle ultrasound measurements and functional muscle parameters in non-dystrophic myotonias suggest structural muscle changes. [electronic resource] by Trip, J Pillen, S Faber, C G van Engelen, B G M Zwarts, M J Drost, G Producer: 20091015 In: Neuromuscular disorders : NMD vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	269.	Alternative splicing of human insulin receptor gene (INSR) in type I and type II skeletal muscle fibers of patients with myotonic dystrophy type 1 and type 2. [electronic resource] by Santoro, Massimo Masciullo, Marcella Bonvissuto, Davide Bianchi, Maria Laura Ester Michetti, Fabrizio Silvestri, Gabriella Producer: 20140207 In: Molecular and cellular biochemistry vol. 380 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	270.	A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24. [electronic resource] by Le Ber, Isabelle Martinez, Maria Campion, Dominique Laquerrière, Annie Bétard, Christine Bassez, Guillaume Girard, Carol Saugier-Veber, Pascale Raux, Gregory Sergeant, Nicolas Magnier, Patrick Maisonobe, Thierry Eymard, Bruno Duyckaerts, Charles Delacourte, André Frebourg, Thierry Hannequin, Didier Producer: 20041015 In: Brain : a journal of neurology vol. 127 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	271.	[Molecular and genetic aspects of the myotonic conditions]. [electronic resource] by Morales Montero, F Cuenca Berger, P Producer: 20040723 In: Revista de neurologia vol. 38 Availability: No items available. Save to lists Add to cart (remove)
	272.	Prevalence study of genetically defined skeletal muscle channelopathies in England. [electronic resource] by Horga, Alejandro Raja Rayan, Dipa L Matthews, Emma Sud, Richa Fialho, Doreen Durran, Siobhan C M Burge, James A Portaro, Simona Davis, Mary B Haworth, Andrea Hanna, Michael G Producer: 20130611 In: Neurology vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	273.	Absence of a differentiation defect in muscle satellite cells from DM2 patients. [electronic resource] by Pelletier, Richard Hamel, Frederic Beaulieu, Daniel Patry, Lysanne Haineault, Caroline Tarnopolsky, Mark Schoser, Benedikt Puymirat, Jack Producer: 20091207 In: Neurobiology of disease vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	274.	A new case of autosomal dominant myotonia associated with the V1589M missense mutation in the muscle sodium channel gene and its phenotypic classification. [electronic resource] by Ferriby, D Stojkovic, T Sternberg, D Hurtevent, J-F Hurtevent, J-P Vermersch, P Producer: 20060809 In: Neuromuscular disorders : NMD vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	275.	Guidelines on clinical presentation and management of nondystrophic myotonias. [electronic resource] by Stunnenberg, Bas C LoRusso, Samantha Arnold, W David Barohn, Richard J Cannon, Stephen C Fontaine, Bertrand Griggs, Robert C Hanna, Michael G Matthews, Emma Meola, Giovanni Sansone, Valeria A Trivedi, Jaya R van Engelen, Baziel G M Vicart, Savine Statland, Jeffrey M Producer: 20201123 In: Muscle & nerve vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	276.	New potent mexiletine and tocainide analogues evaluated in vivo and in vitro as antimyotonic agents on the myotonic ADR mouse. [electronic resource] by De Luca, Annamaria Pierno, Sabata Liantonio, Antonella Desaphy, Jean-François Natuzzi, Fedele Didonna, Maria Paola Ferrannini, Ermanno Jockusch, Harald Franchini, Carlo Lentini, Giovanni Corbo, Filomena Tortorella, Vincenzo Camerino, Diana Conte Producer: 20040913 In: Neuromuscular disorders : NMD vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	277.	Activation of the innate immune response and interferon signalling in myotonic dystrophy type 1 and type 2 cataracts. [electronic resource] by Rhodes, Jeremy D Lott, Martin C Russell, Sarah L Moulton, Vincent Sanderson, Julie Wormstone, I Michael Broadway, David C Producer: 20120709 In: Human molecular genetics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	278.	Muscle weakness in myotonic dystrophy associated with misregulated splicing and altered gating of Ca(V)1.1 calcium channel. [electronic resource] by Tang, Zhen Zhi Yarotskyy, Viktor Wei, Lan Sobczak, Krzysztof Nakamori, Masayuki Eichinger, Katy Moxley, Richard T Dirksen, Robert T Thornton, Charles A Producer: 20120807 In: Human molecular genetics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	279.	[Recommendations of good practices for the genetic diagnosis of myotonic dystrophy. Grupo AEGH/CIBERER]. [electronic resource] by Garcia Planells, Javier Molano, Jesús Borrego, Salud Producer: 20110913 In: Medicina clinica vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	280.	New mutation of the Na channel in the severe form of potassium-aggravated myotonia. [electronic resource] by Kubota, Tomoya Kinoshita, Masanobu Sasaki, Ryogen Aoike, Futoshi Takahashi, Masanori P Sakoda, Saburo Hirose, Kazuhiko Producer: 20090609 In: Muscle & nerve vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 280 results.