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	201.	A Korean family with Arg1448Cys mutation of SCN4A channel causing paramyotonia congenita: electrophysiologic, histopathologic, and molecular genetic studies. [electronic resource] by Kim, Dae-Seong Kim, Eun-Joo Jung, Dae-Soo Park, Kyu-Hyun Kim, In-Joo Kwak, Ki-Young Kim, Cheol-Min Ko, Hyun-Yoon Producer: 20030625 In: Journal of Korean medical science vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	202.	Muscle Na+ channelopathies: MRI detects intracellular 23Na accumulation during episodic weakness. [electronic resource] by Weber, M-A Nielles-Vallespin, S Essig, M Jurkat-Rott, K Kauczor, H-U Lehmann-Horn, F Producer: 20061108 In: Neurology vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	203.	Myotonia congenita and myotonic dystrophy in the same family: coexistence of a CLCN1 mutation and expansion in the CNBP (ZNF9) gene. [electronic resource] by Sun, C Van Ghelue, M Tranebjærg, L Thyssen, F Nilssen, Ø Torbergsen, T Producer: 20120216 In: Clinical genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	204.	Does quantitative EMG differ myotonic dystrophy type 2 and type 1? [electronic resource] by Szmidt-Salkowska, Elzbieta Gawel, Malgorzata Lusakowska, Anna Nojszewska, Monika Lipowska, Marta Sulek, Anna Krysa, Wioletta Rajkiewicz, Marta Seroka, Andrzej Kaminska, Anna M Producer: 20141103 In: Journal of electromyography and kinesiology : official journal of the International Society of Electrophysiological Kinesiology vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	205.	3D radial projection technique with ultrashort echo times for sodium MRI: clinical applications in human brain and skeletal muscle. [electronic resource] by Nielles-Vallespin, Sònia Weber, Marc-André Bock, Michael Bongers, André Speier, Peter Combs, Stephanie E Wöhrle, Johannes Lehmann-Horn, Frank Essig, Marco Schad, Lothar R Producer: 20070302 In: Magnetic resonance in medicine vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	206.	Preferred mexiletine block of human sodium channels with IVS4 mutations and its pH-dependence. [electronic resource] by Mohammadi, Bahram Jurkat-Rott, Karin Alekov, Alexi Dengler, Reinhard Bufler, Johannes Lehmann-Horn, Frank Producer: 20050913 In: Pharmacogenetics and genomics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	207.	Slow inactivation: slow but not dull. [electronic resource] by Ruff, Robert L Producer: 20080403 In: Neurology vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	208.	[Paramyotonia congenita caused by a novel mutation of SCN4A gene in a Chinese family]. [electronic resource] by Li, Wen Chen, Qianting Zhang, Qianjun Li, Xiurong Du, Juan Producer: 20160630 In: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	209.	Proximal myopathy and diffuse white matter involvement in myotonic dystrophy type I. [electronic resource] by Uluc, Kayihan Arsava, E Murat Erdem, Sevim Tan, Ersin Producer: 20020809 In: Journal of neurology vol. 249 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	210.	Temperature-sensitive defects in paramyotonia congenita mutants R1448C and T1313M. [electronic resource] by Dice, Margaret S Abbruzzese, Jennifer L Wheeler, James T Groome, James R Fujimoto, Esther Ruben, Peter C Producer: 20040921 In: Muscle & nerve vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	211.	Comparative transcriptional and biochemical studies in muscle of myotonic dystrophies (DM1 and DM2). [electronic resource] by Salvatori, Sergio Furlan, Sandra Fanin, Marina Picard, Anne Pastorello, Ebe Romeo, Vincenzo Trevisan, Carlo Pietro Angelini, Corrado Producer: 20090914 In: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	212.	Primary periodic paralyses. [electronic resource] by Finsterer, J Producer: 20080304 In: Acta neurologica Scandinavica vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	213.	Diagnosis of pediatric neuromuscular disorders in the era of DNA analysis. [electronic resource] by Darras, B T Jones, H R Producer: 20001220 In: Pediatric neurology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	214.	The myotonias and susceptibility to malignant hyperthermia. [electronic resource] by Parness, Jerome Bandschapp, Oliver Girard, Thierry Producer: 20091001 In: Anesthesia and analgesia vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	215.	Differential effects of paramyotonia congenita mutations F1473S and F1705I on sodium channel gating. [electronic resource] by Groome, James R Larsen, Matthew F Coonts, Allyson Producer: 20081112 In: Channels (Austin, Tex.) vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	216.	Expression and distribution of a small-conductance calcium-activated potassium channel (SK3) protein in skeletal muscles from myotonic muscular dystrophy patients and congenital myotonic mice. [electronic resource] by Kimura, Takashi Takahashi, Masanori P Fujimura, Harutoshi Sakoda, Saburo Producer: 20030818 In: Neuroscience letters vol. 347 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	217.	Paramyotonia congenita due to a de novo mutation: a case report. [electronic resource] by Fukudome, Takayasu Izumoto, Hajime Goto, Hirofumi Matsuo, Hidenori Yoshimura, Toshiro Sakoda, Shun-Ichi Shibuya, Noritoshi Producer: 20030822 In: Muscle & nerve vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	218.	Functional characterization and cold sensitivity of T1313A, a new mutation of the skeletal muscle sodium channel causing paramyotonia congenita in humans. [electronic resource] by Bouhours, Magali Sternberg, Damien Davoine, Claire-Sophie Ferrer, Xavier Willer, Jean Claude Fontaine, Bertrand Tabti, Nacira Producer: 20041116 In: The Journal of physiology vol. 554 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	219.	Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2. [electronic resource] by Cardani, Rosanna Giagnacovo, Marzia Botta, Annalisa Rinaldi, Fabrizio Morgante, Alessandra Udd, Bjarne Raheem, Olayinka Penttilä, Sini Suominen, Tiina Renna, Laura V Sansone, Valeria Bugiardini, Enrico Novelli, Giuseppe Meola, Giovanni Producer: 20130620 In: Journal of neurology vol. 259 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	220.	Restless legs syndrome and daytime sleepiness are prominent in myotonic dystrophy type 2. [electronic resource] by Lam, Erek M Shepard, Paul W St Louis, Erik K Dueffert, Lucas G Slocumb, Nancy McCarter, Stuart J Silber, Michael H Boeve, Bradley F Olson, Eric J Somers, Virend K Milone, Margherita Producer: 20130917 In: Neurology vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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