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	161.	Large SGCE deletion contributes to Taiwanese myoclonus-dystonia syndrome. [electronic resource] by Huang, Chia-Ling Lan, Min-Yu Chang, Yung-Yee Hsu, Chia-Yu Lai, Szu-Chia Chen, Rou-Shayn Chang, Hsiu-Chen Lu, Chin-Song Wu-Chou, Yah-Huei Producer: 20110210 In: Parkinsonism & related disorders vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	162.	Twenty years on: Myoclonus-dystonia and ε-sarcoglycan - neurodevelopment, channel, and signaling dysfunction. [electronic resource] by Menozzi, Elisa Balint, Bettina Latorre, Anna Valente, Enza Maria Rothwell, John C Bhatia, Kailash P Producer: 20200708 In: Movement disorders : official journal of the Movement Disorder Society vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	163.	Analysis on sarcoglycans expression as markers of septic cardiomyopathy in sepsis-related death. [electronic resource] by Ventura Spagnolo, Elvira Mondello, Cristina Di Mauro, Debora Vermiglio, Giovanna Asmundo, Alessio Filippini, Elena Alibrandi, Angela Rizzo, Giuseppina Producer: 20181031 In: International journal of legal medicine vol. 132 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	164.	alpha-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutations. [electronic resource] by Duggan, D J Fanin, M Pegoraro, E Angelini, C Hoffman, E P Producer: 19970103 In: Journal of the neurological sciences vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	165.	Genetic background influences muscular dystrophy. [electronic resource] by Heydemann, Ahlke Huber, Jill M Demonbreun, Alexis Hadhazy, Michele McNally, Elizabeth M Producer: 20051121 In: Neuromuscular disorders : NMD vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	166.	Prominent psychiatric comorbidity in the dominantly inherited movement disorder myoclonus-dystonia. [electronic resource] by Weissbach, Anne Kasten, Meike Grünewald, Anne Brüggemann, Norbert Trillenberg, Peter Klein, Christine Hagenah, Johann Producer: 20130906 In: Parkinsonism & related disorders vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	167.	Impaired saccadic adaptation in DYT11 dystonia. [electronic resource] by Hubsch, Cécile Vidailhet, Marie Rivaud-Péchoux, Sophie Pouget, Pierre Brochard, Vanessa Degos, Bertrand Pélisson, Denis Golmard, Jean-Louis Gaymard, Bertrand Roze, Emmanuel Producer: 20111031 In: Journal of neurology, neurosurgery, and psychiatry vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	168.	Ultrastructural localization of alpha-, beta- and gamma-sarcoglycan and their mutual relation, and their relation to dystrophin, beta-dystroglycan and beta-spectrin in normal skeletal myofiber. [electronic resource] by Wakayama, Y Inoue, M Kojima, H Murahashi, M Shibuya, S Jimi, T Hara, H Oniki, H Producer: 19990630 In: Acta neuropathologica vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	169.	Epsilon-sarcoglycan compensates for lack of alpha-sarcoglycan in a mouse model of limb-girdle muscular dystrophy. [electronic resource] by Imamura, Michihiro Mochizuki, Yasushi Engvall, Eva Takeda, Shin'ichi Producer: 20050728 In: Human molecular genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	170.	Combined deficiency of alpha and epsilon sarcoglycan disrupts the cardiac dystrophin complex. [electronic resource] by Lancioni, Alessio Rotundo, Ida Luisa Kobayashi, Yvonne Monique D'Orsi, Luca Aurino, Stefania Nigro, Gerardo Piluso, Giulio Acampora, Dario Cacciottolo, Mafalda Campbell, Kevin P Nigro, Vincenzo Producer: 20120222 In: Human molecular genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	171.	A novel SGCE gene mutation causing myoclonus dystonia in a family with an unusual phenotype. [electronic resource] by Tedroff, Kristina Rolfs, Arndt Norling, Andreas Producer: 20120416 In: Acta paediatrica (Oslo, Norway : 1992) vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	172.	[A novel missense mutation in the alpha-sarcoglycan gene in a Spanish family with muscular dystrophy]. [electronic resource] by Pinel-González, Ana Montero-Escribano, Paloma Aladro, Yolanda Gil-Fournier, Belén Ramiro-León, Soraya Producer: 20131230 In: Revista de neurologia vol. 56 Availability: No items available. Save to lists Add to cart (remove)
	173.	Familial 7q21.3 microdeletion involving epsilon-sarcoglycan causing myoclonus dystonia, cognitive impairment, and psychosis. [electronic resource] by Dale, Russell C Nasti, Julian J Peters, Greg B Producer: 20111208 In: Movement disorders : official journal of the Movement Disorder Society vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	174.	Finding the sweet spot: assembly and glycosylation of the dystrophin-associated glycoprotein complex. [electronic resource] by Townsend, Dewayne Producer: 20150423 In: Anatomical record (Hoboken, N.J. : 2007) vol. 297 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	175.	[Muscular dystrophy due to a deficit of gamma-sarcoglycan. A report of three patients with the Delta-521t mutation]. [electronic resource] by Eirís-Puñal, J Pintos-Martínez, E Lasa, A Gallano, P Castro-Gago, M Producer: 20021108 In: Revista de neurologia vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	176.	A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies. [electronic resource] by Moreira, E S Vainzof, M Marie, S K Nigro, V Zatz, M Passos-Bueno, M R Producer: 19990204 In: Journal of medical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	177.	Earlier onset of motor deficits in mice with double mutations in Dyt1 and Sgce. [electronic resource] by Yokoi, Fumiaki Yang, Guang Li, Jindong DeAndrade, Mark P Zhou, Tong Li, Yuqing Producer: 20110209 In: Journal of biochemistry vol. 148 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	178.	Molecular and cell biology of the sarcoglycan complex. [electronic resource] by Ozawa, Eijiro Mizuno, Yuji Hagiwara, Yasuko Sasaoka, Toshikuni Yoshida, Mikiharu Producer: 20051206 In: Muscle & nerve vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	179.	Age-related changes in dystrophin-glycoprotein complex and in utrophin are not correlated with intrinsic laryngeal muscles protection in mdx mice. [electronic resource] by Ferretti, Renato Pertille, Adriana Santo Neto, Humberto Marques, Maria Julia Producer: 20120109 In: Muscle & nerve vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	180.	[Clinicopathological characteristics and molecular genetics of adhalin deficiency (severe childhood autosomal recessive muscular dystrophy/SCARMD)]. [electronic resource] by Matsumura, K Producer: 19980324 In: Nihon rinsho. Japanese journal of clinical medicine vol. 55 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 798 results.