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	301.	Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12. [electronic resource] by Azibi, K Bachner, L Beckmann, J S Matsumura, K Hamouda, E Chaouch, M Chaouch, A Ait-Ouarab, R Vignal, A Weissenbach, J Producer: 19931230 In: Human molecular genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	302.	Laminin-alpha2 (merosin), beta-dystroglycan, alpha-sarcoglycan (adhalin), and dystrophin expression in congenital muscular dystrophies: an immunohistochemical study. [electronic resource] by ter Laak, H J Leyten, Q H Gabreëls, F J Kuppen, H Renier, W O Sengers, R C Producer: 19980814 In: Clinical neurology and neurosurgery vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	303.	Smooth muscle trans-membrane sarcoglycan complex in partial bladder outlet obstruction. [electronic resource] by Macarak, Edward J Schulz, Jake Zderic, Stephen A Sado, Yoshikazu Ninomiya, Yoshifumi Polyak, Erzsebet Chacko, Samuel Howard, Pamela S Producer: 20061220 In: Histochemistry and cell biology vol. 126 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	304.	[Clinical and genetic analysis of childhood-onset myoclonus dystonia syndrome caused by SGCE variants]. [electronic resource] by Tian, X J Ding, C H Zhang, Y H Dai, L F Chen, C H Li, J W Wang, X Han, T L Wang, X H Deng, J Producer: 20200316 In: Zhonghua er ke za zhi = Chinese journal of pediatrics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	305.	Primary adhalin deficiency as a cause of muscular dystrophy in patients with normal dystrophin. [electronic resource] by Ljunggren, A Duggan, D McNally, E Boylan, K B Gama, C H Kunkel, L M Hoffman, E P Producer: 19951012 In: Annals of neurology vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	306.	Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy. [electronic resource] by Eymard, B Romero, N B Leturcq, F Piccolo, F Carrié, A Jeanpierre, M Collin, H Deburgrave, N Azibi, K Chaouch, M Merlini, L Thémar-Noël, C Penisson, I Mayer, M Tanguy, O Campbell, K P Kaplan, J C Tomé, F M Fardeau, M Producer: 19970611 In: Neurology vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	307.	Adhalin deficiency: an unusual cause of muscular dystrophy. [electronic resource] by Dua, T Kalra, V Sharma, M C Kabra, M Producer: 20020124 In: Indian journal of pediatrics vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	308.	gamma-Sarcoglycan deficiency increases cell contractility, apoptosis and MAPK pathway activation but does not affect adhesion. [electronic resource] by Griffin, Maureen A Feng, Huisheng Tewari, Manorama Acosta, Pedro Kawana, Masataka Sweeney, H Lee Discher, Dennis E Producer: 20051025 In: Journal of cell science vol. 118 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	309.	Impact of delta-sarcoglycan gene polymorphism on the occurrence of coronary spastic angina in Japanese patients with hypertrophic cardiomyopathy. [electronic resource] by Honda, Tsuyoshi Sugiyama, Seigo Sakamoto, Tomohiro Kaikita, Koichi Ogawa, Hisao Producer: 20070920 In: Circulation journal : official journal of the Japanese Circulation Society vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	310.	Delta-sarcoglycan gene polymorphism frequency in Amerindian and Mestizo populations of Mexico. [electronic resource] by Ordoñez-Razo, Rosa María Canizales-Quinteros, Samuel Rodríguez-Cruz, Maricela Peñaloza, Rosenda Minauro-Sanmiguel, Fernando Canto-Cetina, Thelma Canto, Patricia Coral-Vázquez, Ramón Salamanca-Gómez, Fabio Producer: 20100729 In: Genetic testing and molecular biomarkers vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	311.	A child with myoclonus-dystonia (DYT11) misdiagnosed as atypical opsoclonus myoclonus syndrome. [electronic resource] by Drivenes, Bergitte Born, Alfred Peter Ek, Jakob Dunoe, Morten Uldall, Peter Vilhelm Producer: 20160523 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	312.	Deep brain stimulation for myoclonus-dystonia syndrome with double mutations in DYT1 and DYT11. [electronic resource] by Wang, Jia-Wei Li, Ji-Ping Wang, Yun-Peng Zhang, Xiao-Hua Zhang, Yu-Qing Producer: 20181012 In: Scientific reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	313.	Selective defect in dystrophin-associated glycoproteins 50DAG (A2) and 35DAG (A4) in the dystrophic hamster: an animal model for severe childhood autosomal recessive muscular dystrophy (SCARMD). [electronic resource] by Yamanouchi, Y Mizuno, Y Yamamoto, H Takemitsu, M Yoshida, M Nonaka, I Ozawa, E Producer: 19940608 In: Neuromuscular disorders : NMD vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	314.	Abnormal distribution of sarcoglycan subcomplex in colonic smooth muscle cells of aganglionic bowel. [electronic resource] by Arena, Salvatore Cutroneo, Giuseppina Favaloro, Angelo Sinatra, Maria Teresa Trimarchi, Fabio Scarvaglieri, Silvia Mallamace, Agostino Arena, Francesco Anastasi, Giuseppe Di Benedetto, Vincenzo Producer: 20100412 In: International journal of molecular medicine vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	315.	Novel SGCE gene mutation in a Korean patient with myoclonus-dystonia with unique phenotype mimicking Moya-Moya disease. [electronic resource] by Chung, Eun Joo Lee, Won Yong Kim, Ji-Youn Kim, Jong-Hun Kim, Gyeong-Moon Ki, Chang Seok Kim, In-Suk Producer: 20070907 In: Movement disorders : official journal of the Movement Disorder Society vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	316.	Milder forms of α-sarcoglicanopathies diagnosed in adulthood by NGS analysis. [electronic resource] by Cantero, Diana Hernández-Laín, Aurelio Martínez, Juan Francisco Gonzalo Pérez, María Rabasa Ruano, Yolanda Lleixà, Cinta Gallardo, Eduard Domínguez-González, Cristina Producer: 20190719 In: Journal of the neurological sciences vol. 394 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	317.	A gene-edited mouse model of limb-girdle muscular dystrophy 2C for testing exon skipping. [electronic resource] by Demonbreun, Alexis R Wyatt, Eugene J Fallon, Katherine S Oosterbaan, Claire C Page, Patrick G Hadhazy, Michele Quattrocelli, Mattia Barefield, David Y McNally, Elizabeth M Producer: 20200615 In: Disease models & mechanisms vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	318.	Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation. [electronic resource] by McNally, E M Passos-Bueno, M R Bönnemann, C G Vainzof, M de Sá Moreira, E Lidov, H G Othmane, K B Denton, P H Vance, J M Zatz, M Kunkel, L M Producer: 19961211 In: American journal of human genetics vol. 59 Availability: No items available. Save to lists Add to cart (remove)
	319.	Primary structure and muscle-specific expression of the 50-kDa dystrophin-associated glycoprotein (adhalin). [electronic resource] by Roberds, S L Anderson, R D Ibraghimov-Beskrovnaya, O Campbell, K P Producer: 19931213 In: The Journal of biological chemistry vol. 268 Availability: No items available. Save to lists Add to cart (remove)
	320.	Differential expression of dystrophin, utrophin, and dystrophin-associated proteins in human muscle culture. [electronic resource] by Radojevic, V Lin, S Burgunder, J M Producer: 20001207 In: Cell and tissue research vol. 300 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 798 results.