Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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21 |
Material Type: Artigo
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Autonomic, locomotor and cardiac abnormalities in a mouse model of muscular dystrophy: targeting the renin–angiotensin systemSabharwal, Rasna ; Chapleau, Mark W.Experimental physiology, 2014-04, Vol.99 (4), p.627-631 [Periódico revisado por pares]England: John Wiley & Sons, IncTexto completo disponível |
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22 |
Material Type: Artigo
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A Drosophila model of oculopharyngeal muscular dystrophy reveals intrinsic toxicity of PABPN1Chartier, Aymeric ; Benoit, Béatrice ; Simonelig, MartineThe EMBO journal, 2006-05, Vol.25 (10), p.2253-2262 [Periódico revisado por pares]Chichester, UK: John Wiley & Sons, LtdTexto completo disponível |
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23 |
Material Type: Artigo
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Sarcolemmopathy: Muscular Dystrophies with Cell Membrane DefectsOzawa, Eijiro ; Nishino, Ichizo ; Nonaka, IkuyaBrain pathology (Zurich, Switzerland), 2001-04, Vol.11 (2), p.218-230 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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24 |
Material Type: Artigo
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HIF Activation and VEGF Overexpression are Coupled with ZO-1 Up-phosphorylation in the Brain of Dystrophic MDX MouseNico, Beatrice ; Mangieri, Domenica ; Crivellato, Enrico ; Longo, Vito ; De Giorgis, Michela ; Capobianco, Carmen ; Corsi, Patrizia ; Benagiano, Vincenzo ; Roncali, Luisa ; Ribatti, DomenicoBrain pathology (Zurich, Switzerland), 2007-10, Vol.17 (4), p.399-406 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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25 |
Material Type: Artigo
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9 YEAR OLD GIRL WITH PROGRESSIVE WEAKNESSSeemann, Natashia ; Campbell, Craig ; Hammond, Robert ; Prasad, ChitraBrain pathology (Zurich, Switzerland), 2010-01, Vol.20 (1), p.255-256 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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26 |
Material Type: Artigo
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Non-sarcolemmal Muscular DystrophiesBrown, Susan C. ; Muntoni, Francesco ; Sewry, Caroline A.Brain pathology (Zurich, Switzerland), 2001-04, Vol.11 (2), p.193-205 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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27 |
Material Type: Artigo
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Gene diagnosis of Oculopharyngeal muscular dystrophy in a Chinese family by a genescan methodYou, Pan ; Ma, Qilin ; Tao, TaoJournal of clinical laboratory analysis, 2010, Vol.24 (6), p.422-425 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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28 |
Material Type: Artigo
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Gene diagnosis for nine Chinese patients with DMD/BMD by multiplex ligation-dependent probe amplification and prenatal diagnosis for one of themWu, Yupeng ; Yin, Gengxin ; Fu, Keqin ; Wu, De ; Zhai, Qian ; Du, Huarong ; Huang, Zhongjun ; Niu, YuhuaJournal of clinical laboratory analysis, 2009, Vol.23 (6), p.380-386 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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29 |
Material Type: Artigo
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Introduction: Recent Advances in Hereditary Neuromuscular Diseases of ChildhoodBornemann, Antje ; Goebel, Hans H.Brain pathology (Zurich, Switzerland), 2001-04, Vol.11 (2), p.190-192 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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30 |
Material Type: Artigo
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Myofiber Degeneration in Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (AD-EDMD) (LGMD1B)Mittelbronn, Michel ; Hanisch, Frank ; Gleichmann, Marc ; Stötter, Mechthild ; Korinthenberg, Rudolf ; Wehnert, Manfred ; Bonne, Gisèle ; Rudnik-Schöneborn, Sabine ; Bornemann, AntjeBrain pathology (Zurich, Switzerland), 2006-10, Vol.16 (4), p.266-272 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |