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21
Autonomic, locomotor and cardiac abnormalities in a mouse model of muscular dystrophy: targeting the renin–angiotensin system
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Autonomic, locomotor and cardiac abnormalities in a mouse model of muscular dystrophy: targeting the renin–angiotensin system

Sabharwal, Rasna ; Chapleau, Mark W.

Experimental physiology, 2014-04, Vol.99 (4), p.627-631 [Periódico revisado por pares]

England: John Wiley & Sons, Inc

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22
A Drosophila model of oculopharyngeal muscular dystrophy reveals intrinsic toxicity of PABPN1
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A Drosophila model of oculopharyngeal muscular dystrophy reveals intrinsic toxicity of PABPN1

Chartier, Aymeric ; Benoit, Béatrice ; Simonelig, Martine

The EMBO journal, 2006-05, Vol.25 (10), p.2253-2262 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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23
Sarcolemmopathy: Muscular Dystrophies with Cell Membrane Defects
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Sarcolemmopathy: Muscular Dystrophies with Cell Membrane Defects

Ozawa, Eijiro ; Nishino, Ichizo ; Nonaka, Ikuya

Brain pathology (Zurich, Switzerland), 2001-04, Vol.11 (2), p.218-230 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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24
HIF Activation and VEGF Overexpression are Coupled with ZO-1 Up-phosphorylation in the Brain of Dystrophic MDX Mouse
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HIF Activation and VEGF Overexpression are Coupled with ZO-1 Up-phosphorylation in the Brain of Dystrophic MDX Mouse

Nico, Beatrice ; Mangieri, Domenica ; Crivellato, Enrico ; Longo, Vito ; De Giorgis, Michela ; Capobianco, Carmen ; Corsi, Patrizia ; Benagiano, Vincenzo ; Roncali, Luisa ; Ribatti, Domenico

Brain pathology (Zurich, Switzerland), 2007-10, Vol.17 (4), p.399-406 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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25
9 YEAR OLD GIRL WITH PROGRESSIVE WEAKNESS
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9 YEAR OLD GIRL WITH PROGRESSIVE WEAKNESS

Seemann, Natashia ; Campbell, Craig ; Hammond, Robert ; Prasad, Chitra

Brain pathology (Zurich, Switzerland), 2010-01, Vol.20 (1), p.255-256 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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26
Non-sarcolemmal Muscular Dystrophies
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Non-sarcolemmal Muscular Dystrophies

Brown, 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 Ltd

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27
Gene diagnosis of Oculopharyngeal muscular dystrophy in a Chinese family by a genescan method
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Gene diagnosis of Oculopharyngeal muscular dystrophy in a Chinese family by a genescan method

You, Pan ; Ma, Qilin ; Tao, Tao

Journal of clinical laboratory analysis, 2010, Vol.24 (6), p.422-425 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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28
Gene diagnosis for nine Chinese patients with DMD/BMD by multiplex ligation-dependent probe amplification and prenatal diagnosis for one of them
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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 them

Wu, Yupeng ; Yin, Gengxin ; Fu, Keqin ; Wu, De ; Zhai, Qian ; Du, Huarong ; Huang, Zhongjun ; Niu, Yuhua

Journal of clinical laboratory analysis, 2009, Vol.23 (6), p.380-386 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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29
Introduction: Recent Advances in Hereditary Neuromuscular Diseases of Childhood
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Introduction: Recent Advances in Hereditary Neuromuscular Diseases of Childhood

Bornemann, Antje ; Goebel, Hans H.

Brain pathology (Zurich, Switzerland), 2001-04, Vol.11 (2), p.190-192 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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30
Myofiber Degeneration in Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (AD-EDMD) (LGMD1B)
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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, Antje

Brain pathology (Zurich, Switzerland), 2006-10, Vol.16 (4), p.266-272 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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