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A152T tau allele causes neurodegeneration that can be ameliorated in a zebrafish model by autophagy induction
Lopez, Ana, Lee, Suzee E., Wojta, Kevin, Ramos, Eliana Marisa, Klein, Eric, Chen, Jason, Boxer, Adam L., Gorno-Tempini, Maria Luisa, Geschwind, Daniel H., Schlotawa, Lars, Ogryzko, Nikolay V., Bigio, Eileen H., Rogalski, Emily, Weintraub, Sandra, Mesulam, Marsel M., Fleming, Angeleen, Coppola, Giovanni, Miller, Bruce L., Rubinsztein, David C.
Published in Brain (London, England : 1878) (01.04.2017)
Published in Brain (London, England : 1878) (01.04.2017)
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Huntington's Disease like 2 presenting with isolated Parkinsonism
Vasconcellos, Luiz Felipe Rocha, Macêdo, Philippe Joaquim Oliveira Menezes, Franck, Jéssyca Botelho, Tumas, Vitor, Marques Júnior, Wilson, Spitz, Mariana
Published in Journal of the neurological sciences (15.02.2017)
Published in Journal of the neurological sciences (15.02.2017)
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A Systematic Review of the Huntington Disease-Like 2 Phenotype
Anderson, David G., Walker, Ruth H., Connor, Myles, Carr, Jonathan, Margolis, Russell L., Krause, Amanda
Published in Journal of Huntington's disease (01.01.2017)
Published in Journal of Huntington's disease (01.01.2017)
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Quantification of Ataxin-3 and Ataxin-7 aggregates formed in vivo in Drosophila reveals a threshold of aggregated polyglutamine proteins associated with cellular toxicity
Vinatier, Gérald, Corsi, Jean-Marc, Mignotte, Bernard, Gaumer, Sébastien
Published in Biochemical and biophysical research communications (04.09.2015)
Published in Biochemical and biophysical research communications (04.09.2015)
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G protein-coupled receptor 26 immunoreactivity in intranuclear inclusions associated with polyglutamine and intranuclear inclusion body diseases
Mori, Fumiaki, Tanji, Kunikazu, Miki, Yasuo, Toyoshima, Yasuko, Yoshida, Mari, Kakita, Akiyoshi, Takahashi, Hitoshi, Utsumi, Jun, Sasaki, Hidenao, Wakabayashi, Koichi
Published in Neuropathology (01.02.2016)
Published in Neuropathology (01.02.2016)
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Depletion of mitochondrial DNA in leukocytes of patients with poly-Q diseases
Liu, Chin-San, Cheng, Wen-Ling, Kuo, Shou-Jen, Li, Jie-Yuan, Soong, Bing-Wen, Wei, Yau-Huei
Published in Journal of the neurological sciences (15.01.2008)
Published in Journal of the neurological sciences (15.01.2008)
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Genetic polymorphisms in folate and homocysteine metabolism as risk factors for DNA damage
Botto, Nicoletta, Andreassi, Maria Grazia, Manfredi, Samantha, Masetti, Serena, Cocci, Franca, Colombo, Maria Giovanna, Storti, Simona, Rizza, Antonio, Biagini, Andrea
Published in European journal of human genetics : EJHG (01.09.2003)
Published in European journal of human genetics : EJHG (01.09.2003)
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Neuromelanin and its interaction with iron as a Potential risk : Factor for dopaminergic neurodegeneration underlying Parkinson's disease
Gerlach, Manfred, Double, Kay L, Ben-Shachar, Dorit, Zecca, Luigi, Youdim, Moussa BH, Riederer, Peter
Published in Neurotoxicity research (2003)
Published in Neurotoxicity research (2003)
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A case of megalencephalic leukoencephalopathy with subcortical cysts (van der Knaap disease): molecular genetic study
Saijo, Harumi, Nakayama, Harumi, Ezoe, Takanori, Araki, Katsuhito, Sone, Sui, Hamaguchi, Hiroshi, Suzuki, Hisaharu, Shiroma, Naohide, Kanazawa, Naomi, Tsujino, Seiichi, Hirayama, Yoshito, Arima, Masataka
Published in Brain & development (01.08.2003)
Published in Brain & development (01.08.2003)
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Molecular biology of channelopathies: impact on diagnosis and treatment
Avanzini, Giuliano, Franceschetti, Silvana, Avoni, Patrizia, Liguori, Rocco
Published in Expert review of neurotherapeutics (01.05.2004)
Published in Expert review of neurotherapeutics (01.05.2004)
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Cognitive Deficits Associated With a Recently Reported Familial Neurodegenerative Disease: Familial Encephalopathy With Neuroserpin Inclusion Bodies
Bradshaw, Charles B, Davis, Richard L, Shrimpton, Antony E, Holohan, Peter D, Rea, Cornelia B, Fieglin, David, Kent, Paul, Collins, George H
Published in Archives of neurology (Chicago) (01.09.2001)
Published in Archives of neurology (Chicago) (01.09.2001)
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