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La maladie de Parkinson en France (serveur d'exploration) - Curation (PubMed)

Index « MedMesh.i » - entrée « DNA-Binding Proteins »
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List of bibliographic references

Number of relevant bibliographic references: 9.
Ident.Authors (with country if any)Title
000342 (2015) Takahiro Takeda ; Mutsumi Iijima ; Toshiki Uchihara ; Takashi Ohashi ; Danielle Seilhean ; Charles Duyckaerts ; Shinichiro UchiyamaTDP-43 Pathology Progression Along the Olfactory Pathway as a Possible Substrate for Olfactory Impairment in Amyotrophic Lateral Sclerosis.
000472 (2014) Karim Fifel [Pays-Bas] ; Howard M. Cooper [France]Loss of dopamine disrupts circadian rhythms in a mouse model of Parkinson's disease.
000672 (2013) Thierry Zenone [France] ; Nathalie Streichenberger ; Marie PugetCamptocormia as a clinical manifestation of polymyositis/systemic sclerosis overlap myositis associated with anti-Ku.
000704 (2013) Eric Duplan [France] ; Emilie Giaime ; Julien Viotti ; Jean Sévalle ; Olga Corti ; Alexis Brice ; Hiroyoshi Ariga ; Ling Qi ; Frédéric Checler ; Cristine Alves Da CostaER-stress-associated functional link between Parkin and DJ-1 via a transcriptional cascade involving the tumor suppressor p53 and the spliced X-box binding protein XBP-1.
000A86 (2010) A. Gabelle [France] ; F. Portet ; C. Berr ; J. TouchonNeurodegenerative dementia and parkinsonism.
000A88 (2010) Jean-Baptiste Chanson [France] ; Andoni Echaniz-Laguna ; Thomas Vogel ; Michel Mohr ; Aurélien Benoilid ; Georges Kaltenbach ; Michèle KiesmannTDP43-positive intraneuronal inclusions in a patient with motor neuron disease and Parkinson's disease.
000C03 (2009) N. Le Forestier [France] ; L. Lacomblez ; V. Meininger[Parkinson disease and amyotrophic lateral sclerosis. Tauopathies, TDP-43 and SOD mutations].
000F62 (2004) C. Levecque [France] ; A. Destée ; V. Mouroux ; P. Amouyel ; M-C Chartier-HarlinAssessment of Nurr1 nucleotide variations in familial Parkinson's disease.
000F72 (2004) P. Ibá Ez [France] ; E. Lohmann ; P. Pollak ; F. Durif ; C. Tranchant ; Y. Agid ; A. Dürr ; A. BriceAbsence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease.

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