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Gellera Cinzia
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http://hub.abes.fr/bmj/periodical/jnnp/2013/volume_84/issue_2/B35A17CA23585B19E053120B220AE1F6/authorship/1
http://hub.abes.fr/bmj/periodical/jnnp/2012/volume_83/issue_suppl1/B35A17CA20F75B19E053120B220AE1F6/authorship/3
http://hub.abes.fr/bmj/periodical/jmg/2009/volume_47/issue_3/B3598D6B65AE7CBEE053120B220A90C5/authorship/19
http://hub.abes.fr/bmj/periodical/jnnp/2011/volume_82/issue_11/B35A17CA1D295B19E053120B220AE1F6/authorship/13
http://hub.abes.fr/oup/periodical/brainj/2006/volume_129/issue_1/101093brainawh651/authorship/10
http://hub.abes.fr/oup/periodical/hmg/1999/volume_8/issue_3/101093hmg83425/authorship/3
http://hub.abes.fr/oup/periodical/brainj/2009/volume_132/issue_1/101093brainawn269/authorship/6
http://hub.abes.fr/oup/periodical/brainj/2003/volume_126/issue_4/101093brainawg077/authorship/2
http://hub.abes.fr/oup/periodical/hmg/2000/volume_9/issue_17/101093hmg9172523/authorship/2
http://hub.abes.fr/oup/periodical/humanmoleculargenetics/1995/volume_4/issue_1/101093hmg4119/authorship/8
http://hub.abes.fr/oup/periodical/brainj/2007/volume_130/issue_4/101093brainawm009/authorship/5
http://hub.abes.fr/oup/periodical/hmg/2001/volume_10/issue_19/101093hmg10192099/authorship/4
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Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course
Visual system involvement in patients with Friedreich's ataxia
Frataxin expression rescues mitochondrial dysfunctions in FRDA cells
The A467T and W748S POLG substitutions are a rare cause of adult-onset ataxia in Europe
SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2
Human frataxin maintains mitochondrial iron homeostasis in Saccharomyces cerevisiae
Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutations
The Friedreich's Ataxia Mutation Confers Cellular Sensitivity to Oxidant Stress Which Is Rescued by Chelators of Iron and Calcium and Inhibitors of Apoptosis
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