Autosomal dominant hereditary spastic paraplegia: Novel mutations in the <it>REEP1 </it>gene (SPG31) by Epplen Joerg T, Arning Larissa, Schlang Katharina J, Stemmler Susanne

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Age at onset of Huntington disease is not modulated by the R72P variation in TP53 and the R196K variation in the gene coding for the human caspase activated DNase (hCAD) by Andrich Jürgen, Saft Carsten, Kraus Peter H, Arning Larissa, Epplen Jörg T

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Genomic <it>NGFB </it>variation and multiple sclerosis in a case control study by Arning Larissa, Kruse Niels, Akkad Denis A, Gold Ralf, Epplen Jörg T

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Glutathione S-Transferase Ω 1 variation does not influence age at onset of Huntington's disease by Saft Carsten, Wieczorek Stefan, Jagiello Peter, Arning Larissa, Andrich Jürgen, Epplen Jörg T

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Hepatic mitochondrial dysfunction in Friedreich Ataxia by Stüwe Sven H, Goetze Oliver, Arning Larissa, Banasch Matthias, Schmidt Wolfgang E, Schöls Ludger, Saft Carsten

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PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease by Haghikia Aiden, Wieczorek Stefan, Akkad Denis A, Saft Carsten, Taherzadeh-Fard Elahe, Chan Andrew, Epplen Jörg T, Arning Larissa

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No association between polymorphisms in the <it>BDNF </it>gene and age at onset in Huntington disease by Kraus Peter H, Andrich Jürgen, Saft Carsten, Wieczorek Stefan, Akkad Amer D, Mai Maren, Epplen Jörg T, Arning Larissa

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