Risultati della ricerca - G. Bernhard Landwehrmeyer

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  1. 1
    A single nucleotide polymorphism in the coding region of PGC-1α is a male-specific modifier of Huntington disease age-at-onset in a large European cohort

    A single nucleotide polymorphism in the coding region of PGC-1α is a male-specific modifier of Huntington disease age-at-onset in a large European cohort di Patrick Weydt, Selma M. Soyal, G. Bernhard Landwehrmeyer, Wolfgang Patsch

    Pubblicazione 2014
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  2. 2
    Thalamic Atrophy in Huntington's Disease Co-varies with Cognitive Performance: A Morphometric MRI Analysis

    Thalamic Atrophy in Huntington's Disease Co-varies with Cognitive Performance: A Morphometric MRI Analysis di Jan Kassubek, Freimut D. Juengling, Daniel Ecker, G. Bernhard Landwehrmeyer

    Pubblicazione 2004
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  3. 3
    NMDA receptor subunit mRNA expression by projection neurons and interneurons in rat striatum

    NMDA receptor subunit mRNA expression by projection neurons and interneurons in rat striatum di G. Bernhard Landwehrmeyer, David G. Standaert, CM Testa, JB Penney, AB Young

    Pubblicazione 1995
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  4. 4
    Cortical dysfunction in patients with Huntington's disease during working memory performance

    Cortical dysfunction in patients with Huntington's disease during working memory performance di Robert Christian Wolf, Nenad Vasić, Carlos Schönfeldt‐Lecuona, Daniel Ecker, G. Bernhard Landwehrmeyer

    Pubblicazione 2008
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  5. 5
    Dorsolateral prefrontal cortex dysfunction in presymptomatic Huntington's disease: evidence from event-related fMRI

    Dorsolateral prefrontal cortex dysfunction in presymptomatic Huntington's disease: evidence from event-related fMRI di Robert Christian Wolf, Nenad Vasić, Carlos Schönfeldt‐Lecuona, G. Bernhard Landwehrmeyer, D. Ecker

    Pubblicazione 2007
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  6. 6
    Observing Huntington's Disease: the European Huntington's Disease Network's REGISTRY.

    Observing Huntington's Disease: the European Huntington's Disease Network's REGISTRY. di Michael Orth, Olivia Handley, Carsten Schwenke, Stephen B. Dunnett, Edward J. Wild, Sarah J. Tabrizi, G. Bernhard Landwehrmeyer

    Pubblicazione 2010
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  7. 7
    The gene coding for PGC-1α modifies age at onset in Huntington's Disease

    The gene coding for PGC-1α modifies age at onset in Huntington's Disease di Patrick Weydt, Selma M. Soyal, Cinzia Gellera, Stefano DiDonato, Claus Weidinger, Hannes Oberkofler, G. Bernhard Landwehrmeyer, Wolfgang Patsch

    Pubblicazione 2009
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  8. 8
    Validation of a prognostic index for Huntington's disease

    Validation of a prognostic index for Huntington's disease di Jeffrey D. Long, Douglas R. Langbehn, Sarah J. Tabrizi, G. Bernhard Landwehrmeyer, Jane S. Paulsen, John Harley Warner, Cristina Sampaio

    Pubblicazione 2016
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  9. 9
    Proteases Acting on Mutant Huntingtin Generate Cleaved Products that Differentially Build Up Cytoplasmic and Nuclear Inclusions

    Proteases Acting on Mutant Huntingtin Generate Cleaved Products that Differentially Build Up Cytoplasmic and Nuclear Inclusions di Astrid Lunkes, Katrin S. Lindenberg, Léa Ben-Haı̈em, C. R. Weber, Didier Devys, G. Bernhard Landwehrmeyer, Jean‐Louis Mandel, Yvon Trottier

    Pubblicazione 2002
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  10. 10
    Enroll-HD: An Integrated Clinical Research Platform and Worldwide Observational Study for Huntington's Disease

    Enroll-HD: An Integrated Clinical Research Platform and Worldwide Observational Study for Huntington's Disease di Swati Sathe, Jen Ware, Jamie Levey, Eileen Neacy, Robi Blumenstein, Simon Noble, Alžbeta Mühlbäck, Anne Rosser, G. Bernhard Landwehrmeyer, Cristina Sampaio

    Pubblicazione 2021
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  11. 11
    Huntingtin HTT1a is generated in a CAG repeat-length-dependent manner in human tissues

    Huntingtin HTT1a is generated in a CAG repeat-length-dependent manner in human tissues di Franziska Hoschek, Julia Natan, Maximilian Wagner, Kirupa Sathasivam, Alshaimaa Abdelmoez, Björn von Einem, Gillian P. Bates, G. Bernhard Landwehrmeyer, Andreas Neueder

    Pubblicazione 2024
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  12. 12
    Magnetic resonance perfusion imaging of resting-state cerebral blood flow in preclinical Huntington's disease

    Magnetic resonance perfusion imaging of resting-state cerebral blood flow in preclinical Huntington's disease di Robert Christian Wolf, Georg Grön, Fabio Sambataro, Nenad Vasić, Nadine D. Wolf, Philipp A. Thomann, Carsten Saft, G. Bernhard Landwehrmeyer, Michael Orth

    Pubblicazione 2011
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  13. 13
    Summary of cerebrospinal fluid routine parameters in neurodegenerative diseases

    Summary of cerebrospinal fluid routine parameters in neurodegenerative diseases di Sarah Jesse, Johannes Brettschneider, Sigurd D. Süßmuth, G. Bernhard Landwehrmeyer, Christine A. F. Von Arnim, Albert C. Ludolph, Hayrettin Tumani, Markus Otto

    Pubblicazione 2010
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  14. 14
    Brain activation and functional connectivity in premanifest Huntington's disease during states of intrinsic and phasic alertness

    Brain activation and functional connectivity in premanifest Huntington's disease during states of intrinsic and phasic alertness di Robert Christian Wolf, Georg Grön, Fabio Sambataro, Nenad Vasić, Nadine D. Wolf, Philipp A. Thomann, Carsten Saft, G. Bernhard Landwehrmeyer, Michael Orth

    Pubblicazione 2011
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  15. 15
    Body weight is a robust predictor of clinical progression in Huntington disease

    Body weight is a robust predictor of clinical progression in Huntington disease di Jorien M.M. van der Burg, Sarah L. Gardiner, Albert C. Ludolph, G. Bernhard Landwehrmeyer, Raymund A.C. Roos, N. Ahmad Aziz

    Pubblicazione 2017
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  16. 16
    A greatly extended PPARGC1A genomic locus encodes several new brain-specific isoforms and influences Huntington disease age of onset†

    A greatly extended PPARGC1A genomic locus encodes several new brain-specific isoforms and influences Huntington disease age of onset† di Selma M. Soyal, Thomas K. Felder, Simon Auer, Penelope Hahne, Hannes Oberkofler, Anke Witting, Markus Paulmichl, G. Bernhard Landwehrmeyer, Patrick Weydt, Wolfgang Patsch

    Pubblicazione 2012
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  17. 17
    An Isoform of Ataxin‐3 Accumulates in the Nucleus of Neuronal Cells in Affected Brain Regions of SCA3 Patients

    An Isoform of Ataxin‐3 Accumulates in the Nucleus of Neuronal Cells in Affected Brain Regions of SCA3 Patients di Thorsten Schmidt, G. Bernhard Landwehrmeyer, Ina Schmitt, Yvon Trottier, Georg Auburger, Franco Laccone, Thomas Klockgether, Michael Völpel, Jörg T. Epplen, Lüdger Schöls, Olaf Rieß

    Pubblicazione 1998
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  18. 18
    Five siRNAs Targeting Three SNPs May Provide Therapy for Three-Quarters of Huntington's Disease Patients

    Five siRNAs Targeting Three SNPs May Provide Therapy for Three-Quarters of Huntington's Disease Patients di Edith L. Pfister, Lori Kennington, Juerg Straubhaar, Sujata Wagh, Wanzhou Liu, Marian DiFiglia, G. Bernhard Landwehrmeyer, Jean‐Paul Vonsattel, Phillip D. Zamore, Neil Aronin

    Pubblicazione 2009
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  19. 19
    Data Analytics from Enroll‐<scp>HD</scp>, a Global Clinical Research Platform for Huntington's Disease

    Data Analytics from Enroll‐<scp>HD</scp>, a Global Clinical Research Platform for Huntington's Disease di G. Bernhard Landwehrmeyer, Cheryl Fitzer‐Attas, Joseph Giuliano, Nilza Gonçalves, Karen E. Anderson, Francisco Cardoso, Joaquim J. Ferreira, Tiago Mestre, Julie C. Stout, Cristina Sampaio

    Pubblicazione 2016
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  20. 20
    Impaired Regulation of Brain Mitochondria by Extramitochondrial Ca2+ in Transgenic Huntington Disease Rats

    Impaired Regulation of Brain Mitochondria by Extramitochondrial Ca2+ in Transgenic Huntington Disease Rats di Frank N. Gellerich, Zemfira Gizatullina, Huu Phuc Nguyen, Sonata Trumbeckaitė, Stefan Vielhaber, Enn Seppet, Stephan Zierz, G. Bernhard Landwehrmeyer, Olaf Rieß, Stephan von Hörsten, Frank Striggow

    Pubblicazione 2008
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