检索结果 - Anette Torvin Møller

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  1. 1
    Reproducibility, and sensitivity to motor unit loss in amyotrophic lateral sclerosis, of a novel MUNE method: MScanFit MUNE

    Reproducibility, and sensitivity to motor unit loss in amyotrophic lateral sclerosis, of a novel MUNE method: MScanFit MUNE 由 Anna Bystrup Jacobsen, Hugh Bostock, Anders Fuglsang‐Frederiksen, Lene Duez, Sándor Beniczky, Anette Torvin Møller, Jakob Udby Blicher, Hatice Tankişi

    出版 2017
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    Artigo
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  2. 2
    Early diagnosis of peripheral nervous system involvement in Fabry disease and treatment of neuropathic pain: the report of an expert panel

    Early diagnosis of peripheral nervous system involvement in Fabry disease and treatment of neuropathic pain: the report of an expert panel 由 Alessandro P Burlina, Katherine B. Sims, Juan Politei, Gary J. Bennett, Ralf Baron, Claudia Sommer, Anette Torvin Møller, Max J. Hilz

    出版 2011
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    Revisão
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  3. 3
    Prediction of survival in amyotrophic lateral sclerosis: a nationwide, Danish cohort study

    Prediction of survival in amyotrophic lateral sclerosis: a nationwide, Danish cohort study 由 Anne-Lene Kjældgaard, Katrine Pilely, Karsten Skovgaard Olsen, Anders Hedegaard Jessen, Anne Øberg Lauritsen, Stephen Wørlich Pedersen, Kirsten Svenstrup, Merete Karlsborg, Helle Thagesen, Morten Blaabjerg, Ásta Theódórsdóttir, Elisabeth Gundtoft Elmo, Anette Torvin Møller, Lone Bonefeld, M. van den Berg, Peter Garred, Kirsten Møller

    出版 2021
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    Artigo
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  4. 4
    Haplotypes and gene expression implicate the <i>MAPT</i> region for Parkinson disease

    Haplotypes and gene expression implicate the <i>MAPT</i> region for Parkinson disease 由 Jennifer E. Tobin, Jeanne C. Latourelle, Mark Lew, Christine Klein, Oksana Suchowersky, H. A. Shill, Lawrence I. Golbe, M. H. Mark, John H. Growdon, G. Frederick Wooten, Brad A. Racette, J. S. Perlmutter, Ray L. Watts, Mark Guttman, Kenneth B. Baker, Stefano Goldwurm, Gianni Pezzoli, Carlos Singer, Marie Saint‐Hilaire, Audrey E. Hendricks, Sally Williamson, Michael W. Nagle, Jemma B. Wilk, Tiffany Massood, Jason M. Laramie, Anita L. DeStefano, Irene Litvan, Garth A. Nicholson, Alastair Corbett, Stuart Isaacson, David J. Burn, Patrick F. Chinnery, Peter P. Pramstaller, Scott J. Sherman, Jomana T. Al‐Hinti, Edward Drasby, Martha Nance, Anette Torvin Møller, Karen Østergaard, Richard Roxburgh, B. J. Snow, John T. Slevin, Franca Cambi, James F. Gusella, Richard H. Myers

    出版 2008
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  5. 5
    The Gly2019Ser mutation in LRRK2is not fully penetrant in familial Parkinson's disease: the GenePD study

    The Gly2019Ser mutation in LRRK2is not fully penetrant in familial Parkinson's disease: the GenePD study 由 Jeanne C. Latourelle, Mei Sun, Mark Lew, Oksana Suchowersky, Christine Klein, Lawrence I. Golbe, Margery H. Mark, John H. Growdon, G. Frederick Wooten, Ray L. Watts, Mark Guttman, Brad A. Racette, Joel S. Perlmutter, Anwar Ahmed, Holly A. Shill, Carlos Singer, Stefano Goldwurm, Gianni Pezzoli, Michela Zini, Marie Saint‐Hilaire, Audrey E. Hendricks, Sally Williamson, Michael W. Nagle, Jemma B. Wilk, Tiffany Massood, Karen W. Huskey, Jason M. Laramie, Anita L. DeStefano, Kenneth B. Baker, Ilia Itin, Irene Litvan, Garth A. Nicholson, Alastair Corbett, Martha Nance, Edward Drasby, Stuart Isaacson, David J. Burn, Patrick F. Chinnery, Peter P. Pramstaller, Jomana T. Al‐Hinti, Anette Torvin Møller, Karen Østergaard, Scott J. Sherman, Richard Roxburgh, Barry Snow, John T. Slevin, Franca Cambi, James F. Gusella, Richard H. Myers

    出版 2008
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    Artigo
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