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Common Grounds for Family Maladies

Oexle, Konrad ; Winkelmann, Juliane

Neuron, 16 May 2018, Vol.98(4), pp.671-672 [Rivista Peer Reviewed]

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When Parkinson’s disease patients go to sleep: specific sleep disturbances related to Parkinson’s disease

Schulte, Eva ; Winkelmann, Juliane

Journal of Neurology, 2011, Vol.258(Supplement 2), pp.328-335 [Rivista Peer Reviewed]

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Reply to letter: Novel compound heterozygous mutations in PRKRA cause pure dystonia

Zech, Michael ; Castrop, Florian ; Haslinger, Bernhard ; Winkelmann, Juliane

Movement Disorders, May 2015, Vol.30(6), pp.878-879 [Rivista Peer Reviewed]

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Parkinson's disease risk score: moving to a premotor diagnosis.(Author abstract)(Report)

Winkler, Jurgen ; Ehret, Reinhard ; Buttner, Thomas ; Dillmann, Ulrich ; Fogel, Wolfgang ; Sabolek, Michael ; Winkelmann, Juliane ; Kassubek, Jan

Journal of Neurology, May, 2011, Vol.258(2), p.311(5) [Rivista Peer Reviewed]

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Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls

Zech, Michael ; Gross, Nadine ; Jochim, Angela ; Castrop, Florian ; Kaffe, Maria ; Dresel, Christian ; Lichtner, Peter ; Peters, Annette ; Gieger, Christian ; Meitinger, Thomas ; Haslinger, Bernhard ; Winkelmann, Juliane

Movement Disorders, January 2014, Vol.29(1), pp.143-147 [Rivista Peer Reviewed]

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Myoclonus‐dystonia in 18p deletion syndrome

Kowarik, Markus C. ; Langer, Sabine ; Keri, Corinna ; Hemmer, Bernhard ; Oexle, Konrad ; Winkelmann, Juliane

Movement Disorders, 15 February 2011, Vol.26(3), pp.560-561 [Rivista Peer Reviewed]

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Ferric carboxymaltose in patients with restless legs syndrome and nonanemic iron deficiency: A randomized trial

Trenkwalder, Claudia ; Winkelmann, Juliane ; Oertel, Wolfgang ; Virgin, Garth ; Roubert, Bernard ; Mezzacasa, Anna

Movement Disorders, October 2017, Vol.32(10), pp.1478-1482 [Rivista Peer Reviewed]

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TOR1A, THAP1, and GNAL mutational screening in Austrian patients with primary isolated dystonia

Zech, Michael ; Boesch, Sylvia ; Sycha, Thomas ; Mueller, Joerg ; Poewe, Werner ; Winkelmann, Juliane

Movement Disorders, November 2015, Vol.30(13), pp.1853-1854 [Rivista Peer Reviewed]

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The clinical phenotype of early‐onset isolated dystonia caused by recessive COL6A3 mutations (DYT27

Jochim, Angela ; Zech, Michael ; Gora‐Stahlberg, Gina ; Winkelmann, Juliane ; Haslinger, Bernhard

Movement Disorders, May 2016, Vol.31(5), pp.747-750 [Rivista Peer Reviewed]

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Restless legs syndrome associated with major diseases: A systematic review and new concept

Trenkwalder, Claudia ; Allen, Richard ; Högl, Birgit ; Paulus, Walter ; Winkelmann, Juliane

Neurology, 2016, Vol.86(14), pp.1336-1343 [Rivista Peer Reviewed]

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da questo autore/creatore:

  1. Winkelmann, Juliane
  2. Winkelmann, J.
  3. Trenkwalder, Claudia
  4. Gieger, Christian
  5. Lichtner, Peter

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