Movement Disorders (revue) - Curation (PubMed)

Index « Auteurs » - entrée « Christine Klein »
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Christine Höft < Christine Klein < Christine M. Belden  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 91.
[20-40] [0 - 20][0 - 50][40-60]
Ident.Authors (with country if any)Title
000921 (2013) Alberto Albanese [Italie] ; Kailash Bhatia ; Susan B. Bressman ; Mahlon R. Delong ; Stanley Fahn ; Victor S C. Fung ; Mark Hallett ; Joseph Jankovic ; Hyder A. Jinnah ; Christine Klein ; Anthony E. Lang ; Jonathan W. Mink ; Jan K. TellerPhenomenology and classification of dystonia: a consensus update.
000942 (2013) Benjamin Dehay [France] ; Marta Martinez-Vicente ; Guy A. Caldwell ; Kim A. Caldwell ; Zhenyue Yue ; Mark R. Cookson ; Christine Klein ; Miquel Vila ; Erwan BezardLysosomal impairment in Parkinson's disease.
000A37 (2013) Federica Agosta [Italie] ; Vladimir S. Kostic ; Kristina Davidovic ; Nikola Kresojevi ; Lidia Sarro ; Marina Svetel ; Iva Stankovi ; Giancarlo Comi ; Christine Klein ; Massimo FilippiWhite matter abnormalities in Parkinson's disease patients with glucocerebrosidase gene mutations.
000A77 (2013) Silke Appenzeller ; Claudia Schulte ; Sandra Thier ; Franziska Hopfner ; Manuela Pendziwiat ; Frank Papengut ; Christine Klein ; Johann Hagenah ; Meike Kasten ; Karin Srulijes ; Daniela Berg ; Thomas Gasser ; Andrew Singleton ; Günther Deuschl ; Gregor Kuhlenb UmerNo association between polymorphisms in the glutamate transporter SLC1A2 and Parkinson's disease.
000A91 (2013) Ana Westenberger [Allemagne] ; Raymond L. Rosales ; Sascha Heinitz ; Karen Freimann ; Lilian V. Lee ; Roland D. Jamora ; Arlene R. Ng ; Aloysius Domingo ; Katja Lohmann ; Uwe Walter ; Uta Gölnitz ; Arndt Rolfs ; Inga Nagel ; Gabriele Gillessen-Kaesbach ; Reiner Siebert ; Dirk Dressler ; Christine KleinX-linked Dystonia-Parkinsonism manifesting in a female patient due to atypical turner syndrome.
000B53 (2012) Anne Weissbach [Allemagne] ; Katharina Siegesmund ; Norbert Brüggemann ; Alexander Schmidt ; Meike Kasten ; Irene Pichler ; Hiltrud Muhle ; Ebba Lohmann ; Thora Lohnau ; Eberhard Schwinger ; Johann Hagenah ; Ulrich Stephani ; Peter P. Pramstaller ; Christine Klein ; Katja LohmannExome sequencing in a family with restless legs syndrome.
000C28 (2012) Susanne A. Schneider [Allemagne] ; Laura Drude ; Meike Kasten ; Christine Klein ; Johann HagenahA study of subtle motor signs in early Parkinson's disease.
000C44 (2012) Katja Lohmann [Allemagne] ; Christine KleinFamilial idiopathic basal ganglia calcification: unraveling the first genetic cause.
000C97 (2012) Silke Appenzeller [Allemagne] ; Sandra Thier ; Frank Papengut ; Christine Klein ; Johann Hagenah ; Meike Kasten ; Daniela Berg ; Karin Srulijes ; Thomas Gasser ; Stefan Schreiber ; Günther Deuschl ; Gregor Kuhlenb UmerNo association between NOD2 variants and Parkinson's disease.
000D16 (2014) Kishore R. Kumar [Australie] ; Christine KleinCommentary for "Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy".
000D83 (2012) Meike Kasten [Allemagne] ; Lena Kertelge ; Vera Tadic ; Norbert Brüggemann ; Alexander Schmidt ; Joyce Van Der Vegt ; Hartwig Siebner ; Carsten Buhmann ; Rebekka Lencer ; Kishore R. Kumar ; Katja Lohmann ; Johann Hagenah ; Christine KleinDepression and quality of life in monogenic compared to idiopathic, early-onset Parkinson's disease.
000E92 (2012) Julia Richter ; Silke Appenzeller ; Ole Ammerpohl ; G. Deuschl ; Steffen Paschen ; Norbert Brüggemann ; Christine Klein ; Gregor Kuhlenb UmerNo evidence for differential methylation of α-synuclein in leukocyte DNA of Parkinson's disease patients.
000F32 (2011) Christine Klein [Allemagne]The Wilson films--Huntington's chorea.
001018 (2011) Robert A. Wilcox [Australie] ; Susen Winkler ; Katja Lohmann ; Christine KleinWhispering dysphonia in an Australian family (DYT4): a clinical and genetic reappraisal.
001032 (2011) Sascha Heinitz ; Christine Klein ; Ana DjarmatiThe p.S77N presenilin-associated rhomboid-like protein mutation is not a frequent cause of early-onset Parkinson's disease.
001040 (2011) Beenish Arif [Pakistan] ; Anne Grünewald ; Amara Fatima ; Alfredo Ramirez ; Arif Ali ; Nobert Brüggemann ; Jens Würfel ; Arndt Rolfs ; Katja Lohmann ; Akbar Malik ; Christine Klein ; Sadaf NazAn unusual neurological syndrome of crawling gait, dystonia, pyramidal signs, and limited speech.
001063 (2011) Simone Zittel ; Tobias B Umer ; Norbert Brüggemann ; Christian Gerloff ; Christine Klein ; Alexander MünchauParoxysmal cervical myoclonus.
001088 (2011) Christine Klein [Canada] ; Rosalind Chuang ; Connie Marras ; Anthony E. LangThe curious case of phenocopies in families with genetic Parkinson's disease.
001090 (2011) Sarah Schiebler [Allemagne] ; Alexander Schmidt ; Simone Zittel ; Tobias B Umer ; Christian Gerloff ; Christine Klein ; Alexander MünchauArm tremor in cervical dystonia--is it a manifestation of dystonia or essential tremor?
001150 (2011) Christoph Kamm ; Nils Uflacker ; Friedrich Asmus ; Christoph Schrader ; Alexander Wolters ; Matthias Wittstock ; Jens Pahnke ; Thomas Gasser ; Jens Volkmann ; Alexander Münchau ; Johann Hagenah ; Reiner Benecke ; Christine Klein ; Katja LohmannNo evidence for THAP1/DYT6 variants as disease modifiers in DYT1 dystonia.
001283 (2011) Alma Osmanovic ; Andreas Dendorfer ; Alev Erogullari ; Nils Uflacker ; Diana Braunholz ; Aleksandar Rakovic ; Gudrun Vierke ; Conchi Gil-Rodríguez ; Alexander Münchau ; Melanie Albrecht ; Norbert Brüggemann ; Gabriele Gillessen-Kaesbach ; Christine Klein ; Katja Lohmann ; Frank J. KaiserTruncating mutations in THAP1 define the nuclear localization signal.

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