Norbert Brüggemann

Best Publications

• Clinical manifestations of the anti-IgLON5 disease.

  Carles Gaig;Francesc Graus;Yarko Compta;Birgit Högl

  412
  Citations

• An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA50/ATX-FGF14.

  Unknown

  199
  Citations

• Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study.

  Ana Djarmati;Susanne A Schneider;Katja Lohmann;Susen Winkler

  194
  Citations

• Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene

  Katja Lohmann;Robert A. Wilcox;Susen Winkler;Alfredo Ramirez;Alfredo Ramirez

  182
  Citations

• Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects

  Eunju Seong;Ryan Insolera;Marija Dulovic;Erik Jan Kamsteeg

  177
  Citations

• Mitochondrial damage-associated inflammation highlights biomarkers in PRKN/PINK1 parkinsonism.

  Max Borsche;Inke R König;Sylvie Delcambre;Simona Petrucci;Simona Petrucci

  172
  Citations

• Etiology of musician's dystonia: familial or environmental?

  A. Schmidt;H. C. Jabusch;H. C. Jabusch;E. Altenmüller;J. Hagenah

  150
  Citations

• Short- and long-term outcome of chronic pallidal neurostimulation in monogenic isolated dystonia

  Norbert Brüggemann;Andrea Kühn;Susanne A. Schneider;Christoph Kamm

  139
  Citations

• Dopa-responsive dystonia revisited: diagnostic delay, residual signs, and nonmotor signs.

  Vera Tadic;Meike Kasten;Norbert Brüggemann;Sophie Stiller

  134
  Citations

• Clinical spectrum of Kufor-Rakeb syndrome in the Chilean kindred with ATP13A2 mutations.

  Maria I. Behrens;Maria I. Behrens;Norbert Brüggemann;Pedro Chana;Pablo Venegas

  127
  Citations

• Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease.

  Carles Gaig;Yaroslau Compta;Anna Heidbreder;Maria J Marti

  107
  Citations

• The Rostock International Parkinson's Disease (ROPAD) Study: Protocol and Initial Findings.

  Volha Skrahina;Hanaa Gaber;Eva-Juliane Vollstedt;Toni M Förster

  103
  Citations

• Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype.

  Norbert Brüggemann;Johann Hagenah;Kathrin Reetz;Alexander Schmidt

  99
  Citations

• Mutations in GNAL: A Novel Cause of Craniocervical Dystonia

  Kishore R. Kumar;Katja Lohmann;Ikuo Masuho;Ryosuke Miyamoto

  97
  Citations

• Nonmotor symptoms in genetic Parkinson disease.

  Meike Kasten;Lena Kertelge;Norbert Brüggemann;Joyce van der Vegt

  96
  Citations

• Gaucher Disease Ascertained through a Parkinson’s Center: Imaging and Clinical Characterization

  Rachel Saunders‐Pullman;Rachel Saunders‐Pullman;Johann Hagenah;Vijay Dhawan;Kaili Stanley

  95
  Citations

• Dominantly transmitted focal dystonia in families of patients with musician’s cramp

  A. Schmidt;H. C. Jabusch;E. Altenmüller;J. Hagenah

  94
  Citations

• Psychiatric associations of adult-onset focal dystonia phenotypes

  Brian D. Berman;Johanna Junker;Erika Shelton;Stefan H. Sillau

  93
  Citations

• A hexanucleotide repeat modifies expressivity of X-linked dystonia parkinsonism.

  Ana Westenberger;Charles Jourdan Reyes;Gerard Saranza;Valerija Dobricic

  88
  Citations

• ATP13A2 variants in early-onset Parkinson's disease patients and controls.

  Ana Djarmati;Johann Hagenah;Kathrin Reetz;Susen Winkler

  84
  Citations