Publications by authors named "Julia Schicks"

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Leukodystrophies in idiopathic adult-onset ataxia: frequency and phenotype in 105 patients.
Jennifer Müller Vom Hagen, Matthis Synofzik, Julia Schicks, Ingeborg Krägeloh-Mann, Ludger Schöls

Mov Disord· December 2013

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Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data.
Heike Jacobi, Kathrin Reetz, Sophie Tezenas du Montcel, Peter Bauer, Caterina Mariotti, Julia Schicks

Lancet Neurol· July 2013

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Teaching NeuroImages: MRI guides genetics: leukoencephalopathy with brainstem and spinal cord involvement (LBSL).
Julia Schicks, Ludger Schöls, Marjo S van der Knaap, Matthis Synofzik

Neurology· April 2013

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Niemann-Pick type C is frequent in adult ataxia with cognitive decline and vertical gaze palsy.
Julia Schicks, Jennifer Müller Vom Hagen, Peter Bauer, Stefanie Beck-Wödl, Saskia Biskup

Neurology· March 2013

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Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum.
Matthis Synofzik, Anne S Soehn, Janina Gburek-Augustat, Julia Schicks, Kathrin N Karle

Orphanet J Rare Dis· March 2013

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Decreased retinal sensitivity and loss of retinal nerve fibers in multiple system atrophy.
M Dominik Fischer, Matthis Synofzik, Christoph Kernstock, Janko Dietzsch, Robert Heidlauf, Julia Schicks

Graefes Arch Clin Exp Ophthalmol· January 2013

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Video game-based coordinative training improves ataxia in children with degenerative ataxia.
Winfried Ilg, Cornelia Schatton, Julia Schicks, Martin A Giese, Ludger Schöls

Neurology· November 2012

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POLG and PEO1 (Twinkle) mutations are infrequent in PSP-like atypical parkinsonism: a preliminary screening study.
Matthis Synofzik, Julia Schicks, Karin Srulijes, Claudia Schulte, Franziska Schiele

J Neurol· October 2012

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Charcot-Marie-Tooth hereditary neuropathy due to a mitochondrial ATP6 mutation.
Matthis Synofzik, Julia Schicks, Christian Wilhelm, Antje Bornemann, Ludger Schöls

Eur J Neurol· October 2012

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Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47) .
Peter Bauer, Esther Leshinsky-Silver, Lubov Blumkin, Nina Schlipf, Christopher Schröder, Julia Schicks

Neurogenetics· February 2012

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Acetazolamide-responsive exercise-induced episodic ataxia associated with a novel homozygous DARS2 mutation.
Matthis Synofzik, Julia Schicks, Tobias Lindig, Saskia Biskup, Thorsten Schmidt

J Med Genet· October 2011

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Retinal nerve fiber layer loss in multiple system atrophy.
M Dominik Fischer, Matthis Synofzik, Robert Heidlauf, Julia Schicks, Karin Srulijes

Mov Disord· April 2011

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Atypical juvenile parkinsonism in a consanguineous SPG15 family.
Julia Schicks, Matthis Synofzik, Hjörvar Pétursson, Johanna Huttenlocher, Matthias Reimold

Mov Disord· February 2011

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POLG, but not PEO1, is a frequent cause of cerebellar ataxia in Central Europe.
Julia Schicks, Matthis Synofzik, Claudia Schulte, Ludger Schöls

Mov Disord· November 2010

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