Christine Klein

发表

Direct-to-Consumer Genetic Testing

Alexander Münchau, Kishore R. Kumar, Carolyn M. Sue, 2014 .

Lewy body parkinsonism in a large pedigree with 77 Parkin mutation carriers

Christine Klein, Thomas S. Jacques, Peter P. Pramstaller, 2005 .

Putting Theory into Practice: Compton-Drew Investigative Learning Center

Christine Klein, 1998 .

Ultraschall zur Früherkennung von Parkinson

Til Aach, Alfred Mertins, Christine Klein, 2009, GI Jahrestagung.

Brain parenchyma sonography detects preclinical parkinsonism

Christine Klein, Uwe Walter, Peter P Pramstaller, 2004, Movement disorders : official journal of the Movement Disorder Society.

Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease

Aldo Quattrone, Nobutaka Hattori, Anthony E. Lang, 2011, Neurobiology of Aging.

Transcranial sonography in patients with Parkinson's disease with glucocerebrosidase mutations.

Christine Klein, Marina Svetel, Aleksandra Pavlović, 2013, Parkinsonism & related disorders.

Digitized spiral analysis is a promising early motor marker for Parkinson Disease.

Christine Klein, Seth L. Pullman, Kathrin Reetz, 2010, Parkinsonism & Related Disorders.

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

Alexander Münchau, Christine Klein, Alfredo Ramirez, 2010, Archives of neurology.

BMC Medicine

Christine Klein, Karen Ostergaard, Stuart, 2006 .

LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

Christine Klein, Geetha Senthil, Michele Tagliati, 2006, The New England journal of medicine.

Novel mutation in the TOR1A (DYT1) gene in atypical, early onset dystonia and polymorphisms in dystonia and early onset parkinsonism

Christine Klein, Peter P. Pramstaller, Thomas Gasser, 2001, Neurogenetics.

Pharmacological Rescue of Mitochondrial Deficits in iPSC-Derived Neural Cells from Patients with Familial Parkinson’s Disease

Christine Klein, Karen Marder, Luis Carrillo-Reid, 2012, Science Translational Medicine.

Role of parkin mutations in 111 community‐based patients with early‐onset parkinsonism

Christine Klein, Katja Hedrich, X. Breakefield, 2002, Annals of neurology.

The striatal dopaminergic deficit is dependent on the number of mutant alleles in a family with mutations in the parkin gene: evidence for enzymatic parkin function in humans

Karl Herholz, Christine Klein, Peter P. Pramstaller, 2002, Neuroscience Letters.

Structural Changes Associated with Progression of Motor Deficits in Spinocerebellar Ataxia 17

Christian Gaser, Christine Klein, Uwe Walter, 2009, The Cerebellum.

Neuroanatomical changes extend beyond striatal atrophy in X-linked dystonia parkinsonism.

Thomas F Münte, Marcus Heldmann, Volker Tronnier, 2016, Parkinsonism & related disorders.

CAG Repeats Determine Brain Atrophy in Spinocerebellar Ataxia 17: A VBM Study

Christine Klein, Rebekka Lencer, Kathrin Reetz, 2011, PloS one.

Increased insula-putamen connectivity in X-linked dystonia-parkinsonism☆

Marcus Heldmann, Christine Klein, Thomas F. Münte, 2017, NeuroImage: Clinical.

Parkin gene alterations in hepatocellular carcinoma

Fang Wang, Christine Klein, Norman Kock, 2004, Genes, chromosomes & cancer.

Transcranial sonography as early indicator for genetic Parkinson’s disease

Til Aach, Alfred Mertins, Christine Klein, 2009 .

ε‐sarcoglycan mutations found in combination with other dystonia gene mutations

Christine Klein, Ruth H Walker, Norman Kock, 2002, Annals of neurology.

Focal dystonia as a presenting sign of spinocerebellar ataxia 17

Christine Klein, Wolfgang Heide, W. Heide, 2004, Movement disorders : official journal of the Movement Disorder Society.

The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene.

Alexander Münchau, Christine Klein, William B Dobyns, 2007, Brain : a journal of neurology.

Evidence of TAF1 dysfunction in peripheral models of X-linked dystonia-parkinsonism

Ron Shamir, Christine Klein, Uwe Walter, 2016, Cellular and Molecular Life Sciences.

Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis

Edwin Cuppen, Christine Klein, Dagmar Verbaan, 2011, Annals of neurology.

Rapid-onset dystonia-parkinsonism: case report

Christine Klein, Marina Svetel, Katja Lohmann, 2010, Journal of Neurology.

Dystonia: clinical features, genetics, and treatment

Christine Klein, C. Klein, L. Ozelius, 2002, Current opinion in neurology.

Replication of association between ELAVL4 and Parkinson disease: the GenePD study

Christine Klein, David J. Burn, Kenneth B. Baker, 2008, Human Genetics.

Early-onset parkinsonism associated with PINK1 mutations: Frequency, genotypes, and phenotypes

Christine Klein, Katja Hedrich, C. Klein, 2005 .

Genetics of Parkinson's disease.

Christine Klein, C. Klein, A. Westenberger, 2012, Cold Spring Harbor perspectives in medicine.

Imaging movement-related activity in medicated Parkin-associated and sporadic Parkinson's disease.

Christine Klein, Ferdinand Binkofski, Carsten Buhmann, 2010, Parkinsonism & related disorders.

StemBANCC: Governing Access to Material and Data in a Large Stem Cell Research Consortium

Michael Morrison, Christine Klein, Jane Kaye, 2015, Stem Cell Reviews and Reports.

Mapping preclinical compensation in Parkinson's disease: An imaging genomics approach

Christine Klein, Carsten Buhmann, B. Bloem, 2009, Movement disorders : official journal of the Movement Disorder Society.

A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia.

Deborah Hughes, Christine Klein, Thomas Foltynie, 2015, American journal of human genetics.