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Katja Hedrich

University of Lübeck

69

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3095

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Rapid and reliable detection of exon rearrangements in various movement disorders genes by multiplex ligation‐dependent probe amplification

2007 Movement Disorders
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Morphometric fingerprint of asymptomatic Parkin and PINK1 mutation carriers in the basal ganglia

2007 Neurology
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Somatosensory processing in asymptomatic PINK1- and PARKIN-mutation carriers

2007 Aktuelle Neurologie
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Phenotypic spectrum of PINK1-associated parkinsonism in 15 mutation carriers from 1 family.

2007 Movement Disorders
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Substantia nigra hyperechogenicity correlates with clinical status and number of Parkin mutated alleles

2007 Journal of Neurology
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Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene

2007 Movement Disorders
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Modified somatosensory processing in PINK1 (PARK6)-mutation carriers: Preclinical evidence by the use of quantitative sensory testing (QST)

2007 Clinical Neurophysiology
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Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease: role of a single hit?

2006 JAMA Neurology
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Co-occurrence of affective and schizophrenia spectrum disorders with PINK1 mutations

2006 Journal of Neurology, Neurosurgery, and Psychiatry
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Early-onset parkinsonism associated with PINK1 mutations: Frequency, genotypes, and phenotypes

2006 Neurology
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