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Publications by L. Ishihara-Paul
PINK1 Mutations and Parkinsonism
Neurology
Neurology
Related publications
PINK1, Parkin, and DJ-1 Mutations in Italian Patients With Early-Onset Parkinsonism
European Journal of Human Genetics
Genetics
Parkinsonism Due to Mutations in PINK1, Parkin, and DJ-1 and Oxidative Stress and Mitochondrial Pathways
Cold Spring Harbor perspectives in medicine
Biochemistry
Medicine
Genetics
Molecular Biology
New Perception of Mitochondrial Regulatory Pathway in Parkinsonism €“ Ubiquitin, PINK1, and Parkin
Frontiers in Neurology
Neurology
Juvenile-Onset Parkinsonism as a Result of the First Mutation in the Adenosine Triphosphate Orientation Domain of PINK1
Archives of Neurology
Late-Onset Levodopa Responsive Parkinsonism Due to Polymerase Γ 1 Mutations
Movement Disorders Clinical Practice
Neurology
Clinical Spectrum of Homozygous and Heterozygous PINK1 Mutations in a Large German Family With Parkinson Disease
Archives of Neurology
Enhanced Sensitivity to Group II mGlu Receptor Activation at Corticostriatal Synapses in Mice Lacking the Familial Parkinsonism-Linked Genes PINK1 or Parkin
Experimental Neurology
Developmental Neuroscience
Neurology
Postencephalitic Parkinsonism
The Lancet
Medicine
Monograph on Parkinsonism
BMJ
