A. Hiller

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

F. Binkofski, R. Hilker, R. Lencer, 2006, Archives of neurology.

Phenotypic spectrum of PINK1‐associated parkinsonism in 15 mutation carriers from 1 family

K. Reetz, A. Münchau, C. Klein, 2007, Movement disorders : official journal of the Movement Disorder Society.

Premutations in the FMR1 gene as a modifying factor in Parkin‐associated Parkinson's disease?

J. Volkmann, P. Pramstaller, P. Vieregge, 2005, Movement disorders : official journal of the Movement Disorder Society.

PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism

P. Bauer, P. Pramstaller, G. Abbruzzese, 2005, European Journal of Human Genetics.

McLeod syndrome: Five new pedigrees with novel mutations.

D. Scharre, S. Lakhani, C. Westhoff, 2019, Parkinsonism & related disorders.

Family‐based association study of the restless legs syndrome loci 2 and 3 in a European population

W. Oertel, W. Poewe, T. Meitinger, 2007, Movement disorders : official journal of the Movement Disorder Society.

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

I. König, R. Lencer, C. Klein, 2006, Journal of Neurology, Neurosurgery & Psychiatry.

Bilateral subthalamic stimulation in Parkin and PINK1 parkinsonism

G. Deuschl, A. Lozano, I. König, 2008, Neurology.

Bilateral subthalamic stimulation in Parkin and PINK1 parkinsonism

G. Deuschl, A. Schnitzler, J. Volkmann, 2008, Neurology.