Standard
Recessively inherited parkinsonism : effect of ATP13A2 mutations on the clinical and neuroimaging phenotype. / Brüggemann, Norbert; Hagenah, Johann; Reetz, Kathrin; Schmidt, Alexander; Kasten, Meike; Buchmann, Inga; Eckerle, Susanne; Bähre, Manfred; Münchau, Alexander; Djarmati, Ana; van der Vegt, Joyce; Siebner, Hartwig; Binkofski, Ferdinand; Ramirez, Alfredo; Behrens, Maria I; Klein, Christine.
In:
Archives of Neurology, Vol. 67, No. 11, 01.11.2010, p. 1357-63.
Research output: Contribution to journal › Journal article › Research › peer-review
Harvard
Brüggemann, N, Hagenah, J, Reetz, K, Schmidt, A, Kasten, M, Buchmann, I, Eckerle, S, Bähre, M, Münchau, A, Djarmati, A, van der Vegt, J
, Siebner, H, Binkofski, F, Ramirez, A, Behrens, MI & Klein, C 2010, '
Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype',
Archives of Neurology, vol. 67, no. 11, pp. 1357-63.
https://doi.org/10.1001/archneurol.2010.281APA
Brüggemann, N., Hagenah, J., Reetz, K., Schmidt, A., Kasten, M., Buchmann, I., Eckerle, S., Bähre, M., Münchau, A., Djarmati, A., van der Vegt, J.
, Siebner, H., Binkofski, F., Ramirez, A., Behrens, M. I., & Klein, C. (2010).
Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype.
Archives of Neurology,
67(11), 1357-63.
https://doi.org/10.1001/archneurol.2010.281Vancouver
Brüggemann N, Hagenah J, Reetz K, Schmidt A, Kasten M, Buchmann I et al.
Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype.
Archives of Neurology. 2010 Nov 1;67(11):1357-63.
https://doi.org/10.1001/archneurol.2010.281Author
Brüggemann, Norbert ; Hagenah, Johann ; Reetz, Kathrin ; Schmidt, Alexander ; Kasten, Meike ; Buchmann, Inga ; Eckerle, Susanne ; Bähre, Manfred ; Münchau, Alexander ; Djarmati, Ana ; van der Vegt, Joyce ; Siebner, Hartwig ; Binkofski, Ferdinand ; Ramirez, Alfredo ; Behrens, Maria I ; Klein, Christine. / Recessively inherited parkinsonism : effect of ATP13A2 mutations on the clinical and neuroimaging phenotype. In: Archives of Neurology. 2010 ; Vol. 67, No. 11. pp. 1357-63.
Bibtex
@article{a05af506d10e475192325674310d6f8f,
title = "Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype",
abstract = "To determine clinical features and to identify changes in brain structure and function in compound heterozygous and heterozygous ATP13A2 mutation carriers.",
keywords = "Aged, Brain, Brain Mapping, Color Perception, Discrimination (Psychology), Female, Genetic Predisposition to Disease, Heterozygote, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Mutation, Nerve Degeneration, Olfactory Perception, Parkinsonian Disorders, Pedigree, Phenotype, Prospective Studies, Proton-Translocating ATPases",
author = "Norbert Br{\"u}ggemann and Johann Hagenah and Kathrin Reetz and Alexander Schmidt and Meike Kasten and Inga Buchmann and Susanne Eckerle and Manfred B{\"a}hre and Alexander M{\"u}nchau and Ana Djarmati and {van der Vegt}, Joyce and Hartwig Siebner and Ferdinand Binkofski and Alfredo Ramirez and Behrens, {Maria I} and Christine Klein",
year = "2010",
month = nov,
day = "1",
doi = "10.1001/archneurol.2010.281",
language = "English",
volume = "67",
pages = "1357--63",
journal = "JAMA Neurology",
issn = "2168-6149",
publisher = "The JAMA Network",
number = "11",
}
RIS
TY - JOUR
T1 - Recessively inherited parkinsonism
T2 - effect of ATP13A2 mutations on the clinical and neuroimaging phenotype
AU - Brüggemann, Norbert
AU - Hagenah, Johann
AU - Reetz, Kathrin
AU - Schmidt, Alexander
AU - Kasten, Meike
AU - Buchmann, Inga
AU - Eckerle, Susanne
AU - Bähre, Manfred
AU - Münchau, Alexander
AU - Djarmati, Ana
AU - van der Vegt, Joyce
AU - Siebner, Hartwig
AU - Binkofski, Ferdinand
AU - Ramirez, Alfredo
AU - Behrens, Maria I
AU - Klein, Christine
PY - 2010/11/1
Y1 - 2010/11/1
N2 - To determine clinical features and to identify changes in brain structure and function in compound heterozygous and heterozygous ATP13A2 mutation carriers.
AB - To determine clinical features and to identify changes in brain structure and function in compound heterozygous and heterozygous ATP13A2 mutation carriers.
KW - Aged
KW - Brain
KW - Brain Mapping
KW - Color Perception
KW - Discrimination (Psychology)
KW - Female
KW - Genetic Predisposition to Disease
KW - Heterozygote
KW - Humans
KW - Magnetic Resonance Imaging
KW - Male
KW - Middle Aged
KW - Mutation
KW - Nerve Degeneration
KW - Olfactory Perception
KW - Parkinsonian Disorders
KW - Pedigree
KW - Phenotype
KW - Prospective Studies
KW - Proton-Translocating ATPases
U2 - 10.1001/archneurol.2010.281
DO - 10.1001/archneurol.2010.281
M3 - Journal article
C2 - 21060012
VL - 67
SP - 1357
EP - 1363
JO - JAMA Neurology
JF - JAMA Neurology
SN - 2168-6149
IS - 11
ER -
