Статии с изисквания за обществен достъп - Peter P. Pramstaller, MDНаучете повече
Не е налице никъде: 16
Преглед
Substantia nigra hyperechogenicity correlates with clinical status and number of Parkin mutated alleles
JM Hagenah, IR König, B Becker, R Hilker, M Kasten, K Hedrich, ...
Journal of neurology 254, 1407-1413, 2007
Изисквания: German Research Foundation
Преглед
Impaired sense of smell and color discrimination in monogenic and idiopathic Parkinson's disease
L Kertelge, N Brüggemann, A Schmidt, V Tadic, C Wisse, S Dankert, ...
Movement disorders 25 (15), 2665-2669, 2010
Изисквания: US National Institutes of Health, German Research Foundation
Преглед
Recurrent LRRK2 (Park8) mutations in early‐onset Parkinson's disease
K Hedrich, S Winkler, J Hagenah, K Kabakci, M Kasten, E Schwinger, ...
Movement disorders: official journal of the Movement Disorder Society 21 (9 …, 2006
Изисквания: German Research Foundation
Преглед
Variation in the Uric Acid Transporter Gene SLC2A9 and Its Association with AAO of Parkinson’s Disease
MF Facheris, AA Hicks, C Minelli, JM Hagenah, V Kostic, S Campbell, ...
Journal of Molecular Neuroscience 43, 246-250, 2011
Изисквания: German Research Foundation
Преглед
Structural imaging in the presymptomatic stage of genetically determined parkinsonism
K Reetz, V Tadic, M Kasten, N Brüggemann, A Schmidt, J Hagenah, ...
Neurobiology of disease 39 (3), 402-408, 2010
Изисквания: German Research Foundation
Преглед
Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?
K Lohmann-Hedrich, A Neumann, A Kleensang, T Lohnau, H Muhle, ...
Neurology 70 (9), 686-694, 2008
Изисквания: German Research Foundation
Преглед
Frequency of heterozygous Parkin mutations in healthy subjects: need for careful prospective follow-up examination of mutation carriers
N Brüggemann, M Mitterer, AJ Lanthaler, A Djarmati, J Hagenah, ...
Parkinsonism & related disorders 15 (6), 425-429, 2009
Изисквания: German Research Foundation
Преглед
Co‐occurrence of restless legs syndrome and Parkin mutations in two families
S Adel, A Djarmati, K Kabakci, I Pichler, C Eskelson, T Lohnau, N Kock, ...
Movement disorders 21 (2), 258-263, 2006
Изисквания: German Research Foundation
Преглед
Nonmotor symptoms in Parkin gene‐related parkinsonism
G Kägi, C Klein, NW Wood, SA Schneider, PP Pramstaller, V Tadic, ...
Movement Disorders 25 (9), 1279-1284, 2010
Изисквания: German Research Foundation
Преглед
Exome sequencing in a family with restless legs syndrome
A Weissbach, K Siegesmund, N Brüggemann, A Schmidt, M Kasten, ...
Movement disorders 27 (13), 1686-1689, 2012
Изисквания: German Research Foundation
Преглед
Eye movement disorders are different in Parkin-linked and idiopathic early-onset PD
B Machner, C Klein, A Sprenger, P Baumbach, PP Pramstaller, ...
Neurology 75 (2), 125-128, 2010
Изисквания: German Research Foundation
Преглед
Primary familial brain calcification in the ‘IBGC2’ kindred: All linkage roads lead to SLC20A2
K Grütz, CB Volpato, A Domingo, D Alvarez‐Fischer, U Gebert, ...
Movement Disorders 31 (12), 1901-1904, 2016
Изисквания: US National Institutes of Health, German Research Foundation
Преглед
Abnormal premotor–motor interaction in heterozygous Parkin-and Pink1 mutation carriers
A Weissbach, T Bäumer, PP Pramstaller, N Brüggemann, V Tadic, ...
Clinical neurophysiology 128 (1), 275-280, 2017
Изисквания: German Research Foundation, European Commission
Преглед
Influence of L-dopa on subtle motor signs in heterozygous Parkin-and PINK1 mutation carriers
A Weissbach, IR König, K Hückelheim, PP Pramstaller, E Werner, ...
Parkinsonism & Related Disorders 42, 95-99, 2017
Изисквания: German Research Foundation, European Commission
Преглед
Parkin gene modifies the effect of RLS4 on the age at onset of restless legs syndrome (RLS)
I Pichler, F Marroni, C Pattaro, K Lohmann, A De Grandi, C Klein, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153 …, 2010
Изисквания: German Research Foundation
Преглед
Task matters-challenging the motor system allows distinguishing unaffected Parkin mutation carriers from mutation-free controls
J Prasuhn, M Borsche, AA Hicks, M Gögele, C Egger, C Kritzinger, ...
Parkinsonism & Related Disorders 86, 101-104, 2021
Изисквания: German Research Foundation
Налице някъде: 215
Преглед
Heart disease and stroke statistics—2017 update: a report from the American Heart Association
EJ Benjamin, MJ Blaha, SE Chiuve, M Cushman, SR Das, R Deo, ...
circulation 135 (10), e146-e603, 2017
Изисквания: US National Institutes of Health, American Heart Association
Преглед
Genetic studies of body mass index yield new insights for obesity biology
AE Locke, B Kahali, SI Berndt, AE Justice, TH Pers, FR Day, C Powell, ...
Nature 518 (7538), 197-206, 2015
Изисквания: US National Institutes of Health, British Heart Foundation, Cancer Research …
Преглед
Biological, clinical and population relevance of 95 loci for blood lipids
TM Teslovich, K Musunuru, AV Smith, AC Edmondson, IM Stylianou, ...
Nature 466 (7307), 707-713, 2010
Изисквания: US National Institutes of Health, British Heart Foundation
Преглед
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
EK Speliotes, CJ Willer, SI Berndt, KL Monda, G Thorleifsson, AU Jackson, ...
Nature genetics 42 (11), 937-948, 2010
Изисквания: Swiss National Science Foundation, US National Institutes of Health, German …
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