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Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study
19 auth.
A. Djarmati,
S. Schneider,
K. Lohmann,
Susen Winkler,
H. Pawlack,
J. Hagenah,
N. Brüggemann,
S. Zittel,
Tania Fuchs,
A. Rakovic,
...
A. Schmidt,
H. Jabusch,
R. Wilcox,
V. Kostic,
H. Siebner,
E. Altenmüller,
A. Münchau,
L. Ozelius,
C. Klein
|
7 |
2009 |
7 🐜
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PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism
18 auth.
C. Klein,
A. Djarmati,
K. Hedrich,
N. Schäfer,
C. Scaglione,
R. Marchese,
N. Kock,
B. Schüle,
A. Hiller,
T. Lohnau,
...
Susen Winkler,
Karin Wiegers,
R. Hering,
P. Bauer,
O. Riess,
G. Abbruzzese,
P. Martinelli,
P. Pramstaller
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7 |
2005 |
7 🐜
|
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Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene
29 auth.
K. Lohmann,
R. Wilcox,
Susen Winkler,
A. Ramírez,
A. Rakovic,
Jin-Sung Park,
B. Arns,
T. Lohnau,
J. Groen,
M. Kasten,
N. Brüggemann,
J. Hagenah,
A. Schmidt,
F. Kaiser,
K. Kumar,
...
Katja Zschiedrich,
D. Alvarez-Fischer,
E. Altenmüller,
A. Ferbert,
A. Lang,
A. Münchau,
V. Kostic,
K. Simonyan,
M. Agzarian,
L. Ozelius,
A. Langeveld,
C. Sue,
M. Tijssen,
C. Klein
|
7 |
2013 |
7 🐜
|
🦁
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α-Synuclein and Parkinson disease susceptibility
9 auth.
Susen Winkler,
J. Hagenah,
Sarah Lincoln,
Michael G. Heckman,
K. Haugarvoll,
K. Lohmann‐Hedrich,
...
Vladimir S. Kostić,
M. Farrer,
C. Klein
|
7 |
2007 |
7 🦁
|
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Bilateral subthalamic stimulation in Parkin and PINK1 parkinsonism
18 auth.
E. Moro,
J. Volkmann,
Inke König,
Susen Winkler,
A. Hiller,
S. Hassin-Baer,
J. Herzog,
A. Schnitzler,
K. Lohmann,
M. Pinsker,
...
J. Voges,
A. Djarmatic,
Philip Seibler,
A. Lozano,
E. Rogaeva,
A. Lang,
G. Deuschl,
C. Klein
|
6 |
2008 |
6 🐜
|
🐜
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ATP13A2 variants in early‐onset Parkinson's disease patients and controls
19 auth.
A. Djarmati,
J. Hagenah,
K. Reetz,
Susen Winkler,
M. Behrens,
H. Pawlack,
K. Lohmann,
A. Ramírez,
V. Tadić,
N. Brüggemann,
...
D. Berg,
H. Siebner,
A. Lang,
P. Pramstaller,
F. Binkofski,
V. Kostic,
J. Volkmann,
T. Gasser,
C. Klein
|
6 |
2009 |
6 🐜
|
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Childhood‐onset restless legs syndrome: Clinical and genetic features of 22 families
11 auth.
H. Muhle,
A. Neumann,
K. Lohmann‐Hedrich,
T. Lohnau,
Yang Lu,
Susen Winkler,
...
S. Waltz,
A. Fischenbeck,
P. Kramer,
C. Klein,
U. Stephani
|
5 |
2008 |
5 🐜
|
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Whispering dysphonia in an Australian family (DYT4): A clinical and genetic reappraisal
R. Wilcox,
Susen Winkler,
K. Lohmann,
C. Klein
|
5 |
2011 |
5 🐬
|
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Myoclonus-dystonia due to maternal uniparental disomy.
12 auth.
E. Guettard,
M. Portnoi,
K. Lohmann‐Hedrich,
B. Keren,
S. Rossignol,
Susen Winkler,
...
Imen El Kamel,
Smaranda Leu,
E. Apartis,
M. Vidailhet,
C. Klein,
E. Roze
|
5 |
2008 |
5 🐜
|