G. Wunderlich
发表
B. Wirth,
R. Boostani,
R. Heller,
2018,
Human mutation.
R. Baron,
C. Sommer,
E. Hund,
2020,
Journal of Neurology.
G. Fink,
C. Sommer,
H. Lehmann,
2020,
Neurological Research and Practice.
H. Reichmann,
M. Forsting,
S. Petri,
2020,
The Lancet Neurology.
G. Fink,
A. Brunn,
M. Deckert,
2017,
Journal of Neurology, Neurosurgery, and Psychiatry.
G. Fink,
H. Lehmann,
G. Wunderlich,
2021,
European journal of neurology.
G. Fink,
P. Albrecht,
J. Gielen,
2020,
Journal of Neurology.
V. Visser-Vandewalle,
M. Barbe,
T. Haack,
2022,
Neurological Research and Practice.
B. Schlotter-Weigel,
M. Blankenburg,
P. Huppke,
2022,
Orphanet Journal of Rare Diseases.
D. Maintz,
K. Laukamp,
K. Weiss,
2022,
Journal of Neurology.
G. Fink,
Veronika Dunkl,
H. Lehmann,
2016,
Journal of the Neurological Sciences.
G. Fink,
A. Brunn,
J. Weis,
2018,
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.
B. Wirth,
J. Petry-Schmelzer,
M. Karakaya,
2021,
Movement disorders clinical practice.
G. Fink,
J. Weis,
H. Lehmann,
2020,
Der Nervenarzt.
Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia
M. Kloss,
K. Kiening,
A. Koy,
2019,
Journal of Human Genetics.
S. Çırak,
U. Yiş,
D. Okur,
2019,
The Turkish journal of pediatrics.
G. Wunderlich,
2023,
Neurologie up2date.
E. Puffenberger,
K. Strauss,
B. Wirth,
2020,
The American Journal of Human Genetics.
Katherine R. Smith,
M. B. Pereira,
A. Need,
2021,
Brain : a journal of neurology.
G. Fink,
A. Brunn,
H. Lehmann,
2016,
Fortschritte der Neurologie-Psychiatrie.
M. Sturm,
S. Paus,
S. Ossowski,
2021,
Neurology: Genetics.
B. Wirth,
R. Boostani,
S. Yılmaz,
2021,
Human mutation.
H. Zempel,
G. Wunderlich,
Mohamed AGHYAD AL KABBANI,
2022,
BIOCELL.
F. Klein,
H. Lehmann,
G. Fink,
2022,
European journal of neurology.
G. Fink,
K. Claeys,
A. Brunn,
2018,
Acta Neurologica Belgica.
T. Hagenacker,
B. Braumann,
G. Wunderlich,
2023,
Orphanet Journal of Rare Diseases.
G. Fink,
B. Braumann,
H. Lehmann,
2020,
Frontiers in Neurology.
G. Fink,
C. Kabbasch,
H. Lehmann,
2019,
Practical Neurology.
G. Fink,
E. Neuen‐Jacob,
H. Lehmann,
2017,
Zeitschrift für Rheumatologie.
Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia
M. Kloss,
K. Kiening,
A. Koy,
2019,
Journal of Human Genetics.
B. Wirth,
R. Boostani,
R. Heller,
2018,
Human mutation.