S. Otto
发表
Zacharias Kohl,
Jan Kassubek,
Stephan Züchner,
2016,
Annals of neurology.
L. Schöls,
H. Przuntek,
S. Otto,
1995,
Journal of Neurology.
S. Klebe,
R. Schüle,
L. Schöls,
2013,
Orphanet Journal of Rare Diseases.
R. Gold,
S. Otto,
M. Yoon,
2021,
Therapeutic advances in neurological disorders.
R. Gold,
S. Otto,
M. Yoon,
2021,
Annals of clinical and translational neurology.
R. Schüle,
L. Schöls,
J. Kassubek,
2008,
Journal of Neurology, Neurosurgery, and Psychiatry.
S. Klebe,
P. Bauer,
R. Schüle,
2012,
neurogenetics.
REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31.
M. Pericak-Vance,
H. Smeets,
S. Züchner,
2008,
Brain : a journal of neurology.
J Kassubek,
T. Holland-Letz,
R. Schüle,
2006,
Neurology.
R. Gold,
S. Otto,
M. Yoon,
2020,
European journal of neurology.
O. Witte,
R. Schüle,
L. Schöls,
2006,
Neurology.
S. Klebe,
A. Durr,
P. Bauer,
2010,
European Journal of Human Genetics.
S. Klebe,
R. Schüle,
L. Schöls,
2008,
Journal of the Neurological Sciences.
S. Klebe,
S. Züchner,
P. Bauer,
2016
.
S. Otto,
F. Erbguth,
S. Pittock,
2001,
European journal of neurology.
S. Klebe,
P. Bauer,
R. Schüle,
2012,
neurogenetics.
J. Kassubek,
S. Klebe,
R. Schüle,
2012,
European journal of neurology.
REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31.
M. Pericak-Vance,
H. Smeets,
S. Züchner,
2008,
Brain : a journal of neurology.