S. Cumming
发表
P. Donnan,
J. Glennon,
B. Engelen,
2018
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Jonathan J. Evans,
Jonathan J Evans,
M. Farrugia,
2018,
Front. Neurol..
T. Ashizawa,
S. Rogers,
J. McClure,
2020,
PloS one.
T. Ashizawa,
S. Rogers,
J. McClure,
2019,
bioRxiv.
A. Lucia,
G. Nogales-Gadea,
G. Pintos-Morell,
2020,
Genes.
A. Lucia,
G. Nogales-Gadea,
G. Pintos-Morell,
2020,
Genes.
P. Nopoulos,
J. Long,
V. Magnotta,
2020,
Journal of neuromuscular diseases.
P. Holmans,
S. Tabrizi,
L. Jones,
2019
.
M. Tschannen,
E. Worthey,
P. Herzyk,
2018,
European Journal of Human Genetics.
M. Farrugia,
I. Findlay,
S. Cumming,
2017,
PloS one.
M. Farrugia,
I. Findlay,
S. Cumming,
2017
.
T. Heskes,
P. Donnan,
J. Deux,
2018,
The Lancet Neurology.
Associations Between Variant Repeat Interruptions and Clinical Outcomes in Myotonic Dystrophy Type 1
H. Knoop,
G. Bassez,
H. Lochmüller,
2021,
Neurology: Genetics.
H. Lochmüller,
C. Jimenez-Moreno,
S. Cumming,
2020
.
Hanns Lochmüller,
C. Jimenez-Moreno,
S. Cumming,
2019,
Journal of Neurology.
M. Farrugia,
S. Cumming,
J. Mclean,
2022,
Neuromuscular Disorders.
A. Lucia,
G. Nogales-Gadea,
G. Pintos-Morell,
2020,
Human mutation.
P. Herzyk,
Efthymia Symeonidi,
S. Cumming,
2018,
Protocol Exchange.
M. Willemse,
B. Wieringa,
V. Mouly,
2017,
Molecular therapy : the journal of the American Society of Gene Therapy.
J. Glennon,
S. Treweek,
Hanns Lochmüller,
2022,
BMC Medicine.
A. Morton,
William Tottey,
V. Wheeler,
2021,
Journal of Huntington's disease.
H. Lochmüller,
C. Jimenez-Moreno,
S. Cumming,
2019,
Acta neurologica Scandinavica.
P. Nopoulos,
L. Gutmann,
D. Moser,
2021,
Frontiers in Neurology.
P. Holmans,
R. Roos,
S. Tabrizi,
2019,
EBioMedicine.
Guillaume Bassez,
Arend Heerschap,
Baziel G M van Engelen,
2019,
Neurology.
MSH3 modifies somatic instability and disease severity in Huntington’s and myotonic dystrophy type 1
Nick C Fox,
T. Heskes,
C. Kennard,
2019,
Brain : a journal of neurology.
G. Bassez,
H. Lochmüller,
B. V. van Engelen,
2019,
Neurology.
H. Lochmüller,
C. Jimenez-Moreno,
S. Cumming,
2020,
Journal of Neurology.
P. Nopoulos,
A. Atalaia,
M. Farrugia,
2022,
Neuromuscular Disorders.
M. Farrugia,
I. Findlay,
S. Cumming,
2017,
PLoS ONE.
M. Tschannen,
E. Worthey,
P. Herzyk,
2018,
European Journal of Human Genetics.
P. Nopoulos,
J. Long,
V. Magnotta,
2022,
Frontiers in Neurology.
P. Nopoulos,
V. Magnotta,
L. Gutmann,
2021,
Neurology: Genetics.
P. Nopoulos,
J. Long,
V. Magnotta,
2023,
Neuromuscular Disorders.
T. Heskes,
P. Donnan,
J. Deux,
2018,
The Lancet Neurology.