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Rossor, M
~ 900
results:
Search for persons
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Format
Online
Mediatypes
E-Books
Articles (Online)
OpenAccess-fulltext
Languages
english (879)
french (1)
Sorted by: Relevance
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?
1
Are we prepared for clinical trials in Charcot-Marie-Tooth ..:
Rossor, A.M.
;
Shy, M.E.
;
Reilly, M.M.
Brain Research. 1729 (2020) - p. 146625 , 2020
Link:
https://doi.org/10.1016/..
?
2
Corrigendum to Routine blood monitoring in maintenance Immu..:
Keh, R.
;
Khalil, A.
;
Nihoyannopoulos, L.
...
Journal of the Neurological Sciences. 417 (2020) - p. 116988 , 2020
Link:
https://doi.org/10.1016/..
?
3
Routine blood monitoring in maintenance immunoglobulin trea..:
Keh, R.
;
Kahlil, A.
;
Nihoyannopoulos, L.
...
Journal of the Neurological Sciences. 408 (2020) - p. 116527 , 2020
Link:
https://doi.org/10.1016/..
?
4
Gene replacement therapy after neuropathy onset provides th..:
Kagiava, A
;
Richter, J
;
Tryfonos, C
...
Human Molecular Genetics. 28 (2019) 21 - p. 3528-3542 , 2019
Link:
https://doi.org/10.1093/..
?
5
Plasma neurofilament light chain levels are raised in patie..:
Rossor, A.M.
;
Sandelius, A.
;
Adiutori, R.
...
Neuromuscular Disorders. 28 (2018) - p. S23 , 2018
Link:
https://doi.org/10.1016/..
?
6
Frequency of genetic variants in Charcot-Marie-Tooth diseas..:
Pipis, M.
;
Rossor, A.M.
;
Polke, J.
..
Neuromuscular Disorders. 28 (2018) - p. S22 , 2018
Link:
https://doi.org/10.1016/..
?
7
Functional validation of non-coding variants of GJB1 in pat..:
Cortese, A.
;
Manole, A.
;
Ashokkumar, B.
...
Neuromuscular Disorders. 27 (2017) - p. S25 , 2017
Link:
https://doi.org/10.1016/..
?
8
A Homozygous Reticulon 2 mutation is a cause of DHMN with p..:
Rossor, A.M.
;
Rebelo, A.
;
Horga, A.
...
Neuromuscular Disorders. 27 (2017) - p. S24 , 2017
Link:
https://doi.org/10.1016/..
?
9
Modulation of cytoplasmic dynein and tubulin modification a..:
Green, R.L.
;
Simoes, F.A.
;
Reyes-Aldasoro, C.C.
...
Neuromuscular Disorders. 27 (2017) - p. S1 , 2017
Link:
https://doi.org/10.1016/..
?
10
Thromboembolic risk in inflammatory neuromuscular disease p..:
Spillane, J.
;
Englezou, C.
;
Sarri-Gonzales, S.
...
Neuromuscular Disorders. 27 (2017) - p. S24 , 2017
Link:
https://doi.org/10.1016/..
?
11
Clinical features and genetic findings in patients with Cha..:
Cortese, A.
;
Laurá, M.
;
Polke, J.M.
...
Neuromuscular Disorders. 27 (2017) - p. S25 , 2017
Link:
https://doi.org/10.1016/..
?
12
Neurology: a Queen Square textbook:
Clarke, Charles
;
Howard, Robin
;
Rossor, M
. - Second edition . , 2016
Link:
https://onlinelibrary.wi..
?
13
P56 Whole-exome sequencing in patients with sensory and mot..:
Horga, A.
;
Cottenie, E.
;
Liu, Y-T.
...
Neuromuscular Disorders. 24 (2014) - p. S22 , 2014
Link:
https://doi.org/10.1016/..
?
14
P54 A dominant negative mutation in FBXO38 is a cause of di..:
Rossor, A.M.
;
d'Ydewalle, C.
;
Wooley, J.
...
Neuromuscular Disorders. 24 (2014) - p. S21 , 2014
Link:
https://doi.org/10.1016/..
?
15
P52 A novel p.glu175x premature stop mutation in the C-term..:
Rossor, A.M.
;
Davidson, G.
;
Houlden, H.H.
...
Neuromuscular Disorders. 22 (2012) - p. S21 , 2012
Link:
https://doi.org/10.1016/..
1-15