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De Vriendt, E.
65
results:
Search for persons
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Online (65)
Mediatypes
Articles (Online) (49)
Bookchapter (Online) (1)
OpenAccess-fulltext (15)
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1
Increased prime edit rates in KCNQ2 and SCN1A via single ni..:
Dirkx, N.
;
Weuring, Wout J.
;
De Vriendt, E.
...
BMC Biology. 21 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
?
2
phenotypic and genetic heterogeneity of adult patients with..:
Peric, S.
;
Markovic, V.
;
De Vriendt, E.
...
Journal of the Neurological Sciences. 405 (2019) - p. 59-60 , 2019
Link:
https://doi.org/10.1016/..
?
3
G.P.237:
Peeters, K.
;
Litvinenko, I.
;
Chamova, T.
...
Neuromuscular Disorders. 24 (2014) 9-10 - p. 888 , 2014
Link:
https://doi.org/10.1016/..
?
4
Deficiency of the E3 ubiquitin ligase TRIM2 in early-onset ..:
Ylikallio, E.
;
Poyhonen, R.
;
Zimon, M.
...
Human Molecular Genetics. 22 (2013) 15 - p. 2975-2983 , 2013
Link:
https://doi.org/10.1093/..
?
5
G.O.7 Distal myopathy with upper limb predominance caused b..:
Guergueltcheva, V.
;
Peeters, K.
;
Baets, J.
...
Neuromuscular Disorders. 22 (2012) 9-10 - p. 874-875 , 2012
Link:
https://doi.org/10.1016/..
?
6
Distal myopathy with upper limb predominance caused byfilam..:
Guergueltcheva, V.
;
Peeters, K.
;
Baets, J.
...
Neurology. 77 (2011) 24 - p. 2105-2114 , 2011
Link:
https://doi.org/10.1212/..
?
7
DominantGDAP1mutations cause predominantly mild CMT phenoty..:
Zimoń, M.
;
Baets, J.
;
Fabrizi, G.M.
...
Neurology. 77 (2011) 6 - p. 540-548 , 2011
Link:
https://doi.org/10.1212/..
?
8
Genetic spectrum of hereditary neuropathies with onset in t..:
Baets, J.
;
Deconinck, T.
;
De Vriendt, E.
...
Brain. 134 (2011) 9 - p. 2664-2676 , 2011
Link:
https://doi.org/10.1093/..
?
9
Genes for hereditary sensory and autonomic neuropathies: a ..:
Rotthier, A.
;
Baets, J.
;
Vriendt, E. D.
...
Brain. 132 (2009) 10 - p. 2699-2711 , 2009
Link:
https://doi.org/10.1093/..
?
10
Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie..:
Claeys, K. G.
;
Zuchner, S.
;
Kennerson, M.
...
Brain. 132 (2009) 7 - p. 1741-1752 , 2009
Link:
https://doi.org/10.1093/..
?
11
Relative contribution of mutations in genes for autosomal d..:
Dierick, I.
;
Baets, J.
;
Irobi, J.
...
Brain. 131 (2007) 5 - p. 1217-1227 , 2007
Link:
https://doi.org/10.1093/..
?
12
A novel locus for hereditary spastic paraplegia with thin c..:
Al-Yahyaee, S.
;
Al-Gazali, L. I.
;
De Jonghe, P.
...
Neurology. 66 (2006) 8 - p. 1230-1234 , 2006
Link:
https://doi.org/10.1212/..
?
13
SPTLC1mutation in twin sisters with hereditary sensory neur..:
Verhoeven, K.
;
Coen, K.
;
De Vriendt, E.
...
Neurology. 62 (2004) 6 - p. 1001-1002 , 2004
Link:
https://doi.org/10.1212/..
?
14
Autosomal dominante striatale Degeneration - eine hereditär..:
Kuhlenbäumer, G
;
Schirmacher, A
;
Lüdemann, P
...
Aktuelle Neurologie. 31 (2004) S 1 - p. , 2004
Link:
https://doi.org/10.1055/..
?
15
Autosomal dominant striatal degeneration (ADSD): Clinical d..:
Kuhlenbäumer, G.
;
Lüdemann, P.
;
Schirmacher, A.
...
Neurology. 62 (2004) 12 - p. 2203-2208 , 2004
Link:
https://doi.org/10.1212/..
1-15