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X
De Vriendt, E.
64  Ergebnisse:
Personensuche X
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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9

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/..
 
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10

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/..
 
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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/..
 
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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/..
 
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13

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/..
 
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14

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/..
 
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15

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/..
 
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