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Hotzy, C.
10  Ergebnisse:
Personensuche X
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1

Hereditary spastic paraplegia caused by compound heterozygo..:

Krenn, M. ; Zulehner, G. ; Hotzy, C....
European Journal of Neurology.  24 (2017)  5 - p. 741-747 , 2017
Link: https://doi.org/10.1111/..
 
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2

A splice site variant in the sodium channel geneSCN1Aconfer..:

Schlachter, K. ; Gruber-Sedlmayr, U. ; Stogmann, E....
Neurology.  72 (2009)  11 - p. 974-978 , 2009
Link: https://doi.org/10.1212/..
 
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3

Idiopathic generalized epilepsy phenotypes associated with ..:

Stogmann, E. ; Lichtner, P. ; Baumgartner, C....
Neurology.  67 (2006)  11 - p. 2029-2031 , 2006
Link: https://doi.org/10.1212/..
 
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4

Mutations in the CLCN2 gene are a rare cause of idiopathic ..:

Stogmann, E. ; Lichtner, P. ; Baumgartner, C....
Neurogenetics.  7 (2006)  4 - p. 265-268 , 2006
Link: https://doi.org/10.1007/..
 
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5

TPP2 mutation associated with sterile brain inflammation mi..:

Reinthaler, E.M ; Graf, E ; Zrzavy, T...
info:eu-repo/semantics/altIdentifier/doi/10.1212/NXG.0000000000000285.  , 2018
Link: https://push-zb.helmholt..
 
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6

Evidence that the N-terminal part of the S-layer protein fr..:

Ries, W ; Hotzy, C ; Schocher, I..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC179197.  , 1997
Link: http://www.ncbi.nlm.nih...
 
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7

Rare variants in γ‐aminobutyric acid type A receptor genes ..:

Reinthaler, Eva M. ; Dejanovic, Borislav ; Lal, Dennis...
Annals of Neurology.  77 (2015)  6 - p. 972-986 , 2015
Link: https://doi.org/10.1002/..
 
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8

Replication study of multiple sclerosis (MS) susceptibility..:

Schmied, Mascha C. ; Zehetmayer, Sonja ; Reindl, Markus...
neurogenetics.  13 (2012)  2 - p. 181-187 , 2012
Link: https://doi.org/10.1007/..
 
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9

A Mutation in VPS35, Encoding a Subunit of the Retromer Com..:

Zimprich, Alexander ; Benet-Pagès, Anna ; Struhal, Walter...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135812.  , 2011
Link: http://www.ncbi.nlm.nih...
 
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10

Prescription frequency and development of liraglutide and e..:

Seidel, K ; Jacob, C ; Schwedler, D.
http://dx.doi.org/10.3205/21dkvf068.  , 2021
Link: https://doi.org/10.3205/..
 
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