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X
Cottenie, Ellen
8  Ergebnisse:
Personensuche X
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1

Absence of HINT1 mutations in a UK and Spanish cohort of pa..:

Horga, Alejandro ; Cottenie, Ellen ; Tomaselli, Pedro J....
Journal of Neurology.  262 (2015)  8 - p. 1984-1986 , 2015
Link: https://doi.org/10.1007/..
 
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2

Truncating and Missense Mutations in IGHMBP2 Cause Charcot-..:

Cottenie, Ellen ; Kochanski, Andrzej ; Jordanova, Albena...
The American Journal of Human Genetics.  95 (2014)  5 - p. 590-601 , 2014
Link: https://doi.org/10.1016/..
 
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3

Mutations in gamma adducin are associated with inherited ce..:

Kruer, Michael C. ; Jepperson, Tyler ; Dutta, Sudeshna...
Annals of Neurology.  74 (2013)  6 - p. 805-814 , 2013
Link: https://doi.org/10.1002/..
 
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4

Rapidly progressive asymmetrical weakness in Charcot–Marie–..:

Cottenie, Ellen ; Menezes, Manoj P. ; Rossor, Alexander M....
Neuromuscular Disorders.  23 (2013)  5 - p. 399-403 , 2013
Link: https://doi.org/10.1016/..
 
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5

Genetic dysfunction ofMT-ATP6causes axonal Charcot-Marie-To..:

Pitceathly, Robert D.S. ; Murphy, Sinéad M. ; Cottenie, Ellen...
Neurology.  79 (2012)  11 - p. 1145-1154 , 2012
Link: https://doi.org/10.1212/..
 
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6

Truncating and Missense Mutations in IGHMBP2 Cause Charcot-..:

Cottenie, Ellen ; Kochanski, Andrzej ; Jordanova, Albena...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225647/.  , 2014
Link: http://www.ncbi.nlm.nih...
 
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7

Mutations in gamma adducin are associated with inherited ce..:

Kruer, Michael C ; Jepperson, Tyler ; Dutta, Sudeshna...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3952628.  , 2013
Link: http://www.ncbi.nlm.nih...
 
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8

Genetic dysfunction of MT-ATP6 causes axonal Charcot-Marie-..:

Pitceathly, Robert D.S ; Murphy, Sinéad M ; Cottenie, Ellen...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3525307.  , 2012
Link: http://www.ncbi.nlm.nih...
 
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