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Clementine E Karageorgiou

Showing results (1-10 of 5) with videos related to

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Swiss Medical Weekly|July 17, 2007
A novel CADASIL-causing mutation in a stroke patientMichail Vikelis, John Papatriantafyllou, Clementine E Karageorgiou
Functional Neurology|January 21, 2009
On the calculation of transcallosal conduction time using transcranial magnetic stimulationSpyros N Deftereos, Gregory Panagopoulos, Dimitra Georgonikou, et al.
Annals of Clinical and Laboratory Science|December 21, 2016
Possible Implication of GSTP1 and NQO1 Polymorphisms on Natalizumab Response in Multiple SclerosisAthanasia Alexoudi, Sophia Zachaki, Chrysa Stavropoulou, et al.
The International Journal of Neuroscience|March 5, 2014
Combined GSTP1 and NQO1 germline polymorphisms in the susceptibility to Multiple SclerosisAthanasia Alexoudi, Sophia Zachaki, Chrysa Stavropoulou, et al.
Free Radical Biology & Medicine|May 25, 2011
The C609T inborn polymorphism in NAD(P)H:quinone oxidoreductase 1 is associated with susceptibility to multiple sclerosis and affects the risk of development of the primary progressive form of the diseaseChrysa Stavropoulou, Sophia Zachaki, Athanasia Alexoudi, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Swiss Medical Weekly|July 17, 2007
A novel CADASIL-causing mutation in a stroke patientMichail Vikelis, John Papatriantafyllou, Clementine E Karageorgiou
Functional Neurology|January 21, 2009
On the calculation of transcallosal conduction time using transcranial magnetic stimulationSpyros N Deftereos, Gregory Panagopoulos, Dimitra Georgonikou, et al.
Annals of Clinical and Laboratory Science|December 21, 2016
Possible Implication of GSTP1 and NQO1 Polymorphisms on Natalizumab Response in Multiple SclerosisAthanasia Alexoudi, Sophia Zachaki, Chrysa Stavropoulou, et al.
The International Journal of Neuroscience|March 5, 2014
Combined GSTP1 and NQO1 germline polymorphisms in the susceptibility to Multiple SclerosisAthanasia Alexoudi, Sophia Zachaki, Chrysa Stavropoulou, et al.
Free Radical Biology & Medicine|May 25, 2011
The C609T inborn polymorphism in NAD(P)H:quinone oxidoreductase 1 is associated with susceptibility to multiple sclerosis and affects the risk of development of the primary progressive form of the diseaseChrysa Stavropoulou, Sophia Zachaki, Athanasia Alexoudi, et al.
Pageof 1