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European Journal of Neurology
|
April 21, 2010
EFNS guidelines on the diagnostic approach to pauci- or asymptomatic hyperCKemia
T Kyriakides, C Angelini, J Schaefer, et al.
Biochemistry and Biophysics Reports
|
September 29, 2017
Genetic background modifies amyloidosis in a mouse model of ATTR neuropathy
E Panayiotou, R Papacharalambous, A Antoniou, et al.
Genetic Testing
|
August 28, 1999
Neonatal screening for Duchenne muscular dystrophy: a novel semiquantitative application of the bioluminescence test for creatine kinase in a pilot national program in Cyprus
A Drousiotou, P Ioannou, T Georgiou, et al.
Electromyography and Clinical Neurophysiology
|
November 25, 2003
Click evoked neurogenic vestibular potentials (NVESTEPs): a method of assessing the function of the vestibular system
E Papathanasiou, E Zamba-Papanicolaou, M Pantziaris, et al.
Electromyography and Clinical Neurophysiology
|
August 9, 2005
Vestibular symptoms and signs are correlated with abnormal neurogenic vestibular evoked potentials in patients with multiple sclerosis
E S Papathanasiou, C Piperidou, M Pantzaris, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
May 29, 2015
Genetic findings of Cypriot spinal muscular atrophy patients
L Theodorou, P Nicolaou, P Koutsou, et al.
Electromyography and Clinical Neurophysiology
|
September 24, 2004
Neurogenic vestibular evoked potentials in the diagnosis of multiple sclerosis
E S Papathanasiou, M Pantzaris, E Zamba-Papanicolaou, et al.
Revue Neurologique
|
December 25, 2002
[Hereditary Motor Neuronopathies]
E. Zamba-Papanicolaou[[sup]][[/sup, K. Christodoulou[[sup]][[/sup, C. Christodoulou[[sup]][[/sup, et al.
Neurology
|
February 16, 2006
Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X
K A Kleopa, E Zamba-Papanicolaou, X Alevra, et al.
Muscle & Nerve
|
April 1, 1993
The clinical significance of type 1 fiber predominance
T Kyriakides, J M Silberstein, S Jongpiputvanich, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 47) with videos related to
Sort By:
Page
of 5
European Journal of Neurology
|
April 21, 2010
EFNS guidelines on the diagnostic approach to pauci- or asymptomatic hyperCKemia
T Kyriakides, C Angelini, J Schaefer, et al.
Biochemistry and Biophysics Reports
|
September 29, 2017
Genetic background modifies amyloidosis in a mouse model of ATTR neuropathy
E Panayiotou, R Papacharalambous, A Antoniou, et al.
Genetic Testing
|
August 28, 1999
Neonatal screening for Duchenne muscular dystrophy: a novel semiquantitative application of the bioluminescence test for creatine kinase in a pilot national program in Cyprus
A Drousiotou, P Ioannou, T Georgiou, et al.
Electromyography and Clinical Neurophysiology
|
November 25, 2003
Click evoked neurogenic vestibular potentials (NVESTEPs): a method of assessing the function of the vestibular system
E Papathanasiou, E Zamba-Papanicolaou, M Pantziaris, et al.
Electromyography and Clinical Neurophysiology
|
August 9, 2005
Vestibular symptoms and signs are correlated with abnormal neurogenic vestibular evoked potentials in patients with multiple sclerosis
E S Papathanasiou, C Piperidou, M Pantzaris, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
May 29, 2015
Genetic findings of Cypriot spinal muscular atrophy patients
L Theodorou, P Nicolaou, P Koutsou, et al.
Electromyography and Clinical Neurophysiology
|
September 24, 2004
Neurogenic vestibular evoked potentials in the diagnosis of multiple sclerosis
E S Papathanasiou, M Pantzaris, E Zamba-Papanicolaou, et al.
Revue Neurologique
|
December 25, 2002
[Hereditary Motor Neuronopathies]
E. Zamba-Papanicolaou[[sup]][[/sup, K. Christodoulou[[sup]][[/sup, C. Christodoulou[[sup]][[/sup, et al.
Neurology
|
February 16, 2006
Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X
K A Kleopa, E Zamba-Papanicolaou, X Alevra, et al.
Muscle & Nerve
|
April 1, 1993
The clinical significance of type 1 fiber predominance
T Kyriakides, J M Silberstein, S Jongpiputvanich, et al.
Page
of 5