Search research articles
Contact Us
Filters
Showing results (241-250 of 248) with videos related to
Page
of 25
Sort By:
You have reached the last page of results.
This site can display upto 248 results.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
May 18, 2007
Headache and anxiety-depressive disorder comorbidity: the HADAS study
E Beghi, G Allais, P Cortelli, et al.
European Journal of Neurology
|
March 23, 2012
Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern?
C La Morgia, P Barboni, G Rizzo, et al.
The Journal of Headache and Pain
|
May 31, 2012
Cost of healthcare for patients with migraine in five European countries: results from the International Burden of Migraine Study (IBMS)
L M Bloudek, M Stokes, D C Buse, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
December 13, 2018
Red Flags for early referral of people with symptoms suggestive of narcolepsy: a report from a national multidisciplinary panel
L Vignatelli, E Antelmi, I Ceretelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
May 18, 2007
Validation of AIDA Cefalee, a computer-assisted diagnosis database for the management of headache patients
R De Simone, G Coppola, A Ranieri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
January 28, 2003
PARK6 is a common cause of familial parkinsonism
E M Valente, F Brancati, V Caputo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 16, 2015
New insights into orthostatic hypotension in multiple system atrophy: a European multicentre cohort study
A Pavy-Le Traon, A Piedvache, S Perez-Lloret, et al.
Science (New York, N.Y.)
|
March 3, 2009
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis
T J Kwiatkowski, D A Bosco, A L Leclerc, et al.
Page
of 25
Search research articles
Search
Showing results (241-250 of 248) with videos related to
Sort By:
Page
of 25
You have reached the last page of results.
This site can display upto 248 results.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
May 18, 2007
Headache and anxiety-depressive disorder comorbidity: the HADAS study
E Beghi, G Allais, P Cortelli, et al.
European Journal of Neurology
|
March 23, 2012
Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern?
C La Morgia, P Barboni, G Rizzo, et al.
The Journal of Headache and Pain
|
May 31, 2012
Cost of healthcare for patients with migraine in five European countries: results from the International Burden of Migraine Study (IBMS)
L M Bloudek, M Stokes, D C Buse, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
December 13, 2018
Red Flags for early referral of people with symptoms suggestive of narcolepsy: a report from a national multidisciplinary panel
L Vignatelli, E Antelmi, I Ceretelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
May 18, 2007
Validation of AIDA Cefalee, a computer-assisted diagnosis database for the management of headache patients
R De Simone, G Coppola, A Ranieri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
January 28, 2003
PARK6 is a common cause of familial parkinsonism
E M Valente, F Brancati, V Caputo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 16, 2015
New insights into orthostatic hypotension in multiple system atrophy: a European multicentre cohort study
A Pavy-Le Traon, A Piedvache, S Perez-Lloret, et al.
Science (New York, N.Y.)
|
March 3, 2009
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis
T J Kwiatkowski, D A Bosco, A L Leclerc, et al.
Page
of 25