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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
February 7, 2016
Eye movement abnormalities in a patient with Zellweger spectrum disorder
F Rosini, C Vinciguerra, A Mignarri, et al.
Neurology
|
December 28, 2006
Pulsating enophthalmos in an adult patient with type 1 neurofibromatosis
A Rufa, E Zicari, A Cerase, et al.
Journal of the Neurological Sciences
|
June 19, 2007
Recurrent venous thrombosis including cerebral venous sinus thrombosis in a patient taking sildenafil for erectile dysfunction
A Rufa, A Cerase, L Monti, et al.
Journal of the Neurological Sciences
|
June 10, 2008
Acute vestibular syndrome in a patient with cerebral autosomal dominant leukoencephalopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
A Rufa, A Cerase, L Monti, et al.
Journal of Neurology
|
June 9, 1998
A case of ethambutol-induced optic neuropathy harbouring the primary mitochondrial LHON mutation at nt 11778
M T Dotti, K Plewnia, E Cardaioli, et al.
Journal of Neuroscience Methods
|
May 24, 2014
Nonlinear analysis of saccade speed fluctuations during combined action and perception tasks
C Stan, C Astefanoaei, E Pretegiani, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
April 3, 2004
Wilson's disease with Leu492Ser mutation and arylsulfatase A pseudodeficiency: just a coincidence?
C Battisti, M T Dotti, G Loudianos, et al.
European Journal of Neurology
|
April 21, 2010
Four novel CYP27A1 mutations in seven Italian patients with CTX
G N Gallus, M T Dotti, A Mignarri, et al.
The International Journal of Neuroscience
|
January 20, 2011
Wernicke encephalopathy after gastrointestinal surgery for cancer: causes of diagnostic failure or delay
A Rufa, F Rosini, A Cerase, et al.
American Journal of Medical Genetics
|
July 16, 1999
Detection of a rare Wilson disease mutation associated with arylsulfatase A pseudodeficiency
C Battisti, G Loudianos, A Rufa, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 36) with videos related to
Sort By:
Page
of 4
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
February 7, 2016
Eye movement abnormalities in a patient with Zellweger spectrum disorder
F Rosini, C Vinciguerra, A Mignarri, et al.
Neurology
|
December 28, 2006
Pulsating enophthalmos in an adult patient with type 1 neurofibromatosis
A Rufa, E Zicari, A Cerase, et al.
Journal of the Neurological Sciences
|
June 19, 2007
Recurrent venous thrombosis including cerebral venous sinus thrombosis in a patient taking sildenafil for erectile dysfunction
A Rufa, A Cerase, L Monti, et al.
Journal of the Neurological Sciences
|
June 10, 2008
Acute vestibular syndrome in a patient with cerebral autosomal dominant leukoencephalopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
A Rufa, A Cerase, L Monti, et al.
Journal of Neurology
|
June 9, 1998
A case of ethambutol-induced optic neuropathy harbouring the primary mitochondrial LHON mutation at nt 11778
M T Dotti, K Plewnia, E Cardaioli, et al.
Journal of Neuroscience Methods
|
May 24, 2014
Nonlinear analysis of saccade speed fluctuations during combined action and perception tasks
C Stan, C Astefanoaei, E Pretegiani, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
April 3, 2004
Wilson's disease with Leu492Ser mutation and arylsulfatase A pseudodeficiency: just a coincidence?
C Battisti, M T Dotti, G Loudianos, et al.
European Journal of Neurology
|
April 21, 2010
Four novel CYP27A1 mutations in seven Italian patients with CTX
G N Gallus, M T Dotti, A Mignarri, et al.
The International Journal of Neuroscience
|
January 20, 2011
Wernicke encephalopathy after gastrointestinal surgery for cancer: causes of diagnostic failure or delay
A Rufa, F Rosini, A Cerase, et al.
American Journal of Medical Genetics
|
July 16, 1999
Detection of a rare Wilson disease mutation associated with arylsulfatase A pseudodeficiency
C Battisti, G Loudianos, A Rufa, et al.
Page
of 4