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Neurology
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August 26, 1998
Giant dystrophin deletion associated with congenital cataract and mild muscular dystrophy
M Mirabella, G Galluzzi, G Manfredi, et al.
Experimental Brain Research
|
August 11, 2001
Inhibition of biceps brachii muscle motor area by painful heat stimulation of the skin
M Valeriani, D Restuccia, V Di Lazzaro, et al.
Neuromuscular Disorders : NMD
|
June 14, 2002
Hypermyelinating neuropathy, mental retardation and epilepsy in a case of merosin deficiency
F Deodato, M Sabatelli, E Ricci, et al.
Journal of the Neurological Sciences
|
March 1, 1993
Manifesting heterozygotes in McArdle's disease: clinical, morphological and biochemical studies in a family
G Manfredi, G Silvestri, S Servidei, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 1, 1996
Changes in spinal cord excitability in a patient with rhythmic segmental myoclonus
V Di Lazzaro, D Restuccia, R Nardone, et al.
Neuromuscular Disorders : NMD
|
February 5, 2008
Natural history of CMT1A including QoL: a 2-year prospective study
L Padua, D Pareyson, I Aprile, et al.
Journal of Neurology
|
December 24, 1997
Ocular palsies in the absence of other neurological or ocular symptoms: analysis of 105 cases
A P Batocchi, A Evoli, L Majolini, et al.
European Journal of Neurology
|
August 28, 2003
Incidence of first-ever ischemic and hemorrhagic stroke in a well-defined community of southern Italy, 1993-1995
D Intiso, P Stampatore, M M Zarrelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
August 7, 2001
Neurophysiological classification of ulnar entrapment across the elbow
L Padua, I Aprile, O Mazza, et al.
Neurology
|
April 13, 2000
A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiency
G Silvestri, T Mongini, F Odoardi, et al.
Page
of 32
Search research articles
Search
Showing results (261-270 of 320) with videos related to
Sort By:
Page
of 32
Neurology
|
August 26, 1998
Giant dystrophin deletion associated with congenital cataract and mild muscular dystrophy
M Mirabella, G Galluzzi, G Manfredi, et al.
Experimental Brain Research
|
August 11, 2001
Inhibition of biceps brachii muscle motor area by painful heat stimulation of the skin
M Valeriani, D Restuccia, V Di Lazzaro, et al.
Neuromuscular Disorders : NMD
|
June 14, 2002
Hypermyelinating neuropathy, mental retardation and epilepsy in a case of merosin deficiency
F Deodato, M Sabatelli, E Ricci, et al.
Journal of the Neurological Sciences
|
March 1, 1993
Manifesting heterozygotes in McArdle's disease: clinical, morphological and biochemical studies in a family
G Manfredi, G Silvestri, S Servidei, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 1, 1996
Changes in spinal cord excitability in a patient with rhythmic segmental myoclonus
V Di Lazzaro, D Restuccia, R Nardone, et al.
Neuromuscular Disorders : NMD
|
February 5, 2008
Natural history of CMT1A including QoL: a 2-year prospective study
L Padua, D Pareyson, I Aprile, et al.
Journal of Neurology
|
December 24, 1997
Ocular palsies in the absence of other neurological or ocular symptoms: analysis of 105 cases
A P Batocchi, A Evoli, L Majolini, et al.
European Journal of Neurology
|
August 28, 2003
Incidence of first-ever ischemic and hemorrhagic stroke in a well-defined community of southern Italy, 1993-1995
D Intiso, P Stampatore, M M Zarrelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
August 7, 2001
Neurophysiological classification of ulnar entrapment across the elbow
L Padua, I Aprile, O Mazza, et al.
Neurology
|
April 13, 2000
A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiency
G Silvestri, T Mongini, F Odoardi, et al.
Page
of 32