Search research articles
Contact Us
Filters
Showing results (31-40 of 84) with videos related to
Page
of 9
Sort By:
Brain : a Journal of Neurology
|
January 29, 2000
Synergistic effect of beta-amyloid protein and interferon gamma on nitric oxide production by C2C12 muscle cells
P Baron, D Galimberti, L Meda, et al.
Journal of Neurology
|
February 1, 1995
Ryanodine receptor gene point mutation and malignant hyperthermia susceptibility
I Moroni, E F Gonano, G P Comi, et al.
Journal of the Neurological Sciences
|
May 1, 1994
Chronic progressive external ophthalmoplegia: a correlative study of quantitative molecular data and histochemical and biochemical profile
A Fassati, A Bordoni, P Amboni, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
May 11, 2010
Guillain-Barré syndrome after rtPA therapy for acute stroke
A Bersano, D Santoro, A Prelle, et al.
AJNR. American Journal of Neuroradiology
|
June 18, 2011
The topography of brain microstructural damage in amyotrophic lateral sclerosis assessed using diffusion tensor MR imaging
E Canu, F Agosta, N Riva, et al.
Neuromuscular Disorders : NMD
|
January 1, 1992
Congenital myopathy associated with abnormal accumulation of desmin and dystrophin
A Prelle, M Moggio, G P Comi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 22, 2008
A longitudinal diffusion tensor MRI study of the cervical cord and brain in amyotrophic lateral sclerosis patients
F Agosta, M A Rocca, P Valsasina, et al.
Clinical Neuropathology
|
April 10, 2009
Severe acute multineuropathy in Churg-Strauss syndrome in a patient with a history of melanoma
M E Fruguglietti, L Napoli, M Sciacco, et al.
The New England Journal of Medicine
|
January 8, 1987
Is nebulin the defective gene product in Duchenne muscular dystrophy?
D S Wood, M Zeviani, A Prelle, et al.
American Journal of Medical Genetics
|
April 27, 2002
Clinical and genetic variability of glycogen storage disease type IIIa: seven novel AGL gene mutations in the Mediterranean area
S Lucchiari, I Fogh, A Prelle, et al.
Page
of 9
Search research articles
Search
Showing results (31-40 of 84) with videos related to
Sort By:
Page
of 9
Brain : a Journal of Neurology
|
January 29, 2000
Synergistic effect of beta-amyloid protein and interferon gamma on nitric oxide production by C2C12 muscle cells
P Baron, D Galimberti, L Meda, et al.
Journal of Neurology
|
February 1, 1995
Ryanodine receptor gene point mutation and malignant hyperthermia susceptibility
I Moroni, E F Gonano, G P Comi, et al.
Journal of the Neurological Sciences
|
May 1, 1994
Chronic progressive external ophthalmoplegia: a correlative study of quantitative molecular data and histochemical and biochemical profile
A Fassati, A Bordoni, P Amboni, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
May 11, 2010
Guillain-Barré syndrome after rtPA therapy for acute stroke
A Bersano, D Santoro, A Prelle, et al.
AJNR. American Journal of Neuroradiology
|
June 18, 2011
The topography of brain microstructural damage in amyotrophic lateral sclerosis assessed using diffusion tensor MR imaging
E Canu, F Agosta, N Riva, et al.
Neuromuscular Disorders : NMD
|
January 1, 1992
Congenital myopathy associated with abnormal accumulation of desmin and dystrophin
A Prelle, M Moggio, G P Comi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 22, 2008
A longitudinal diffusion tensor MRI study of the cervical cord and brain in amyotrophic lateral sclerosis patients
F Agosta, M A Rocca, P Valsasina, et al.
Clinical Neuropathology
|
April 10, 2009
Severe acute multineuropathy in Churg-Strauss syndrome in a patient with a history of melanoma
M E Fruguglietti, L Napoli, M Sciacco, et al.
The New England Journal of Medicine
|
January 8, 1987
Is nebulin the defective gene product in Duchenne muscular dystrophy?
D S Wood, M Zeviani, A Prelle, et al.
American Journal of Medical Genetics
|
April 27, 2002
Clinical and genetic variability of glycogen storage disease type IIIa: seven novel AGL gene mutations in the Mediterranean area
S Lucchiari, I Fogh, A Prelle, et al.
Page
of 9