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Human Mutation
|
November 21, 2002
Molecular characterisation of GSD III subjects and identification of six novel mutations in AGL
S Lucchiari, M A Donati, R Parini, 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.
Headache
|
August 1, 1988
Mitochondrial abnormalities in migraine. Preliminary findings
P Montagna, T Sacquegna, P Martinelli, 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.
European Journal of Neurology
|
August 29, 2012
Atypical adult onset complicated spastic paraparesis with thin corpus callosum in two patients carrying a novel FA2H mutation
A Tonelli, M G D'Angelo, F Arrigoni, et al.
European Journal of Neurology
|
March 29, 2007
IP-10 serum levels are not increased in mild cognitive impairment and Alzheimer's disease
D Galimberti, E Venturelli, C Fenoglio, 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.
Clinical Neuropathology
|
July 1, 1991
Muscle biopsy in Alzheimer's disease: morphological and biochemical findings
C Mariani, N Bresolin, E Farina, et al.
Neurology
|
June 1, 1985
Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscle
N Bresolin, M Zeviani, E Bonilla, et al.
Neurology
|
June 1, 1988
Clinical and biochemical correlations in mitochondrial myopathies treated with coenzyme Q10
N Bresolin, L Bet, A Binda, et al.
Page
of 21
Search research articles
Search
Showing results (91-100 of 206) with videos related to
Sort By:
Page
of 21
Human Mutation
|
November 21, 2002
Molecular characterisation of GSD III subjects and identification of six novel mutations in AGL
S Lucchiari, M A Donati, R Parini, 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.
Headache
|
August 1, 1988
Mitochondrial abnormalities in migraine. Preliminary findings
P Montagna, T Sacquegna, P Martinelli, 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.
European Journal of Neurology
|
August 29, 2012
Atypical adult onset complicated spastic paraparesis with thin corpus callosum in two patients carrying a novel FA2H mutation
A Tonelli, M G D'Angelo, F Arrigoni, et al.
European Journal of Neurology
|
March 29, 2007
IP-10 serum levels are not increased in mild cognitive impairment and Alzheimer's disease
D Galimberti, E Venturelli, C Fenoglio, 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.
Clinical Neuropathology
|
July 1, 1991
Muscle biopsy in Alzheimer's disease: morphological and biochemical findings
C Mariani, N Bresolin, E Farina, et al.
Neurology
|
June 1, 1985
Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscle
N Bresolin, M Zeviani, E Bonilla, et al.
Neurology
|
June 1, 1988
Clinical and biochemical correlations in mitochondrial myopathies treated with coenzyme Q10
N Bresolin, L Bet, A Binda, et al.
Page
of 21