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Journal of Neurology, Neurosurgery, and Psychiatry
|
June 30, 2001
Paraneoplastic opsoclonus-myoclonus associated with renal cell carcinoma and responsive to tumour ablation
M C Vigliani, L Palmucci, P Polo, et al.
European Neurology
|
January 1, 1992
Lipid storage myopathy in multiple acyl-CoA dehydrogenase deficiency: an adult case
T Mongini, C Doriguzzi, L Palmucci, et al.
Italian Journal of Neurological Sciences
|
January 1, 1981
Epidemiology of Duchenne muscular dystrophy in the province of Turin
A Bertolotto, M De Marchi, C Doriguzzi, 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.
European Neurology
|
January 1, 1993
Congenital muscular dystrophy associated with familial junctional epidermolysis bullosa letalis
C Doriguzzi, L Palmucci, T Mongini, et al.
Human Mutation
|
August 3, 2000
A new polymorphism, g119A>G, in the integrin alpha 7 (ITGA7) gene
D Pirulli, S Zezlina, L Vatta, et al.
Neurology
|
March 23, 2007
Phenotypic clustering of lamin A/C mutations in neuromuscular patients
S Benedetti, I Menditto, M Degano, et al.
Page
of 8
Search research articles
Search
Showing results (71-80 of 77) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 77 results.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 30, 2001
Paraneoplastic opsoclonus-myoclonus associated with renal cell carcinoma and responsive to tumour ablation
M C Vigliani, L Palmucci, P Polo, et al.
European Neurology
|
January 1, 1992
Lipid storage myopathy in multiple acyl-CoA dehydrogenase deficiency: an adult case
T Mongini, C Doriguzzi, L Palmucci, et al.
Italian Journal of Neurological Sciences
|
January 1, 1981
Epidemiology of Duchenne muscular dystrophy in the province of Turin
A Bertolotto, M De Marchi, C Doriguzzi, 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.
European Neurology
|
January 1, 1993
Congenital muscular dystrophy associated with familial junctional epidermolysis bullosa letalis
C Doriguzzi, L Palmucci, T Mongini, et al.
Human Mutation
|
August 3, 2000
A new polymorphism, g119A>G, in the integrin alpha 7 (ITGA7) gene
D Pirulli, S Zezlina, L Vatta, et al.
Neurology
|
March 23, 2007
Phenotypic clustering of lamin A/C mutations in neuromuscular patients
S Benedetti, I Menditto, M Degano, et al.
Page
of 8