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Journal of the Neurological Sciences
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December 24, 2008
Emotional Lability in MND: Relationship to cognition and psychopathology and impact on caregivers
A Palmieri, S Abrahams, G Sorarù, et al.
European Review for Medical and Pharmacological Sciences
|
February 3, 2022
OAS1 gene, Spike protein variants and persistent COVID-19-related anosmia: may the olfactory disfunction be a harbinger of future neurodegenerative disease?
A Di Stadio, E Bernitsas, M Ralli, et al.
Italian Journal of Neurological Sciences
|
February 1, 1996
Clinical and hormonal aspects of male hypogonadism in myotonic dystrophy
I Mastrogiacomo, G Bonanni, E Menegazzo, et al.
Il Giornale Di Chirurgia
|
June 1, 1997
[Hernioplasty using a Lichtenstein polypropylene mesh]
F Uggeri, L Erba, C Franciosi, et al.
Neuromuscular Disorders : NMD
|
March 1, 1993
Dystrophin-positive myotubes in innervated muscle cultures from Duchenne and Becker muscular dystrophy patients
M Fanin, E P Hoffman, F A Saad, et al.
Neurology
|
April 22, 2009
Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes
M Fanin, A C Nascimbeni, S Aurino, et al.
Neurological Research
|
January 23, 2010
The clinical course of calpainopathy (LGMD2A) and dysferlinopathy (LGMD2B)
C Angelini, L Nardetto, C Borsato, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 18, 2008
Sphingomonas paucimobilis associated with localised calf myositis
E Pegoraro, C Borsato, F Dal Bello, et al.
The Journal of Nervous and Mental Disease
|
December 1, 1989
Intellectual impairment and cognitive evoked potentials in myotonic dystrophy
G I Perini, G Colombo, M Armani, et al.
Minerva Chirurgica
|
October 1, 1994
[Description of two cases of retrobrachiocephalic thymus gland]
M R Pelizzo, R Grigoletto, D Fiore, et al.
Page
of 54
Search research articles
Search
Showing results (161-170 of 531) with videos related to
Sort By:
Page
of 54
Journal of the Neurological Sciences
|
December 24, 2008
Emotional Lability in MND: Relationship to cognition and psychopathology and impact on caregivers
A Palmieri, S Abrahams, G Sorarù, et al.
European Review for Medical and Pharmacological Sciences
|
February 3, 2022
OAS1 gene, Spike protein variants and persistent COVID-19-related anosmia: may the olfactory disfunction be a harbinger of future neurodegenerative disease?
A Di Stadio, E Bernitsas, M Ralli, et al.
Italian Journal of Neurological Sciences
|
February 1, 1996
Clinical and hormonal aspects of male hypogonadism in myotonic dystrophy
I Mastrogiacomo, G Bonanni, E Menegazzo, et al.
Il Giornale Di Chirurgia
|
June 1, 1997
[Hernioplasty using a Lichtenstein polypropylene mesh]
F Uggeri, L Erba, C Franciosi, et al.
Neuromuscular Disorders : NMD
|
March 1, 1993
Dystrophin-positive myotubes in innervated muscle cultures from Duchenne and Becker muscular dystrophy patients
M Fanin, E P Hoffman, F A Saad, et al.
Neurology
|
April 22, 2009
Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes
M Fanin, A C Nascimbeni, S Aurino, et al.
Neurological Research
|
January 23, 2010
The clinical course of calpainopathy (LGMD2A) and dysferlinopathy (LGMD2B)
C Angelini, L Nardetto, C Borsato, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 18, 2008
Sphingomonas paucimobilis associated with localised calf myositis
E Pegoraro, C Borsato, F Dal Bello, et al.
The Journal of Nervous and Mental Disease
|
December 1, 1989
Intellectual impairment and cognitive evoked potentials in myotonic dystrophy
G I Perini, G Colombo, M Armani, et al.
Minerva Chirurgica
|
October 1, 1994
[Description of two cases of retrobrachiocephalic thymus gland]
M R Pelizzo, R Grigoletto, D Fiore, et al.
Page
of 54