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Clinical Nutrition (Edinburgh, Scotland)
|
June 20, 2008
Nutrition in care homes and home care: how to implement adequate strategies (report of the Brussels Forum (22-23 November 2007))
M Arvanitakis, A Beck, P Coppens, et al.
Journal of Neurology
|
October 31, 2014
A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutation
Rita Barone, M Carrozzi, R Parini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
June 4, 2025
Delphi consensus finding on paediatric-adult transition: results from the epilepsy transition working group of the italian league against epilepsy (LICE)
F Darra, P Biermann Klaus, D Audenino, et al.
Acta Neurologica Scandinavica
|
January 25, 2018
Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15)
S Matricardi, F Darra, A Spalice, et al.
Molecular Psychiatry
|
July 20, 2005
Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions
M D'Amelio, I Ricci, R Sacco, et al.
Neurology
|
July 20, 2007
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy
P Striano, A Coppola, M Pezzella, et al.
Psychiatric Genetics
|
May 29, 2004
Enhanced APOE2 transmission rates in families with autistic probands
A M Persico, L D'Agruma, L Zelante, et al.
Molecular Psychiatry
|
July 9, 2008
Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1
L Palmieri, V Papaleo, V Porcelli, et al.
European Journal of Neurology
|
October 2, 2012
Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution
S Agostinelli, M Traverso, P Accorsi, et al.
Neurology
|
June 25, 2003
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy
R Nabbout, E Gennaro, B Dalla Bernardina, et al.
Page
of 35
Search research articles
Search
Showing results (331-340 of 343) with videos related to
Sort By:
Page
of 35
Clinical Nutrition (Edinburgh, Scotland)
|
June 20, 2008
Nutrition in care homes and home care: how to implement adequate strategies (report of the Brussels Forum (22-23 November 2007))
M Arvanitakis, A Beck, P Coppens, et al.
Journal of Neurology
|
October 31, 2014
A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutation
Rita Barone, M Carrozzi, R Parini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
June 4, 2025
Delphi consensus finding on paediatric-adult transition: results from the epilepsy transition working group of the italian league against epilepsy (LICE)
F Darra, P Biermann Klaus, D Audenino, et al.
Acta Neurologica Scandinavica
|
January 25, 2018
Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15)
S Matricardi, F Darra, A Spalice, et al.
Molecular Psychiatry
|
July 20, 2005
Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions
M D'Amelio, I Ricci, R Sacco, et al.
Neurology
|
July 20, 2007
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy
P Striano, A Coppola, M Pezzella, et al.
Psychiatric Genetics
|
May 29, 2004
Enhanced APOE2 transmission rates in families with autistic probands
A M Persico, L D'Agruma, L Zelante, et al.
Molecular Psychiatry
|
July 9, 2008
Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1
L Palmieri, V Papaleo, V Porcelli, et al.
European Journal of Neurology
|
October 2, 2012
Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution
S Agostinelli, M Traverso, P Accorsi, et al.
Neurology
|
June 25, 2003
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy
R Nabbout, E Gennaro, B Dalla Bernardina, et al.
Page
of 35