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Clinical and Experimental Medicine
|
August 13, 2005
HLA DR/DQ alleles and risk of type I diabetes in childhood: a population-based case-control study
E Altobelli, A Blasetti, R Petrocelli, et al.
American Journal of Medical Genetics. Part A
|
June 5, 2003
Deletion of the SHOX gene in patients with short stature of unknown cause
E Morizio, L Stuppia, V Gatta, et al.
Tissue Antigens
|
January 9, 2008
Association between PTPN22 C1858T and type 1 diabetes: a replication in continental Italy
P Saccucci, E Del Duca, N Rapini, et al.
European Journal of Neurology
|
July 30, 2010
Rufinamide in refractory childhood epileptic encephalopathies other than Lennox-Gastaut syndrome
G Coppola, S Grosso, E Franzoni, et al.
Current Pediatric Reviews
|
September 17, 2016
Child Abuse and Neglect and its Psycho-Physical and Social Consequences: A Review of the Literature
P Ferrara, C Guadagno, A Sbordone, 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.
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.
European Journal of Neurology
|
October 27, 2015
Clinical dissection of childhood occipital epilepsy of Gastaut and prognostic implication
A Verrotti, D Laino, V E Rinaldi, et al.
Epilepsy Research
|
August 30, 2016
Effectiveness and tolerability of perampanel in children and adolescents with refractory epilepsies-An Italian observational multicenter study
P De Liso, F Vigevano, N Specchio, et al.
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of 24
Search research articles
Search
Showing results (231-240 of 239) with videos related to
Sort By:
Page
of 24
You have reached the last page of results.
This site can display upto 239 results.
Clinical and Experimental Medicine
|
August 13, 2005
HLA DR/DQ alleles and risk of type I diabetes in childhood: a population-based case-control study
E Altobelli, A Blasetti, R Petrocelli, et al.
American Journal of Medical Genetics. Part A
|
June 5, 2003
Deletion of the SHOX gene in patients with short stature of unknown cause
E Morizio, L Stuppia, V Gatta, et al.
Tissue Antigens
|
January 9, 2008
Association between PTPN22 C1858T and type 1 diabetes: a replication in continental Italy
P Saccucci, E Del Duca, N Rapini, et al.
European Journal of Neurology
|
July 30, 2010
Rufinamide in refractory childhood epileptic encephalopathies other than Lennox-Gastaut syndrome
G Coppola, S Grosso, E Franzoni, et al.
Current Pediatric Reviews
|
September 17, 2016
Child Abuse and Neglect and its Psycho-Physical and Social Consequences: A Review of the Literature
P Ferrara, C Guadagno, A Sbordone, 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.
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.
European Journal of Neurology
|
October 27, 2015
Clinical dissection of childhood occipital epilepsy of Gastaut and prognostic implication
A Verrotti, D Laino, V E Rinaldi, et al.
Epilepsy Research
|
August 30, 2016
Effectiveness and tolerability of perampanel in children and adolescents with refractory epilepsies-An Italian observational multicenter study
P De Liso, F Vigevano, N Specchio, et al.
Page
of 24