Detalhe da pesquisa
1.
NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders.
Curr Genomics
; 19(6): 431-443, 2018 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-30258275
2.
Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease.
J Neural Transm (Vienna)
; 121(5): 533-42, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24292895
3.
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man.
Mult Scler
; 17(6): 763-6, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21685233
4.
Presenilin enhancer-2 gene: identification of a novel promoter mutation in a patient with early-onset familial Alzheimer's disease.
Alzheimers Dement
; 7(6): 574-8, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22055974
5.
Association between the M129V variant allele of PRNP gene and mild temporal lobe epilepsy in women.
Neurosci Lett
; 421(1): 1-4, 2007 Jun 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-17092648
6.
Copy Number Variants in Alzheimer's Disease.
J Alzheimers Dis
; 55(1): 37-52, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-27662298
7.
Interaction between Apolipoprotein epsilon 4 and traumatic brain injury in patients with Alzheimer's disease and Mild Cognitive Impairment.
Funct Neurol
; 21(4): 223-8, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-17367583
8.
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms.
Arch Neurol
; 61(3): 341-4, 2004 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-15023809
9.
Association between Synapsin III gene promoter polymorphisms and multiple sclerosis.
J Neurol
; 251(2): 165-70, 2004 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-14991350
10.
Gender-related effect of clinical and genetic variables on the cognitive impairment in multiple sclerosis.
J Neurol
; 251(10): 1208-14, 2004 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-15503099
11.
Apolipoprotein E genotype does not influence the progression of multiple sclerosis.
J Neurol
; 250(9): 1094-8, 2003 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-14504972
12.
Lack of association between estrogen receptor 1 gene polymorphisms and multiple sclerosis in southern Italy in humans.
Neurosci Lett
; 327(2): 115-8, 2002 Jul 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-12098649
13.
A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation.
J Neurol
; 255(1): 127-9, 2008 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-18204809
14.
Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study.
J Neuroimmunol
; 225(1-2): 175-9, 2010 Aug 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-20471697
15.
Fas antigen and sporadic Alzheimer's disease in Southern Italy: evaluation of two polymorphisms in the TNFRSF6 gene.
Neurochem Res
; 32(9): 1445-9, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17406980
16.
ApoE epsilon4 allele and disease duration affect verbal learning in mild temporal lobe epilepsy.
Epilepsia
; 46(1): 110-7, 2005 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-15660776
17.
Prodynorphin gene promoter polymorphism and temporal lobe epilepsy.
Epilepsia
; 44(9): 1255-6, 2003 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-12919401