|
rs1799969
|
|
|
0.020 |
GeneticVariation |
BEFREE |
We found a significant protective association between heterozygous GA genotype in ICAM1 (241Gly/Arg) and GBS (p < .047).
|
31464097 |
2019 |
|
rs4986790
|
|
|
0.020 |
GeneticVariation |
BEFREE |
However, no associations were observed between the genotypes of the Asp299Gly and Thr399Ile SNPs and antecedent <i>C. jejuni</i> infection or disease severity in Bangladeshi patients with GBS.
|
31019995 |
2019 |
|
rs4986791
|
|
|
0.020 |
GeneticVariation |
BEFREE |
However, no associations were observed between the genotypes of the Asp299Gly and Thr399Ile SNPs and antecedent <i>C. jejuni</i> infection or disease severity in Bangladeshi patients with GBS.
|
31019995 |
2019 |
|
rs1799969
|
|
|
0.020 |
GeneticVariation |
BEFREE |
IL-17 (Glu126Gly) mutant and ICAM-1 (Gly241Arg) heterozygous genotypes were strongly associated with increased risk of GBS (p < 0.016; OR = 3.706, 95% CI = 1.28-10.67; p < 0.001; OR = 4.148, 95% CI = 2.119-8.119, respectively).
|
27595159 |
2017 |
|
rs397514767
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Neurological symptoms of patients with p.Cys89Tyr mutation in the CD59 gene include recurrent peripheral neuropathy resembling Guillain-Barré syndrome, characterized by sensory-motor demyelinating neuropathy with secondary axonal damage and moderate enhancement of the nerve roots on spine MRI, together with recurrent strokes and retinal involvement.
|
28622911 |
2017 |
|
rs397514767
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The Cys89Tyr mutation in CD59 was clinically manifested in infancy, and associated with chronic hemolysis and relapsing peripheral demyelinating disease resembling recurrent Guillain-Barré syndrome (GBS) or chronic inflammatory demyelinating polyneuropathy (CIDP).
|
25818314 |
2015 |
|
rs4986790
|
|
|
0.020 |
GeneticVariation |
BEFREE |
In conclusion, TLR4 (Asp299Gly) polymorphism is associated with an increased susceptibility to GBS.
|
19913922 |
2010 |
|
rs4986791
|
|
|
0.020 |
GeneticVariation |
BEFREE |
TLR4 (Asp299Gly) polymorphism was significantly associated with GBS (p, 0.045; OR, 8.75; 95% CI, 1.05-72.88); only acute motor axonal neuropathy (AMAN) was associated with Gly299Gly homozygote (p, 0.027; OR, 12.40; 95% CI, 1.33-115.77) and Thr399Ile (p, 0.019; OR, 3.42; 95% CI, 1.22-9.54) heterozygote, and TLR4-399Ile allele (p, 0.045; OR, 2.63; 95% CI, 1.02-6.75) compared to controls.
|
19913922 |
2010 |
|
rs746073437
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We found a significant protective association between heterozygous GA genotype in ICAM1 (241Gly/Arg) and GBS (p < .047).
|
31464097 |
2019 |
|
rs1801274
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We assessed whether polymorphisms rs1801274 in FCGR2A and rs396991 in FCGR3A were associated with GBS in a Brazilian population.
|
27609290 |
2016 |
|
rs2066844
|
|
|
0.010 |
GeneticVariation |
BEFREE |
NOD1 (Glu266Lys) and NOD2 (Arg702Trp and Gly908Arg) polymorphisms were associated with an increased susceptibility to GBS.
|
27000222 |
2016 |
|
rs2066845
|
|
|
0.010 |
GeneticVariation |
BEFREE |
NOD1 (Glu266Lys) and NOD2 (Arg702Trp and Gly908Arg) polymorphisms were associated with an increased susceptibility to GBS.
|
27000222 |
2016 |
|
rs2075820
|
|
|
0.010 |
GeneticVariation |
BEFREE |
NOD1 (Glu266Lys) and NOD2 (Arg702Trp and Gly908Arg) polymorphisms were associated with an increased susceptibility to GBS.
|
27000222 |
2016 |
|
rs396991
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We assessed whether polymorphisms rs1801274 in FCGR2A and rs396991 in FCGR3A were associated with GBS in a Brazilian population.
|
27609290 |
2016 |
|
rs1445335859
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The Cys89Tyr mutation in CD59 was clinically manifested in infancy, and associated with chronic hemolysis and relapsing peripheral demyelinating disease resembling recurrent Guillain-Barré syndrome (GBS) or chronic inflammatory demyelinating polyneuropathy (CIDP).
|
25818314 |
2015 |
|
rs1253159682
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Subgroup analysis further provided evidence of significant association between TNF-α 308 G/A</span> and risk of the GBS in Asian population (GG+GA vs. AA: OR=32, 95%CI=0.11-0.93; GG vs. AA: OR=0.32, 95%CI=0.15-0.68).
|
22236374 |
2012 |
|
rs762142186
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Subgroup analysis further provided evidence of significant association between TNF-α 308 G/A</span> and risk of the GBS in Asian population (GG+GA vs. AA: OR=32, 95%CI=0.11-0.93; GG vs. AA: OR=0.32, 95%CI=0.15-0.68).
|
22236374 |
2012 |