Detalhe da pesquisa
1.
Feasibility of newborn screening for guanidinoacetate methyltransferase (GAMT) deficiency.
J Inherit Metab Dis
; 37(2): 231-6, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24276113
2.
Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children.
Genet Med
; 12(8): 512-6, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20613545
3.
Expert testimony and the effects of a biological approach, psychopathy, and juror attitudes in cases of insanity.
Behav Sci Law
; 28(3): 411-25, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20014145
4.
Autoimmune disease in a DFNA6/14/38 family carrying a novel missense mutation in WFS1.
Am J Med Genet A
; 146A(17): 2258-65, 2008 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18688868
5.
Green tea epigallocatechin-3-gallate (EGCG) reduces beta-amyloid mediated cognitive impairment and modulates tau pathology in Alzheimer transgenic mice.
Brain Res
; 1214: 177-87, 2008 Jun 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-18457818
6.
A novel mutation in COCH-implications for genotype-phenotype correlations in DFNA9 hearing loss.
Laryngoscope
; 120(12): 2489-93, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21046548