Detalhe da pesquisa
1.
Development and validation of next generation sequencing based 35-gene hereditary cancer panel.
Hered Cancer Clin Pract
; 18: 9, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32368312
2.
CYP2D6 allele frequencies, copy number variants, and tandems in the population of Hong Kong.
J Clin Lab Anal
; 33(1): e22634, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-30069923
3.
Relationship between aberrant brain connectivity and clinical features in Angelman Syndrome: a new method using tract based spatial statistics of DTI color-coded orientation maps.
Neuroimage
; 59(1): 349-55, 2012 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-21827860
4.
Sensitive diffusion tensor imaging quantification method to identify language pathway abnormalities in children with developmental delay.
J Pediatr
; 160(1): 147-51, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21839473
5.
Exome sequencing of a pedigree with Tourette syndrome or chronic tic disorder.
Ann Neurol
; 69(5): 901-4, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21520241
6.
GNAQ Mutation in the Venous Vascular Malformation and Underlying Brain Tissue in Sturge-Weber Syndrome.
Neuropediatrics
; 48(5): 385-389, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28571101
7.
Alterations in frontal lobe tracts and corpus callosum in young children with autism spectrum disorder.
Cereb Cortex
; 20(9): 2103-13, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20019145
8.
Mortality Prediction of COVID-19 Patients at Intensive Care Unit Admission.
Cureus
; 13(11): e19690, 2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-34976472
9.
Diffusion tensor imaging of frontal lobe in autism spectrum disorder.
Cereb Cortex
; 18(11): 2659-65, 2008 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-18359780
10.
Absence of arcuate fasciculus in children with global developmental delay of unknown etiology: a diffusion tensor imaging study.
J Pediatr
; 152(2): 250-5, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18206698
11.
Diffusion tensor analysis of temporal and extra-temporal lobe tracts in temporal lobe epilepsy.
Epilepsy Res
; 80(1): 30-41, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18436432
12.
Quantification of protein synthesis in the human brain using L-[1-11C]-leucine PET: incorporation of factors for large neutral amino acids in plasma and for amino acids recycled from tissue.
J Nucl Med
; 47(11): 1787-95, 2006 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17079811
13.
Simplified kinetic analysis of tumor 18F-FDG uptake: a dynamic approach.
J Nucl Med
; 45(8): 1328-33, 2004 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-15299057
14.
Infantile spasms are associated with abnormal copy number variations.
J Child Neurol
; 28(10): 1191-6, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22914377
15.
SCN2A mutation is associated with infantile spasms and bitemporal glucose hypometabolism.
Pediatr Neurol
; 49(1): 46-9, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23827426
16.
Increased L-[1-11 C] leucine uptake in the leptomeningeal angioma of sturge-weber syndrome: a PET study.
J Neuroimaging
; 22(2): 177-83, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21223431
17.
Abnormal brain protein synthesis in language areas of children with pervasive developmental disorder: a L-[1-11C]-leucine PET study.
J Child Neurol
; 26(11): 1347-54, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21636781
18.
Arcuate fasciculus and speech in congenital bilateral perisylvian syndrome.
Pediatr Neurol
; 44(4): 270-4, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21397168
19.
Abnormal language pathway in children with Angelman syndrome.
Pediatr Neurol
; 44(5): 350-6, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21481743
20.
Tourette syndrome is associated with recurrent exonic copy number variants.
Neurology
; 74(20): 1583-90, 2010 May 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-20427753