Detalhe da pesquisa
1.
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.
Hum Mol Genet
; 23(10): 2752-68, 2014 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24381304
2.
Risk factors for reading disability in families with rolandic epilepsy.
Epilepsy Behav
; 53: 174-9, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26580214
3.
Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.
Brain
; 133(Pt 3): 655-70, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20129935
4.
Vici syndrome associated with sensorineural hearing loss and evidence of neuromuscular involvement on muscle biopsy.
Am J Med Genet A
; 152A(3): 741-7, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20186778
5.
A microRNA-328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy.
Ann Clin Transl Neurol
; 3(7): 512-22, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27386500
6.
'Oral injury in child abuse'.
Arch Dis Child
; 99(3): 207, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24311189
7.
Broad-range polymerase chain reaction for the diagnosis of Bartonella henselae endocarditis.
J Paediatr Child Health
; 42(7-8): 469-71, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-16898887
8.
The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits.
Neurobiol Dis
; 20(3): 799-804, 2005 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-15964197