Detalhe da pesquisa
1.
Phenotypic insights into ADCY5-associated disease.
Mov Disord
; 31(7): 1033-40, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27061943
2.
Intravenous immunoglobulin in acute Sydenham's chorea: A systematic review.
J Paediatr Child Health
; 51(12): 1235-8, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26633611
3.
Movement disorders in children with anti-NMDAR encephalitis and other autoimmune encephalopathies.
Mov Disord
; 29(12): 1539-42, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25154478
4.
Investigation of suspected Guillain-Barre syndrome in childhood: what is the role for gadolinium enhanced magnetic resonance imaging of the spine?
J Paediatr Child Health
; 50(10): E72-6, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20626577
5.
GNAO1-related movement disorder with life-threatening exacerbations: movement phenomenology and response to DBS.
J Neurol Neurosurg Psychiatry
; 89(2): 221-222, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28668776
6.
Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2.
Am J Hum Genet
; 84(1): 44-51, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19118815
7.
Microdeletions detected using chromosome microarray in children with suspected genetic movement disorders: a single-centre study.
Dev Med Child Neurol
; 54(7): 618-23, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22515636
8.
Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis.
Brain
; 133(Pt 6): 1810-22, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20430833
9.
Neuronal intranuclear inclusion disease: two cases of dopa-responsive juvenile parkinsonism with drug-induced dyskinesia.
Mov Disord
; 25(9): 1274-9, 2010 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20629123
10.
Familial paroxysmal exercise-induced dystonia: atypical presentation of autosomal dominant GTP-cyclohydrolase 1 deficiency.
Dev Med Child Neurol
; 52(6): 583-6, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20187889
11.
Acquired facial palsy with hypertension secondary to Guillain-Barre syndrome.
J Paediatr Child Health
; 46(3): 125-7, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20158600
12.
Defective responses to DNA single- and double-strand breaks in spinocerebellar ataxia.
DNA Repair (Amst)
; 7(7): 1061-76, 2008 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18467193
13.
Mutations in the cyclic adenosine monophosphate response element of the tyrosine hydroxylase gene.
Ann Neurol
; 62(4): 422-6, 2007 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17696123
14.
Defective p53 response and apoptosis associated with an ataxia-telangiectasia-like phenotype.
Cancer Res
; 66(6): 2907-12, 2006 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-16540636
15.
Legal clarification of "loss of chance of a better outcome" in Australia.
Med J Aust
; 197(5): 273, 2012 Sep 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-22938116
16.
Genetic epilepsy with febrile seizures plus: Refining the spectrum.
Neurology
; 89(12): 1210-1219, 2017 Sep 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-28842445
17.
Perceived practice change in Australian doctors as a result of medicolegal concerns.
Med J Aust
; 194(6): 325; author reply 325-6, 2011 Mar 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-21426293
18.
Response to Zhang et al.
J Paediatr Child Health
; 47(12): 928, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22171837
19.
Neuroepithelial cysts in a patient with Joubert syndrome plus renal cysts.
J Child Neurol
; 19(3): 227-31, 2004 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-15119486
20.
Paroxysmal dyskinesias with drowsiness and thalamic lesions in GABA transaminase deficiency.
Neurology
; 92(2): 94-97, 2019 01 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30617166