Detalhe da pesquisa
1.
KCC3 axonopathy: neuropathological features in the central and peripheral nervous system.
Mod Pathol
; 29(9): 962-76, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27230413
2.
The histopathology of polymicrogyria: a series of 71 brain autopsy studies.
Dev Med Child Neurol
; 58(1): 39-48, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26179148
3.
An atypical case of SCN9A mutation presenting with global motor delay and a severe pain disorder.
Muscle Nerve
; 49(1): 134-8, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23893323
4.
Cerebral microsporidiosis manifesting as progressive multifocal leukoencephalopathy in an HIV-infected individual - a case report.
AIDS Res Ther
; 11: 20, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25057277
5.
Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies.
Am J Hum Genet
; 86(2): 213-21, 2010 Feb 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-20096397
6.
Coronary artery dilatation and vasculitis in a case of rabies: similarity with Kawasaki disease?
Pediatr Int
; 55(2): 237-40, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23679164
7.
Cardiovascular Risk Factors and Adherence to Cardiovascular Protection Practice Guidelines in Adults With Type 1 Diabetes: A BETTER Registry Cross-sectional Analysis.
Can J Diabetes
; 47(6): 473-481.e1, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37059389
8.
LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency.
J Med Genet
; 48(3): 183-9, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21266382
9.
The clinical spectrum of nodular heterotopias in children: report of 31 patients.
Epilepsia
; 52(4): 728-37, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21320118
10.
c-Met activation in medulloblastoma induces tissue factor expression and activity: effects on cell migration.
Carcinogenesis
; 30(7): 1089-96, 2009 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-19359592
11.
Lethal respiratory failure and mild primary hypothyroidism in a term girl with a de novo heterozygous mutation in the TITF1/NKX2.1 gene.
J Clin Endocrinol Metab
; 94(1): 197-203, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-18957494
12.
Involvement of paraoxonase 1 genetic variants in Alzheimer's disease neuropathology.
Eur J Neurosci
; 30(9): 1823-30, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19863653
13.
Prenatal head growth and white matter injury in hypoplastic left heart syndrome.
Pediatr Res
; 64(4): 364-9, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18552707
14.
Congenital axonal neuropathy and encephalopathy.
Pediatr Neurol
; 38(4): 261-6, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18358405
15.
A newborn with spinal muscular atrophy type 0 presenting with a clinicopathological picture suggestive of myotubular myopathy.
J Child Neurol
; 22(11): 1301-4, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-18006961
16.
Atorvastatin-induced necrotizing autoimmune myositis: An emerging dominant entity in patients with autoimmune myositis presenting with a pure polymyositis phenotype.
Medicine (Baltimore)
; 96(3): e5694, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-28099331
17.
Pelizaeus-Merzbacher disease.
J Neuropathol Exp Neurol
; 61(9): 747-59, 2002 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-12230321
18.
Declining expression of neprilysin in Alzheimer disease vasculature: possible involvement in cerebral amyloid angiopathy.
J Neuropathol Exp Neurol
; 61(10): 849-56, 2002 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-12387451
19.
More than meets the eyes in focal epilepsy.
Can J Neurol Sci
; 36(5): 542, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19831120
20.
TAU mutations are not a predominant cause of frontotemporal dementia in Canadian patients.
Can J Neurol Sci
; 31(3): 363-7, 2004 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-15376481