Detalhe da pesquisa
1.
Hypercapnia is a possible determinant of the function of the blood-cerebrospinal fluid barrier in amyotrophic lateral sclerosis.
Neurochem Res
; 35(7): 1071-4, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20333464
2.
Amygdala size reduction is associated with memory deficits in complicated hereditary spastic paraparesis: an MRI study.
Eur Neurol
; 64(2): 117-23, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20664204
3.
Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridization.
Amyotroph Lateral Scler
; 10(3): 162-9, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18985462
4.
Widespread white matter changes in Kennedy disease: a voxel based morphometry study.
J Neurol Neurosurg Psychiatry
; 78(11): 1209-12, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17332050
5.
Different regional brain volume loss in pure and complicated hereditary spastic paraparesis: a voxel-based morphometric study.
Amyotroph Lateral Scler
; 8(6): 328-36, 2007 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-17852008
6.
Diffusion tensor imaging and tractwise fractional anisotropy statistics: quantitative analysis in white matter pathology.
Biomed Eng Online
; 6: 42, 2007 Nov 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-17996104
7.
Spastin related hereditary spastic paraplegia with dysplastic corpus callosum.
J Neurol Sci
; 236(1-2): 9-12, 2005 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-16009377
8.
The effect of tau genotype on clinical features in FTDP-17.
Parkinsonism Relat Disord
; 11(4): 205-8, 2005 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-15878580
9.
X-linked bulbospinal neuronopathy: Kennedy disease.
Arch Neurol
; 59(12): 1921-6, 2002 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-12470181
10.
TDP-43 in cerebrospinal fluid of patients with frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Arch Neurol
; 65(11): 1481-7, 2008 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19001167
11.
A novel nonsense mutation in the ABC1 gene causes a severe syringomyelia-like phenotype of Tangier disease.
Brain
; 126(Pt 4): 920-7, 2003 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-12615648
12.
Intracerebral hemorrhage in a patient with glycogenosis type II (Pompe disease): is there a pathophysiological relationship?
Muscle Nerve
; 38(3): 1211-2, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18642382