Detalhe da pesquisa
1.
SPG11-related parkinsonism: Clinical profile, molecular imaging and l-dopa response.
Mov Disord
; 33(10): 1650-1656, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30306626
2.
ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease.
Brain
; 139(Pt 1): 73-85, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26556829
3.
Spastic paraplegia type 31: A novel REEP1 splice site donor variant and expansion of the phenotype variability.
Parkinsonism Relat Disord
; 46: 79-83, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29107646
4.
SPG11 mutations cause widespread white matter and basal ganglia abnormalities, but restricted cortical damage.
Neuroimage Clin
; 19: 848-857, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29946510
5.
Phenotype variability and allelic heterogeneity in KMT2B-Associated disease.
Parkinsonism Relat Disord
; 52: 55-61, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29653907
6.
Spastic paraplegia type 4: A novel SPAST splice site donor mutation and expansion of the phenotype variability.
J Neurol Sci
; 380: 92-97, 2017 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28870597
7.
Trans-crocetin improves amyloid-ß degradation in monocytes from Alzheimer's Disease patients.
J Neurol Sci
; 372: 408-412, 2017 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27865556
8.
Long-term miR-669a therapy alleviates chronic dilated cardiomyopathy in dystrophic mice.
J Am Heart Assoc
; 2(4): e000284, 2013 Aug 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-23963759