Detalhe da pesquisa
1.
Observation of Masturbation After Visual Sexual Stimuli From Conspecifics in a Captive Male Bearded Capuchin (Sapajus libidinosus).
Arch Sex Behav
; 52(3): 1333-1337, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36422729
2.
Chemical composition, antioxidant, and antimicrobial activities of six commercial essential oils.
Lett Appl Microbiol
; 76(1)2023 Jan 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-36688786
3.
Chemical Composition of Macroalgae Polysaccharides from Galician and Portugal Coasts: Seasonal Variations and Biological Properties.
Mar Drugs
; 21(11)2023 Nov 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37999413
4.
Zimbro (Juniperus communis L.) as a Promising Source of Bioactive Compounds and Biomedical Activities: A Review on Recent Trends.
Int J Mol Sci
; 23(6)2022 Mar 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-35328621
5.
Single-implant mandibular overdentures: Clinical, radiographic, and patient-reported outcomes after a 5-year follow-up.
J Prosthet Dent
; 128(5): 949-955, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-33640091
6.
A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia.
Am J Hum Genet
; 101(1): 87-103, 2017 Jul 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28686858
7.
Mutational mechanism for DAB1 (ATTTC)n insertion in SCA37: ATTTT repeat lengthening and nucleotide substitution.
Hum Mutat
; 40(4): 404-412, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30588707
8.
Mutations in PNKP cause recessive ataxia with oculomotor apraxia type 4.
Am J Hum Genet
; 96(3): 474-9, 2015 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-25728773
9.
Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia.
Am J Hum Genet
; 94(2): 268-77, 2014 Feb 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-24388663
10.
Signal-dependent incorporation of MyoD-BAF60c into Brg1-based SWI/SNF chromatin-remodelling complex.
EMBO J
; 31(2): 301-16, 2012 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-22068056
11.
Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia.
Am J Hum Genet
; 93(1): 118-23, 2013 Jul 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-23746551
12.
Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia.
Brain
; 138(Pt 8): 2191-205, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26026163
13.
Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum.
Nat Genet
; 39(3): 366-72, 2007 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-17322883
14.
Modifiers of (CAG)(n) instability in Machado-Joseph disease (MJD/SCA3) transmissions: an association study with DNA replication, repair and recombination genes.
Hum Genet
; 133(10): 1311-8, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25026993
15.
The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies.
Neuroepidemiology
; 42(3): 174-83, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24603320
16.
Optimization of liquid overlay technique to formulate heterogenic 3D co-cultures models.
Biotechnol Bioeng
; 111(8): 1672-85, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24615162
17.
Familial hemiplegic migraine due to L263V SCN1A mutation: discordance for epilepsy between two kindreds from Douro Valley.
Cephalalgia
; 34(12): 1015-20, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24646837
18.
Nystagmus as an early ocular alteration in Machado-Joseph disease (MJD/SCA3).
BMC Neurol
; 14: 17, 2014 Jan 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-24450306
19.
The prevalence of familial hemiplegic migraine with cerebellar ataxia and spinocerebellar ataxia type 6 in Portugal.
Headache
; 54(5): 911-5, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24898624
20.
Web-based cognitive training: patient adherence and intensity of treatment in an outpatient memory clinic.
J Med Internet Res
; 16(5): e122, 2014 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-24808451