Detalhe da pesquisa
1.
First splicing variant in HECW2 with an autosomal recessive pattern of inheritance and associated with NDHSAL.
Hum Mutat
; 43(10): 1361-1367, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35753050
2.
Glioblastoma Treatment: State-of-the-Art and Future Perspectives.
Int J Mol Sci
; 23(13)2022 Jun 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-35806212
3.
Pharmacological evaluation of the anxiolytic-like effects of Lippia graveolens and bioactive compounds.
Pharm Biol
; 55(1): 1569-1576, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28385098
4.
Carbon Material-Reinforced Polymer Composites for Bipolar Plates in Polymer Electrolyte Membrane Fuel Cells.
Polymers (Basel)
; 16(5)2024 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38475354
5.
Antinociceptive effects of Raphanus sativus sprouts involve the opioid and 5-HT1A serotonin receptors, cAMP/cGMP pathways, and the central activity of sulforaphane.
Food Funct
; 15(9): 4773-4784, 2024 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38469873
6.
Radiation therapy for optic nerve sheath meningiomas: Local control and treatment related visual changes.
World Neurosurg X
; 23: 100291, 2024 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-38523881
7.
Pharmacological evaluation of the anxiolytic-like effects of an aqueous extract of the Raphanus sativus L. sprouts in mice.
Biomed Pharmacother
; 162: 114579, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-36989714
8.
Primary Spinal Cord Glioblastoma.
Cureus
; 13(10): e18464, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34754630
9.
The Thalamic Arteriovenous Malformations Have Better Prognosis than Basal Ganglia Malformations Regarding Obliteration: Prognostic Factors Analysis.
World Neurosurg
; 150: e750-e755, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33812069
10.
A novel de novo mutation in the PURA gene associated with a new clinical finding: large brainstem.
J Genet
; 992020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32089526
11.
A novel de novo MTOR gain-of-function variant in a patient with Smith-Kingsmore syndrome and Antiphospholipid syndrome.
Eur J Hum Genet
; 27(9): 1369-1378, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31053780