Detalhe da pesquisa
1.
Development of an online calculator for the prediction of seizure freedom following pediatric hemispherectomy using the Hemispherectomy Outcome Prediction Scale (HOPS).
Epilepsia
; 65(1): 46-56, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37347512
2.
Predictive models for starting antiseizure medication withdrawal following epilepsy surgery in adults.
Brain
; 146(6): 2389-2398, 2023 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36415957
3.
Multi-conformers caused by conformational change of A-ring in the C18- and C19-N-dealkyl diterpenoid alkaloids.
J Asian Nat Prod Res
; 25(9): 819-833, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-36632044
4.
Synthesis of Three-Dimensionally Fascinating Diterpenoid Alkaloids and Related Diterpenes.
Acc Chem Res
; 54(1): 22-34, 2021 01 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33351595
5.
Comparison of the real-world effectiveness of vertical versus lateral functional hemispherotomy techniques for pediatric drug-resistant epilepsy: A post hoc analysis of the HOPS study.
Epilepsia
; 62(11): 2707-2718, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34510448
6.
Hemispherectomy Outcome Prediction Scale: Development and validation of a seizure freedom prediction tool.
Epilepsia
; 62(5): 1064-1073, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33713438
7.
Total Synthesis of Liangshanone.
Angew Chem Int Ed Engl
; 59(52): 23609-23614, 2020 12 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32902096
8.
Degradation of high-concentration simulated organic wastewater by DBD plasma.
Water Sci Technol
; 80(8): 1413-1420, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31961804
9.
New C20-diterpenoid alkaloids from Aconitum vilmorrianum and structural revision of 2-O-acetylorochrine and orochrine.
J Asian Nat Prod Res
; 18(4): 315-27, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26479584
10.
Collective Total Syntheses of Atisane-Type Diterpenes and Atisine-Type Diterpenoid Alkaloids: (±)-Spiramilactoneâ B, (±)-Spiraminol, (±)-Dihydroajaconine, and (±)-Spiraminesâ C andâ D.
Angew Chem Int Ed Engl
; 55(1): 392-6, 2016 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-26545636
11.
Synthesis of Atisine, Ajaconine, Denudatine, and Hetidine Diterpenoid Alkaloids by a Bioinspired Approach.
Angew Chem Int Ed Engl
; 55(50): 15667-15671, 2016 12 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27860043
12.
Generating skeletal diversity from the C19 -diterpenoid alkaloid deltaline: a ring-distortion approach.
Chemistry
; 21(24): 8946-50, 2015 Jun 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-25950550
13.
Reversal of P-glycoprotein-mediated multidrug resistance by the novel tetrandrine derivative W6.
J Asian Nat Prod Res
; 17(6): 638-48, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26235354
14.
[Identification of aminoalcohol-diterpenoid alkaloids in Aconiti Lateralis Radix Praeparata and study of their cardiac effects].
Yao Xue Xue Bao
; 49(12): 1699-704, 2014 Dec.
Artigo
em Chinês
| MEDLINE | ID: mdl-25920200
15.
Diversity-oriented synthesis of diterpenoid alkaloids yields a potent anti-inflammatory agent.
Phytomedicine
; 117: 154907, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37295024
16.
Mesaconine alleviates doxorubicin-triggered cardiotoxicity and heart failure by activating PINK1-dependent cardiac mitophagy.
Front Pharmacol
; 14: 1118017, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37124193
17.
A novel D-ring modified taxoid: synthesis and biological evaluation of a γ-lactone analogue of docetaxel.
Org Biomol Chem
; 10(2): 361-6, 2012 Jan 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-22080402
18.
Oxidative dearomatization/intramolecular Diels-Alder cycloaddition cascade for the syntheses of (±)-atisine and (±)-isoazitine.
Org Biomol Chem
; 10(7): 1411-7, 2012 Feb 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-22193953
19.
A selective intramolecular transacylation of taxoids accompanying with the oxetane ring opening.
Chem Pharm Bull (Tokyo)
; 60(3): 415-8, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22382426
20.
Cardioactive C19-diterpenoid alkaloids from the lateral roots of Aconitum carmichaeli "Fu Zi".
Chem Pharm Bull (Tokyo)
; 60(1): 144-9, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22223386