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12篇 您的检索式:作者名="Bortolozzi F"
    题名 作者 年代 出处 被引量
1Automatic recognition of handwritten numerical strings: A recognition and verification strategy 显示文摘Oliveira L S Sabourin R Bortolozzi F 2002IEEE Trans on PAMI2002,24,11:1
2A comparison of SVM and HMM classifiers in the off-line signature verification显示文摘Justino E J R Bortolozzi F Sabourin R 2005Pattern recognition letters2005,26,9:1
3Neuronal apoptosis and reversible motor deficit in dominant-negative GSK-3 conditional transgenic mice 显示文摘Gomez-Sintes R Hernandez F Bortolozzi A 2007EMBO J2007,26,11:1
4Serotonin5-HT1A recep- tors as targets for agents to treat psychiatric disorders: ration- ale and current status of research显示文摘Celada P Bortolozzi A Artigas F 2013CNS Drugs2013,27,9:1
5Catecholamine/Serotonin inter- actions:systems thinking for brain function and disease显示文摘Hensler JG Artigas F Bortolozzi A 2013Adv Pharma- col2013,68,1:1
6Serotonin 5-HTIA receptors as targets for agents to treat psychiatric disorders: rationale and current status of research显示文摘Celada P Bortolozzi A Artigas F 2013CNS Drugs2013,27,9:1
7Serotonin 5-HTIA receptors as targets for agents to treat psychiatric disorders : rationale and cur- rent status of research显示文摘Celada P Bortolozzi A Artigas F 2013CNS Drugs2013,27,9:1
8The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing loss显示文摘Spiden SL Bortolozzi M Di Leva F 2008PLoS One2008,4,10:1
9A functional study of plasma-membrane calcium-pump isoform 2 mutants causing digenie deafness显示文摘Ficarella R Di Leva F Bortolozzi M 2007Proe Natl Acad Sci USA2007,104,5:1
10A comparison of SVM and HMM classifiers in the off-line signature verification显示文摘 Bortolozzi F Sabourin R 2005Pattern Recognition Lettersm2005,26,:1
11Serotonin5-HT1A receptors as targets for agents to treat psychiatric disorders:rationale and current status of research显示文摘CELADA P BORTOLOZZI A ARTIGAS F 2013CNS Drugs2013,27,9:1
12The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing loss 显示文摘Spiden S L Bortolozzi M Di Leva F 2008PLoS Genet2008,4,10:1
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