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31篇 您的检索式：作者名="Proukakis"

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	题名	作者	年代	出处	被引量
1	Modeling and Estimation of Ambi-guities in Linear Arrays显示文摘	Manikas A Proukakis C	1998	IEEE Transactions on signal process- ing1998，46，8：	1
2	Investigative study of planar array ambiguities based on 'Hyperhelical' parameterization 显示文摘	Manikas A Proukakis C Lefkaditis V	1999	IEEE Tmns on Signal Processing1999，47，6：	1
3	Modeling and estimation of ambiguities in linear arrays显示文摘	MANIKAS A PROUKAKIS C	1998	IEEE Trans on Signal Processing1998，46，8：	1
4	Investigative study of planar array ambiguities based on 'hyperhelical' parameterization 显示文摘	MANIKAS A PROUKAKIS C LEFKADITIS V	1999	IEEE Trans on Signal processing1999，47，6：	1
5	Modeling and Estima- tion of Am-Biguities in Linear arrays显示文摘	MANIKAS A PROUKAKIS C	1998	IEEE Transac- tions on SignalProcessing1998，46，8：	1
6	Investi- gative Study of Planar Array Ambiguities Based on' Hy- perhelical' parameterization 显示文摘	MANIKAS A PROUKAKIS C LEFKADITIS V	1999	IEEE Trans on Signal Processing1999，47，6：	1
7	Investigative study of planar array ambiguities based on ' hyper-helical' parameterization 显示文摘	A Manikas C Proukakis V Lefkaditis	1999	IEEE trans on signal processing1999，47，6：	1
8	Modeling and estimation of ambiguities in linear Arrays显示文摘	A Manikas C Proukakis	1998	IEEE Trans on signal and propagation1998，46，8：	1
9	Hereditary spastic paraplegia:clinical features and path ogenetic mechanisms显示文摘	Salinas S Proukakis C Crosby A		0，，：	1
10	Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase 显示文摘	Simpson M A Cross H Proukakis C	2004	Nat Genet2004，36，：	1
11	Detection of novel mutations and review of published data suggests that hereditary spastic paraplegia caused by spastin(SPAST)mutations is found more often in males显示文摘	Proukakis C Moore D Labrum R		0，，：	1
12	Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms 显示文摘	Salinas S Proukakis C Crosby A	2008	Lancet Neurol2008，7，12：	1
13	Evolution of prodromal clinical markers of Parkinson disease in a GBA mutation-positive cohort显示文摘	Beavan M McNeill A Proukakis C	2015	JAMA Neurol2015，72，2：	1
14	Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms 显示文摘	Salinas S Proukakis C Crosby A Warner T	2008	Lancet Neurol2008，7，12：	1
15	Spastin and microtubules:Functions in health and disease显示文摘	Salinas S Carazo-Salas RE Proukakis C		0，，：	1
16	SPG20 is mutated inTroyer syndrome, an hereditary spastic paraplegia 显示文摘	Patel H Cross H Proukakis C	2002	Nat Genet2002，31，4：	1
17	Dark soliton decay due to trap anharmonicity in atomic Bose-Einstein condensates 显示文摘	Parker N G Proukakis N P Adams C S	2010	Phys Rev A2010，81，03：	1
18	Dark soliton decay due to trap anharmonicity in atomic Bose-Einstein condensates 显示文摘	Parker N G Proukakis N P Adams C S	2010	Phys Rev A2010，81，03：	1
19	Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase显示文摘	Simpson M A Cross H Proukakis C	2004	Nat GeneU2004，36，11：	1
20	Modeling and estimation of ambiguities in linear arrays显示文摘	Manikas A Proukakis C	1998	IEEE Transactions on Signal Processing1998，46，8：	1

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