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18篇 您的检索式：作者名="Edvardson"

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		题名	作者	年代	出处	被引量
	1	Exome-se- quencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic para- paresis显示文摘	Erlich Y Edvardson S Hodges E	2011	Genome Res2011，21，5：	1
	2	Excited states in odd Sn nuclei, A=109-125显示文摘	ch MADUEME G EDVARDSON L O WEST- ERBERG L	1976	Physica Scripta1976，13，1：	1
	3	Deleterious mutation in the mitochondrial arginyl-transfer RNA synthetase gene is associated with pontocerebellar hypoplasia 显示文摘	Edvardson S Shaag A Kolesnikova O	2007	Am J Hum Genet2007，81，4：	1
	4	Sotalol versus quinidine for the maintenance of sinus rhythm after direct current conversion of atrial fibrillation显示文摘	Edvardson N Rdhnqvist-Ahlberg N	1990	Circulation1990，82，：	1
	5	Service quality: Beyond cognitive assessment 显示文摘	Edvardson B	2005	Managing Service Quality2005，15，2：	1
	6	Noninvasive myocardial strain measurement by speckle tracking echocardiography:validation against sonomicrometry and tagged magnetic resonance imaging 显示文摘	Amundsen BH Helle-Valle T Edvardson T	2006	J Am Coll Cardiol2006，47，4：	1
	7	A deleterious mutation in the LOXHD1gene causes autosomal recessive hearing loss in Ashkenazi Jews显示文摘	EDVARDSON S JALAS C SHAAG A	2011	Am J Med Genet A2011，155，：	1
	8	West syn- drome caused by ST3Gal- Ⅲ deficiency 显示文摘	Edvardson S Baumann AM Mtihlenhoff M	2013	Epilepsia2013，54，2：	1
	9	SLC25A19 mutation as a cause of neuropathy and bilateral striatal necrosis显示文摘	Spiegel R Shaag A Edvardson S	2009	Ann Neurol2009，66，3：	1
	10	Joubert syndrome 2 (JBTS2) in Ashkenazi Jews is associated with a TMEM216 mutation显示文摘	Edvardson S Shaag A Zenvirt S	2010	Am J Hum Genet2010，86，1：	1
	11	Noninvasive myocardial strain measurement by speckle tracking echocardiography validation against sonomicrometry and tagged magnetic resonance imaging显示文摘	AMUNDSEN B H HELLE-VALLE T EDVARDSON T	2006	J Am Coll Cardiol2006，47，：	1
	12	显示文摘	Skulstad H Aakhus S	2001	J Am Coll Cardiol2001，37，3：	1
	13	Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis显示文摘	Erlich Y Edvardson S Hodges E Zenvirt S Thekkat P Shaag A Dor T Hannon GJ Elpeleg O		0，，：	1
	14	Left ventricular coneen tric remodeling is associated with decreased global and regional systolic function:the Multi Ethnic Study of Atheroselerosis 显示文摘	Rosen BD Edvardson T Lai S	2005	Circulation2005，112，7：	1
	15	Noninvasive myo- cardial strain measurement by spcclde tracking cchocardJography: validation against sonomicrometry and tagged magnetJcmsonance imaging 显示文摘	Amundsen BH Helle Valle T Edvardson T otal	2006	J Am Cell Cardiol2006，47，4：	1
	16	A deleterious mutation in DNAJC6 encoding the neuronal-specific elathrin- uneoating co-chaperone auxilin, is associated with juvenile parkinsonism显示文摘	Edvardson S Cinnamon Y Ta-Shma A	2012	PLoS One2012，7，36：	1
	17	Deleterious mutation inthe mitochondrial arginyl-transfer RNA synthetase gene is associatedwith pontocerebellar hypoplasia 显示文摘	Edvardson S Shaag A Kolesnikova O	2007	AmJ Hum Genet2007，81，4：	1
	18	Early infantile epilep- tic encephalopathy associated with a high voltage gated calci- um channelopathy 显示文摘	Edvardson S Oz S Abulhijaa FA	2013	J Med Genet2013，50，2：	1

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