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84篇 您的检索式：作者名="VALENTE EM"

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	题名	作者	年代	出处	被引量
1	Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1显示文摘	Abou-Sleiman PM Caputo V	2004	Science2004，304，：	1
2	Severe infantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4A显示文摘	Brancati F Valente EM Davies NP	2003	J Neurol Neurosurg Psychiatry2003，74，9：	1
3	Computerized gait analysis of botulinum toxin treatment in children with cerebral palsy显示文摘	Galli M Cimolin V Valente EM	2007	Disabil Rehabil2007，29，8：	1
4	PINKI mutations are associated with sporadic early-onset parkinsonism显示文摘	Salvi S Ialongo T	2004	Ann Neurol2004，56，3：	1
5	Role of the dopamine D5 receptor (DRD5) as a susceptibility gene for cervical dystonia 显示文摘	Brancati F Valente EM Castori M	2003	Journal of Neurology Neurosurgery and Psychiatry2003，74，：	1
6	Computerized gait analysis of botulinum toxin treatment in children with cere- bral palsy显示文摘	Galli M Cimolin V Valente EM	2007	Disabil Rehabi12007，29，8：	1
7	Clinical and subclinical dopaminergic dysfunction in PARK6- linked parkinsonism: an lSF-dopa PET study显示文摘	Khan NL Valente EM Bentivoglio AR	2002	Ann Neurol2002，52，6：	1
8	Joubert syndrome and relat- ed disorders显示文摘	Brancati F Dallapieeola B Valente EM	2010	Orphanet J Rare Dis2010，5，：	1
9	Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36显示文摘	Valente EM Bentivoglio AR Dixon PH	2001	AmJ Hum Genet2001，68，4：	1
10	Genotypes and phenotypes of Joubert syndrome and related disorders 显示文摘	Valente EM Brancati F Dallapiccola B	2008	Eur J Med Genet2008，51，：	1
11	Hereditarry earlyonset Parkinson's disease caused by mutations in PINKI 显示文摘	Valente EM Abou-Sleiman PM Caputo V	2004	Science2004，304，5674：	1
12	Joubert syndrome and re latect disorders显示文摘	Brancati F Dallapiccola B Valente EM	2010	Orphanet J Rare Dis2010，5，1：	1
13	PINK1 mutations are associated with sporadic early-onset parkinsonism显示文摘	Valente EM Salvi S Ialongo T		0，，03：	1
14	DJ-1 mutations in Parkinson's disease显示文摘	Abou-Sleiman PM Valente EM	2004	J Neurol Neurosurg Psychiatry2004，75，：	1
15	Hereditary early-onset Parkinson's disease caused by mutations in PINK1显示文摘	Valente EM Abou-Sleiman PM Caputo V	2004	Science2004，304，5674：	1
16	Acneiform follicular mucinosis显示文摘	Passaro EM Silveira MT Valente NY	2004	Clin Exp Dermatol2004，29，4：	1
17	Hereditary early-onset Parkinson disease caused by mutations in PINKI 显示文摘	Valente EM Abou-Sleiman PM Caputo V	2004	Science2004，304，5674：	1
18	Pallidal stimulation improves pantothenate kinase-associated neurodegeneration显示文摘	Castelnau P Cif L Valente EM	2005	Ann Neurol2005，57，5：	1
19	Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene显示文摘	Spacey SD Valente EM Wali GM	2002	Mov Disord2002，17，4：	1
20	Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evi- dence for a third EKD gene显示文摘	SPACEY SD VALENTE EM WALl GM	2002	Mov Disord2002，17，4：	1

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