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20篇 您的检索式：作者名="Camuzat"

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	题名	作者	年代	出处	被引量
1	Atlastin1 mutations are frequent in young-onset autosomal dominant spastic paraplegia显示文摘	Dürr A Camuzat A Colin E	2004	Arch Neurol2004，61，12：	1
2	Prevalence of dentatorubral-pallidoluysian atrophy in a large series of white patients with cerebellar ataxia 显示文摘	Ber IL Camuzat A Castelnovo G	2003	Arch Neurol2003，60，8：	1
3	Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease显示文摘	Le Ber I Camuzat A Berger E		0，，：	1
4	Reaction of phosphonium ylides and aromatic nitriles under Lewis acid conditions: an easy access to aryl-substituted α-methoxyacetophenones 显示文摘	Camuzat D B Provot O	1999	Synthesis1999，9，：	1
5	Atlastin 1 mutations are frequent in young-onset autosomal dominant spastic paraplegia显示文摘	Durr A Camuzat A Colin E	2004	Arch Neurol2004，61，12：	1
6	Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?显示文摘	P Charles A Camuzat N Benammar F Sellal A Destée A-M Bonnet S Lesage I Le Ber G Stevanin A Dürr A Brice	2007	Neurology2007，，21：	1
7	SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family显示文摘	Fujigasaki H Verma I C Camuzat A	2001	Ann Neurol2001，49，1：	1
8	Association between the extended tau haplotype and frontotemporal dementia显示文摘	Camuzat A Hannequin D	2002	Arch Neurol2002，59，：	1
9	Are interrupted SCA2 CAG repeat expansions responsible for Parkinsonlsm? 显示文摘	Charles P Camuzat A Benammar N	2007	Neurology2007，69，21：	1
10	Are interrupted SCA2 CAG repeat expansions responsible tbr parkinsonism? 显示文摘	Charles P Camuzat A Benammar N	2007	Neurology2007，69，21：	1
11	Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron dise ase显示文摘	Le Ber I Camuzat A Berger E	2009	Neurology2009，72，19：	1
12	Segregation of on in the microtubule-associated protein tau gene with familial frontotemporal dementia and par- kinsonism显示文摘	Dumanchin C Camuzat A Campion D	1998	Hum Mol Genet1998，7，1：	1
13	Chromosome 9p- linked families with frontotemporal dementia associated with motor neuron disease显示文摘	Le Ber I Camuzat A Berger E	2009	Neurology2009，72，19：	1
14	SQSTM1 mutations in French patients with frontotemporal dementia or frontotem- poral dementia with amyotrophic lateral sclerosis显示文摘	Le Ber I Camuzat A Guerreiro R	2013	JAMA Neurol2013，70，11：	1
15	TARDBP mutations inmotoneuron disease with frontotemporal lobar degeneration 显示文摘	Benajiba L Le Ber I Camuzat A	2009	Ann Neurol2009，65，47：	1
16	SCA12 is a rare locus fnr autosomal dominant cerebellar ataxia:a study of an Indian family显示文摘	Fujigasaki H Verma IC Camuzat A et aI	2001	Ann-Neurol2001，49，1：	1
17	Extensive white matter involvement in patients with frontotemporal lobar degeneration: think progranulin 显示文摘	Caroppo P Le Bet I Camuzat A	2014	JAMA Neurol2014，71，12：	1
18	Frequency of the DYT1 mutation in primary torsion dystonia without family histo- ry显示文摘	Brassat D Camuzat A Vidailhet M	2000	Arch Neurol2000，57，3：	1
19	SCA12 is a rarelocus for autosoma dominant eerehellar ataxia:a study of an Indian family 显示文摘	Fujigasaki H Verma IC Camuzat A	2001	Ann Neurol2001，49，1：	1
20	A phenotype of atypical apraxia of speech in a family carrying SQSTM1 mutation 显示文摘	BOUTOLEAU-BRETONNI RE C CAMUZAT A LE BER I	2015	J Alzheimers Dis2015，43，2：	1

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