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23篇 您的检索式：作者名="LE BER I"

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	题名	作者	年代	出处	被引量
1	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
2	C9orf72 repeat expansions are a rare genetic cause of parkinsonism 显示文摘	Lesage S Le Ber I Condmyer C	2013	Brain2013，1362，：	1
3	Genetics of frontotemporal lobar degeneration : An up-date and diagnosis algorithm 显示文摘	Le Ber I	2013	Rev Neurol ( Paris )2013，169，10：	1
4	New autosomal recessive cerebellar ataxias with oculomotor apraxia显示文摘	Le Ber I Brice A Durr A	2005	Curr Neurol Neurosci Rep2005，5，5：	1
5	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
6	Demographic, neurological and behavioural characteristics and brain perfusion SPECT in frontal variant of frontotemporal dementia 显示文摘	Le Ber I Guedj E Gabelle A	2006	Brain2006，129，11：	1
7	A non-DM1, non-DM2 multisystem myotonie disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24 显示文摘	Le Ber I Martinez M Campion D	2004	Brain2004，127，：	1
8	hnRNPA2B1 and hnRNPA1 mutations are rare in patients with ' multisystem proteinopathy' and frontotemporal lobar degeneration phenotypes 显示文摘	Le Ber I Van Bortel I Nicolas G	2014	Neurobiol Aging2014，35，4：	1
9	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
10	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
11	Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosis显示文摘	CIURA S LATTANTE S LE BER I etal	2013	Annals of Neurology2013，74，2：	1
12	Neuropsychological and18F1Xj-PET studies in a family with idiopathic basal gangliacalcifications显示文摘	Le Ber I Marie RM Chabot B	2007	J Neurol Sci2007，258，12：	1
13	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
14	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
15	Catalytic wet-air oxidation of industrial effluents: total mineralization of organics and lumped kinetic modelling显示文摘	Albin Pintar Gorazd Ber?i? Michèle Besson Pierre Gallezot	2003	Applied Catalysis B Environmental2003，，3：	1
16	A non-DM1,non-DM2multisystem myotonic disorder with frontotemporal dementia : phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24 显示文摘	LE BER I MARTINEZ M CAMPION D	2004	Brain2004，127，9：	1
17	Neuropsychological and 18FDG-PET studies in a family with idiopathic basal ganglia calcifications显示文摘	Le Ber I Marie RM Chabot B	2007	Journal of the Neurological Sciences2007，258，：	1
18	C9orf72 repeat expansionsare a rare genetic cause of Parkinsonism显示文摘	Lesage S Le Ber I Condroyer C	2013	Brain2013，136，：	1
19	Familial idiopathic striato-pallido-dentate calcifications: clinical and brain imaging study in a family显示文摘	Le Ber I Marie RM Lalevee C	2003	Rev Neurol (Paris)2003，159，1：	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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