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14篇 您的检索式：作者名="Wokke"

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		题名	作者	年代	出处	被引量
	1	Riluzole 显示文摘	Wokke J	1996	Lancet1996，348，9030：	1
	2	查看详情显示文摘	Wokke J H Ausems M G E M Van den Boo gaard M T H		0，，03：	1
	3	Multifo cal motor neuropathy:diagnostic criteria that predict the response to immunoglobulin treatment显示文摘	Van den Berg-Vos RM Franssen H Wokke JH	2000	Ann Neurol2000，48，6：	1
	4	Juvenile and adult-onset acid maltase deficiency in France: genotype-phenotypecorrelation显示文摘	Ausems MG Wokke JH Reuser AJ	2001	Neurology2001，57，10：	1
	5	Increase of sural nerve T cells in progressive axonal polyneuropathy and monoclonal gammopathy显示文摘	Eurelings M van den Berg LH Wokke JHJ	2003	Neurology2003，71，：	1
	6	Bullying and victimization of primary school children in England and Germany:Prevalence and school factors显示文摘	WOKKE D WOODS S STANFORD K	2001	Br J Psychol2001，92，4：	1
	7	The influence of temperature on conduction block 显示文摘	Franssen H Wieneke GH Wokke JHJ	1999	Muscle & Nerve1999，22，：	1
	8	Exercise-induced muscle damage in the rat: the effect of vitamin E deficiency显示文摘	Amelink G J van der Wal WA Wokke JH	1991	Pflügers Arch1991，419，：	1
	9	Rilizole显示文摘		1996	Lancet1996，348，：	1
	10	Recombinant human insulin-like growth factor Ⅰ (rhIGF-Ⅰ) for the treatment of amyotrophic lateral sclerosis/motor neuron disease显示文摘	Beauverd M Mitchell JD Wokke JH		0，，：	1
	11	Comparison o f dixon and T1-weighted MR methods to assess the degree of fat infiltration in duchenne muscular dystrophy patients显示文摘	Wokke BH Bos C Monique Reijnierse MD	2013	J Magn Reson Imaging2013，38，3：	1
	12	Botulinum and Guillain-Barre syndrome显示文摘	Nortermans SHW Wokke JHJ Van den Bero LH	1992	Lacet1992，340，8814：	1
	13	家族性ALS表型表现为原发性侧索硬化症	Brugman F. Wokke J.H.J. De Jong J.M.B.V. 李一明	2005	世界核心医学期刊文摘(神经病学分册)2005，0，9：	0
	14	散发上运动神经元综合征成年患者的spastin基因突变显示文摘Mutation of the spastin gene is the single most common cause of pure hereditary spastic paraparesis. In patients with an unexplained sporadic upper motor neuron (UMN) syndrome, clinical distinction between primary lateral sclerosis and sporadic hereditary spastic paraparesis may be problematic. To investigate whether spastin mutations are present in patients with primary lateral sclerosis and sporadic hereditary spastic paraparesis, we screened the spastin gene in 99 Dutch patients with an unexplained, apparently sporadic, adult-onset UMN syndrome. We found 6 mutations, of which 4 were novel, in the subgroup of 47 patients with UMN symptoms restricted to the legs (13% ). Another novel spastin mutation was found in a patient with a rapidly progressive spinal and bulbar UMN syndrome that progressed to amyotrophic lateral sclerosis. In the patients with arm or bulbar UMN symptoms and slow progression, no spastin mutations were found. Our study shows that spastin mutations are a frequent cause of apparently sporadic spastic paraparesis but not of primary lateral sclerosis.	Brugman F Wokke J.H.J Scheffer H. 江山	2006	世界核心医学期刊文摘(神经病学分册)2006，2，5：	0

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