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57篇 您的检索式：作者名="MAISONOBE"

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	题名	作者	年代	出处	被引量
1	Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the musclesodium channel gene SCN4A显示文摘	STERNBERG D MAISONOBE T JURKAT-ROTT K		0，，06：	1
2	Severe perturbations of the blood T cell repertoire in polymyositis, but not dermatomyositis patients显示文摘	Benveniste O Cherin P Maisonobe T	2001	J Immunol2001，167，6：	1
3	Neuropathy in lymphoma:a relationship between the pattern of neuropathy,type of lymphoma and prognosis?显示文摘	B6hin A Maisonobe T	2008	J Neurol Neurosurg Psychiatry2008，79，7：	1
4	Idiopathic lumbosacral plexopathy显示文摘	Seror P Maisonobe T Viala K	2005	Presse Med2005，34，12：	1
5	Genotype-pheno- type relationship in 2 SMA III patients with novel muta- tions in the Tudor domain 显示文摘	Fraidakis M J Drunat S Maisonobe T	2012	Neurology2012，78，8：	1
6	Hypokalemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A显示文摘	Sternberg D Maisonobe T Jurkat-Rott K	2001	Brain2001，124，6：	1
7	Diagnostic value of markers of muscle degeneration in sporadic inclusion body myositis 显示文摘	Dubourg O Wansehitz J Maisonobe T	2011	Acta Myol2011，30，：	1
8	Role of matrix metalloproteinases, proinflammatory cytokines, and oxidative stress-derived molecules in hepatitis C virusassociated mixed cryoglobulinemia vasculitis neuropathy 显示文摘	Saadoun D Bieche I Authier FJ Laurendeau 1 J ambou F Piette JC Vidaud M Maisonobe T Cacoub P	2007	Arthritis Rheum2007，56，4：	1
9	Diagnostic value of markers of muscle degeneration in sporadic inclusion body myositis 显示文摘	Dubourg O Wanschitz J Maisonobe T	2011	Acta Myol2011，30，：	1
10	Proposed revised elec- trophysiological criteria for chronic inflammatory demyelinating polyra- diculoneuropathy 显示文摘	Nicolas G Maisonobe T Le Forestier N	2002	Muscle Nerve2002，25，：	1
11	Proposed revised elec- trophysiologieal criteria for chronic inflammatory demyelinating polyradiculoneuropathy显示文摘	Nicolas G Maisonobe T Le Forestier N	2002	Muscle Nerve2002，25，1：	1
12	Electrophysiological determination of the site involved in generating abnormal muscle responses in hemifacial spasm显示文摘	Tankere F Maisonobe T Lamas G	1998	Muscle Nerve1998，21，：	1
13	Diagnostic value of markers of muscle degeneration in sporadic inclusion body myositis显示文摘	Dubourg O Wanschitz J Maisonobe T	2011	Acta Myol2011，30，2：	1
14	Polyneuropathy associated with IgG/IgA monoclonal gammopathy:a clinical and electrophysiological study of 15 cases显示文摘	Magy L Chassande B Maisonobe T	2003	Eur J Neurol2003，10，6：	1
15	Cryoglobulinemic peripheral neuropathy in hepatitis C virus infection: clinical and anatomical correlations of 22 cases显示文摘	Taieb G Maisonobe T Musset L	2010	Rev Neurol (Paris)2010，166，5：	1
16	Neurogenic involvement in a case of oculopharyngeal muscular dystrophy显示文摘	Boukriche Y Maisonobe T Masson C	2002	Muscle Nerve2002，25，1：	1
17	Does primary lateral sclerosis exist? A study of 20 patients and a review of the literature显示文摘	Le Forestier N Maisonobe T Piquard A	2001	Brain2001，124，10：	1
18	Hypokalemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A显示文摘	Sternberg D Maisonobe T Jurkat-Rott K		0，，06：	1
19	Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A显示文摘	Sternberg D Maisonobe T Jurkat-Rott K	2001	Brain2001，124，6：	1
20	Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A显示文摘	Sternberg D Maisonobe T Jurkat Rott K	2001	Brain2001，124，6：	1

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