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20篇 您的检索式：作者名="Sewry C"

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	题名	作者	年代	出处	被引量
1	Late onset muscular dystrophy with cerebral white matter changes to partial merosin deficiency显示文摘	Tan E Topaloglu H Sewry C	1997	Neuromuscular Disorders1997，7，2：	1
2	Defining alpha-skeletaland alpha-cardiac actin expression in human heart andskeletal muscle explains the absence of cardiac involvementin ACTA1 nemaline myopathy显示文摘	Ilkovski B Clement S Sewry C		0，，12：	1
3	Defining alpha-skeletaland alpha -cardiac actin expression in human heart and skeletalmuscle explains the absence of cardiac involvement in ACTA1nemaline myopathy 显示文摘	llkovski B Clement S Sewry C	2005	Neuromuscul Disord2005，15，12：	1
4	Deletions in the 5' region of dystrophin and resulting phenotypes显示文摘	Muntoni F Gobbi P Sewry C	1994	J Med Genet1994，31，：	1
5	Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1 显示文摘	Sehessl J Taratuto AL Sewry C	2009	Brain2009，132，：	1
6	Expression of dystrophin-associated glycoproteins and utrophin in carriers of Duchenne muscular dystrophy显示文摘	Sewry C A Matsumura K Campbell K P	1994	Neuromuscular Disorders1994，4，5：	1
7	Defining alpha-skeletal and alpha-cardiac actin expression in human heart and skeletal muscle explains the absence of cardiac involvement in ACTA1 nemaline myopathy显示文摘	Ilkovski B Clement S Sewry C		0，，12：	1
8	Infantile onsetmyofibrillar myopathy due to recessive CRYAB mutations 显示文摘	FORREST KM AL SARRAJ S SEWRY C	2011	Neuromuscul Disord2011，21，1：	1
9	The spectrum of pathology in central core disease显示文摘	Muller C Davis M	2002	Neuromuscu[Disord2002，12，10：	1
10	Mutations in the nebulin gene can cause severe congenital nemaline myopathy 显示文摘	Wallgren-Pettersson C Donner K Sewry C	2002	Neuromuscul Disord2002，12，：	1
11	Minicore myopathy in chil- dren: a clinical and histopathological study of 19 cases 显示文摘	Jungbluth H Sewry C Brown SC	2000	Neuro- muscul Disorder2000，10，45：	1
12	Nemaline rnyopathies 显示文摘	Wallgren-Pettemson C Sewry CA Nowak KJ	2011	Semin Pediatr Neurol2011，18，4：	1
13	The spectrum of pathology in central core disease显示文摘	Sewry CA Muller C Davis M	2002	Neuromusc Disord2002，12，：	1
14	Infantile onset myofibrillar myopathy due to recessive CRYAB mutations显示文摘	Forrest KM Al-Sarraj S Sewry C		0，，01：	1
15	Absence of neuronal nitric oxide synthase (nNOS) as a pathological marker for the diagnosis of Becket muscular dystrophy with rod domain deletions 显示文摘	ToreBi S Brown SC Jimenez-Mallebrera C Feng L Muntoni F Sewry CA	2004	Neuropathol Appl Neurobiol2004，30，5：	1
16	lmmunohistological intensity measurements as a tool to assess sarcolemma-associated protein expression显示文摘	Areehavala Gomeza V Kinali M Feng L Brown SC Sewry C Morgan JE	2010	Neuropathol Appl Neurobiol2010，36，4：	1
17	Deletions in the 5'region of dystrophin and resulting phenotypes显示文摘	GOBBI P SEWRY C	1994	J Med Genet1994，31，：	1
18	Minicore myopathy in children:a clinical and histopathological study of 19 cases显示文摘	Jungbluth H Sewry C Brown SC		0，，：	1
19	Nemaline myopathy caused by absence of alpha-skeletal muscle actin 显示文摘	Nowak KJ Sewry CA Navarro C	2007	Ann Neurol2007，61，2：	1
20	The spectrum of pathology in central core disease显示文摘	Sewry CA Muller C Davis M	2002	Neuromuscul Disord2002，12，10：	1

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