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86篇 您的检索式：作者名="Engel AG"

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	题名	作者	年代	出处	被引量
1	Fingerprint body myopathy,a newly recognized congenital muscle disease显示文摘	Engel AG Angelini C Gomez MR	1972	Mayo Clinic Proc1972，47，6：	1
2	Clinical and electro-myograpnic studies in a patient with primary hypokalemic periodic paralysis显示文摘	ENGEL AG LAMBERT EH ROSEVEAR JW	1965	Am J Med1965，38，：	1
3	Mierovaseular changes in earlly andadvaneed dermatomyositis: a quantitatie study 显示文摘	Emslie-Smith AM Engel AG	1990	Ann Neurol1990，27，4：	1
4	Mutations in myotilin cause myofibrillar myopathy显示文摘	Selcen D Engel AG	2004	Neurology2004，62，：	1
5	Myofibrillar myopathy caused by novel dominant negative alphaB-crystallin mutations 显示文摘	Selcen D Engel AG	2003	Ann Neurol2003，54，：	1
6	Myofibrillar myopathy : clinical, morphological and genetic studies in 63 patients 显示文摘	Selcen D Ohno K Engel AG	2004	Brain2004，127，：	1
7	Ultrastructural localization of the acetylcholine receptor in myasthenia gravis and in its experimental autoimmune model显示文摘	Engel AG Lindstrom JM Lambert EH	1977	Neurology1977，27，：	1
8	Unexpected sarcolemmal complement membrane attack complex deposits on non-necrotic muscle fibers in nmscular dystrophies显示文摘	Spuler S Engel AG	1998	Neurology1998，50，1：	1
9	Mutations in myotilin cause myoflbrillar myopathy显示文摘	Selcen D Engel AG	2004	Neurology2004，62，：	1
10	Immunohistochemical study of CD45 T cell isoforms ininflammatory myopathies显示文摘	De Bleeker JL Engel AG	1995	Am J Pathol1995，146，：	1
11	Mutations in ZASP define a novel form of muscular dystrophy in humans显示文摘	Selcen D Engel AG	2005	Ann Neurol2005，57，：	1
12	The earliest pathologic alterations in dysferlinopathy 显示文摘	Selcen D Stilling G Engel AG	2001	Neurology2001，1256，11：	1
13	Carnitine deficiency of human skeletal muscle with associated lipid storage myopathy: a new syndrome显示文摘	Engel AG Angelini C	1973	Science1973，179，76：	1
14	Expression of cell adhesion molecule in inflammatory myopathiesand Duchenne dystrophy显示文摘	Bleecker Engel AG	1994	J Neuropathol Exp Neurol1994，53，4：	1
15	Major histocompatibility complex class I antigen localization of interferon subtypes,and T cell-mediated cytotoxicity in myopathies 显示文摘	Emslie-Smith AM Arahata K Engel AG	1989	Hum Pathol1989，20，3：	1
16	Carnitine metabolism and inborn errors显示文摘	Engel AG Rebouche CJ	1984	J Inherit Metab Dis1984，7，1：	1
17	Congenital myasthenic syndromes: recent advances显示文摘	Engel AG Ohno K Sine SM	1999	Arch Neurol1999，56，2：	1
18	Mutations in ZASP define a novel form of muscular dystrophy in humans显示文摘	Selcen D Engel AG	2005	Ann Neurol2005，57，2：	1
19	New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congential myasthenic syndrome显示文摘	Engel AG Ohno K Milone M	1996	Hum Molec Genet1996，5，9：	1
20	Myofibrillar myopathy caused by novel dominant negative alpha-B-crystallin mutations显示文摘	Selcen D Engel AG	2003	Ann Neurol2003，54，：	1

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