The therapy of congenital myasthenic syndromes

Por Engel, Andrew G.
Publicado em 2007

Current Status of the Congenital Myasthenic Syndromes

Por Engel, Andrew G.
Publicado em 2011

Why does acetylcholine exacerbate myasthenia caused by anti-MuSK antibodies?

Por Engel, Andrew G
Publicado em 2013

Congenital Myasthenic Syndromes in 2012

Por Engel, Andrew G.
Publicado em 2012

Acid maltase levels in muscle in heterozygous acid maltase deficiency and in non-weak and neuromuscular disease controls

Por Engel, Andrew G., Gomez, Manuel R.
Publicado em 1970

Serum choline activates mutant acetylcholine receptors that cause slow channel congenital myasthenic syndromes

Por Zhou, Ming, Engel, Andrew G., Auerbach, Anthony
Publicado em 1999

OBSERVATIONS ON ORGANIZATION OF Z-DISK COMPONENTS AND ON ROD-BODIES OF Z-DISK ORIGIN

Por MacDonald, Ronald D., Engel, Andrew G.
Publicado em 1971

BENEFICIAL EFFECTS OF ALBUTEROL IN CONGENITAL ENDPLATE ACETYLCHOLINESTERASE DEFICIENCY AND DOK-7 MYASTHENIA

Por Liewluck, Teerin, Selcen, Duygu, Engel, Andrew G.
Publicado em 2011

Teaching NeuroImages: Hydroxychloroquine-induced vacuolar myopathy

Por Ghosh, Partha S., Swift, David, Engel, Andrew G.
Publicado em 2013

BENEFICIAL EFFECT OF ALBUTEROL IN CONGENTIAL MYASTHENIC SYNDROME WITH EPSILON SUBUINT MUTATIONS

Por Sadeh, Menachem, Shen, Xin-Ming, Engel, Andrew G.
Publicado em 2011

Human endplate acetylcholinesterase deficiency caused by mutations in the collagen-like tail subunit (ColQ) of the asymmetric enzyme

Por Ohno, Kinji, Brengman, Joan, Tsujino, Akira, Engel, Andrew G.
Publicado em 1998

Muscle blood flow in Duchenne type muscular dystrophy, limb-girdle dystrophy, polymyositis, and in normal controls

Por Paulson, Olaf B., Engel, Andrew G., Gomez, Manuel R.
Publicado em 1974

Endplate Structure and Parameters of Neuromuscular Transmission in Sporadic Centronuclear Myopathy Associated with Myasthenia

Por Liewluck, Teerin, Shen, Xin-Ming, Milone, Margherita, Engel, Andrew G.
Publicado em 2011

Reducing bodies and myofibrillar myopathy features in FHL1 muscular dystrophy

Por Selcen, Duygu, Bromberg, Mark B., Chin, Steven S., Engel, Andrew G.
Publicado em 2011

New horizons for congenital myasthenic syndromes

Por Engel, Andrew G., Shen, Xin-Ming, Selcen, Duygu, Sine, Steven
Publicado em 2012

Mutant SNAP25B causes myasthenia, cortical hyperexcitability, ataxia, and intellectual disability

Por Shen, Xin-Ming, Selcen, Duygu, Brengman, Joan, Engel, Andrew G.
Publicado no Neurology (2014)

Neuromuscular Junction Acetylcholinesterase Deficiency Responsive to Albuterol

Por Chan, Sophelia H. S., Wong, Virginia C. N., Engel, Andrew G.
Publicado no Pediatr Neurol (2012)

The human adult subtype ACh receptor channel has high Ca(2+) permeability and predisposes to endplate Ca(2+) overloading

Por Fucile, Sergio, Sucapane, Antonietta, Grassi, Francesca, Eusebi, Fabrizio, Engel, Andrew G
Publicado em 2006

Sporadic Centronuclear Myopathy with Muscle Pseudohypertrophy, Neutropenia, and Necklace Fibers due to a DNM2 mutation

Por Liewluck, Teerin, Lovell, Tracy L., Bite, Anna V., Engel, Andrew G.
Publicado em 2010

What Have We Learned from the Congenital Myasthenic Syndromes

Por Engel, Andrew G., Shen, Xin-Ming, Selcen, Duygu, Sine, Steven M.
Publicado em 2009