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Annals of the New York Academy of Sciences|January 1, 1976
The motor end plate in myasthenia gravis and in experimental autoimmune myasthenia gravis. A quantitative ultrastructural studyA G Engel, M Tsujihata, J M Lindstrom, et al.
Neurology|November 19, 2011
Reducing bodies and myofibrillar myopathy features in FHL1 muscular dystrophyDuygu Selcen, Mark B Bromberg, Steven S Chin, et al.
Neuromuscular Disorders : NMD|March 24, 2004
Novel truncating RAPSN mutations causing congenital myasthenic syndrome responsive to 3,4-diaminopyridineBrenda L Banwell, Kinji Ohno, Joern P Sieb, et al.
Brain : a Journal of Neurology|December 24, 2004
Subunit-specific contribution to agonist binding and channel gating revealed by inherited mutation in muscle acetylcholine receptor M3-M4 linkerXin-Ming Shen, Kinji Ohno, Steven M Sine, et al.
Human Molecular Genetics|November 1, 1994
Human muscle glycogenosis due to phosphorylase kinase deficiency associated with a nonsense mutation in the muscle isoform of the alpha subunitM Wehner, P R Clemens, A G Engel, et al.
Biochimica Et Biophysica Acta|April 20, 1983
Characterization of beta-adrenergic receptor subtypes in androgen-induced mouse kidney hypertrophy using a new high-affinity ligand, [125I]iodocyanopindololS L Petrovic, G Engel, R P Haugland, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|June 1, 1984
Labelling of Ri adenosine receptors in rat fat cell membranes with (-)-[125iodo]N6-hydroxyphenylisopropyladenosineD Ukena, R Furler, M J Lohse, et al.
The International Journal of Eating Disorders|October 25, 2008
Health-related quality of life and eating disorders: a review and updateScott G Engel, Carol E Adair, Carlota Las Hayas, et al.
Annals of the New York Academy of Sciences|June 24, 2008
Further observations in congenital myasthenic syndromesAndrew G Engel, Xin-Ming Shen, Duygu Selcen, et al.
Deutsche Medizinische Wochenschrift (1946)|April 4, 1980
[Carnitine deficiency myopathy (author's transl)]F Jerusalem, A G Engel, C Sengupta, et al.
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