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Birth Defects Original Article Series|January 1, 1979
Anxiety engendered by amniocentesisD Beeson, M S Golbus
Annals of Neurology|February 16, 1999
Early-onset myasthenia gravis: a recurring T-cell epitope in the adult-specific acetylcholine receptor epsilon subunit presented by the susceptibility allele HLA-DR52aM Hill, D Beeson, P Moss, et al.
The Journal of Clinical Investigation|November 15, 1996
Association of arthrogryposis multiplex congenita with maternal antibodies inhibiting fetal acetylcholine receptor functionS Riemersma, A Vincent, D Beeson, et al.
Journal of the American Medical Directors Association|December 25, 2018
Medical Cannabis in the Skilled Nursing Facility: A Novel Approach to Improving Symptom Management and Quality of LifeZachary J Palace, Daniel A Reingold
Neurology|December 14, 2005
Serum antibodies in epilepsy and seizure-associated disordersK McKnight, Y Jiang, Y Hart, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|December 26, 2008
Dok-7/MuSK signaling and a congenital myasthenic syndromeY Yamanashi, O Higuch, D Beeson
The Journal of Clinical Investigation|July 4, 2001
Acetylcholine receptor delta subunit mutations underlie a fast-channel myasthenic syndrome and arthrogryposis multiplex congenitaS Brownlow, R Webster, R Croxen, et al.
Proceedings. Biological Sciences|October 22, 1993
Detection of alpha-subunit isoforms in human muscle acetylcholine receptor by specific T cells from a myasthenia gravis patientG Harcourt, A P Batocchi, S Hawke, et al.
Multiple Sclerosis Journal - Experimental, Translational and Clinical|January 17, 2022
The use of OCT in good visual acuity MOGAD and AQP4-NMOSD patients; with and without optic neuritisA Roca-Fernández, V Camera, G Loncarevic-Whitaker, et al.
Neuromuscular Disorders : NMD|October 19, 2010
Congenital fibre type disproportion associated with mutations in the tropomyosin 3 (TPM3) gene mimicking congenital myastheniaP Munot, D Lashley, H Jungbluth, et al.
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