Myotonic dystrophy with unilateral bulbar involvement.

Author:

Giladi N,Bazak I,Harel D

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference7 articles.

1. Myotonic Muscular Dystrophy;Harper, P.S.,1979

2. Myotonic muscular dystrophy systemic manifestation;Welsh, J.D.; Haase, G.R.; Bynum, T.E.;Arch Int Med,1964

3. Sir: In 1984 Roth and Egloff-Baer described the motor axon loop, a new kind of response of the motor unit to stimulation of the peripheral motor nerve.' We would like to report a case in which a motor axon loop may have caused an error in the motor nerve conduction velocity measurement. A 72 year old man developed weakness and atrophy in his right hand muscles in January, 1985. The weakness and atrophy slowly progressed, and in September, 1986, when he visited our outpatient clinic, he had severe weakness and atrophy in his right upper extremity muscles and moderate weakness and atrophy in his left hand;Ballenger, J.J.,1985

4. Pharyngolaryngeal manifestation in myasthenia and myotonic dystrophy;Mesolella, C.; Pezzarossa, G.;Arch Ital Laryngol,1968

5. Electromyography in Otolaryngology;Carceni, T.; Zibordi, F.;Arch Ital Otol,1966

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