{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,27]],"date-time":"2025-09-27T21:49:51Z","timestamp":1759009791290},"reference-count":7,"publisher":"BMJ","issue":"11","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of Neurology, Neurosurgery & Psychiatry"],"published-print":{"date-parts":[[1988,11,1]]},"DOI":"10.1136\/jnnp.51.11.1462","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T21:16:40Z","timestamp":1226351800000},"page":"1462-1462","source":"Crossref","is-referenced-by-count":11,"title":["Sixth cranial nerve palsy complicating psittacosis."],"prefix":"10.1136","volume":"51","author":[{"given":"A","family":"Zumla","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G","family":"Lipscomb","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D","family":"Lewis","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","reference":[{"key":"ref_1","article-title":"Myotonic Muscular Dystrophy","author":"Harper, P.S.","year":"1979","unstructured":"Harper PS. Myotonic Muscular Dystrophy. Philadelphia: WB Saunders, 1979."},{"key":"ref_2","doi-asserted-by":"crossref","first-page":"669","DOI":"10.1001\/archinte.1964.03860110139016","article-title":"Myotonic muscular dystrophy systemic manifestation","volume":"114","author":"Welsh, J.D.; Haase, G.R.; Bynum, T.E.","year":"1964","unstructured":"Welsh JD, Haase GR, Bynum TE. Myotonic muscular dystrophy systemic manifestation. Arch Int Med 1964;114:669-79.","journal-title":"Arch Int Med"},{"key":"ref_3","first-page":"544","article-title":"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","volume-title":"Disease of the Nose, by the diplopia and was unwilling to use muscles. Sensation was intact. Electromyo-Throat and Ear. Philadelphia: Lea and Febiger","author":"Ballenger, J.J.","year":"1985","unstructured":"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 In: Ballenger JJ, ed. Disease of the Nose, by the diplopia and was unwilling to use muscles. Sensation was intact. Electromyo-Throat and Ear. Philadelphia: Lea and Febiger, 1985:544-5."},{"key":"ref_4","first-page":"1","article-title":"Pharyngolaryngeal manifestation in myasthenia and myotonic dystrophy","volume":"1","author":"Mesolella, C.; Pezzarossa, G.","year":"1968","unstructured":"Mesolella C, Pezzarossa G. Pharyngolaryngeal manifestation in myasthenia and myotonic dystrophy. Arch Ital Laryngol 1968;Supp 1: 1-15.","journal-title":"Arch Ital Laryngol"},{"key":"ref_5","first-page":"48","article-title":"Electromyography in Otolaryngology","volume":"1","author":"Carceni, T.; Zibordi, F.","year":"1966","unstructured":"Carceni T, Zibordi F. Electromyography in Otolaryngology. Arch Ital Otol 1966;Supp 1:48.","journal-title":"Arch Ital Otol"},{"key":"ref_6","article-title":"Laryngeal paralysis of vocal cords in Steinert disease. Les Maladies du Larynx","author":"Piquet, J.; Teprracol, J.","year":"1958","unstructured":"Piquet J, Teprracol J. Laryngeal paralysis of vocal cords in Steinert disease. Les Maladies du Larynx. Paris: Masson, ed. 1958."},{"key":"ref_7","article-title":"XIIth4 cranial nerve palsies have been graphy revealed neurogenic abnormalities in the facial, sternocleidomastoid, tongue, and upper and lower limb muscles. A diagnosis of amyotrophic lateral sclerosis was made. A motor nerve conduction study was carried out on the right median nerve. Recording was made with surface electrodes placed on the belly of the thenar muscle (cathode) and the base of the thumb (anode). Electrical pulses of 0-2 ms in duration were delivered. Only one motor unit potential (MUP) was Accped I July 1988 rtaecpoosrits.edUninliskeevetrheeseen, cetphhearleitwiecrceanseos soifgnpssiot-f evoked in the thenar muscle, in an \"all-ornone\" manner. When the median nerve was encephalitis or raised intracranial pressure stimulated at the elbow, the latency of the in our patient. Rare as it may be, the prog-MUP shortened abruptly by increasing the nosis appears excellent","unstructured":"XIIth4 cranial nerve palsies have been graphy revealed neurogenic abnormalities in the facial, sternocleidomastoid, tongue, and upper and lower limb muscles. A diagnosis of amyotrophic lateral sclerosis was made. A motor nerve conduction study was carried out on the right median nerve. Recording was made with surface electrodes placed on the belly of the thenar muscle (cathode) and the base of the thumb (anode). Electrical pulses of 0-2 ms in duration were delivered. Only one motor unit potential (MUP) was Accped I July 1988 rtaecpoosrits.edUninliskeevetrheeseen,cetphhearleitwiecrceanseos soifgnpssiot-f evoked in the thenar muscle, in an \"all-ornone\" manner. When the median nerve was encephalitis or raised intracranial pressure stimulated at the elbow, the latency of the in our patient. Rare as it may be, the prog-MUP shortened abruptly by increasing the nosis appears excellent."}],"container-title":["Journal of Neurology, Neurosurgery & Psychiatry"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/jnnp.51.11.1462","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,9,26]],"date-time":"2020-09-26T04:20:44Z","timestamp":1601094044000},"score":1,"resource":{"primary":{"URL":"https:\/\/jnnp.bmj.com\/lookup\/doi\/10.1136\/jnnp.51.11.1462"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1988,11,1]]},"references-count":7,"journal-issue":{"issue":"11","published-print":{"date-parts":[[1988,11,1]]}},"URL":"https:\/\/doi.org\/10.1136\/jnnp.51.11.1462","relation":{},"ISSN":["0022-3050"],"issn-type":[{"value":"0022-3050","type":"print"}],"subject":[],"published":{"date-parts":[[1988,11,1]]}}}