Zobrazeno 1 - 10 of 47 pro vyhledávání: '"H R, Jones"'
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Topical Review: Childhood Guillain-Barré Syndrome: Clinical Presentation, Diagnosis, and Therapy
Autor: H R Jones
Publikováno v: Journal of Child Neurology. 11:4-12
A rapidly progressive, generally symmetric, ascending flaccid paraparesis or quadriparesis that develops in an infant or child constitutes an uncommon but important pediatric neurologic emergency that requires immediate evaluation and treatment. The
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1c22132cc9db69c1423f908ccfb4a012
https://doi.org/10.1177/088307389601100102
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4
Case 8-1995
Autor: M. A. Edgar, H. R. Jones
Publikováno v: New England Journal of Medicine. 332:730-737
Presentation of Case A 75-year-old man was admitted to the hospital because of cranial-nerve deficits and a footdrop. The patient had been well until the age of 74 years and 3 months, when an erythematous, nonpruritic rash developed on the scalp, acc
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a33ded34841a21edadf6d9c401eeaea5
https://doi.org/10.1056/nejm199503163321108
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5
Reversible Kernohan notch
Autor: B. Tronic, P. Hildenbrand, H. R. Jones, G. R. Cosgrove, Joel M. Oster
Publikováno v: Neurology. 68(5)
A 55-year-old patient experienced episodic headaches, left facial twitching, and increasing falls over 2 years. Multiple yearly brain MRs (figure 1, top panels) revealed a large right frontal arachnoid cyst with evolving …
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b33c65a57d2f0d450f1964daa7bfe49a
https://pubmed.ncbi.nlm.nih.gov/17261684
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6
Clinically disparate stiff-person syndrome with GAD65 autoantibody in a father and daughter
Autor: Vanda A. Lennon, Henry A. Erlich, Ted M. Burns, Teodorica L. Bugawan, Lawrence H. Phillips, H. R. Jones
Publikováno v: Neurology. 61(9)
Stiff-person syndrome (SPS) is a sporadic autoimmune disorder characterized by muscle stiffness with painful spasms and usually a high level of GAD65 antibody. The authors report familial SPS associated with GAD65 antibody. The clinical presentations
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea17e5904143506390158a622675fbd6
https://pubmed.ncbi.nlm.nih.gov/14610143
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9
Familial polyneuropathy with anti-myelin-associated glycoprotein antibodies
Autor: Elijah W. Stommel, D. Yang, V. G. Tseng, Brent T. Harris, H. R. Jones, Jayashri Srinivasan
Publikováno v: Neurology. 64:1983-1984
We describe the occurrence of the anti-myelin-associated glycoprotein (anti-MAG) syndrome, a well-recognized variant of chronic inflammatory demyelinating polyneuropathy (CIDP) with distinct clinical and electrophysiologic characteristics, in two bro
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20ff5cae43d4c2e66a0a2d9779d94b4f
https://doi.org/10.1212/01.wnl.0000163994.27792.18
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10
Stiff person syndrome does not always occur with maternal passive transfer of GAD65 antibodies
Autor: T. M. Burns, L. H. Phillips, H. R. Jones, R. Nemni, L.M. Caniatti, M. Gironi, E. Bazzigaluppi, D. D. Grandis
Publikováno v: Neurology. 64:399-400
The authors report the presence of high titer antibodies to glutamic acid decarboxylase (anti-GAD65) until age 24 months in two asymptomatic newborns of a woman with stiff-person syndrome (SPS). No signs of SPS were detectable in the two children at
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d3ac0879d731728adb41600be1e3710b
https://doi.org/10.1212/wnl.64.2.399-a
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