A case of neuralgic amyotrophy with extension disturbance of fingers after Cushing’s syndrome remission
Author:
Affiliation:
1. Department of Neurology, Niigata Prefectural Shibata Hospital
Publisher
Societas Neurologica Japonica
Subject
Neurology (clinical)
Link
https://www.jstage.jst.go.jp/article/clinicalneurol/62/8/62_cn-001759/_pdf
Reference13 articles.
1. 1) Gstoettner C, Mayer JA, Rassam S, et al. Neuralgic amyotrophy: a paradigm shift in diagnosis and treatment. J Neurol Neurosurg Psychiatry 2020;91:879-888.
2. 2) van Alfen N, van Engelen BG. The clinical spectrum of neuralgic amyotrophy in 246 cases. Brain 2006;129:438-450.
3. 3) van Alfen N, van der Werf SP, van Engelen BG. Long-term pain, fatigue, and impairment in neuralgic amyotrophy. Arch Phys Med Rehabil 2009;90:435-439.
4. 4) van Eijk JJ, van Alfen N, Tio-Gillen AP, et al. Screening for antecedent Campylobacter jejuni infections and anti-ganglioside antibodies in idiopathic neuralgic amyotrophy. J Peripher Nerv Syst 2011;16:153-156.
5. 5) van Eijk JJ, van Alfen N, Berrevoets M, et al. Evaluation of prednisolone treatment in the acute phase of neuralgic amyotrophy: an observational study. J Neurol Neurosurg Psychiatry 2009;80:1120-1124.
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