Familial Creutzfeldt-Jakob Disease with early onset myoclonus: A case for fulminant progression.
作者信息
Naskar Indira, Sharma Pooja, Goyal Nishant
机构信息
Department of Psychiatry, Central Institute of Psychiatry, Ranchi, Jharkhand, India E-mail:
出版信息
Indian J Psychiatry. 2023 Jul;65(7):795-796. doi: 10.4103/indianjpsychiatry.indianjpsychiatry_261_23. Epub 2023 Jul 12.
Abstract
摘要
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本文引用的文献
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Atypical and early symptoms of sporadic Creutzfeldt - Jakob disease: case series and review of the literature.散发型 Creutzfeldt-Jakob 病的非典型和早期症状：病例系列和文献复习。
Int J Neurosci. 2021 Sep;131(9):927-938. doi: 10.1080/00207454.2020.1759594. Epub 2020 Apr 29.
2
Familial Creutzfeldt-Jakob Disease in an Indian Kindred.一个印度家族中的家族性克雅氏病
Ann Indian Acad Neurol. 2019 Oct-Dec;22(4):458-461. doi: 10.4103/aian.AIAN_214_19. Epub 2019 Oct 25.
3
Familial Creutzfeldt-Jakob Disease: The First Reported Kindred from South-East Asia.家族性克雅氏病：东南亚首例报道的家族病例
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Unusual Clinical Presentations Challenging the Early Clinical Diagnosis of Creutzfeldt-Jakob Disease.不常见的临床特征对克雅氏病早期临床诊断的挑战。
J Alzheimers Dis. 2018;64(4):1051-1065. doi: 10.3233/JAD-180123.
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Characterization of movement disorders in patients with familial Creutzfeldt-Jakob disease carrying the E200K mutation.携带E200K突变的家族性克雅氏病患者运动障碍的特征
Isr Med Assoc J. 2012 Mar;14(3):162-5.
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Symptomatic myoclonus.症状性肌阵挛
Neurophysiol Clin. 2006 Sep-Dec;36(5-6):309-18. doi: 10.1016/j.neucli.2006.12.006. Epub 2007 Jan 17.
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