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Familial Creutzfeldt-Jakob Disease with M232R Mutation Progressed Slowly like Alzheimer's Disease.
2017
SulKi Lee, and Hee Won Bae, and YoungSoon Yang
Department of Neurology, Veterans Health Service Medical Center, Seoul, Korea.
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SulKi Lee, and Hee Won Bae, and YoungSoon Yang
Familial Creutzfeldt-Jakob disease with M232R mutation presented with corticobasal syndrome.
July 2015, Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology,
SulKi Lee, and Hee Won Bae, and YoungSoon Yang
Diffusion-weighted imaging negative M232R familial Creutzfeldt-Jakob disease.
June 2019, Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia,
SulKi Lee, and Hee Won Bae, and YoungSoon Yang
Creutzfeldt-Jakob disease with homozygous M232R mutation: A case report.
May 2015, Journal of the neurological sciences,
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Familial Creutzfeldt-Jakob disease with V180I mutation.
July 2010, Journal of Korean medical science,
SulKi Lee, and Hee Won Bae, and YoungSoon Yang
[Slowly developing Creutzfeldt-Jakob disease].
May 1995, Neurologia (Barcelona, Spain),
SulKi Lee, and Hee Won Bae, and YoungSoon Yang
Creutzfeldt-Jakob disease with an M232R substitution: report of a patient showing slowly progressive disease with abundant plaque-like PrP deposits in the cerebellum.
December 2009, Neuropathology : official journal of the Japanese Society of Neuropathology,
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A case of M232R genetic Creutzfeldt-Jakob disease with Lewy bodies.
February 2020, Journal of the neurological sciences,
SulKi Lee, and Hee Won Bae, and YoungSoon Yang
[A case of Creutzfeldt-Jakob disease with a double mutation (V180I/M232R) in the PRNP gene].
January 2015, Rinsho shinkeigaku = Clinical neurology,
SulKi Lee, and Hee Won Bae, and YoungSoon Yang
Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution.
November 2007, Journal of neurology,
SulKi Lee, and Hee Won Bae, and YoungSoon Yang
Familial Creutzfeldt-Jakob disease (codon 200 mutation) with supranuclear palsy.
November 1992, JAMA,
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