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11. Clinical features and diagnosis of the MM2 cortical subtype of sporadic Creutzfeldt-Jakob disease. Krasnianski A; Meissner B; Schulz-Schaeffer W; Kallenberg K; Bartl M; Heinemann U; Varges D; Kretzschmar HA; Zerr I Arch Neurol; 2006 Jun; 63(6):876-80. PubMed ID: 16769870 [TBL] [Abstract][Full Text] [Related]
12. The midbrain-to-pons ratio distinguishes progressive supranuclear palsy from non-fluent primary progressive aphasias. Silsby M; Tweedie-Cullen RY; Murray CR; Halliday GM; Hodges JR; Burrell JR Eur J Neurol; 2017 Jul; 24(7):956-965. PubMed ID: 28510312 [TBL] [Abstract][Full Text] [Related]
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15. Pure Prosodic Type of Primary Progressive Apraxia of Speech Mimicking Nonfluent Aphasia and Later Progressing to Corticobasal Syndrome. Kwon M; Shim WH; Jo Y; Park S; Lim JS; Lee JH Alzheimer Dis Assoc Disord; 2022 Oct-Dec 01; 36(4):365-367. PubMed ID: 35288519 [TBL] [Abstract][Full Text] [Related]
16. Creutzfeldt-Jakob disease presenting as isolated aphasia. Mandell AM; Alexander MP; Carpenter S Neurology; 1989 Jan; 39(1):55-8. PubMed ID: 2642613 [TBL] [Abstract][Full Text] [Related]
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19. An autopsy-verified case of FTLD-TDP type A with upper motor neuron-predominant motor neuron disease mimicking MM2-thalamic-type sporadic Creutzfeldt-Jakob disease. Hayashi Y; Iwasaki Y; Takekoshi A; Yoshikura N; Asano T; Mimuro M; Kimura A; Satoh K; Kitamoto T; Yoshida M; Inuzuka T Prion; 2016 Nov; 10(6):492-501. PubMed ID: 27929803 [TBL] [Abstract][Full Text] [Related]
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