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Clinical/Scientific Notes
October 29, 2007

FRONTOTEMPORAL LOBAR DEGENERATION WITH UPPER MOTOR NEURON DISEASE/ PRIMARY LATERAL SCLEROSIS

October 30, 2007 issue
69 (18) 1800-1801

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Josephs KA, Parisi JE, Knopman DS, Boeve BF, Petersen RC, Dickson DW. Clinically undetected motor neuron disease in pathologically proven frontotemporal lobar degeneration with motor neuron disease. Arch Neurol 2006;63:506–512.
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Information & Authors

Information

Published In

Neurology®
Volume 69Number 18October 30, 2007
Pages: 1800-1801
PubMed: 17967995

Publication History

Published online: October 29, 2007
Published in print: October 30, 2007

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Authors

Affiliations & Disclosures

Keith A. Josephs, MST, MD
From the Department of Neurology (K.A.J.), Mayo Clinic, Rochester, MN, and Department of Neuroscience (Neuropathology) (D.W.D.), Mayo Clinic, Jacksonville, FL.
Dennis W. Dickson, MD
From the Department of Neurology (K.A.J.), Mayo Clinic, Rochester, MN, and Department of Neuroscience (Neuropathology) (D.W.D.), Mayo Clinic, Jacksonville, FL.

Notes

Address correspondence and reprint requests to Dr Josephs, Divisions of Behavioral Neurology and Movement Disorders, Department of Neurology, Mayo Clinic, Rochester, MN 55905; [email protected].

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Cited By
  1. Motor neuron disease beginning with frontotemporal dementia: clinical features and progression, Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 22, 7-8, (508-516), (2021).https://doi.org/10.1080/21678421.2021.1910309
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  2. Atypical Motor Neuron Disease variants: Still a diagnostic challenge in Neurology, Revue Neurologique, 175, 4, (221-232), (2019).https://doi.org/10.1016/j.neurol.2018.04.016
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  3. Hereditary primary lateral sclerosis and progressive nonfluent aphasia, Journal of Neurology, 266, 5, (1079-1090), (2019).https://doi.org/10.1007/s00415-019-09235-x
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  4. Primary lateral sclerosis and the amyotrophic lateral sclerosis–frontotemporal dementia spectrum, Journal of Neurology, 265, 8, (1819-1828), (2018).https://doi.org/10.1007/s00415-018-8917-5
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  5. A case series of PLS patients with frontotemporal dementia and overview of the literature, Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 18, 7-8, (534-548), (2017).https://doi.org/10.1080/21678421.2017.1354996
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  6. Progressive hemiparesis in a 75-year-old man, Practical Neurology, 15, 1, (63-71), (2014).https://doi.org/10.1136/practneurol-2014-000950
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  7. Significance and limitation of the pathological classification of TDP ‐43 proteinopathy , Neuropathology, 34, 6, (578-588), (2014).https://doi.org/10.1111/neup.12138
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  8. Corticospinal tract degeneration associated with TDP-43 type C pathology and semantic dementia, Brain, 136, 2, (455-470), (2013).https://doi.org/10.1093/brain/aws324
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  9. ALS and Frontotemporal Dysfunction: A Review, Neurology Research International, 2012, (1-9), (2012).https://doi.org/10.1155/2012/806306
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  10. Right temporal variant frontotemporal dementia with motor neuron disease, Journal of Clinical Neuroscience, 19, 1, (85-91), (2012).https://doi.org/10.1016/j.jocn.2011.06.007
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