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Motor neuron disease beginning with frontotemporal dementia: clinical features and progression.

Amyotrophic lateral sclerosis & frontotemporal degeneration - 1 Nov 2021

Gromicho Marta, Kuzma-Kozakiewicz Magdalena, Szacka Katarzyna, Nieporecki Krzysztof, Andersen Peter M, Grosskreutz Julian, Petri Susanne, Pinto Susana, Uysal Hilmi, Swash Michael, De Carvalho Mamede

Abstract excerpt

Objective: To study disease characteristics, progression and outcome in a group of motor neuron disease (MND) patients beginning with frontotemporal dementia (FTD) by comparing them with patients with the typical motor-onset. Methods: 849 patients recruited from tertiary centers were studied according to FTD-onset and motor-onset. We studied clinical data, functional decline and survival. Results: Twenty six...

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PMID: 34229542
DOI: 10.1080/21678421.2021.1910309

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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