Michael D Geschwind
Overview
Explore the profile of Michael D Geschwind including associated specialties, affiliations and a list of published articles.
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126
Citations
4395
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Recent Articles
1.
Burt A, LItalien G, Perlman S, Rosenthal L, Kuo S, Ashizawa T, et al.
Mov Disord
. 2025 Mar;
PMID: 40035484
Background: The Patient-Reported Outcome Measure of Ataxia (PROM-Ataxia) has been validated cross-sectionally but not longitudinally. Objective: We aimed to validate PROM-Ataxia as a measure of patient experience of disease over...
2.
Harrison K, Morgan B, Friend J, Garrett S, Looi D, Halim M, et al.
J Am Geriatr Soc
. 2025 Feb;
PMID: 39907502
Background: One in three older adults in the United States dies with or from dementia. Little is known about whether end-of-life caregiving experiences differ by dementia diagnosis. Methods: We conducted...
3.
Morrison M, Yao J, Bhalerao R, Jakary A, Glueck J, Driscoll T, et al.
medRxiv
. 2025 Jan;
PMID: 39867412
Background: There are no disease modifying therapies for Huntington's disease (HD), a rare but fatal genetic neurodegenerative condition. To develop and test new management strategies, a better understanding of the...
4.
Kucukali F, Hill E, Watzeels T, Hummerich H, Campbell T, Darwent L, et al.
Brain
. 2025 Jan;
PMID: 39865733
Prions are assemblies of misfolded prion protein that cause several fatal and transmissible neurodegenerative diseases, with the most common phenotype in humans being sporadic Creutzfeldt-Jakob disease (sCJD). Aside from variation...
5.
Piura Y, Corriveau-Lecavalier N, Abu Dabrh A, Geschwind M, Brigham T, Day G
J Neurol
. 2024 Dec;
272(1):67.
PMID: 39680209
Background And Objectives: The term rapid progressive dementia (RPD) may be applied to patients who develop dementia within 1 year or complete incapacitation within 2 years of the first symptom...
6.
Hummerich H, Speedy H, Campbell T, Darwent L, Hill E, Collins S, et al.
PLoS One
. 2024 Jul;
19(7):e0304528.
PMID: 39079175
Human prion diseases are rare, transmissible and often rapidly progressive dementias. The most common type, sporadic Creutzfeldt-Jakob disease (sCJD), is highly variable in clinical duration and age at onset. Genetic...
7.
Petit E, Schmitz-Hubsch T, Coarelli G, Jacobi H, Heinzmann A, Figueroa K, et al.
J Neurol
. 2024 Jun;
271(7):3743-3753.
PMID: 38822840
Background: The Scale for Assessment and Rating of Ataxia (SARA) is a widely used clinical scale to assess cerebellar ataxia but faces some criticisms about the relevancy of all its...
8.
Bateman J, Josephy-Hernandez S, Apostolova L, Benjamin S, Barrett A, Boeve B, et al.
Cogn Behav Neurol
. 2024 May;
37(2):49-56.
PMID: 38717325
Behavioral neurology & neuropsychiatry (BNNP) is a field that seeks to understand brain-behavior relationships, including fundamental brain organization principles and the many ways that brain structures and connectivity can be...
9.
Gibbons C, Levine T, Adler C, Bellaire B, Wang N, Stohl J, et al.
JAMA
. 2024 Mar;
331(15):1298-1306.
PMID: 38506839
Importance: Finding a reliable diagnostic biomarker for the disorders collectively known as synucleinopathies (Parkinson disease [PD], dementia with Lewy bodies [DLB], multiple system atrophy [MSA], and pure autonomic failure [PAF])...
10.
Karvelas N, Oh B, Wang E, Cobigo Y, Tsuei T, Fitzsimons S, et al.
Brain Commun
. 2024 Mar;
6(2):fcae071.
PMID: 38495305
Enlarged perivascular spaces have been previously reported in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, but their significance and pathophysiology remains unclear. We investigated associations of white matter...