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Page 1
Subtypes of cognitive impairment in cerebellar disease identified by cross-diagnostic cluster-analysis: results from a German multicenter study.
Liu Q, Rubarth K, Faber J, Sulzer P, Dogan I, Barkhoff M, Minnerop M, Berlijn AM, Elben S, Jacobi H, Aktories JE, Huvermann DM, Erdlenbruch F, Van der Veen R, Müller J, Nio E, Frank B, Köhrmann M, Wondzinski E, Siebler M, Reetz K, Konczak J, Konietschke F, Klockgether T, Synofzik M, Röske S, Timmann D, Thieme A. Liu Q, et al. Among authors: synofzik m. J Neurol. 2024 Dec 21;272(1):83. doi: 10.1007/s00415-024-12831-1. J Neurol. 2024. PMID: 39708269 Free PMC article.
Regional distribution of polymorphisms associated to the disease-causing gene of spinocerebellar ataxia type 3.
Elter TL, Sturm D, Santana MM, Schaprian T, Raposo M, Melo ARV, Lima M, Koyak B, Oender D, Grobe-Einsler M, Lopes S, Silva P, de Almeida LP, Giunti P, Garcia-Moreno H, Nethisinhe S, de Vries J, van de Warrenburg BP, van Gaalen J, Synofzik M, Schöls L, Reetz K, Erdlenbruch F, Jacobi H, Infante J, Riess O, Klockgether T; ESMI study group; Faber J, Hübener-Schmid J. Elter TL, et al. Among authors: synofzik m. J Neurol. 2024 Dec 12;272(1):54. doi: 10.1007/s00415-024-12829-9. J Neurol. 2024. PMID: 39666145 Free PMC article.
Artificial intelligence-based rapid brain volumetry substantially improves differential diagnosis in dementia.
Rudolph J, Rueckel J, Döpfert J, Ling WX, Opalka J, Brem C, Hesse N, Ingenerf M, Koliogiannis V, Solyanik O, Hoppe BF, Zimmermann H, Flatz W, Forbrig R, Patzig M, Rauchmann BS, Perneczky R, Peters O, Priller J, Schneider A, Fliessbach K, Hermann A, Wiltfang J, Jessen F, Düzel E, Buerger K, Teipel S, Laske C, Synofzik M, Spottke A, Ewers M, Dechent P, Haynes JD, Levin J, Liebig T, Ricke J, Ingrisch M, Stoecklein S. Rudolph J, et al. Among authors: synofzik m. Alzheimers Dement (Amst). 2024 Dec 11;16(4):e70037. doi: 10.1002/dad2.70037. eCollection 2024 Oct-Dec. Alzheimers Dement (Amst). 2024. PMID: 39665087 Free PMC article.
Patient-Relevant Digital-Motor Outcomes for Clinical Trials in Hereditary Spastic Paraplegia Type 7: A Multicenter PROSPAX Study.
Beichert L, Seemann J, Kessler C, Traschütz A, Müller D, Dillmann-Jehn K, Ricca I, Satolli S, Basak NA, Coarelli G, Timmann D, Gagnon C, van de Warrenburg BPC; PROSPAX Consortium; Ilg W, Synofzik M, Schüle R. Beichert L, et al. Among authors: synofzik m. Neurology. 2024 Dec 24;103(12):e209887. doi: 10.1212/WNL.0000000000209887. Epub 2024 Dec 2. Neurology. 2024. PMID: 39621946 Free PMC article.
Sensitivity and specificity of a seed amplification assay for diagnosis of multiple system atrophy: a multicentre cohort study.
Ma Y, Farris CM, Weber S, Schade S, Nguyen H, Pérez-Soriano A, Giraldo DM, Fernández M, Soto M, Cámara A, Painous C, Muñoz E, Valldeoriola F, Martí MJ, Clarimon J, Kallunki P, Ma TC, Alcalay RN, Gomes BF, Blennow K, Zetterberg H, Constantinescu J, Mengel D, Kadam V, Parchi P, Brockmann K, Tropea TF, Siderowf A, Synofzik M, Kang UJ, Compta Y, Svenningsson P, Mollenhauer B, Concha-Marambio L. Ma Y, et al. Among authors: synofzik m. Lancet Neurol. 2024 Dec;23(12):1225-1237. doi: 10.1016/S1474-4422(24)00395-8. Lancet Neurol. 2024. PMID: 39577923
Association of Changes in Cerebral and Hypothalamic Structure With Sleep Dysfunction in Patients With Genetic Frontotemporal Dementia.
Best PT, Van Swieten JC, Jiskoot LC, Moreno F, Sánchez-Valle R, Laforce R Jr, Graff C, Masellis M, Tartaglia C, Rowe JB, Borroni B, Finger E, Synofzik M, Galimberti D, Vandenberghe R, de Mendonça A, Butler C, Gerhard A, Le Ber I, Tiraboschi P, Santana I, Pasquier F, Levin J, Otto M, Sorbi S, Seelaar H, Bouzigues A, Cash DM, Russell LL, Bocchetta M, Rohrer JD, Devenyi GA, Chakravarty M, Ducharme S; Genetic Frontotemporal Dementia Initiative (GENFI). Best PT, et al. Among authors: synofzik m. Neurology. 2024 Dec 10;103(11):e209829. doi: 10.1212/WNL.0000000000209829. Epub 2024 Nov 11. Neurology. 2024. PMID: 39527773 Free article.
Association of Initial Side of Brain Atrophy With Clinical Features and Disease Progression in Patients With GRN Frontotemporal Dementia.
Borrego-Ecija S, Juncà-Parella J, Vandebergh M, Pérez Millan A, Balasa M, Llado A, Bouzigues A, Russell LL, Foster PH, Ferry-Bolder E, Van Swieten JC, Jiskoot LC, Seelaar H, Laforce R Jr, Graff C, Galimberti D, Vandenberghe R, de Mendonça A, Tiraboschi P, Santana I, Gerhard A, Levin J, Sorbi S, Otto M, Pasquier F, Ducharme S, Butler C, Le Ber I, Finger E, Tartaglia MC, Masellis M, Rowe JB, Synofzik M, Moreno F, Borroni B, Rademakers R, Rohrer JD, Sánchez-Valle R; Genetic Frontotemporal Initiative (GENFI). Borrego-Ecija S, et al. Among authors: synofzik m. Neurology. 2024 Dec 10;103(11):e209944. doi: 10.1212/WNL.0000000000209944. Epub 2024 Nov 11. Neurology. 2024. PMID: 39527772 Free PMC article.
488 results