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Page 1
Dissecting neural correlates of theory of mind and executive functions in behavioral variant frontotemporal dementia.
Weise CM, Engel A, Polyakova M, Wu Q, Mueller K, Herzig S, Jech R, Diehl-Schmid J, Riedl L, Anderl-Straub S, Kornhuber J, Fassbender K, Wiltfang J, Fliessbach K, Prudlo J, Synofzik M, Danek A, Otto M, Schroeter ML; FTLD Consortium Germany. Weise CM, et al. Among authors: jech r. Alzheimers Res Ther. 2024 Oct 26;16(1):237. doi: 10.1186/s13195-024-01596-4. Alzheimers Res Ther. 2024. PMID: 39462381 Free PMC article.
Clinical Outcome Assessments for Spasticity: Review, Critique, and Recommendations.
Gal O, Baude M, Deltombe T, Esquenazi A, Gracies JM, Hoskovcova M, Rodriguez-Blazquez C, Rosales R, Satkunam L, Wissel J, Mestre T, Sánchez-Ferro Á, Skorvanek M, Tosin MHS, Jech R; members of the MDS Clinical Outcome Assessments Scientific Evaluation Committee and MDS Spasticity Study group. Gal O, et al. Among authors: jech r. Mov Disord. 2024 Dec 4. doi: 10.1002/mds.30062. Online ahead of print. Mov Disord. 2024. PMID: 39629752 Review.
Acute polyneuropathy: a serious complication of levodopa/ /carbidopa intestinal gel treatment for Parkinson's Disease.
Havránková P, Roth J, Čapek V, Klempíř J, Baláž M, Rektorová I, Haň V, Skorvanek M, Gmitterová K, Minár M, Valkovič P, Kaiserová M, Kaňovský P, Grofik M, Kurča E, Necpál J, Jech R. Havránková P, et al. Among authors: jech r. Neurol Neurochir Pol. 2024;58(6):586-592. doi: 10.5603/pjnns.100132. Epub 2024 Nov 20. Neurol Neurochir Pol. 2024. PMID: 39564873 Free article.
Spastic Paresis: A Treatable Movement Disorder.
Gracies JM, Alter KE, Biering-Sørensen B, Dewald JPA, Dressler D, Esquenazi A, Franco JH, Jech R, Kaji R, Jin L, Lim ECH, Raghavan P, Rosales R, Shalash AS, Simpson DM, Suputtitada A, Vecchio M, Wissel J; Spasticity Study Group of the International Parkinson and Movement Disorders Society. Gracies JM, et al. Among authors: jech r. Mov Disord. 2024 Nov 16. doi: 10.1002/mds.30038. Online ahead of print. Mov Disord. 2024. PMID: 39548808 No abstract available.
Loss-of-Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder.
Blackburn PR, Ebstein F, Hsieh TC, Motta M, Radio FC, Herkert JC, Rinne T, Thiffault I, Rapp M, Alders M, Maas S, Gerard B, Smol T, Vincent-Delorme C, Cogné B, Isidor B, Vincent M, Bachmann-Gagescu R, Rauch A, Joset P, Ferrero GB, Ciolfi A, Husson T, Guerrot AM, Bacino C, Macmurdo C, Thompson SS, Rosenfeld JA, Faivre L, Mau-Them FT, Deb W, Vignard V, Agrawal PB, Madden JA, Goldenberg A, Lecoquierre F, Zech M, Prokisch H, Necpál J, Jech R, Winkelmann J, Koprušáková MT, Konstantopoulou V, Younce JR, Shinawi M, Mighton C, Fung C, Morel CF, Lerner-Ellis J, DiTroia S, Barth M, Bonneau D, Krapels I, Stegmann APA, van der Schoot V, Brunet T, Bußmann C, Mignot C, Zampino G, Wortmann SB, Mayr JA, Feichtinger RG, Courtin T, Ravelli C, Keren B, Ziegler A, Hasadsri L, Pichurin PN, Klee EW, Grand K, Sanchez-Lara PA, Krüger E, Bézieau S, Klinkhammer H, Krawitz PM, Eichler EE, Tartaglia M, Küry S, Wang T. Blackburn PR, et al. Among authors: jech r. Ann Neurol. 2024 Sep 20. doi: 10.1002/ana.27077. Online ahead of print. Ann Neurol. 2024. PMID: 39301775
Genetic Risk Factors in Isolated Dystonia Escape Genome-Wide Association Studies.
Laabs BH, Lohmann K, Vollstedt EJ, Reinberger T, Nuxoll LM, Kilic-Berkmen G, Perlmutter JS, Loens S, Cruchaga C, Franke A, Dobricic V, Hinrichs F, Grözinger A, Altenmüller E, Bellows S, Boesch S, Bressman SB, Duque KR, Espay AJ, Ferbert A, Feuerstein JS, Frank S, Gasser T, Haslinger B, Jech R, Kaiser F, Kamm C, Kollewe K, Kühn AA, LeDoux MS, Lohmann E, Mahajan A, Münchau A, Multhaupt-Buell T, Pantelyat A, Pirio Richardson SE, Raymond D, Reich SG, Saunders Pullman R, Schormair B, Sharma N, Sichani AH, Simonyan K, Volkmann J, Wagle Shukla A, Winkelmann J, Wright LJ, Zech M, Zeuner KE, Zittel S, Kasten M, Sun YV, Bäumer T, Brüggemann N, Ozelius LJ, Jinnah HA, Klein C, König IR. Laabs BH, et al. Among authors: jech r. Mov Disord. 2024 Nov;39(11):2110-2116. doi: 10.1002/mds.29968. Epub 2024 Sep 17. Mov Disord. 2024. PMID: 39287592
Dystonia: A novel sign of the Smith-Magenis syndrome - A three-case report.
Kunc L, Havránková P, Škorvánek M, Příhodová I, Poláková K, Nosková L, Tesařová M, Honzík T, Zech M, Jech R. Kunc L, et al. Among authors: jech r. Clin Park Relat Disord. 2024 Aug 6;11:100267. doi: 10.1016/j.prdoa.2024.100267. eCollection 2024. Clin Park Relat Disord. 2024. PMID: 39224875 Free PMC article. No abstract available.
220 results