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COVID19-associated new-onset movement disorders: a follow-up study.
Schneider SA, Desai S, Phokaewvarangkul O, Rosca EC, Sringean J, Anand P, Bravo GÁ, Cardoso F, Cervantes-Arslanian AM, Chovatiya H, Crosiers D, Dijkstra F, Fearon C, Grandas F, Guedj E, Méndez-Guerrero A, Hassan M, Jankovic J, Lang AE, Makhoul K, Muccioli L, O'Shea SA, Ostovan VR, Perez-Sanchez JR, Ramdhani R, Ros-Castelló V, Schulte C, Shah P, Wojtecki L, Pal PK. Schneider SA, et al. Among authors: lang ae. J Neurol. 2023 May;270(5):2409-2415. doi: 10.1007/s00415-023-11661-x. Epub 2023 Mar 21. J Neurol. 2023. PMID: 36943516 Free PMC article.
Investigating differences in young- and late-onset progressive supranuclear palsy.
AlWazan BA, Garcia-Cordero I, Couto B, Monteiro ML, Tsang MY, Antwi J, Sasitharan J, Bhakta P, Kovacs GG, Fox S, Tang-Wai DF, Lang AE, Tartaglia MC. AlWazan BA, et al. Among authors: lang ae. J Neurol. 2023 Dec;270(12):6103-6112. doi: 10.1007/s00415-023-11976-9. Epub 2023 Sep 5. J Neurol. 2023. PMID: 37670149
Coprophenomena in Tourette syndrome.
Freeman RD, Zinner SH, Müller-Vahl KR, Fast DK, Burd LJ, Kano Y, Rothenberger A, Roessner V, Kerbeshian J, Stern JS, Jankovic J, Loughin T, Janik P, Shady G, Robertson MM, Lang AE, Budman C, Magor A, Bruun R, Berlin CM Jr. Freeman RD, et al. Among authors: lang ae. Dev Med Child Neurol. 2009 Mar;51(3):218-27. doi: 10.1111/j.1469-8749.2008.03135.x. Epub 2008 Dec 4. Dev Med Child Neurol. 2009. PMID: 19183216 Free article.
Distinct involvement of the cranial and spinal nerves in progressive supranuclear palsy.
Tanaka H, Martinez-Valbuena I, Forrest SL, Couto B, Reyes NG, Morales-Rivero A, Lee S, Li J, Karakani AM, Tang-Wai DF, Tator C, Khadadadi M, Sadia N, Tartaglia MC, Lang AE, Kovacs GG. Tanaka H, et al. Among authors: lang ae. Brain. 2024 Apr 4;147(4):1399-1411. doi: 10.1093/brain/awad381. Brain. 2024. PMID: 37972275 Free PMC article.
Genetic Diversity and Expanded Phenotypes in Dystonia: Insights From Large-Scale Exome Sequencing.
Thomsen M, Ott F, Loens S, Kilic-Berkmen G, Tan AH, Lim SY, Lohmann E, Schröder KM, Ipsen L, Nothacker LA, Welzel L, Rudnik AS, Hinrichs F, Odorfer T, Zeuner KE, Schumann F, Kühn AA, Zittel S, Moeller M, Pfister R, Kamm C, Lang AE, Tay YW, de Almeida Marcelino AL, Vidailhet M, Roze E, Perlmutter JS, Feuerstein JS, Fung VSC, Chang F, Barbano RL, Bellows S, Wagle Shukla AA, Espay AJ, LeDoux MS, Berman BD, Reich S, Deik A, Franke A, Wittig M, Franzenburg S, Volkmann J, Brüggemann N, Jinnah HA, Bäumer T, Klein C, Busch H, Lohmann K. Thomsen M, et al. Among authors: lang ae. Ann Clin Transl Neurol. 2025 Jun 18. doi: 10.1002/acn3.70100. Online ahead of print. Ann Clin Transl Neurol. 2025. PMID: 40533913 Free article.
Mitochondrial DNA heteroplasmy distinguishes disease manifestation in PINK1/PRKN-linked Parkinson's disease.
Trinh J, Hicks AA, König IR, Delcambre S, Lüth T, Schaake S, Wasner K, Ghelfi J, Borsche M, Vilariño-Güell C, Hentati F, Germer EL, Bauer P, Takanashi M, Kostić V, Lang AE, Brüggemann N, Pramstaller PP, Pichler I, Rajput A, Hattori N, Farrer MJ, Lohmann K, Weissensteiner H, May P, Klein C, Grünewald A. Trinh J, et al. Among authors: lang ae. Brain. 2023 Jul 3;146(7):2753-2765. doi: 10.1093/brain/awac464. Brain. 2023. PMID: 36478228 Free PMC article.
1,204 results