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Cited by in F6Publishing
For: Lange LM, Gonzalez-Latapi P, Rajalingam R, Tijssen MAJ, Ebrahimi-Fakhari D, Gabbert C, Ganos C, Ghosh R, Kumar KR, Lang AE, Rossi M, van der Veen S, van de Warrenburg B, Warner T, Lohmann K, Klein C, Marras C; on behalf of the Task Force on Genetic Nomenclature in Movement Disorders. Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force - An Update. Mov Disord 2022. [PMID: 35481685 DOI: 10.1002/mds.28982] [Cited by in Crossref: 4] [Cited by in F6Publishing: 7] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
1 Vidailhet M. The multiple twists in the tale: Brain iron accumulation, facial jerks, and truncal dystonia: Expert commentary. Parkinsonism & Related Disorders 2022. [DOI: 10.1016/j.parkreldis.2022.11.015] [Reference Citation Analysis]
2 Nishide M, Marquand KL, Davis M, Halmágyi GM, Fellner A, Narayanan RK, Kennerson ML, Reddel SW, Worgan L, Kumar KR. A family study and literature review of ELOVL4-associated spinocerebellar ataxia type 34.. [DOI: 10.21203/rs.3.rs-2198569/v1] [Reference Citation Analysis]
3 Rafehi H, Read J, Szmulewicz DJ, Davies KC, Snell P, Fearnley LG, Scott L, Thomsen M, Gillies G, Pope K, Bennett MF, Munro JE, Ngo KJ, Chen L, Wallis MJ, Butler EG, Kumar KR, Wu KH, Tomlinson SE, Tisch S, Malhotra A, Lee-archer M, Dolzhenko E, Eberle MA, Roberts LJ, Fogel BL, Brüggemann N, Lohmann K, Delatycki MB, Bahlo M, Lockhart PJ. A novel intronic GAA repeat expansion inFGF14causes autosomal dominant adult-onset ataxia (SCA50, ATX-FGF14).. [DOI: 10.1101/2022.10.21.22281020] [Reference Citation Analysis]
4 Stephen CD. The Dystonias. CONTINUUM: Lifelong Learning in Neurology 2022;28:1435-1475. [DOI: 10.1212/con.0000000000001159] [Reference Citation Analysis]
5 Mo A, Saffari A, Kellner M, Döbler‐neumann M, Jordan C, Srivastava S, Zhang B, Sahin M, Fink JK, Smith L, Posey JE, Alter KE, Toro C, Blackstone C, Soldatos AG, Christie M, Schüle R, Ebrahimi‐fakhari D. Early‐Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST. Movement Disorders. [DOI: 10.1002/mds.29225] [Reference Citation Analysis]
6 Greiten B, Brüggemann N, Spielmann M, Klein C. Gendiagnostik bei neurodegenerativen Erkrankungen. InFo Neurologie 2022;24:46-61. [DOI: 10.1007/s15005-022-2446-6] [Reference Citation Analysis]
7 Shafique A, Arif B, Chu ML, Moran E, Hussain T, Zamora FM, Wohler E, Sobreira N, Klein C, Lohmann K, Naz S. MRM2 variants in families with complex dystonic syndromes: evidence for phenotypic heterogeneity. J Med Genet 2022:jmedgenet-2022-108521. [PMID: 36002240 DOI: 10.1136/jmg-2022-108521] [Reference Citation Analysis]