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Page 1
Association of Cortical Atrophy Patterns With Clinical Phenotypes and Histopathological Findings in Patients With Rasmussen Syndrome.
Bauer T, Held NR, Walger L, Hoppe C, Reiter J, Tietze A, Borger V, Pitsch J, Specht-Riemenschneider L, Kaindl AM, Bernhardt BC, Vatter H, Klotz KA, Helmstaedter C, Becker AJ, Radbruch A, Surges R, Rüber T. Bauer T, et al. Among authors: tietze a. Neurology. 2025 May 27;104(10):e213629. doi: 10.1212/WNL.0000000000213629. Epub 2025 May 2. Neurology. 2025. PMID: 40315396
Epilepsy surgery in early infancy: A retrospective, multicenter study.
Makridis KL, Klotz KA, Ramantani G, Becker LL, San Antonio-Arce V, Syrbe S, Wagner K, Shah MJ, Thomale UW, Tietze A, Elger CE, Borggraefe I, Kaindl AM. Makridis KL, et al. Among authors: tietze a. Epilepsia Open. 2023 Sep;8(3):1182-1189. doi: 10.1002/epi4.12791. Epub 2023 Jul 23. Epilepsia Open. 2023. PMID: 37458529 Free PMC article.
The importance of routine genetic testing in pediatric epilepsy surgery.
Becker LL, Makridis KL, Abad-Perez AT, Thomale UW, Tietze A, Elger CE, Horn D, Kaindl AM. Becker LL, et al. Among authors: tietze a. Epilepsia Open. 2024 Apr;9(2):800-807. doi: 10.1002/epi4.12916. Epub 2024 Feb 17. Epilepsia Open. 2024. PMID: 38366963 Free PMC article.
Detection of Epileptogenic Focal Cortical Dysplasia Using Graph Neural Networks: A MELD Study.
Ripart M, Spitzer H, Williams LZJ, Walger L, Chen A, Napolitano A, Rossi-Espagnet C, Foldes ST, Hu W, Mo J, Likeman M, Rüber T, Caligiuri ME, Gambardella A, Guttler C, Tietze A, Lenge M, Guerrini R, Cohen NT, Wang I, Kloster A, Pinborg LH, Hamandi K, Jackson G, Tortora D, Tisdall M, Conde-Blanco E, Pariente JC, Perez-Enriquez C, Gonzalez-Ortiz S, Mullatti N, Vecchiato K, Liu Y, Kalviainen R, Sokol D, Shetty J, Sinclair B, Vivash L, Willard A, Winston GP, Yasuda C, Cendes F, Shinohara RT, Duncan JS, Cross JH, Baldeweg T, Robinson EC, Iglesias JE, Adler S, Wagstyl K; MELD FCD writing group. Ripart M, et al. Among authors: tietze a. JAMA Neurol. 2025 Feb 24;82(4):397-406. doi: 10.1001/jamaneurol.2024.5406. Online ahead of print. JAMA Neurol. 2025. PMID: 39992650 Free PMC article.
MRI in LARS1 deficiency-Spectrum, patterns, and correlation with acute neurological deterioration.
Hammann N, Lenz D, Bianzano A, Husain RA, Forman E, Bernstein JA, Dattner T, Engelen M, Hanson-Kahn AK, Isidor B, Kotzaeridou U, Tietze A, Trollmann R, Weiß C, Wolffenbuttel BHR, Kölker S, Hoffmann GF, Crushell E, Staufner C, Mohr A, Harting I. Hammann N, et al. Among authors: tietze a. J Inherit Metab Dis. 2024 Sep;47(5):1028-1046. doi: 10.1002/jimd.12764. Epub 2024 Jul 1. J Inherit Metab Dis. 2024. PMID: 38951950
168 results