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ATP synthase deficiency due to TMEM70 mutation leads to ultrastructural mitochondrial degeneration and is amenable to treatment.
Braczynski AK, Vlaho S, Müller K, Wittig I, Blank AE, Tews DS, Drott U, Kleinle S, Abicht A, Horvath R, Plate KH, Stenzel W, Goebel HH, Schulze A, Harter PN, Kieslich M, Mittelbronn M. Braczynski AK, et al. Among authors: vlaho s. Biomed Res Int. 2015;2015:462592. doi: 10.1155/2015/462592. Epub 2015 Oct 13. Biomed Res Int. 2015. PMID: 26550569 Free PMC article.
T-cell homeostasis in pediatric multiple sclerosis: old cells in young patients.
Balint B, Haas J, Schwarz A, Jarius S, Fürwentsches A, Engelhardt K, Bussmann C, Ebinger F, Fritzsching B, Paul F, Seidel U, Vlaho S, Huppke P, Gärtner J, Wildemann B. Balint B, et al. Among authors: vlaho s. Neurology. 2013 Aug 27;81(9):784-92. doi: 10.1212/WNL.0b013e3182a2ce0e. Epub 2013 Aug 2. Neurology. 2013. PMID: 23911752
Rasmussen encephalitis: incidence and course under randomized therapy with tacrolimus or intravenous immunoglobulins.
Bien CG, Tiemeier H, Sassen R, Kuczaty S, Urbach H, von Lehe M, Becker AJ, Bast T, Herkenrath P, Karenfort M, Kruse B, Kurlemann G, Rona S, Schubert-Bast S, Vieker S, Vlaho S, Wilken B, Elger CE. Bien CG, et al. Among authors: vlaho s. Epilepsia. 2013 Mar;54(3):543-50. doi: 10.1111/epi.12042. Epub 2012 Dec 6. Epilepsia. 2013. PMID: 23216622 Free article. Clinical Trial.
Febrile infection-related epilepsy syndrome without detectable autoantibodies and response to immunotherapy: a case series and discussion of epileptogenesis in FIRES.
van Baalen A, Häusler M, Plecko-Startinig B, Strautmanis J, Vlaho S, Gebhardt B, Rohr A, Abicht A, Kluger G, Stephani U, Probst C, Vincent A, Bien CG. van Baalen A, et al. Among authors: vlaho s. Neuropediatrics. 2012 Aug;43(4):209-16. doi: 10.1055/s-0032-1323848. Epub 2012 Aug 21. Neuropediatrics. 2012. PMID: 22911482
23 results