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Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation.
Hartig MB, Iuso A, Haack T, Kmiec T, Jurkiewicz E, Heim K, Roeber S, Tarabin V, Dusi S, Krajewska-Walasek M, Jozwiak S, Hempel M, Winkelmann J, Elstner M, Oexle K, Klopstock T, Mueller-Felber W, Gasser T, Trenkwalder C, Tiranti V, Kretzschmar H, Schmitz G, Strom TM, Meitinger T, Prokisch H. Hartig MB, et al. Among authors: trenkwalder c. Am J Hum Genet. 2011 Oct 7;89(4):543-50. doi: 10.1016/j.ajhg.2011.09.007. Am J Hum Genet. 2011. PMID: 21981780 Free PMC article.
[Restless leg syndrome].
Winkelmann J, Collado-Seidel V, Trenkwalder C. Winkelmann J, et al. Among authors: trenkwalder c. Med Monatsschr Pharm. 1999 Mar;22(3):67-71. Med Monatsschr Pharm. 1999. PMID: 10097580 Review. German. No abstract available.
Magnetic resonance imaging findings in corticobasal degeneration.
Winkelmann J, Auer DP, Lechner C, Elbel G, Trenkwalder C. Winkelmann J, et al. Among authors: trenkwalder c. Mov Disord. 1999 Jul;14(4):669-73. doi: 10.1002/1531-8257(199907)14:4<669::aid-mds1018>3.0.co;2-y. Mov Disord. 1999. PMID: 10435506
489 results