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ARX mutations in X-linked lissencephaly with abnormal genitalia.
Uyanik G, Aigner L, Martin P, Gross C, Neumann D, Marschner-Schäfer H, Hehr U, Winkler J. Uyanik G, et al. Among authors: aigner l. Neurology. 2003 Jul 22;61(2):232-5. doi: 10.1212/01.wnl.0000079371.19562.ba. Neurology. 2003. PMID: 12874405
Transient expression of doublecortin during adult neurogenesis.
Brown JP, Couillard-Després S, Cooper-Kuhn CM, Winkler J, Aigner L, Kuhn HG. Brown JP, et al. Among authors: aigner l. J Comp Neurol. 2003 Dec 1;467(1):1-10. doi: 10.1002/cne.10874. J Comp Neurol. 2003. PMID: 14574675
Functional imaging in PNH caused by a new FilaminA mutation.
Lange M, Winner B, Müller JL, Marienhagen J, Schröder M, Aigner L, Uyanik G, Winkler J. Lange M, et al. Among authors: aigner l. Neurology. 2004 Jan 13;62(1):151-2. doi: 10.1212/01.wnl.0000103170.00899.8d. Neurology. 2004. PMID: 14718723 No abstract available.
Location and type of mutation in the LIS1 gene do not predict phenotypic severity.
Uyanik G, Morris-Rosendahl DJ, Stiegler J, Klapecki J, Gross C, Berman Y, Martin P, Dey L, Spranger S, Korenke GC, Schreyer I, Hertzberg C, Neumann TE, Burkart P, Spaich C, Meng M, Holthausen H, Adès L, Seidel J, Mangold E, Buyse G, Meinecke P, Schara U, Zeschnigk C, Muller D, Helland G, Schulze B, Wright ML, Kortge-Jung S, Hehr A, Bogdahn U, Schuierer G, Kohlhase J, Aigner L, Wolff G, Hehr U, Winkler J. Uyanik G, et al. Among authors: aigner l. Neurology. 2007 Jul 31;69(5):442-7. doi: 10.1212/01.wnl.0000266629.98503.d0. Neurology. 2007. PMID: 17664403
Neuronal precursor-specific activity of a human doublecortin regulatory sequence.
Karl C, Couillard-Despres S, Prang P, Munding M, Kilb W, Brigadski T, Plötz S, Mages W, Luhmann H, Winkler J, Bogdahn U, Aigner L. Karl C, et al. Among authors: aigner l. J Neurochem. 2005 Jan;92(2):264-82. doi: 10.1111/j.1471-4159.2004.02879.x. J Neurochem. 2005. PMID: 15663475 Free article.
211 results