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Page 1
Somatic mosaicism and variable penetrance in doublecortin-associated migration disorders.
Aigner L, Uyanik G, Couillard-Despres S, Ploetz S, Wolff G, Morris-Rosendahl D, Martin P, Eckel U, Spranger S, Otte J, Woerle H, Holthausen H, Apheshiotis N, Fluegel D, Winkler J. Aigner L, et al. Among authors: winkler j. Neurology. 2003 Jan 28;60(2):329-32. doi: 10.1212/01.wnl.0000042091.90361.d2. Neurology. 2003. PMID: 12552055
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: winkler j. 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: winkler j. Neurology. 2007 Jul 31;69(5):442-7. doi: 10.1212/01.wnl.0000266629.98503.d0. Neurology. 2007. PMID: 17664403
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: winkler j. Neurology. 2003 Jul 22;61(2):232-5. doi: 10.1212/01.wnl.0000079371.19562.ba. Neurology. 2003. PMID: 12874405
1,564 results