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Year Number of Results
1963 1
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1995 2
1996 1
1997 1
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2002 1
2005 1
2006 3
2008 1
2010 1
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2017 1
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26 results

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Page 1
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy.
Muona M, Berkovic SF, Dibbens LM, Oliver KL, Maljevic S, Bayly MA, Joensuu T, Canafoglia L, Franceschetti S, Michelucci R, Markkinen S, Heron SE, Hildebrand MS, Andermann E, Andermann F, Gambardella A, Tinuper P, Licchetta L, Scheffer IE, Criscuolo C, Filla A, Ferlazzo E, Ahmad J, Ahmad A, Baykan B, Said E, Topcu M, Riguzzi P, King MD, Ozkara C, Andrade DM, Engelsen BA, Crespel A, Lindenau M, Lohmann E, Saletti V, Massano J, Privitera M, Espay AJ, Kauffmann B, Duchowny M, Møller RS, Straussberg R, Afawi Z, Ben-Zeev B, Samocha KE, Daly MJ, Petrou S, Lerche H, Palotie A, Lehesjoki AE. Muona M, et al. Among authors: lindenau m. Nat Genet. 2015 Jan;47(1):39-46. doi: 10.1038/ng.3144. Epub 2014 Nov 17. Nat Genet. 2015. PMID: 25401298 Free PMC article.
The neuroimaging and clinical spectrum of neurofibromatosis 2.
Mautner VF, Lindenau M, Baser ME, Hazim W, Tatagiba M, Haase W, Samii M, Wais R, Pulst SM. Mautner VF, et al. Among authors: lindenau m. Neurosurgery. 1996 May;38(5):880-5; discussion 885-6. doi: 10.1097/00006123-199605000-00004. Neurosurgery. 1996. PMID: 8727812
Skin abnormalities in neurofibromatosis 2.
Mautner VF, Lindenau M, Baser ME, Kluwe L, Gottschalk J. Mautner VF, et al. Among authors: lindenau m. Arch Dermatol. 1997 Dec;133(12):1539-43. Arch Dermatol. 1997. PMID: 9420538
Unusual variability of PRRT2 linked phenotypes within a family.
Brueckner F, Kohl B, Puest B, Gassner S, Osseforth J, Lindenau M, Stodieck S, Biskup S, Lohmann E. Brueckner F, et al. Among authors: lindenau m. Eur J Paediatr Neurol. 2014 Jul;18(4):540-2. doi: 10.1016/j.ejpn.2014.03.012. Epub 2014 Apr 8. Eur J Paediatr Neurol. 2014. PMID: 24755245
26 results