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Long-term efficiency of intravenously administered immunoglobulin in anti-Yo syndrome with paraneoplastic cerebellar degeneration.
J Neurol. 2011 May;258(5):946-7. doi: 10.1007/s00415-010-5859-y. Epub 2010 Dec 21.
J Neurol. 2011.
PMID: 21174114
No abstract available.
Facioscapulohumeral muscular dystrophy presenting with unusual phenotypes and atypical morphological features of vacuolar myopathy.
Reilich P, Schramm N, Schoser B, Schneiderat P, Strigl-Pill N, Müller-Höcker J, Kress W, Ferbert A, Rudnik-Schöneborn S, Noth J, Lochmüller H, Weis J, Walter MC.
Reilich P, et al. Among authors: strigl pill n.
J Neurol. 2010 Jul;257(7):1108-18. doi: 10.1007/s00415-010-5471-1. Epub 2010 Feb 10.
J Neurol. 2010.
PMID: 20146070
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Prediction of response to IVIg treatment in patients with lower motor neurone disorders.
Strigl-Pill N, König A, Schröder M, Beranek H, Schoser BG, Spaeth M, Pongratz D, Müller-Felber W.
Strigl-Pill N, et al.
Eur J Neurol. 2006 Feb;13(2):135-40. doi: 10.1111/j.1468-1331.2006.01142.x.
Eur J Neurol. 2006.
PMID: 16490043
Clinical Trial.
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Enzyme replacement therapy with alglucosidase alfa in 44 patients with late-onset glycogen storage disease type 2: 12-month results of an observational clinical trial.
Strothotte S, Strigl-Pill N, Grunert B, Kornblum C, Eger K, Wessig C, Deschauer M, Breunig F, Glocker FX, Vielhaber S, Brejova A, Hilz M, Reiners K, Müller-Felber W, Mengel E, Spranger M, Schoser B.
Strothotte S, et al. Among authors: strigl pill n.
J Neurol. 2010 Jan;257(1):91-7. doi: 10.1007/s00415-009-5275-3. Epub 2009 Aug 1.
J Neurol. 2010.
PMID: 19649685
Clinical Trial.
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Toward deconstructing the phenotype of late-onset Pompe disease.
Schüller A, Wenninger S, Strigl-Pill N, Schoser B.
Schüller A, et al. Among authors: strigl pill n.
Am J Med Genet C Semin Med Genet. 2012 Feb 15;160C(1):80-8. doi: 10.1002/ajmg.c.31322. Epub 2012 Jan 17.
Am J Med Genet C Semin Med Genet. 2012.
PMID: 22253010
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36 months observational clinical study of 38 adult Pompe disease patients under alglucosidase alfa enzyme replacement therapy.
Regnery C, Kornblum C, Hanisch F, Vielhaber S, Strigl-Pill N, Grunert B, Müller-Felber W, Glocker FX, Spranger M, Deschauer M, Mengel E, Schoser B.
Regnery C, et al. Among authors: strigl pill n.
J Inherit Metab Dis. 2012 Sep;35(5):837-45. doi: 10.1007/s10545-012-9451-8. Epub 2012 Jan 31.
J Inherit Metab Dis. 2012.
PMID: 22290025
Clinical Trial.
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Ephedrine therapy in eight patients with congenital myasthenic syndrome due to DOK7 mutations.
Schara U, Barisic N, Deschauer M, Lindberg C, Straub V, Strigl-Pill N, Wendt M, Abicht A, Müller JS, Lochmüller H.
Schara U, et al. Among authors: strigl pill n.
Neuromuscul Disord. 2009 Dec;19(12):828-32. doi: 10.1016/j.nmd.2009.09.008. Epub 2009 Oct 17.
Neuromuscul Disord. 2009.
PMID: 19837590
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