Wenninger S - Search Results

1

Assessing the influence of age and gender on the phenotype of myotonic dystrophy type 2.

Montagnese F, Mondello S, Wenninger S, Kress W, Schoser B. Montagnese F, et al. Among authors: wenninger s. J Neurol. 2017 Dec;264(12):2472-2480. doi: 10.1007/s00415-017-8653-2. Epub 2017 Oct 30. J Neurol. 2017. PMID: 29086017

2

[Congenital and endogenous endocrine myopathy].

Wenninger S, Schoser B. Wenninger S, et al. Z Rheumatol. 2011 Nov;70(9):760-2, 764-6. doi: 10.1007/s00393-011-0787-5. Z Rheumatol. 2011. PMID: 21904835 German.

3

Toward deconstructing the phenotype of late-onset Pompe disease.

Schüller A, Wenninger S, Strigl-Pill N, Schoser B. Schüller A, et al. Among authors: wenninger s. 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

4

The impact of antibodies in late-onset Pompe disease: a case series and literature review.

Patel TT, Banugaria SG, Case LE, Wenninger S, Schoser B, Kishnani PS. Patel TT, et al. Among authors: wenninger s. Mol Genet Metab. 2012 Jul;106(3):301-9. doi: 10.1016/j.ymgme.2012.04.027. Epub 2012 May 9. Mol Genet Metab. 2012. PMID: 22613277

5

Pregnancy and delivery in women with Pompe disease.

Karabul N, Berndt J, Kornblum C, Kley RA, Wenninger S, Tiling N, Mengel E, Plöckinger U, Vorgerd M, Deschauer M, Schoser B, Hanisch F. Karabul N, et al. Among authors: wenninger s. Mol Genet Metab. 2014 Jun;112(2):148-53. doi: 10.1016/j.ymgme.2014.03.010. Epub 2014 Mar 30. Mol Genet Metab. 2014. PMID: 24726296

6

Urge incontinence and gastrointestinal symptoms in adult patients with pompe disease: a cross-sectional survey.

Karabul N, Skudlarek A, Berndt J, Kornblum C, Kley RA, Wenninger S, Tiling N, Mengel E, Plöckinger U, Vorgerd M, Deschauer M, Schoser B, Hanisch F. Karabul N, et al. Among authors: wenninger s. JIMD Rep. 2014;17:53-61. doi: 10.1007/8904_2014_334. Epub 2014 Aug 26. JIMD Rep. 2014. PMID: 25155777 Free PMC article.

7

Sleep-related symptoms and sleep-disordered breathing in adult Pompe disease.

Boentert M, Karabul N, Wenninger S, Stubbe-Dräger B, Mengel E, Schoser B, Young P. Boentert M, et al. Among authors: wenninger s. Eur J Neurol. 2015 Feb;22(2):369-76, e27. doi: 10.1111/ene.12582. Epub 2014 Nov 4. Eur J Neurol. 2015. PMID: 25367349

8

Cognitive behaviour therapy plus aerobic exercise training to increase activity in patients with myotonic dystrophy type 1 (DM1) compared to usual care (OPTIMISTIC): study protocol for randomised controlled trial.

van Engelen B; OPTIMISTIC Consortium. van Engelen B, et al. Trials. 2015 May 23;16:224. doi: 10.1186/s13063-015-0737-7. Trials. 2015. PMID: 26002596 Free PMC article. Clinical Trial.

9

Homozygosity for the common GAA gene splice site mutation c.-32-13T>G in Pompe disease is associated with the classical adult phenotypical spectrum.

Musumeci O, Thieme A, Claeys KG, Wenninger S, Kley RA, Kuhn M, Lukacs Z, Deschauer M, Gaeta M, Toscano A, Gläser D, Schoser B. Musumeci O, et al. Among authors: wenninger s. Neuromuscul Disord. 2015 Sep;25(9):719-24. doi: 10.1016/j.nmd.2015.07.002. Epub 2015 Jul 10. Neuromuscul Disord. 2015. PMID: 26231297

10

[The Spectrum of Neuromyotonia: Clinics, Therapy and Outcome].

Wenninger S, Schoser B. Wenninger S, et al. Fortschr Neurol Psychiatr. 2015 Aug;83(8):457-62. doi: 10.1055/s-0035-1553512. Epub 2015 Sep 1. Fortschr Neurol Psychiatr. 2015. PMID: 26327478 German.

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