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1

Expanding the Clinical Spectrum of IgLON5-Syndrome

Wenninger, Stephan

Journal:

Journal of Neuromuscular Diseases

Year:

2017

Language:

english

File:

PDF, 321 KB

english, 2017

2

Cognitive behavioural therapy with optional graded exercise therapy in patients with severe fatigue with myotonic dystrophy type 1: a multicentre, single-blind, randomised trial

Okkersen, Kees, Jimenez-Moreno, Cecilia, Wenninger, Stephan, Daidj, Ferroudja, Glennon, Jeffrey, Cumming, Sarah, Littleford, Roberta, Monckton, Darren G, Lochmüller, Hanns, Catt, Michael, Faber, Catha

Journal:

The Lancet Neurology

Year:

2018

Language:

english

File:

PDF, 185 KB

english, 2018

3

Toward deconstructing the phenotype of late-onset Pompe disease

Angela Schüller, Stephan Wenninger, Nicola Strigl-Pill, Benedikt Schoser

Journal:

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

Year:

2012

Language:

english

File:

PDF, 246 KB

english, 2012

4

Functional neuroanatomy of CCK-4-induced panic attacks in healthy volunteers

Daniela Eser, Gregor Leicht, Jürgen Lutz, Stephan Wenninger, Valerie Kirsch, Cornelius Schüle, Susanne Karch, Thomas Baghai, Oliver Pogarell, Christine Born, Rainer Rupprecht, Christoph Mulert

Journal:

Human Brain Mapping

Year:

2009

Language:

english

File:

PDF, 384 KB

english, 2009

5

Impact of state and trait anxiety on the panic response to CCK-4

Daniela Eser, Stephan Wenninger, Thomas Baghai, Cornelius Schüle, Rainer Rupprecht

Journal:

Journal of Neural Transmission

Year:

2008

Language:

english

File:

PDF, 178 KB

english, 2008

6

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

Trusha T. Patel, Suhrad G. Banugaria, Laura E. Case, Stephan Wenninger, Benedikt Schoser, Priya S. Kishnani

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 822 KB

english, 2012

7

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, Olimpia, Thieme, Andrea, Claeys, Kristl G., Wenninger, Stephan, Kley, Rudolf A., Kuhn, Marius, Lukacs, Zoltan, Deschauer, Marcus, Gaeta, Michele, Toscano, Antonio, Gläser, Dieter, Schoser, B

Journal:

Neuromuscular Disorders

Year:

2015

Language:

english

File:

PDF, 563 KB

english, 2015

8

Utility of a next-generation sequencing-based gene panel investigation in German patients with genetically unclassified limb-girdle muscular dystrophy

Kuhn, Marius, Gläser, Dieter, Joshi, Pushpa Raj, Zierz, Stephan, Wenninger, Stephan, Schoser, Benedikt, Deschauer, Marcus

Journal:

Journal of Neurology

Year:

2016

Language:

english

File:

PDF, 470 KB

english, 2016

9

Prospective exploratory muscle biopsy, imaging, and functional assessment in patients with late-onset Pompe disease treated with alglucosidase alfa: The EMBASSY Study

van der Ploeg, Ans, Carlier, Pierre G., Carlier, Robert-Yves, Kissel, John T., Schoser, Benedikt, Wenninger, Stephan, Pestronk, Alan, Barohn, Richard J., Dimachkie, Mazen M., Goker-Alpan, Ozlem, Mozaf

Journal:

Molecular Genetics and Metabolism

Year:

2016

Language:

english

File:

PDF, 970 KB

english, 2016

10

Multimodales Monitoring und Therapie der Myotonen Dystrophien

Schüller, Angela, Wenninger, Stephan, Montagnese, Federica, Schoser, Benedikt

Journal:

DNP - Der Neurologe und Psychiater

Year:

2016

Language:

german

File:

PDF, 480 KB

german, 2016

11

Long-term whole-body vibration training in two late-onset Pompe disease patients

Montagnese, Federica, Thiele, Simone, Wenninger, Stephan, Schoser, Benedikt

Journal:

Neurological Sciences

Year:

2016

Language:

english

File:

PDF, 592 KB

english, 2016

12

Respiratory involvement in neuromuscular disorders

Boentert, Matthias, Wenninger, Stephan, Sansone, Valeria A.

Journal:

Current Opinion in Neurology

Year:

2017

Language:

english

File:

PDF, 283 KB

english, 2017

13

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

Montagnese, Federica, Mondello, Stefania, Wenninger, Stephan, Kress, Wolfram, Schoser, Benedikt

Journal:

Journal of Neurology

Year:

2017

Language:

english

File:

PDF, 986 KB

english, 2017

14

Falls and resulting fractures in myotonic dystrophy: results from a multinational retrospective survey.

Jimenez-Moreno, Aura Cecilia, Raaphorst, Joost, Babačić, Haris, Wood, Libby, van Engelen, Baziel, Lochmüller, Hanns, Schoser, Benedikt, Wenninger, Stephan

Journal:

Neuromuscular Disorders

Year:

2017

Language:

english

File:

PDF, 1.26 MB

english, 2017

15

Ventilationsstörungen erkennen und richtig handeln

Wenninger, Stephan, Schoser, Benedikt

Journal:

DNP - Der Neurologe und Psychiater

Year:

2018

Language:

german

File:

PDF, 643 KB

german, 2018

16

Practical Recommendations for Diagnosis and Management of Respiratory Muscle Weakness in Late-Onset Pompe Disease

Boentert, Matthias, Prigent, Hélène, Várdi, Katalin, Jones, Harrison, Mellies, Uwe, Simonds, Anita, Wenninger, Stephan, Barrot Cortés, Emilia, Confalonieri, Marco

Journal:

International Journal of Molecular Sciences

Year:

2016

Language:

english

File:

PDF, 1006 KB

english, 2016

17

Core Clinical Phenotypes in Myotonic Dystrophies

Wenninger, Stephan, Montagnese, Federica, Schoser, Benedikt

Journal:

Frontiers in Neurology

Year:

2018

Language:

english

File:

PDF, 648 KB

english, 2018

18

First impressions of two new brilliant biomarkers for Pompe disease in plasma and urine in comparison to Hex4 and Glc4 in urine

Mascher, Hermann, Schoser, Benedikt, Wenninger, Stephan

Journal:

Molecular Genetics and Metabolism

Year:

2018

Language:

english

File:

PDF, 50 KB

english, 2018

19

First impressions of two new brilliant biomarkers for Pompe disease (LSD) in plasma and urine in comparison to Hex4 and Glc4 in urine

Mascher, Hermann, Schoser, Benedikt, Wenninger, Stephan

Journal:

Year:

2018

Language:

english

File:

PDF, 52 KB

english, 2018

20

Myasthenia gravis: aktuelle Antikörperdiagnostik und Aspekte zum therapierefraktären Verlauf

Wenninger, Stephan, Schoser, Benedikt

Journal:

Fortschritte der Neurologie · Psychiatrie

Year:

2018

File:

PDF, 495 KB

2018

21

Das Anti-IgLON5-Syndrom – Was ist unser aktueller Wissensstand?

Wenninger, Stephan, Schoser, Benedikt

Journal:

Fortschritte der Neurologie · Psychiatrie

Year:

2018

File:

PDF, 312 KB

2018

22

Evidence of mild founder LMOD3 mutations causing nemaline myopathy 10 in Germany and Austria

Schatz, Ulrich A., Weiss, Simone, Wenninger, Stephan, Schoser, Benedikt, Muss, Wolfgang H., Bittner, Reginald E., Schmidt, Wolfgang M., Schossig, Anna S., Rudnik-Schöneborn, Sabine, Baumann, Matthias

Journal:

Year:

2018

Language:

english

File:

PDF, 587 KB

english, 2018

23

How to Interpret Abnormal Findings of Spirometry and Manometry in Myotonic Dystrophies?

Haris, Babačić, Olga, Goldina, Kristina, Stahl, Federica, Montagnese, Vindi, Jurinović, Benedikt, Schoser, Stephan, Wenninger

Journal:

Journal of Neuromuscular Diseases

Year:

2018

Language:

english

File:

PDF, 326 KB

english, 2018

24

Safety and efficacy of short- and long-term inspiratory muscle training in late-onset Pompe disease (LOPD): a pilot study

Wenninger, Stephan, Greckl, Eva, Babačić, Haris, Stahl, Kristina, Schoser, Benedikt

Journal:

Journal of Neurology

Year:

2018

Language:

english

File:

PDF, 2.11 MB

english, 2018

25

Cannabis use in myotonic dystrophy patients in Germany and USA: a pilot survey

Montagnese, Federica, White, Molly, Klein, Anke, Stahl, Kristina, Wenninger, Stephan, Schoser, Benedikt

Journal:

Journal of Neurology

Year:

2018

Language:

english

File:

PDF, 1.02 MB

english, 2018

26

Safety and Treatment Effects of Nusinersen in Longstanding Adult 5q-SMA Type 3 – A Prospective Observational Study

Walter, Maggie C., Wenninger, Stephan, Thiele, Simone, Stauber, Julia, Hiebeler, Miriam, Greckl, Eva, Stahl, Kristina, Pechmann, Astrid, Lochmüller, Hanns, Kirschner, Janbernd, Schoser, Benedikt

Journal:

Journal of Neuromuscular Diseases

Year:

2019

Language:

english

File:

PDF, 315 KB

english, 2019

27

Safety and Treatment Effects of Nusinersen in Longstanding Adult 5q-SMA Type 3 – A Prospective Observational Study

Walter, Maggie C., Wenninger, Stephan, Thiele, Simone, Stauber, Julia, Hiebeler, Miriam, Greckl, Eva, Stahl, Kristina, Pechmann, Astrid, Lochmüller, Hanns, Kirschner, Janbernd, Schoser, Benedikt

Journal:

Journal of Neuromuscular Diseases

Year:

2019

File:

PDF, 315 KB

2019

28

Utility of maximum inspiratory and expiratory pressures as a screening method for respiratory insufficiency in slowly progressive neuromuscular disorders

Wenninger, Stephan, Stahl, Kristina, Wirner, Corinna, Einvag, Krisztina, Thiele, Simone, Walter, Maggie C., Schoser, Benedikt

Journal:

Neuromuscular Disorders

Year:

2020

File:

PDF, 1.23 MB

2020

29

Genetic determinants of disease severity in the myotonic dystrophy type 1 OPTIMISTIC cohort

Cumming, Sarah A., Jimenez-Moreno, Cecilia, Okkersen, Kees, Wenninger, Stephan, Daidj, Ferroudja, Hogarth, Fiona, Littleford, Roberta, Gorman, GrÃ¡inne, Bassez, Guillaume, Schoser, Benedikt, LochmÃ¼ll

Journal:

Year:

2019

File:

PDF, 1.12 MB

2019

30

Utility and Results from a Patient-Reported Online Survey in Myotonic Dystrophies Types 1 and 2

Wenninger, Stephan, Stahl, Kristina, Montagnese, Federica, Schoser, Benedikt

Journal:

European Neurology

Year:

2020

File:

PDF, 286 KB

2020