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Journal of Neurology
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November 1, 2017
Assessing the influence of age and gender on the phenotype of myotonic dystrophy type 2
Federica Montagnese, Stefania Mondello, Stephan Wenninger, et al.
Neuromuscular Disorders : NMD
|
September 5, 2020
How to capture activities of daily living in myotonic dystrophy type 2?
Federica Montagnese, Emanuele Rastelli, Kristina Stahl, et al.
Journal of Neurology
|
February 24, 2021
The impact of interrupting enzyme replacement therapy in late-onset Pompe disease
Stephan Wenninger, Kristina Gutschmidt, Corinna Wirner, et al.
Frontiers in Neurology
|
May 7, 2020
Validation of Motor Outcome Measures in Myotonic Dystrophy Type 2
Federica Montagnese, Emanuele Rastelli, Nina Khizanishvili, et al.
Frontiers in Neurology
|
August 28, 2024
Characterization of the neuropathic pain component contributing to myalgia in patients with myotonic dystrophy type 1 and 2
Viviane Schmitt, Petra Baeumler, Anne Schänzer, et al.
Neuromuscular Disorders : NMD
|
July 3, 2023
Prediction of respiratory impairment in myotonic dystrophies using the 'Respiratory involvement symptom checklist' (Respicheck)
Kristina Gutschmidt, Corinna Wirner-Piotrowski, Natalia García Angarita, et al.
Journal of Neuromuscular Diseases
|
October 5, 2018
How to Interpret Abnormal Findings of Spirometry and Manometry in Myotonic Dystrophies?
Haris Babačić, Olga Goldina, Kristina Stahl, et al.
Muscle & Nerve
|
November 23, 2016
Two patients with GMPPB mutation: The overlapping phenotypes of limb-girdle myasthenic syndrome and limb-girdle muscular dystrophy dystroglycanopathy
Federica Montagnese, Elisabeth Klupp, Dimitrios C Karampinos, et al.
Neuromuscular Disorders : NMD
|
September 28, 2015
Clinical and pathophysiological clues of respiratory dysfunction in late-onset Pompe disease: New insights from a comparative study by MRI and respiratory function assessment
Michele Gaeta, Olimpia Musumeci, Stefania Mondello, et al.
Journal of Inherited Metabolic Disease
|
February 3, 2016
Intracranial arterial abnormalities in patients with late onset Pompe disease (LOPD)
Federica Montagnese, Francesca Granata, Olimpia Musumeci, et al.
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Search research articles
Search
Showing results (11-20 of 38) with videos related to
Sort By:
Page
of 4
Journal of Neurology
|
November 1, 2017
Assessing the influence of age and gender on the phenotype of myotonic dystrophy type 2
Federica Montagnese, Stefania Mondello, Stephan Wenninger, et al.
Neuromuscular Disorders : NMD
|
September 5, 2020
How to capture activities of daily living in myotonic dystrophy type 2?
Federica Montagnese, Emanuele Rastelli, Kristina Stahl, et al.
Journal of Neurology
|
February 24, 2021
The impact of interrupting enzyme replacement therapy in late-onset Pompe disease
Stephan Wenninger, Kristina Gutschmidt, Corinna Wirner, et al.
Frontiers in Neurology
|
May 7, 2020
Validation of Motor Outcome Measures in Myotonic Dystrophy Type 2
Federica Montagnese, Emanuele Rastelli, Nina Khizanishvili, et al.
Frontiers in Neurology
|
August 28, 2024
Characterization of the neuropathic pain component contributing to myalgia in patients with myotonic dystrophy type 1 and 2
Viviane Schmitt, Petra Baeumler, Anne Schänzer, et al.
Neuromuscular Disorders : NMD
|
July 3, 2023
Prediction of respiratory impairment in myotonic dystrophies using the 'Respiratory involvement symptom checklist' (Respicheck)
Kristina Gutschmidt, Corinna Wirner-Piotrowski, Natalia García Angarita, et al.
Journal of Neuromuscular Diseases
|
October 5, 2018
How to Interpret Abnormal Findings of Spirometry and Manometry in Myotonic Dystrophies?
Haris Babačić, Olga Goldina, Kristina Stahl, et al.
Muscle & Nerve
|
November 23, 2016
Two patients with GMPPB mutation: The overlapping phenotypes of limb-girdle myasthenic syndrome and limb-girdle muscular dystrophy dystroglycanopathy
Federica Montagnese, Elisabeth Klupp, Dimitrios C Karampinos, et al.
Neuromuscular Disorders : NMD
|
September 28, 2015
Clinical and pathophysiological clues of respiratory dysfunction in late-onset Pompe disease: New insights from a comparative study by MRI and respiratory function assessment
Michele Gaeta, Olimpia Musumeci, Stefania Mondello, et al.
Journal of Inherited Metabolic Disease
|
February 3, 2016
Intracranial arterial abnormalities in patients with late onset Pompe disease (LOPD)
Federica Montagnese, Francesca Granata, Olimpia Musumeci, et al.
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of 4