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Federica Montagnese

Showing results (21-30 of 38) with videos related to

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Journal of Neurology|February 13, 2015
Clinical and molecular aspects of 30 patients with late-onset Pompe disease (LOPD): unusual features and response to treatmentFederica Montagnese, E Barca, O Musumeci, et al.
Plos One|April 16, 2025
Deep learning-based acceleration of muscle water T2 mapping in patients with neuromuscular diseases by more than 50% - translating quantitative MRI from research to clinical routineJoachim Schmitt, Dominik Weidlich, Kilian Weiss, et al.
Neuromuscular Disorders : NMD|January 8, 2021
Location matters - Genotype-phenotype correlation in LRSAM1 mutations associated with rare Charcot-Marie-Tooth neuropathy CMT2PPeter Reilich, Beate Schlotter, Federica Montagnese, et al.
NMR in Biomedicine|June 11, 2019
Decreased water T<sub>2</sub> in fatty infiltrated skeletal muscles of patients with neuromuscular diseasesSarah Schlaeger, Dominik Weidlich, Elisabeth Klupp, et al.
Journal of Magnetic Resonance Imaging : JMRI|December 26, 2019
Water T<sub>2</sub> Mapping in Fatty Infiltrated Thigh Muscles of Patients With Neuromuscular Diseases Using a T<sub>2</sub> -Prepared 3D Turbo Spin Echo With SPAIRSarah Schlaeger, Dominik Weidlich, Elisabeth Klupp, et al.
NMR in Biomedicine|July 27, 2022
Beyond mean value analysis - a voxel-based analysis of the quantitative MR biomarker water T<sub>2</sub> in the presence of fatty infiltration in skeletal muscle tissue of patients with neuromuscular diseasesSarah Schlaeger, Dominik Weidlich, Agnes Zoffl, et al.
Journal of Neurology|October 1, 2014
Recurrent rhabdomyolysis due to muscle β-enolase deficiency: very rare or underestimated?Olimpia Musumeci, Stefen Brady, Carmelo Rodolico, et al.
Journal of Neurology|February 5, 2021
STIG study: real-world data of long-term outcomes of adults with Pompe disease under enzyme replacement therapy with alglucosidase alfaKristina Gutschmidt, Olimpia Musumeci, Jordi Díaz-Manera, et al.
Diagnostics (Basel, Switzerland)|July 2, 2021
Quantitative Muscle MRI in Patients with Neuromuscular Diseases-Association of Muscle Proton Density Fat Fraction with Semi-Quantitative Grading of Fatty Infiltration and Muscle Strength at the Thigh RegionSarah Schlaeger, Nico Sollmann, Agnes Zoffl, et al.
BMC Neurology|June 16, 2026
Exploring the impact of myotonia on daily functioning in myotonic dystrophy: a patient-reported surveyValeria A Sansone, Utkarsh J Dang, Linda Edmondson, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Journal of Neurology|February 13, 2015
Clinical and molecular aspects of 30 patients with late-onset Pompe disease (LOPD): unusual features and response to treatmentFederica Montagnese, E Barca, O Musumeci, et al.
Plos One|April 16, 2025
Deep learning-based acceleration of muscle water T2 mapping in patients with neuromuscular diseases by more than 50% - translating quantitative MRI from research to clinical routineJoachim Schmitt, Dominik Weidlich, Kilian Weiss, et al.
Neuromuscular Disorders : NMD|January 8, 2021
Location matters - Genotype-phenotype correlation in LRSAM1 mutations associated with rare Charcot-Marie-Tooth neuropathy CMT2PPeter Reilich, Beate Schlotter, Federica Montagnese, et al.
NMR in Biomedicine|June 11, 2019
Decreased water T<sub>2</sub> in fatty infiltrated skeletal muscles of patients with neuromuscular diseasesSarah Schlaeger, Dominik Weidlich, Elisabeth Klupp, et al.
Journal of Magnetic Resonance Imaging : JMRI|December 26, 2019
Water T<sub>2</sub> Mapping in Fatty Infiltrated Thigh Muscles of Patients With Neuromuscular Diseases Using a T<sub>2</sub> -Prepared 3D Turbo Spin Echo With SPAIRSarah Schlaeger, Dominik Weidlich, Elisabeth Klupp, et al.
NMR in Biomedicine|July 27, 2022
Beyond mean value analysis - a voxel-based analysis of the quantitative MR biomarker water T<sub>2</sub> in the presence of fatty infiltration in skeletal muscle tissue of patients with neuromuscular diseasesSarah Schlaeger, Dominik Weidlich, Agnes Zoffl, et al.
Journal of Neurology|October 1, 2014
Recurrent rhabdomyolysis due to muscle β-enolase deficiency: very rare or underestimated?Olimpia Musumeci, Stefen Brady, Carmelo Rodolico, et al.
Journal of Neurology|February 5, 2021
STIG study: real-world data of long-term outcomes of adults with Pompe disease under enzyme replacement therapy with alglucosidase alfaKristina Gutschmidt, Olimpia Musumeci, Jordi Díaz-Manera, et al.
Diagnostics (Basel, Switzerland)|July 2, 2021
Quantitative Muscle MRI in Patients with Neuromuscular Diseases-Association of Muscle Proton Density Fat Fraction with Semi-Quantitative Grading of Fatty Infiltration and Muscle Strength at the Thigh RegionSarah Schlaeger, Nico Sollmann, Agnes Zoffl, et al.
BMC Neurology|June 16, 2026
Exploring the impact of myotonia on daily functioning in myotonic dystrophy: a patient-reported surveyValeria A Sansone, Utkarsh J Dang, Linda Edmondson, et al.
Pageof 4