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Showing results (41-50 of 83) with videos related to

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Neuromuscular Disorders : NMD|June 17, 2011
Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathyMontse Olivé, Zagaa Odgerel, Amaia Martínez, et al.
Journal of Neurology|March 14, 2022
Muscle MRI characteristic pattern for late-onset TK2 deficiency diagnosisCristina Domínguez-González, Roberto Fernández-Torrón, Ursula Moore, et al.
Journal of Cachexia, Sarcopenia and Muscle|August 15, 2025
High-Density Lipoprotein-Associated Cholesterol Abnormalities in a Clinical Outcomes Study of Dysferlin-Deficient Limb-Girdle Muscular Dystrophy Type R2Zoe White, Laura Rufibach, Heather Gordish Dressman, et al.
Orphanet Journal of Rare Diseases|October 25, 2012
Prognostic value of X-chromosome inactivation in symptomatic female carriers of dystrophinopathyJonàs Juan-Mateu, Maria José Rodríguez, Andrés Nascimento, et al.
Frontiers in Cell and Developmental Biology|May 25, 2023
Loss of the matrix metalloproteinase-10 causes premature features of aging in satellite cellsMiriam Bobadilla Muñoz, Josune Orbe, Gloria Abizanda, et al.
Journal of Neurology|May 26, 2026
Identification of prognostic biomarkers in a large cohort of patients with LGMD R2Carla F Bolano-Diaz, Jose Verdu-Diaz, Dan Hao, et al.
Scientific Reports|June 24, 2020
Growth Differentiation Factor 15 is a potential biomarker of therapeutic response for TK2 deficient myopathyCristina Dominguez-Gonzalez, Carmen Badosa, Marcos Madruga-Garrido, et al.
Acta Neuropathologica|January 4, 2020
POGLUT1 biallelic mutations cause myopathy with reduced satellite cells, α-dystroglycan hypoglycosylation and a distinctive radiological patternE Servián-Morilla, M Cabrera-Serrano, K Johnson, et al.
EMBO Molecular Medicine|November 4, 2016
A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell lossEmilia Servián-Morilla, Hideyuki Takeuchi, Tom V Lee, et al.
Neuromuscular Disorders : NMD|March 27, 2023
Expanding the muscle imaging spectrum in dysferlinopathy: description of an outlier population from the classical MRI patternLaura Llansó, Ursula Moore, Carla Bolano-Diaz, et al.
Pageof 9

Showing results (41-50 of 83) with videos related to

Sort By:
Pageof 9
Neuromuscular Disorders : NMD|June 17, 2011
Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathyMontse Olivé, Zagaa Odgerel, Amaia Martínez, et al.
Journal of Neurology|March 14, 2022
Muscle MRI characteristic pattern for late-onset TK2 deficiency diagnosisCristina Domínguez-González, Roberto Fernández-Torrón, Ursula Moore, et al.
Journal of Cachexia, Sarcopenia and Muscle|August 15, 2025
High-Density Lipoprotein-Associated Cholesterol Abnormalities in a Clinical Outcomes Study of Dysferlin-Deficient Limb-Girdle Muscular Dystrophy Type R2Zoe White, Laura Rufibach, Heather Gordish Dressman, et al.
Orphanet Journal of Rare Diseases|October 25, 2012
Prognostic value of X-chromosome inactivation in symptomatic female carriers of dystrophinopathyJonàs Juan-Mateu, Maria José Rodríguez, Andrés Nascimento, et al.
Frontiers in Cell and Developmental Biology|May 25, 2023
Loss of the matrix metalloproteinase-10 causes premature features of aging in satellite cellsMiriam Bobadilla Muñoz, Josune Orbe, Gloria Abizanda, et al.
Journal of Neurology|May 26, 2026
Identification of prognostic biomarkers in a large cohort of patients with LGMD R2Carla F Bolano-Diaz, Jose Verdu-Diaz, Dan Hao, et al.
Scientific Reports|June 24, 2020
Growth Differentiation Factor 15 is a potential biomarker of therapeutic response for TK2 deficient myopathyCristina Dominguez-Gonzalez, Carmen Badosa, Marcos Madruga-Garrido, et al.
Acta Neuropathologica|January 4, 2020
POGLUT1 biallelic mutations cause myopathy with reduced satellite cells, α-dystroglycan hypoglycosylation and a distinctive radiological patternE Servián-Morilla, M Cabrera-Serrano, K Johnson, et al.
EMBO Molecular Medicine|November 4, 2016
A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell lossEmilia Servián-Morilla, Hideyuki Takeuchi, Tom V Lee, et al.
Neuromuscular Disorders : NMD|March 27, 2023
Expanding the muscle imaging spectrum in dysferlinopathy: description of an outlier population from the classical MRI patternLaura Llansó, Ursula Moore, Carla Bolano-Diaz, et al.
Pageof 9