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Marina Mora

Showing results (31-40 of 122) with videos related to

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International Journal of Molecular Sciences|March 10, 2022
Molecular Fingerprint of BMD Patients Lacking a Portion in the Rod Domain of DystrophinDaniele Capitanio, Manuela Moriggi, Pietro Barbacini, et al.
Muscle & Nerve|April 28, 2009
Fukutin gene mutations in an Italian patient with early onset muscular dystrophy but no central nervous system involvementSimona Saredi, Alessandra Ruggieri, Elisa Mottarelli, et al.
European Journal of Pediatrics|January 19, 2016
SEPN1-related myopathy in three patients: novel mutations and diagnostic cluesAnna Ardissone, Cinzia Bragato, Flavia Blasevich, et al.
Biochimica Et Biophysica Acta|April 21, 2015
Opposing roles of miR-21 and miR-29 in the progression of fibrosis in Duchenne muscular dystrophySimona Zanotti, Sara Gibertini, Maurizio Curcio, et al.
Muscle & Nerve|May 5, 2020
Myopathic changes associated with psychomotor delay and seizures caused by a novel homozygous mutation in TBCKSimona Saredi, Edmund S Cauley, Alessandra Ruggieri, et al.
Human Molecular Genetics|September 27, 2008
Early-onset liver mtDNA depletion and late-onset proteinuric nephropathy in Mpv17 knockout miceCarlo Viscomi, Antonella Spinazzola, Marco Maggioni, et al.
BMC Medical Genetics|September 13, 2013
Novel PTRF mutation in a child with mild myopathy and very mild congenital lipodystrophyAnna Ardissone, Cinzia Bragato, Lorella Caffi, et al.
Frontiers in Pediatrics|May 22, 2023
Management of hypocalcemia following thyroid surgery in childrenAndrea Romera, Lourdes Barragán, Lucía Álvarez-Baena, et al.
Journal of Voice : Official Journal of the Voice Foundation|January 7, 2026
Voice-Based Prediction of Survival in Amyotrophic Lateral Sclerosis (ALS) Patients Using Biomechanical Acoustic MarkersMargarita Pérez-Bonilla, Paola Díaz Borrego, Marina Mora-Ortiz, et al.
Journal of Neuroimmunology|September 27, 2003
Muscle inflammation and MHC class I up-regulation in muscular dystrophy with lack of dysferlin: an immunopathological studyPaolo Confalonieri, Laura Oliva, Francesca Andreetta, et al.
Pageof 13

Showing results (31-40 of 122) with videos related to

Sort By:
Pageof 13
International Journal of Molecular Sciences|March 10, 2022
Molecular Fingerprint of BMD Patients Lacking a Portion in the Rod Domain of DystrophinDaniele Capitanio, Manuela Moriggi, Pietro Barbacini, et al.
Muscle & Nerve|April 28, 2009
Fukutin gene mutations in an Italian patient with early onset muscular dystrophy but no central nervous system involvementSimona Saredi, Alessandra Ruggieri, Elisa Mottarelli, et al.
European Journal of Pediatrics|January 19, 2016
SEPN1-related myopathy in three patients: novel mutations and diagnostic cluesAnna Ardissone, Cinzia Bragato, Flavia Blasevich, et al.
Biochimica Et Biophysica Acta|April 21, 2015
Opposing roles of miR-21 and miR-29 in the progression of fibrosis in Duchenne muscular dystrophySimona Zanotti, Sara Gibertini, Maurizio Curcio, et al.
Muscle & Nerve|May 5, 2020
Myopathic changes associated with psychomotor delay and seizures caused by a novel homozygous mutation in TBCKSimona Saredi, Edmund S Cauley, Alessandra Ruggieri, et al.
Human Molecular Genetics|September 27, 2008
Early-onset liver mtDNA depletion and late-onset proteinuric nephropathy in Mpv17 knockout miceCarlo Viscomi, Antonella Spinazzola, Marco Maggioni, et al.
BMC Medical Genetics|September 13, 2013
Novel PTRF mutation in a child with mild myopathy and very mild congenital lipodystrophyAnna Ardissone, Cinzia Bragato, Lorella Caffi, et al.
Frontiers in Pediatrics|May 22, 2023
Management of hypocalcemia following thyroid surgery in childrenAndrea Romera, Lourdes Barragán, Lucía Álvarez-Baena, et al.
Journal of Voice : Official Journal of the Voice Foundation|January 7, 2026
Voice-Based Prediction of Survival in Amyotrophic Lateral Sclerosis (ALS) Patients Using Biomechanical Acoustic MarkersMargarita Pérez-Bonilla, Paola Díaz Borrego, Marina Mora-Ortiz, et al.
Journal of Neuroimmunology|September 27, 2003
Muscle inflammation and MHC class I up-regulation in muscular dystrophy with lack of dysferlin: an immunopathological studyPaolo Confalonieri, Laura Oliva, Francesca Andreetta, et al.
Pageof 13