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Journal of Biological Engineering
|
March 6, 2023
Customized biofilm device for antibiofilm and antibacterial screening of newly developed nanostructured silver and zinc coatings
Daniele Ghezzi, Marco Boi, Enrico Sassoni, et al.
Orphanet Journal of Rare Diseases
|
May 16, 2024
A novel MT-ATP6 variant associated with complicated ataxia in two unrelated Italian patients: case report and functional studies
Daniele Sala, Silvia Marchet, Lorenzo Nanetti, et al.
Frontiers in Neurology
|
March 21, 2022
Diagnostic Challenges in Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: Clinical, Morphological, and Genetic Aspects
Antonino Lupica, Rosaria Oteri, Sara Volta, et al.
Journal of Materials Chemistry. B
|
August 28, 2024
A natural multifunction and multiscale hierarchical matrix as a drug-eluting scaffold for biomedical applications
Gabriela Graziani, Carla Triunfo, Giulia Magnabosco, et al.
Journal of Medical Genetics
|
September 30, 2016
COA7 (C1orf163/RESA1) mutations associated with mitochondrial leukoencephalopathy and cytochrome c oxidase deficiency
Anabel Martinez Lyons, Anna Ardissone, Aurelio Reyes, et al.
Metabolic Brain Disease
|
January 24, 2018
Neonatal mitochondrial leukoencephalopathy with brain and spinal involvement and high lactate: expanding the phenotype of ISCA2 gene mutations
Irene Toldo, Margherita Nosadini, Chiara Boscardin, et al.
Frontiers in Genetics
|
March 28, 2015
Mitochondrial dysfunction in Parkinson disease: evidence in mutant PARK2 fibroblasts
Maria C Zanellati, Valentina Monti, Chiara Barzaghi, et al.
Environmental Microbiome
|
April 24, 2024
The microbiota characterizing huge carbonatic moonmilk structures and its correlation with preserved organic matter
Daniele Ghezzi, Nicasio Tomás Jiménez-Morillo, Lisa Foschi, et al.
International Journal of Molecular Sciences
|
August 26, 2023
Evaluation of Mitochondrial Dysfunction and Idebenone Responsiveness in Fibroblasts from Leber's Hereditary Optic Neuropathy (LHON) Subjects
Mirko Baglivo, Alessia Nasca, Eleonora Lamantea, et al.
Acta Neurologica Scandinavica
|
May 19, 2019
Epileptic phenotypes in children with early-onset mitochondrial diseases
Sara Matricardi, Laura Canafoglia, Anna Ardissone, et al.
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of 15
Search research articles
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Showing results (41-50 of 143) with videos related to
Sort By:
Page
of 15
Journal of Biological Engineering
|
March 6, 2023
Customized biofilm device for antibiofilm and antibacterial screening of newly developed nanostructured silver and zinc coatings
Daniele Ghezzi, Marco Boi, Enrico Sassoni, et al.
Orphanet Journal of Rare Diseases
|
May 16, 2024
A novel MT-ATP6 variant associated with complicated ataxia in two unrelated Italian patients: case report and functional studies
Daniele Sala, Silvia Marchet, Lorenzo Nanetti, et al.
Frontiers in Neurology
|
March 21, 2022
Diagnostic Challenges in Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: Clinical, Morphological, and Genetic Aspects
Antonino Lupica, Rosaria Oteri, Sara Volta, et al.
Journal of Materials Chemistry. B
|
August 28, 2024
A natural multifunction and multiscale hierarchical matrix as a drug-eluting scaffold for biomedical applications
Gabriela Graziani, Carla Triunfo, Giulia Magnabosco, et al.
Journal of Medical Genetics
|
September 30, 2016
COA7 (C1orf163/RESA1) mutations associated with mitochondrial leukoencephalopathy and cytochrome c oxidase deficiency
Anabel Martinez Lyons, Anna Ardissone, Aurelio Reyes, et al.
Metabolic Brain Disease
|
January 24, 2018
Neonatal mitochondrial leukoencephalopathy with brain and spinal involvement and high lactate: expanding the phenotype of ISCA2 gene mutations
Irene Toldo, Margherita Nosadini, Chiara Boscardin, et al.
Frontiers in Genetics
|
March 28, 2015
Mitochondrial dysfunction in Parkinson disease: evidence in mutant PARK2 fibroblasts
Maria C Zanellati, Valentina Monti, Chiara Barzaghi, et al.
Environmental Microbiome
|
April 24, 2024
The microbiota characterizing huge carbonatic moonmilk structures and its correlation with preserved organic matter
Daniele Ghezzi, Nicasio Tomás Jiménez-Morillo, Lisa Foschi, et al.
International Journal of Molecular Sciences
|
August 26, 2023
Evaluation of Mitochondrial Dysfunction and Idebenone Responsiveness in Fibroblasts from Leber's Hereditary Optic Neuropathy (LHON) Subjects
Mirko Baglivo, Alessia Nasca, Eleonora Lamantea, et al.
Acta Neurologica Scandinavica
|
May 19, 2019
Epileptic phenotypes in children with early-onset mitochondrial diseases
Sara Matricardi, Laura Canafoglia, Anna Ardissone, et al.
Page
of 15