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The Journal of Physiology
|
May 5, 2025
Pathogenic TNNT1 variants are associated with aberrant thin filament compliance and myofibre hyper-contractility
Jenni Laitila, Christopher T A Lewis, Anthony L Hessel, et al.
European Journal of Neurology
|
September 19, 2023
Serum neurofilament light chain: a promising early diagnostic biomarker for hereditary transthyretin amyloidosis?
Angela Romano, Guido Primiano, Giovanni Antonini, et al.
Neurology. Genetics
|
May 25, 2026
Compound Heterozygous <i>COA7</i> Variants Presenting With Childhood-Onset Axonal Neuropathy in 2 Siblings
Gianpaolo Cicala, Elisa Rolleri, Beatrice Berti, et al.
EMBO Molecular Medicine
|
May 24, 2023
A coordinated multiorgan metabolic response contributes to human mitochondrial myopathy
Nneka Southwell, Guido Primiano, Viraj Nadkarni, et al.
Cell Metabolism
|
April 17, 2018
Rewiring of Glutamine Metabolism Is a Bioenergetic Adaptation of Human Cells with Mitochondrial DNA Mutations
Qiuying Chen, Kathryne Kirk, Yevgeniya I Shurubor, et al.
Orphanet Journal of Rare Diseases
|
October 10, 2021
Clinical, imaging, biochemical and molecular features in Leigh syndrome: a study from the Italian network of mitochondrial diseases
Anna Ardissone, Claudio Bruno, Daria Diodato, et al.
Frontiers in Neurology
|
March 16, 2019
Lipomatosis Incidence and Characteristics in an Italian Cohort of Mitochondrial Patients
Olimpia Musumeci, Emanuele Barca, Costanza Lamperti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
May 3, 2024
Serum neurofilament light chain levels correlate with small fiber related parameters in patients with hereditary transthyretin amyloidosis with polyneuropathy (ATTRv-PN)
Eleonora Galosi, Rocco Costanzo, Francesca Forcina, et al.
Molecules (Basel, Switzerland)
|
June 10, 2022
Personalized Medicine in Mitochondrial Health and Disease: Molecular Basis of Therapeutic Approaches Based on Nutritional Supplements and Their Analogs
Vincenzo Tragni, Guido Primiano, Albina Tummolo, et al.
Nature
|
December 5, 2024
Macrophages excite muscle spindles with glutamate to bolster locomotion
Yuyang Yan, Nuria Antolin, Luming Zhou, et al.
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of 9
Search research articles
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Showing results (51-60 of 84) with videos related to
Sort By:
Page
of 9
The Journal of Physiology
|
May 5, 2025
Pathogenic TNNT1 variants are associated with aberrant thin filament compliance and myofibre hyper-contractility
Jenni Laitila, Christopher T A Lewis, Anthony L Hessel, et al.
European Journal of Neurology
|
September 19, 2023
Serum neurofilament light chain: a promising early diagnostic biomarker for hereditary transthyretin amyloidosis?
Angela Romano, Guido Primiano, Giovanni Antonini, et al.
Neurology. Genetics
|
May 25, 2026
Compound Heterozygous <i>COA7</i> Variants Presenting With Childhood-Onset Axonal Neuropathy in 2 Siblings
Gianpaolo Cicala, Elisa Rolleri, Beatrice Berti, et al.
EMBO Molecular Medicine
|
May 24, 2023
A coordinated multiorgan metabolic response contributes to human mitochondrial myopathy
Nneka Southwell, Guido Primiano, Viraj Nadkarni, et al.
Cell Metabolism
|
April 17, 2018
Rewiring of Glutamine Metabolism Is a Bioenergetic Adaptation of Human Cells with Mitochondrial DNA Mutations
Qiuying Chen, Kathryne Kirk, Yevgeniya I Shurubor, et al.
Orphanet Journal of Rare Diseases
|
October 10, 2021
Clinical, imaging, biochemical and molecular features in Leigh syndrome: a study from the Italian network of mitochondrial diseases
Anna Ardissone, Claudio Bruno, Daria Diodato, et al.
Frontiers in Neurology
|
March 16, 2019
Lipomatosis Incidence and Characteristics in an Italian Cohort of Mitochondrial Patients
Olimpia Musumeci, Emanuele Barca, Costanza Lamperti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
May 3, 2024
Serum neurofilament light chain levels correlate with small fiber related parameters in patients with hereditary transthyretin amyloidosis with polyneuropathy (ATTRv-PN)
Eleonora Galosi, Rocco Costanzo, Francesca Forcina, et al.
Molecules (Basel, Switzerland)
|
June 10, 2022
Personalized Medicine in Mitochondrial Health and Disease: Molecular Basis of Therapeutic Approaches Based on Nutritional Supplements and Their Analogs
Vincenzo Tragni, Guido Primiano, Albina Tummolo, et al.
Nature
|
December 5, 2024
Macrophages excite muscle spindles with glutamate to bolster locomotion
Yuyang Yan, Nuria Antolin, Luming Zhou, et al.
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of 9