Found: 13
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Mitochondrial Parkinsonism: A Practical Guide to Genes and Clinical Diagnosis.
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- Movement Disorders Clinical Practice, 2024, v. 11, n. 8, p. 948, doi. 10.1002/mdc3.14148
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- Article
SARS-CoV-2-related myelitis: two cases from a major neurological clinic in Central Italy.
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- Neurological Sciences, 2024, v. 45, n. 5, p. 1845, doi. 10.1007/s10072-024-07370-6
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- Article
Red Flags in Primary Mitochondrial Diseases: What Should We Recognize?
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- International Journal of Molecular Sciences, 2023, v. 24, n. 23, p. 16746, doi. 10.3390/ijms242316746
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- Article
Pathophysiology and Management of Fatigue in Neuromuscular Diseases.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 5, p. 5005, doi. 10.3390/ijms24055005
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- Article
A Multisystem Mitochondrial Disease Caused by a Novel MT-TL1 mtDNA Variant: A Case Report.
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- Journal of Neuromuscular Diseases, 2023, v. 10, n. 1, p. 119, doi. 10.3233/JND-221526
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- Article
Iron-sensitive MR imaging of the primary motor cortex to differentiate hereditary spastic paraplegia from other motor neuron diseases.
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- European Radiology, 2022, v. 32, n. 12, p. 8058, doi. 10.1007/s00330-022-08865-6
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- Article
Mitochondrial Epilepsy, a Challenge for Neurologists.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 21, p. 13216, doi. 10.3390/ijms232113216
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- Article
Mitochondrial Ataxias: Molecular Classification and Clinical Heterogeneity.
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- Neurology International, 2022, v. 14, n. 2, p. 337, doi. 10.3390/neurolint14020028
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- Article
A Single mtDNA Deletion in Association with a LMNA Gene New Frameshift Variant: A Case Report.
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- Journal of Neuromuscular Diseases, 2022, v. 9, n. 3, p. 457, doi. 10.3233/JND-220802
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- Article
3D Printing of a Self-Healing Thermoplastic Polyurethane through FDM: From Polymer Slab to Mechanical Assessment.
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- Polymers (20734360), 2021, v. 13, n. 2, p. 305, doi. 10.3390/polym13020305
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- Article
Therapeutical Management and Drug Safety in Mitochondrial Diseases—Update 2020.
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- Journal of Clinical Medicine, 2021, v. 10, n. 1, p. 94, doi. 10.3390/jcm10010094
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- Article
Fibroblast growth factor 21 and grow differentiation factor 15 are sensitive biomarkers of mitochondrial diseases due to mitochondrial transfer-RNA mutations and mitochondrial DNA deletions.
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- Neurological Sciences, 2020, v. 41, n. 12, p. 3653, doi. 10.1007/s10072-020-04422-5
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- Article
NEWS and VIEWS: mitochondrial encephalomyopathies.
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- Acta Myologica, 2016, v. 35, p. 135
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- Article