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Correction to: Preventive migraine treatment in mitochondrial diseases: a case report of erenumab efficacy and literature review.
- Published in:
- Neurological Sciences, 2023, v. 44, n. 2, p. 789, doi. 10.1007/s10072-022-06462-5
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- Publication type:
- Article
Preventive migraine treatment in mitochondrial diseases: a case report of erenumab efficacy and literature review.
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- Neurological Sciences, 2022, v. 43, n. 12, p. 6955, doi. 10.1007/s10072-022-06391-3
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- Publication type:
- Article
Impact of COVID-19 vaccine on epilepsy in adult subjects: an Italian multicentric experience.
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- Neurological Sciences, 2022, v. 43, n. 8, p. 4627, doi. 10.1007/s10072-022-06100-0
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- Publication type:
- Article
Neurofilament light chain as a disease severity biomarker in ATTRv: data from a single-centre experience.
- Published in:
- 2022
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- Publication type:
- journal article
Expanding the spectrum of congenital myopathies: prenatal onset with extreme hyperextension of the neck.
- Published in:
- Neurological Sciences, 2021, v. 42, n. 4, p. 1549, doi. 10.1007/s10072-020-04937-x
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- Publication type:
- Article
Awareness of rare and genetic neurological diseases among italian neurologist. A national survey.
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- 2020
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- Publication type:
- journal article
Rasmussen encephalitis: an unusual cause for intractable seizures in elderly.
- Published in:
- 2014
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- Publication type:
- Letter
An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene.
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- Neurological Sciences, 2010, v. 31, n. 6, p. 837, doi. 10.1007/s10072-010-0388-0
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- Publication type:
- Article
Acute auditory agnosia as the presenting hearing disorder in MELAS.
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- Neurological Sciences, 2008, v. 29, n. 6, p. 459, doi. 10.1007/s10072-008-1028-9
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- Publication type:
- Article
Hearing Impairment and Neuroimaging Results in Mitochondrial Diseases.
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- Journal of Personalized Medicine, 2023, v. 13, n. 9, p. 1329, doi. 10.3390/jpm13091329
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- Publication type:
- Article
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report.
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- Frontiers in Neurology, 2019, p. N.PAG, doi. 10.3389/fneur.2019.00619
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- Publication type:
- Article
Lipomatosis Incidence and Characteristics in an Italian Cohort of Mitochondrial Patients.
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- Frontiers in Neurology, 2019, p. N.PAG, doi. 10.3389/fneur.2019.00160
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- Publication type:
- Article
A coordinated multiorgan metabolic response contributes to human mitochondrial myopathy.
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- EMBO Molecular Medicine, 2023, v. 15, n. 7, p. 1, doi. 10.15252/emmm.202216951
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- Publication type:
- Article
Genotype-phenotype correlation in Pompe disease, a step forward.
- Published in:
- Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 1, doi. 10.1186/s13023-014-0102-z
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- Publication type:
- Article
Genotype-phenotype correlation in Pompe disease, a step forward.
- Published in:
- 2014
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- Publication type:
- journal article
Vitamin D in Neurological Diseases.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 1, p. 87, doi. 10.3390/ijms24010087
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- Publication type:
- Article
Novel KCND3 Variant Underlying Nonprogressive Congenital Ataxia or SCA19/22 Disrupt K V 4.3 Protein Expression and K+ Currents with Variable Effects on Channel Properties.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 9, p. 4986, doi. 10.3390/ijms22094986
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- Publication type:
- Article
Spinal Cord Involvement in Adult Mitochondrial Diseases: A Cohort Study.
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- Life (2075-1729), 2022, v. 12, n. 1, p. 5, doi. 10.3390/life12010005
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- Publication type:
- Article
Migraine in mitochondrial disorders: Prevalence and characteristics.
- Published in:
- 2018
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- Publication type:
- journal article
Clinical utility of genetic testing in the early diagnosis of Danon disease mimicking hypertrophic cardiomyopathy: a case report.
- Published in:
- 2020
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- Publication type:
- Case Study
Response to Therapy in Myasthenia Gravis with Anti-MuSK Antibodies.
- Published in:
- Annals of the New York Academy of Sciences, 2008, v. 1132, p. 76, doi. 10.1196/annals.1405.012
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- Publication type:
- Article
Nerve Growth Factor Eye Drop Administration Improves Visual Function in a Patient With Optic Glioma.
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- Neurorehabilitation & Neural Repair, 2011, v. 25, n. 4, p. 386, doi. 10.1177/1545968310395601
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- Publication type:
- Article
Sleep Disorders in Mitochondrial Diseases.
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- Current Neurology & Neuroscience Reports, 2021, v. 21, n. 7, p. 1, doi. 10.1007/s11910-021-01121-2
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- Publication type:
- Article
New motor outcome function measures in evaluation of Late-Onset Pompe disease before and after enzyme replacement therapy.
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- Muscle & Nerve, 2012, v. 45, n. 6, p. 831, doi. 10.1002/mus.23340
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- Publication type:
- Article
Functional involvement of cerebral cortex in Duchenne muscular dystrophy.
- Published in:
- 1998
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- Publication type:
- journal article
Maternally inherited cardiomyopathy: a new phenotype associated with the A to G AT nt.3243 of mitochondrial DNA (MELAS mutation).
- Published in:
- 1997
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- Publication type:
- journal article
Instrumental Evaluation of COVID-19 Related Dysautonomia in Non-Critically-Ill Patients: An Observational, Cross-Sectional Study.
- Published in:
- Journal of Clinical Medicine, 2021, v. 10, n. 24, p. 5861, doi. 10.3390/jcm10245861
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- Publication type:
- Article
Emerging multisystem biomarkers in hereditary transthyretin amyloidosis: a pilot study.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-69123-x
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- Publication type:
- Article
Nerve Conduction Studies of Dorsal Sural Nerve: Normative Data and Its Potential Application in ATTRv Pre-Symptomatic Subjects.
- Published in:
- Brain Sciences (2076-3425), 2022, v. 12, n. 8, p. 1037, doi. 10.3390/brainsci12081037
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- Publication type:
- Article
Enzyme Replacement Therapy Improves Respiratory Outcomes in Patients with Late-Onset Type II Glycogenosis and High Ventilator Dependency.
- Published in:
- Lung, 2013, v. 191, n. 5, p. 537, doi. 10.1007/s00408-013-9489-x
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- Publication type:
- Article
Personalized Medicine in Mitochondrial Health and Disease: Molecular Basis of Therapeutic Approaches Based on Nutritional Supplements and Their Analogs.
- Published in:
- Molecules, 2022, v. 27, n. 11, p. 3494, doi. 10.3390/molecules27113494
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- Publication type:
- Article
Macular impairment in mitochondrial diseases: a potential biomarker of disease severity.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-65482-3
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- Publication type:
- Article
Genetic testing offer for inherited neuromuscular diseases within the EURO-NMD reference network: A European survey study.
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- PLoS ONE, 2020, v. 15, n. 9, p. 1, doi. 10.1371/journal.pone.0239329
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- Publication type:
- Article
Clinical, imaging, biochemical and molecular features in Leigh syndrome: a study from the Italian network of mitochondrial diseases.
- Published in:
- 2021
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- Publication type:
- journal article
Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy.
- Published in:
- Brain: A Journal of Neurology, 2009, v. 132, n. 11, p. 3165, doi. 10.1093/brain/awp221
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- Publication type:
- Article
Subacute combined degeneration.
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- Acta Neurologica Belgica, 2014, v. 114, n. 3, p. 221, doi. 10.1007/s13760-013-0231-5
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- Publication type:
- Article
Disorders Associated with Depletion of Mitochondrial DNA.
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- Brain Pathology, 1992, v. 2, n. 2, p. 141, doi. 10.1111/j.1750-3639.1992.tb00682.x
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- Publication type:
- Article
Intestinal pseudo-obstruction in mitochondrial diseases.
- Published in:
- 2017
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- Publication type:
- Letter
Constitutive activation of MAPK cascade in acute quadriplegic myopathy.
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- Annals of Neurology, 2004, v. 55, n. 2, p. 195
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- Publication type:
- Article
Microvascular involvement in migraine: an optical coherence tomography angiography study.
- Published in:
- Journal of Neurology, 2023, v. 270, n. 8, p. 4024, doi. 10.1007/s00415-023-11697-z
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- Publication type:
- Article
Defining the clinical-genetic and neuroradiological features in SPG54: description of eight additional cases and nine novel DDHD2 variants.
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- Journal of Neurology, 2019, v. 266, n. 11, p. 2657, doi. 10.1007/s00415-019-09466-y
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- Publication type:
- Article
Muscle pain in mitochondrial diseases: a picture from the Italian network.
- Published in:
- Journal of Neurology, 2019, v. 266, n. 4, p. 953, doi. 10.1007/s00415-019-09219-x
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- Publication type:
- Article
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort.
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- Journal of Neurology, 2018, v. 265, n. 3, p. 542, doi. 10.1007/s00415-018-8741-y
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- Publication type:
- Article
Erratum to: Redefining phenotypes associated with mitochondrial DNA single deletion.
- Published in:
- 2015
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- Publication type:
- Erratum
Redefining phenotypes associated with mitochondrial DNA single deletion.
- Published in:
- Journal of Neurology, 2015, v. 262, n. 5, p. 1301, doi. 10.1007/s00415-015-7710-y
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- Publication type:
- Article
'Myo-cardiomyopathy' is commonly associated with the A8344G 'MERRF' mutation.
- Published in:
- Journal of Neurology, 2015, v. 262, n. 3, p. 701, doi. 10.1007/s00415-014-7632-0
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- Publication type:
- Article
The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?
- Published in:
- Journal of Neurology, 2014, v. 261, n. 3, p. 504, doi. 10.1007/s00415-013-7225-3
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- Publication type:
- Article
Neurological involvement during legionellosis, look beyond the lung.
- Published in:
- 2012
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- Publication type:
- Letter
Spontaneous recovery from anti-NMDAR encephalitis.
- Published in:
- 2012
- By:
- Publication type:
- Letter
Author response: A severe linezolid‐induced rhabdomyolysis and lactic acidosis in Leigh syndrome.
- Published in:
- Journal of Inherited Metabolic Disease, 2021, v. 44, n. 1, p. 8, doi. 10.1002/jimd.12333
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- Publication type:
- Article