about
The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study.Coenzyme Q10 and Neurological Diseases."Cardioembolic profile" in patients with ischemic stroke: data from the analysis of 1037 cases.Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease.The genetics of ataxia: through the labyrinth of the Minotaur, looking for Ariadne's thread.Neurology residency training in Europe: an Italian perspective.Lack of association between nuclear factor erythroid-derived 2-like 2 promoter gene polymorphisms and oxidative stress biomarkers in amyotrophic lateral sclerosis patients.Myopathic involvement and mitochondrial pathology in Kennedy disease and in other motor neuron diseases.Epidemiology and cerebrovascular events related to cervical and intracranial arteries dissection: the experience of the city of Pisa.Redefining phenotypes associated with mitochondrial DNA single deletion.Robotic gait training improves motor skills and quality of life in hereditary spastic paraplegia.Carotid ultrasound imaging in a patient with acute ischemic stroke and aortic dissection: a lesson for the management of ischemic stroke?Levetiracetam-responsive myoclonus in spinocerebellar ataxia type 15.Hereditary spastic paraparesis in adults. A clinical and genetic perspective from Tuscany.The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene.Oxidative stress biomarkers in patients with untreated obstructive sleep apnea syndrome.Myocardial damage in a mitochondrial myopathy patient with increased ergoreceptor sensitivity and sympatho-vagal imbalance.Myoclonus in mitochondrial disorders.An "inflammatory" mitochondrial myopathy. A case report.Erratum: Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's diseaseNovelMTCYBmutation in a young patient with recurrent stroke-like episodes and status epilepticusProximal Myopathy due to m.5835G>A Mutation in Mitochondrial MT-TY GeneGenetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processingCPEO and Mitochondrial Myopathy in a Patient with Compound Heterozygous Pathogenetic Variant and mtDNA Multiple DeletionsEncephalomyopathy with multiple mitochondrial DNA deletions and multiple symmetric lipomatosis: further evidence of a possible associationEpidemiology of dystrophinopathies in North-West Tuscany: a molecular genetics-based revisitationCardiac involvement in chronic progressive external ophthalmoplegiaConsensus-based statements for the management of mitochondrial stroke-like episodesMonogenic cerebral small-vessel diseases: diagnosis and therapy. Consensus recommendations of the European Academy of NeurologyAuthor Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processingAwareness of rare and genetic neurological diseases among italian neurologist. A national survey
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P50
description
researcher
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wetenschapper
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հետազոտող
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name
Michelangelo Mancuso
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Michelangelo Mancuso
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Michelangelo Mancuso
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Michelangelo Mancuso
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type
label
Michelangelo Mancuso
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Michelangelo Mancuso
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Michelangelo Mancuso
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Michelangelo Mancuso
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prefLabel
Michelangelo Mancuso
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Michelangelo Mancuso
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Michelangelo Mancuso
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Michelangelo Mancuso
@nl
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P1153
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0000-0003-2738-8562