Lista de obras - Michelangelo Mancuso - Dominio Público Uruguay

"Cardioembolic profile" in patients with ischemic stroke: data from the analysis of 1037 cases.

artículo científico publicado en 2015

An "inflammatory" mitochondrial myopathy. A case report

artículo científico publicado en 2013

Anticoagulation After Stroke in Patients With Atrial Fibrillation

artículo científico publicado en 2019

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Autonomic, functional, skeletal muscle, and cardiac abnormalities are associated with increased ergoreflex sensitivity in mitochondrial disease

artículo científico publicado en 2017

Awareness of rare and genetic neurological diseases among italian neurologist. A national survey

artículo científico publicado en 2020

CPEO and Mitochondrial Myopathy in a Patient with Compound Heterozygous Pathogenetic Variant and mtDNA Multiple Deletions

scientific article published on 06 March 2019

Cardiac involvement in chronic progressive external ophthalmoplegia

artículo científico publicado en 2014

Carotid ultrasound imaging in a patient with acute ischemic stroke and aortic dissection: a lesson for the management of ischemic stroke?

artículo científico publicado en 2013

Catatonia as prominent feature of stroke-like episode in MELAS

artículo científico publicado en 2020

Coenzyme Q10 and Neurological Diseases

artículo científico publicado en 2009

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

artículo científico publicado en 2011

Consensus-based statements for the management of mitochondrial stroke-like episodes

artículo científico publicado en 2019

Current and emerging treatment options in the management of Friedreich ataxia

artículo científico publicado en 2010

Early Recurrence and Major Bleeding in Patients With Acute Ischemic Stroke and Atrial Fibrillation Treated With Non-Vitamin-K Oral Anticoagulants (RAF-NOACs) Study.

artículo científico publicado en 2017

Early recurrence in paroxysmal versus sustained atrial fibrillation in patients with acute ischaemic stroke.

artículo científico publicado en 2018

Encephalomyopathy with multiple mitochondrial DNA deletions and multiple symmetric lipomatosis: further evidence of a possible association

scientific article published on 01 December 1999

Epidemiology and cerebrovascular events related to cervical and intracranial arteries dissection: the experience of the city of Pisa.

artículo científico publicado en 2017

Epidemiology of dystrophinopathies in North-West Tuscany: a molecular genetics-based revisitation

artículo científico publicado en 1999

Erratum: Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

article

Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations.

artículo científico publicado en 2011

Functional and radiological outcomes after bridging therapy versus direct thrombectomy in stroke patients with unknown onset

artículo científico publicado en 2020

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

artículo científico publicado en 2014

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

artículo científico publicado en 2019

Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

artículo científico publicado en 2009

Hemorrhagic Transformation in Patients With Acute Ischemic Stroke and Atrial Fibrillation: Time to Initiation of Oral Anticoagulant Therapy and Outcomes.

artículo científico publicado en 2018

Hereditary spastic paraparesis in adults. A clinical and genetic perspective from Tuscany

artículo científico publicado en 2014

Implication of a Genetic Variant at PICALM in Alzheimer's Disease Patients and Centenarians

artículo científico publicado en 2011

Lack of association between nuclear factor erythroid-derived 2-like 2 promoter gene polymorphisms and oxidative stress biomarkers in amyotrophic lateral sclerosis patients

artículo científico publicado en 2014

Levetiracetam-responsive myoclonus in spinocerebellar ataxia type 15.

artículo científico publicado en 2013

Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene

artículo científico publicado en 2003

Monogenic cerebral small-vessel diseases: diagnosis and therapy. Consensus recommendations of the European Academy of Neurology

scientific article published on 20 March 2020

Myocardial damage in a mitochondrial myopathy patient with increased ergoreceptor sensitivity and sympatho-vagal imbalance.

artículo científico publicado en 2014

Myoclonus in mitochondrial disorders

artículo científico publicado en 2014

Myopathic involvement and mitochondrial pathology in Kennedy disease and in other motor neuron diseases.

artículo científico

Neurohormonal modulation for treatment of cardiac involvement in dystrophinopathies and mitochondrial disease

artículo científico publicado en 2017

Neurology residency training in Europe: an Italian perspective.

artículo científico publicado en 2005

No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort

artículo científico publicado en 2009

NovelMTCYBmutation in a young patient with recurrent stroke-like episodes and status epilepticus

artículo científico publicado en 2014

Oxidative stress biomarkers in Fabry disease: is there a room for them?

artículo científico publicado en 2020

Oxidative stress biomarkers in patients with untreated obstructive sleep apnea syndrome

artículo científico publicado en 2012

Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society

artículo científico publicado en 2017

Prediction of Early Recurrent Thromboembolic Event and Major Bleeding in Patients With Acute Stroke and Atrial Fibrillation by a Risk Stratification Schema: The ALESSA Score Study.

artículo científico publicado en 2017

Primary mitochondrial myopathy: Clinical features and outcome measures in 118 cases from Italy

scientific article published on 20 October 2020

Proximal Myopathy due to m.5835G>A Mutation in Mitochondrial MT-TY Gene

article

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

artículo científico publicado en 2017

Redefining phenotypes associated with mitochondrial DNA single deletion

artículo científico publicado en 2015

Response to Newman et al.

artículo científico publicado en 2017

Robotic gait training improves motor skills and quality of life in hereditary spastic paraplegia.

artículo científico publicado en 2015

Safety of Anticoagulation in Patients Treated With Urgent Reperfusion for Ischemic Stroke Related to Atrial Fibrillation

scientific article published on 10 July 2020

The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study

artículo científico publicado en 2010

The genetics of ataxia: through the labyrinth of the Minotaur, looking for Ariadne's thread

artículo científico publicado en 2014

The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?

artículo científico publicado en 2013

Therapeutical Management and Drug Safety in Mitochondrial Diseases-Update 2020

artículo científico publicado en 2020

Timing of initiation of oral anticoagulants in patients with acute ischemic stroke and atrial fibrillation comparing posterior and anterior circulation strokes

artículo científico publicado en 2020

Lista de obras de Michelangelo Mancuso

"Cardioembolic profile" in patients with ischemic stroke: data from the analysis of 1037 cases.

An "inflammatory" mitochondrial myopathy. A case report

Anticoagulation After Stroke in Patients With Atrial Fibrillation

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Autonomic, functional, skeletal muscle, and cardiac abnormalities are associated with increased ergoreflex sensitivity in mitochondrial disease

Awareness of rare and genetic neurological diseases among italian neurologist. A national survey

CPEO and Mitochondrial Myopathy in a Patient with Compound Heterozygous Pathogenetic Variant and mtDNA Multiple Deletions

Cardiac involvement in chronic progressive external ophthalmoplegia

Carotid ultrasound imaging in a patient with acute ischemic stroke and aortic dissection: a lesson for the management of ischemic stroke?

Catatonia as prominent feature of stroke-like episode in MELAS

Coenzyme Q10 and Neurological Diseases

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

Consensus-based statements for the management of mitochondrial stroke-like episodes

Current and emerging treatment options in the management of Friedreich ataxia

Early Recurrence and Major Bleeding in Patients With Acute Ischemic Stroke and Atrial Fibrillation Treated With Non-Vitamin-K Oral Anticoagulants (RAF-NOACs) Study.

Early recurrence in paroxysmal versus sustained atrial fibrillation in patients with acute ischaemic stroke.

Encephalomyopathy with multiple mitochondrial DNA deletions and multiple symmetric lipomatosis: further evidence of a possible association

Epidemiology and cerebrovascular events related to cervical and intracranial arteries dissection: the experience of the city of Pisa.

Epidemiology of dystrophinopathies in North-West Tuscany: a molecular genetics-based revisitation

Erratum: Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations.

Functional and radiological outcomes after bridging therapy versus direct thrombectomy in stroke patients with unknown onset

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

Hemorrhagic Transformation in Patients With Acute Ischemic Stroke and Atrial Fibrillation: Time to Initiation of Oral Anticoagulant Therapy and Outcomes.

Hereditary spastic paraparesis in adults. A clinical and genetic perspective from Tuscany

Implication of a Genetic Variant at PICALM in Alzheimer's Disease Patients and Centenarians

Lack of association between nuclear factor erythroid-derived 2-like 2 promoter gene polymorphisms and oxidative stress biomarkers in amyotrophic lateral sclerosis patients

Levetiracetam-responsive myoclonus in spinocerebellar ataxia type 15.

Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene

Monogenic cerebral small-vessel diseases: diagnosis and therapy. Consensus recommendations of the European Academy of Neurology

Myocardial damage in a mitochondrial myopathy patient with increased ergoreceptor sensitivity and sympatho-vagal imbalance.

Myoclonus in mitochondrial disorders

Myopathic involvement and mitochondrial pathology in Kennedy disease and in other motor neuron diseases.

Neurohormonal modulation for treatment of cardiac involvement in dystrophinopathies and mitochondrial disease

Neurology residency training in Europe: an Italian perspective.

No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort

NovelMTCYBmutation in a young patient with recurrent stroke-like episodes and status epilepticus

Oxidative stress biomarkers in Fabry disease: is there a room for them?

Oxidative stress biomarkers in patients with untreated obstructive sleep apnea syndrome

Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society

Prediction of Early Recurrent Thromboembolic Event and Major Bleeding in Patients With Acute Stroke and Atrial Fibrillation by a Risk Stratification Schema: The ALESSA Score Study.

Primary mitochondrial myopathy: Clinical features and outcome measures in 118 cases from Italy

Proximal Myopathy due to m.5835G>A Mutation in Mitochondrial MT-TY Gene

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

Redefining phenotypes associated with mitochondrial DNA single deletion

Response to Newman et al.

Robotic gait training improves motor skills and quality of life in hereditary spastic paraplegia.

Safety of Anticoagulation in Patients Treated With Urgent Reperfusion for Ischemic Stroke Related to Atrial Fibrillation

The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study

The genetics of ataxia: through the labyrinth of the Minotaur, looking for Ariadne's thread

The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?

Therapeutical Management and Drug Safety in Mitochondrial Diseases-Update 2020

Timing of initiation of oral anticoagulants in patients with acute ischemic stroke and atrial fibrillation comparing posterior and anterior circulation strokes