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Genetics of synucleins in neurodegenerative diseases

Acta neuropathologica, 2021-04, Vol.141 (4), p.471-490

2021

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SnapShot: Genetics of Parkinson’s Disease

Cell, 2015-01, Vol.160 (3), p.570-570.e1

2015

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SnapShot: Genetics of ALS and FTD

Cell, 2015-02, Vol.160 (4), p.798-798.e1

2015

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SnapShot: Genetics of Alzheimer’s Disease

Cell, 2013-11, Vol.155 (4), p.968-968.e1

2013

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Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement

JAMA neurology, 2013-01, Vol.70 (1), p.78

2013

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Intelligent Process Automation and Business Continuity: Areas for Future Research

Information (Basel), 2023-02, Vol.14 (2), p.122

2023

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A novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like family

Neurobiology of aging, 2013-12, Vol.34 (12), p.2890.e1-2890.e5

2013

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Co-creative epiphany of citizenship and health in the 1820 Liberal Revolution in Portugal

Paedagogica historica, 2023-09, Vol.59 (5), p.723-742

2023

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An AARS variant as the likely cause of Swedish type hereditary diffuse leukoencephalopathy with spheroids

Acta neuropathologica communications, 2019-11, Vol.7 (1), p.188-188, Article 188

2019

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Reconsidering the role of blood-brain barrier in Alzheimer's disease: From delivery to target

Frontiers in aging neuroscience, 2023-02, Vol.15, p.1102809-1102809

2023

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Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associations

Human molecular genetics, 2014-09, Vol.23 (R1), p.R47-R53

2014

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Alzheimer’s Disease Genetics: Review of Novel Loci Associated with Disease

Current genetic medicine reports, 2020-03, Vol.8 (1), p.1-16

2020

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A nonsense mutation in PRNP associated with clinical Alzheimer's disease

Neurobiology of aging, 2014-11, Vol.35 (11), p.2656.e13-2656.e16

2014

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Network analysis and wine routes: the case of the Bairrada Wine Route

The Service industries journal, 2010-08, Vol.30 (10), p.1621-1641

2010

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Molecular Characterization of Portuguese Patients with Hereditary Cerebellar Ataxia

Cells (Basel, Switzerland), 2022-03, Vol.11 (6), p.981

2022

Volltextzugriff (PDF)

Vasculitic peripheral neuropathy in deficiency of adenosine deaminase 2

Neuromuscular disorders : NMD, 2021-09, Vol.31 (9), p.891-895

2021

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The association of circulating amylin with β‐amyloid in familial Alzheimer's disease

Alzheimer's & dementia : translational research & clinical interventions, 2021, Vol.7 (1), p.e12130-n/a

2021

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Whole-exome sequencing reveals PSEN1 and ATP7B combined variants as a possible cause of early-onset Lewy body dementia: a case study of genotype–phenotype correlation

Neurogenetics, 2022-10, Vol.23 (4), p.279-283

2022

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Physiological and morphological responses of Arabica coffee cultivars to soil compaction

Revista Brasileira de Ciência do Solo, 2023-01, Vol.47

2023

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Adenosine Deaminase Two and Immunoglobulin M Accurately Differentiate Adult Sneddon’s Syndrome of Unknown Cause

Cerebrovascular diseases (Basel, Switzerland), 2019-02, Vol.46 (5-6), p.257-264

2019

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Novel MAG Variant Causes Cerebellar Ataxia with Oculomotor Apraxia: Molecular Basis and Expanded Clinical Phenotype

Journal of clinical medicine, 2020-04, Vol.9 (4), p.1212

2020

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Advances in auditing and business continuity: A study in financial companies

Journal of open innovation, 2024-06, Vol.10 (2), p.100304, Article 100304

2024

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The Jesuits in Portugal: the communion of science and religion

Historia social y de la educación, 2018-02, Vol.7 (1), p.1-25

2018

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Peripheral Inflammatory Cytokines as Biomarkers in Alzheimer’s Disease and Mild Cognitive Impairment

Neuro-degenerative diseases, 2007-01, Vol.4 (6), p.406-412

2007

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Energy Performance of a Service Building: Comparison Between EnergyPlus and Revit

Computational Science and Its Applications – ICCSA 2020, p.201-213

Volltextzugriff (PDF)

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Genetics of synucleins in neurodegenerative diseases

SnapShot: Genetics of Parkinson’s Disease

SnapShot: Genetics of ALS and FTD

SnapShot: Genetics of Alzheimer’s Disease

Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement

Intelligent Process Automation and Business Continuity: Areas for Future Research

A novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like family

Co-creative epiphany of citizenship and health in the 1820 Liberal Revolution in Portugal

An AARS variant as the likely cause of Swedish type hereditary diffuse leukoencephalopathy with spheroids

Reconsidering the role of blood-brain barrier in Alzheimer's disease: From delivery to target

Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associations

Alzheimer’s Disease Genetics: Review of Novel Loci Associated with Disease

A nonsense mutation in PRNP associated with clinical Alzheimer's disease

Network analysis and wine routes: the case of the Bairrada Wine Route

Molecular Characterization of Portuguese Patients with Hereditary Cerebellar Ataxia

Vasculitic peripheral neuropathy in deficiency of adenosine deaminase 2

The association of circulating amylin with β‐amyloid in familial Alzheimer's disease

Whole-exome sequencing reveals PSEN1 and ATP7B combined variants as a possible cause of early-onset Lewy body dementia: a case study of genotype–phenotype correlation

Physiological and morphological responses of Arabica coffee cultivars to soil compaction

Adenosine Deaminase Two and Immunoglobulin M Accurately Differentiate Adult Sneddon’s Syndrome of Unknown Cause

Novel MAG Variant Causes Cerebellar Ataxia with Oculomotor Apraxia: Molecular Basis and Expanded Clinical Phenotype

Advances in auditing and business continuity: A study in financial companies

The Jesuits in Portugal: the communion of science and religion

Peripheral Inflammatory Cytokines as Biomarkers in Alzheimer’s Disease and Mild Cognitive Impairment

Energy Performance of a Service Building: Comparison Between EnergyPlus and Revit

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