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Lysosomal alterations in peripheral blood mononuclear cells of Parkinson's disease patients

Movement disorders, 2015-11, Vol.30 (13), p.1830-1834

2015

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a-Synuclein and lipids in erythrocytes of Gaucher disease carriers and patients before and after enzyme replacement therapy

PloS one, 2023-02, Vol.18 (2), p.e0277602-e0277602

2023

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Evidence of an association between the scavenger receptor class B member 2 gene and Parkinson's disease

Movement disorders, 2012-03, Vol.27 (3), p.400-405

2012

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Gaucher disease: Biochemical and molecular findings in 141 patients diagnosed in Greece

Molecular genetics and metabolism reports, 2020-09, Vol.24, p.100614-100614, Article 100614

2020

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Increased dimerization of alpha-synuclein in erythrocytes in Gaucher disease and aging

Neuroscience letters, 2012-10, Vol.528 (2), p.205-209

2012

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A novel mutation deep within intron 7 of the GBA gene causes Gaucher disease

Molecular genetics & genomic medicine, 2020-03, Vol.8 (3), p.e1090-n/a

2020

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Parasitic Oscillations in Coaxial Gyrotron Beam Tunnels

IEEE transactions on electron devices, 2013-04, Vol.60 (4), p.1469-1475

2013

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Smart Health Caring Home: A Systematic Review of Smart Home Care for Elders and Chronic Disease Patients

GeNeDis 2016, 2017-01, Vol.989, p.255-264

2017

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Alpha-synuclein dimerization in erythrocytes of patients with genetic and non-genetic forms of Parkinson’s Disease

Neuroscience letters, 2018-04, Vol.672, p.145-149

2018

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Circulating Brain‐enriched MicroRNAs for detection and discrimination of idiopathic and genetic Parkinson's disease

Movement disorders, 2020-03, Vol.35 (3), p.457-467

2020

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α-Synuclein dimerization in erythrocytes of Gaucher disease patients: correlation with lipid abnormalities and oxidative stress

Neuroscience letters, 2016-02, Vol.613, p.1-5

2016

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Gaucher disease: Plasmalogen levels in relation to primary lipid abnormalities and oxidative stress

Blood cells, molecules, & diseases, 2014-06, Vol.53 (1-2), p.30-33

2014

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Synergistic use of glycomics and single‐molecule molecular inversion probes for identification of congenital disorders of glycosylation type‐1

Journal of inherited metabolic disease, 2022-07, Vol.45 (4), p.769-781

2022

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Phenotypic Characteristics in GBA-Associated Parkinson’s Disease: A Study in a Greek Population

Journal of Parkinson's disease, 2018-01, Vol.8 (1), p.101-105

2018

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PEX1 deficiency presenting as Leber congenital amaurosis

Pediatric neurology, 2004-08, Vol.31 (2), p.146-149

2004

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a-Synuclein and lipids in erythrocytes of Gaucher disease carriers and patients before and after enzyme replacement therapy

PloS one, 2023-01, Vol.18 (2), p.e0277602

2023

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Toward understanding tissue‐specific symptoms in dolichol‐phosphate‐mannose synthesis disorders; insight from DPM3‐CDG

Journal of inherited metabolic disease, 2019-09, Vol.42 (5), p.984-992

2019

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β-Glucocerebrosidase gene mutations in two cohorts of Greek patients with sporadic Parkinson's disease

Molecular genetics and metabolism, 2011-09, Vol.104 (1-2), p.149-152

2011

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Transferrin isoelectric focusing and plasma lysosomal enzyme activities in the diagnosis and follow‐up of hereditary fructose intolerance

Clinica chimica acta, 2012-10, Vol.413 (19-20), p.1714-1715

2012

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Plasma lysosomal enzyme activities in congenital disorders of glycosylation, galactosemia and fructosemia

Clinica chimica acta, 2009-03, Vol.401 (1), p.81-83

2009

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Plasmalogen levels in Gaucher disease

Blood cells, molecules, & diseases, 2008-09, Vol.41 (2), p.196-199

2008

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Danon disease: Further clinical and molecular heterogeneity

Muscle & nerve, 2009-06, Vol.39 (6), p.837-844

2009

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Persistent Massive Splenomegaly: Gaucher Disease Masquerading as Visceral Leishmaniasis

Medical & Clinical Case Reports Journal, 2024-07, Vol.2 (3), p.379-381

2024

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Lysosomal alterations in peripheral blood mononuclear cells of Parkinson's disease patients

a-Synuclein and lipids in erythrocytes of Gaucher disease carriers and patients before and after enzyme replacement therapy

Evidence of an association between the scavenger receptor class B member 2 gene and Parkinson's disease

Gaucher disease: Biochemical and molecular findings in 141 patients diagnosed in Greece

Increased dimerization of alpha-synuclein in erythrocytes in Gaucher disease and aging

A novel mutation deep within intron 7 of the GBA gene causes Gaucher disease

Parasitic Oscillations in Coaxial Gyrotron Beam Tunnels

Smart Health Caring Home: A Systematic Review of Smart Home Care for Elders and Chronic Disease Patients

Alpha-synuclein dimerization in erythrocytes of patients with genetic and non-genetic forms of Parkinson’s Disease

Circulating Brain‐enriched MicroRNAs for detection and discrimination of idiopathic and genetic Parkinson's disease

α-Synuclein dimerization in erythrocytes of Gaucher disease patients: correlation with lipid abnormalities and oxidative stress

Impact of APOE Genotype on Cognition in Idiopathic and Genetic Forms of Parkinson's Disease

TMEM199 Deficiency Is a Disorder of Golgi Homeostasis Characterized by Elevated Aminotransferases, Alkaline Phosphatase, and Cholesterol and Abnormal Glycosylation

Gaucher disease: Plasmalogen levels in relation to primary lipid abnormalities and oxidative stress

Synergistic use of glycomics and single‐molecule molecular inversion probes for identification of congenital disorders of glycosylation type‐1

Phenotypic Characteristics in GBA-Associated Parkinson’s Disease: A Study in a Greek Population

PEX1 deficiency presenting as Leber congenital amaurosis

a-Synuclein and lipids in erythrocytes of Gaucher disease carriers and patients before and after enzyme replacement therapy

Toward understanding tissue‐specific symptoms in dolichol‐phosphate‐mannose synthesis disorders; insight from DPM3‐CDG

β-Glucocerebrosidase gene mutations in two cohorts of Greek patients with sporadic Parkinson's disease

Transferrin isoelectric focusing and plasma lysosomal enzyme activities in the diagnosis and follow‐up of hereditary fructose intolerance

Plasma lysosomal enzyme activities in congenital disorders of glycosylation, galactosemia and fructosemia

Plasmalogen levels in Gaucher disease

Danon disease: Further clinical and molecular heterogeneity

Persistent Massive Splenomegaly: Gaucher Disease Masquerading as Visceral Leishmaniasis

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