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Nuclear localization and phosphorylation modulate pathological effects of alpha-synuclein

Human molecular genetics, 2019-01, Vol.28 (1), p.31-50

2019

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Convergence of miRNA expression profiling, α-synuclein interacton and GWAS in Parkinson's disease

PloS one, 2011-10, Vol.6 (10), p.e25443-e25443

2011

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Quality assurance for next-generation sequencing diagnostics of rare neurological diseases in the European Reference Network

European journal of human genetics : EJHG, 2024-06, Vol.32 (8), p.1014-1021

2024

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IL-1β, IL-6, IL-10, and TNFα Single Nucleotide Polymorphisms in Human Influence the Susceptibility to Alzheimer's Disease Pathology

Journal of Alzheimer's disease, 2020-01, Vol.75 (3), p.1029

2020

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Early-onset Alzheimer’s disease due to novel LDLR gene mutation

Acta neurologica Belgica, 2024-02, Vol.124 (1), p.325-327

2024

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Relationship between Brain-Derived Neurotrophic Factor and Cognitive Decline in Patients with Mild Cognitive Impairment and Dementia

Biomolecules (Basel, Switzerland), 2023-03, Vol.13 (3), p.570

2023

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Gene Expression Differences in Peripheral Blood of Parkinson's Disease Patients with Distinct Progression Profiles

PloS one, 2016-06, Vol.11 (6), p.e0157852-e0157852

2016

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Relationships of Cerebrospinal Fluid Alzheimer's Disease Biomarkers and COMT, DBH, and MAOB Single Nucleotide Polymorphisms

Journal of Alzheimer's disease, 2020-01, Vol.73 (1), p.135

2020

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Aberrant expression of shared master-key genes contributes to the immunopathogenesis in patients with juvenile spondyloarthritis

PloS one, 2014-12, Vol.9 (12), p.e115416-e115416

2014

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Genome-Wide Expression Profile in People with Optic Neuritis Associated with Multiple Sclerosis

Biomedicines, 2023-08, Vol.11 (8), p.2209

2023

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Juvenile-onset Mitochondrial-membrane Protein-associated Neurodegeneration with Late Diagnosis

Türk nöroloji dergisi, 2022-06, Vol.28 (2), p.118-121

2022

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A non-invasive hidden-goal test for spatial orientation deficit detection in subjects with suspected mild cognitive impairment

Journal of neuroscience methods, 2020-02, Vol.332, p.108547-108547, Article 108547

2020

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Genetics of Pediatric Epilepsy: Next-Generation Sequencing in Clinical Practice

Genes, 2022-08, Vol.13 (8), p.1466

2022

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BMP7, a Putative Regulator of Epithelial Homeostasis in the Human Prostate, Is a Potent Inhibitor of Prostate Cancer Bone Metastasis in Vivo

The American journal of pathology, 2007-09, Vol.171 (3), p.1047-1057

2007

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Overlap of the Pitt–Hopkins and Lennox–Gastaut syndromes

Acta neurologica Belgica, 2020-04, Vol.120 (2), p.399-401

2020

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Evaluation of cerebrospinal fluid phosphorylated tau231 as a biomarker in the differential diagnosis of Alzheimer's disease and vascular dementia

CNS neuroscience & therapeutics, 2018-08, Vol.24 (8), p.734-740

2018

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Prophylactic therapeutic plasma exchange in pregnant woman with Familial Chylomicronemia Syndrome – A case report

Transfusion and apheresis science, 2022-06, Vol.61 (3), p.103346-103346, Article 103346

2022

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Congenital factor XI deficiency caused by a novel F11 missense variant: a case report

Croatian medical journal, 2020-02, Vol.61 (1), p.62-65

2020

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Correction: Gene Expression Differences in Peripheral Blood of Parkinson's Disease Patients with Distinct Progression Profiles

PloS one, 2017-12, Vol.12 (12), p.e0190552-e0190552

2017

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De novo mutation in desmin gene causing dilated cardiomyopathy requiring ECMO treatment: A clinical report

Human gene (Amsterdam, Netherlands), 2024-02, Vol.39, p.201265, Article 201265

2024

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EEG Analysis and Spect Imaging in Alzheimer's Disease, Vascular Dementia and Mild Cognitive Impairment

Psychiatria Danubina, 2019-03, Vol.31 (1), p.111-115

2019

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Association of MAPT haplotype‐tagging polymorphisms with cerebrospinal fluid biomarkers of Alzheimer's disease: A preliminary study in a Croatian cohort

Brain and behavior, 2018-11, Vol.8 (11), p.e01128-n/a

2018

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Epigenetics, Resilience, Comorbidity and Treatment Outcome

Psychiatria Danubina, 2018-10, Vol.30 (3), p.242-253

2018

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Development of novel genomic blood biomarkers for neurodegenerative diseases

CNS & neurological disorders drug targets, 2010-12, Vol.9 (6), p.669

2010

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Harris JR, Korolchuk VI, eds. Biochemistry and Cell Biology of Aging: Part II Clinical Science

Croatian medical journal, 2020-04, Vol.61 (2), p.208

2020

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Nuclear localization and phosphorylation modulate pathological effects of alpha-synuclein

Convergence of miRNA expression profiling, α-synuclein interacton and GWAS in Parkinson's disease

Quality assurance for next-generation sequencing diagnostics of rare neurological diseases in the European Reference Network

IL-1β, IL-6, IL-10, and TNFα Single Nucleotide Polymorphisms in Human Influence the Susceptibility to Alzheimer's Disease Pathology

Early-onset Alzheimer’s disease due to novel LDLR gene mutation

Relationship between Brain-Derived Neurotrophic Factor and Cognitive Decline in Patients with Mild Cognitive Impairment and Dementia

Gene Expression Differences in Peripheral Blood of Parkinson's Disease Patients with Distinct Progression Profiles

Relationships of Cerebrospinal Fluid Alzheimer's Disease Biomarkers and COMT, DBH, and MAOB Single Nucleotide Polymorphisms

Aberrant expression of shared master-key genes contributes to the immunopathogenesis in patients with juvenile spondyloarthritis

Genome-Wide Expression Profile in People with Optic Neuritis Associated with Multiple Sclerosis

Juvenile-onset Mitochondrial-membrane Protein-associated Neurodegeneration with Late Diagnosis

A non-invasive hidden-goal test for spatial orientation deficit detection in subjects with suspected mild cognitive impairment

Genetics of Pediatric Epilepsy: Next-Generation Sequencing in Clinical Practice

BMP7, a Putative Regulator of Epithelial Homeostasis in the Human Prostate, Is a Potent Inhibitor of Prostate Cancer Bone Metastasis in Vivo

Overlap of the Pitt–Hopkins and Lennox–Gastaut syndromes

Evaluation of cerebrospinal fluid phosphorylated tau231 as a biomarker in the differential diagnosis of Alzheimer's disease and vascular dementia

Prophylactic therapeutic plasma exchange in pregnant woman with Familial Chylomicronemia Syndrome – A case report

Congenital factor XI deficiency caused by a novel F11 missense variant: a case report

Correction: Gene Expression Differences in Peripheral Blood of Parkinson's Disease Patients with Distinct Progression Profiles

De novo mutation in desmin gene causing dilated cardiomyopathy requiring ECMO treatment: A clinical report

EEG Analysis and Spect Imaging in Alzheimer's Disease, Vascular Dementia and Mild Cognitive Impairment

Association of MAPT haplotype‐tagging polymorphisms with cerebrospinal fluid biomarkers of Alzheimer's disease: A preliminary study in a Croatian cohort

Epigenetics, Resilience, Comorbidity and Treatment Outcome

Development of novel genomic blood biomarkers for neurodegenerative diseases

Harris JR, Korolchuk VI, eds. Biochemistry and Cell Biology of Aging: Part II Clinical Science

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