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Genetic background of cognitive decline in Parkinson's disease

Frontiers in Cognition, 2024-07, Vol.3

2024

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

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

2022

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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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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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The influence of dopamine-beta-hydroxylase and catechol O -methyltransferase gene polymorphism on the efficacy of insulin detemir therapy in patients with type 2 diabetes mellitus

Diabetology and metabolic syndrome, 2017-12, Vol.9 (1), p.97-97, Article 97

2017

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Psychiatric Comorbidities in Parkinson's Disease Seen through the Prism of Genomics and Epigenetics

Psychiatria Danubina, 2021-01, Vol.33, p.456-462

2021

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Neurosyphilis: The shape of a rising threat

International journal of infectious diseases, 2018-11, Vol.76, p.1-3

2018

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SNCA 3' UTR Genetic Variants in Patients with Parkinson's Disease

Biomolecules (Basel, Switzerland), 2021-11, Vol.11 (12), p.1799

2021

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Genotype-phenotype correlation in contactin-associated protein-like 2

Human genetics, 2023-07, Vol.142 (7), p.909

2023

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Diagnostic and Therapeutic Dilemmas in the Management of Intracranial Aneurysms

Acta clinica Croatica (Tisak), 2021, Vol.60 (4), p.758-764

Radić, Borislav

2021

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DIAGNOSTIC AND THERAPEUTIC DILEMMAS IN THE MANAGEMENT OF INTRACRANIAL ANEURYSMS/DIJAGNOSTICKE I TERAPIJSKE NEDOUMICE U LIJECENJU INTRAKRANIJSKIH ANEURIZMA

Acta clinica Croatica (Tisak), 2021-12, Vol.60 (4), p.758

2021

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Genotype–phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder

Human genetics, 2023-07, Vol.142 (7), p.909-925

2023

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Harris JR, Korolchuk VI, eds. Biochemistry and Cell Biology of Aging: Part II Clinical ScienceSubcellular Biochemistry; Volume 91; Springer Nature Singapore Pte Ltd 2019;499 pages; ISBN 978-981-13-3680-5; ISBN 978-981-13-3681-2 (eBook)

Croatian medical journal, 2020-04, Vol.61 (2), p.208-209

2020

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Dijagnostičke i terapijske nedoumice u liječenju intrakranijskih aneurizma

Acta clinica Croatica (Tisak), 2021-12, Vol.60. (4.), p.764

2021

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Could Mental and Physical Exercise Alleviate Alzheimer's Disease?

Psychiatria Danubina, 2021, Vol.33 (Suppl 4), p.1267-1273

2021

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Evaluation of cerebrospinal fluid phosphorylated tau 231 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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Epigenetic Alterations in Juvenile Spondyloarthritis Patients: a Preliminary Study of Selected Genes Promoter Methylation and Silencing

SN comprehensive clinical medicine, 2019-07, Vol.1 (7), p.496-501

2019

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Efficacy of insulin detemir treatment in type 2 diabetes mellitus is associated with a allele od the catechol o-methyltransferase polymorphism

Endocrine Abstracts, 2017-05

2017

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

Croatian Medical Journal, 2020, Vol.61 (6), p.62

2020

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

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

2020

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Harris JR, Korolchuk VI, eds. Biochemistry and Cell Biology of Aging: Part II Clinical Science: Subcellular Biochemistry; Volume 91; Springer Nature Singapore Pte Ltd 2019;499 pages; ISBN 978-981-13-3680-5; ISBN 978-981-13-3681-2 (eBook)

Croatian Medical Journal, 2020, Vol.61 (2), p.208-209

2020

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Genetic background of cognitive decline in Parkinson's disease

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

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

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

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

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

The influence of dopamine-beta-hydroxylase and catechol O -methyltransferase gene polymorphism on the efficacy of insulin detemir therapy in patients with type 2 diabetes mellitus

Psychiatric Comorbidities in Parkinson's Disease Seen through the Prism of Genomics and Epigenetics

Neurosyphilis: The shape of a rising threat

SNCA 3' UTR Genetic Variants in Patients with Parkinson's Disease

Genotype-phenotype correlation in contactin-associated protein-like 2

Diagnostic and Therapeutic Dilemmas in the Management of Intracranial Aneurysms

DIAGNOSTIC AND THERAPEUTIC DILEMMAS IN THE MANAGEMENT OF INTRACRANIAL ANEURYSMS/DIJAGNOSTICKE I TERAPIJSKE NEDOUMICE U LIJECENJU INTRAKRANIJSKIH ANEURIZMA

Genotype–phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder

Harris JR, Korolchuk VI, eds. Biochemistry and Cell Biology of Aging: Part II Clinical ScienceSubcellular Biochemistry; Volume 91; Springer Nature Singapore Pte Ltd 2019;499 pages; ISBN 978-981-13-3680-5; ISBN 978-981-13-3681-2 (eBook)

Dijagnostičke i terapijske nedoumice u liječenju intrakranijskih aneurizma

Could Mental and Physical Exercise Alleviate Alzheimer's Disease?

Evaluation of cerebrospinal fluid phosphorylated tau 231 as a biomarker in the differential diagnosis of Alzheimer's disease and vascular dementia

Epigenetic Alterations in Juvenile Spondyloarthritis Patients: a Preliminary Study of Selected Genes Promoter Methylation and Silencing

Efficacy of insulin detemir treatment in type 2 diabetes mellitus is associated with a allele od the catechol o-methyltransferase polymorphism

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

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

Harris JR, Korolchuk VI, eds. Biochemistry and Cell Biology of Aging: Part II Clinical Science: Subcellular Biochemistry; Volume 91; Springer Nature Singapore Pte Ltd 2019;499 pages; ISBN 978-981-13-3680-5; ISBN 978-981-13-3681-2 (eBook)

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