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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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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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Genetic background of cognitive decline in Parkinson's disease

Frontiers in Cognition, 2024-07, Vol.3

2024

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A first report of a rare TP53 variant associated with Li-Fraumeni syndrome manifesting as invasive breast cancer and malignant solitary fibrous tumor

World journal of surgical oncology, 2021-08, Vol.19 (1), p.1-254, Article 254

2021

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Comparable Genomic Copy Number Aberrations Differ across Astrocytoma Malignancy Grades

International journal of molecular sciences, 2019-03, Vol.20 (5), p.1251

2019

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Characterization of M116.1p, a Murine Cytomegalovirus Protein Required for Efficient Infection of Mononuclear Phagocytes

Journal of virology, 2022-01, Vol.96 (2), p.e0087621-e0087621

2022

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Alpha-synuclein deregulates the expression of COL4A2 and impairs ER-Golgi function

Neurobiology of disease, 2018-11, Vol.119, p.121-135

2018

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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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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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Clinical and pathohistological characteristics of Alport spectrum disorder caused by COL4A4 mutation c.193-2A>C: a case series

Croatian Medical Journal, 2021-06, Vol.62 (3), p.204-214

2021

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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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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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Non-motor symptoms of Parkinson`s disease-insights from genetics

Journal of Neural Transmission, 2024-11, Vol.131 (11), p.1277-1284

2024

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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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Rare GRN mutation in a patient diagnosed with primary progressive aphasia and parkinsonism

Acta neurologica Belgica, 2023-04, Vol.123 (2), p.727-729

2023

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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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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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Juvenile-onset Mitochondrial-membrane Protein-associated Neurodegeneration with Late Diagnosis/Geç Tani Konan Juvenil Baslangiçli Mitokondriyal Membran Proteini ile Iliskili Nörodejenerasyon

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

2022

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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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Clinical and pathohistological characteristics of Alport spectrum disorder caused by COL4A4 mutation c.193-2AC: a case series

Croatian medical journal, 2021-06, Vol.62 (3), p.204

2021

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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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A novel disease-causing NF1 variant in a Croatian family with neurofibromatosis type 1

Molecular and experimental biology in medicine, 2019-10, Vol.2 (2), p.21-27

2019

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

Nuclear localization and phosphorylation modulate pathological effects of alpha-synuclein

Genetic background of cognitive decline in Parkinson's disease

A first report of a rare TP53 variant associated with Li-Fraumeni syndrome manifesting as invasive breast cancer and malignant solitary fibrous tumor

Comparable Genomic Copy Number Aberrations Differ across Astrocytoma Malignancy Grades

Characterization of M116.1p, a Murine Cytomegalovirus Protein Required for Efficient Infection of Mononuclear Phagocytes

Alpha-synuclein deregulates the expression of COL4A2 and impairs ER-Golgi function

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

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

Clinical and pathohistological characteristics of Alport spectrum disorder caused by COL4A4 mutation c.193-2A>C: a case series

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

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

Non-motor symptoms of Parkinson`s disease-insights from genetics

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

Rare GRN mutation in a patient diagnosed with primary progressive aphasia and parkinsonism

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

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

Juvenile-onset Mitochondrial-membrane Protein-associated Neurodegeneration with Late Diagnosis/Geç Tani Konan Juvenil Baslangiçli Mitokondriyal Membran Proteini ile Iliskili Nörodejenerasyon

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

Clinical and pathohistological characteristics of Alport spectrum disorder caused by COL4A4 mutation c.193-2AC: a case series

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

A novel disease-causing NF1 variant in a Croatian family with neurofibromatosis type 1

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

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