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Genetic and Clinical Characterization of Patients with HNF1B-Related MODY in Croatia

Journal of personalized medicine, 2023-06, Vol.13 (7), p.1063

2023

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Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness

Genetics in medicine, 2020-09, Vol.22 (9), p.1478-1488

2020

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Is there any association of apolipoprotein E gene polymorphisms with metabolic syndrome in a young population of Croatian origin?

Annals of human biology, 2017-05, Vol.44 (3), p.287-294

2017

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Jesu li bubrežne malformacije jedno od obilježja sindroma MEN2B? – prikaz bolesnika i pregled literature

Liječnički vjesnik, 2023-01, Vol.145 (5-6), p.212-215

2023

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Metabolic syndrome and serum homocysteine in patients with bipolar disorder and schizophrenia treated with second generation antipsychotics

Psychiatry research, 2011-08, Vol.189 (1), p.21-25

2011

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Signal hyperintensities on brain magnetic resonance imaging in patients with primary Sjögren syndrome and frequent episodic tension-type headache: relation to platelet serotonin level and disease activity

Journal of rheumatology, 2013-08, Vol.40 (8), p.1360

2013

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Is Apolipoprotein E ε2 Associated with Delayed Onset of Non-Lesional Temporal Lobe Epilepsy?

Acta clinica Croatica (Tisak), 2017, Vol.56 (1), p.10-13

2017

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Adiponectin Level and Gene Variability Are Obesity and Metabolic Syndrome Markers in a Young Population

Archives of medical research, 2012-02, Vol.43 (2), p.145-153

2012

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Angiotensin-Converting Enzyme Genotype Is Not a Significant Genetic Risk Factor for Idiopathic Nephrotic Syndrome in Croatian Children

Nephron (2015), 2015-01, Vol.130 (1), p.29-34

2015

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Estrogen receptor 1 gene (TA)n polymorphism is associated with lone atrial fibrillation in men

Croatian medical journal, 2014-02, Vol.55 (1), p.38-44

2014

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Interaction of genetic risk factors confers increased risk for metabolic syndrome: the role of peroxisome proliferator-activated receptor γ

Genetic testing and molecular biomarkers, 2014-01, Vol.18 (1), p.32

2014

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Mutation detection in Croatian patients with Familial Hypercholesterolemia

Annals of human genetics, 2013-01, Vol.77 (1), p.22-30

2013

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Effects of lipoprotein lipase and peroxisome proliferator-activated receptor-gamma gene variants on metabolic syndrome traits

Collegium antropologicum, 2013-09, Vol.37 (3), p.801-808

2013

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Molecular Biomarkers for the Diagnosis, Prognosis, and Pharmacodynamics of Spinal Muscular Atrophy

Journal of clinical medicine, 2023-08, Vol.12 (15), p.5060

2023

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Total tau in cerebrospinal fluid detects treatment responders among spinal muscular atrophy types 1–3 patients treated with nusinersen

CNS neuroscience & therapeutics, 2024-03, Vol.30 (3), p.e14051-n/a

2024

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Ethylene glycol poisoning

Forensic science international, 2007-08, Vol.170 (2), p.213-215

2007

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Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness

Genetics in medicine, 2020-09, Vol.22 (9), p.1478-1488

2020

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CRANIOCERVICAL DYSTONIA INDUCED BY OXYCODONE-ESCITALOPRAM: POSSIBLE ROLE OF GENE POLYMORPHISM AND DRUG-DRUG INTERACTIONS

Psychiatria Danubina, 2022, Vol.34 (3), p.506-508

2022

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METOCLOPRAMIDE-INDUCED ACUTE DYSTONIC REACTION IN TWO PATIENTS, CYP2D6 4/4, 10/10 (POOR) AND 1/5 (INTERMEDIATE) METABOLIZERS

Psychiatria Danubina, 2023, Vol.35 (2), p.269-271

2023

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FCγRIIIA and FCγRIIA polymorphisms are not associated with response to rituximab and CHOP in patients with diffuse large B-cell lymphoma

Haematologica (Roma), 2007-07, Vol.92 (7)

2007

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Angiotensin-Converting Enzyme Gene Polymorphism and N-Acetyl-β-D-Glucosaminidase Excretion in Endemic Nephropathy

Nephron. Clinical practice, 2011-09, Vol.119 (2), p.c105-c112

2011

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Interactions of MinK and e-NOS gene polymorphisms appear to be inconsistent predictors of atrial fibrillation propensity, but long alleles of ESR1 promoter TA repeat may be a promising marker

Collegium antropologicum, 2009-09, Vol.33 (3), p.933-937

2009

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Association of angiotensin-converting enzyme insertion-deletion polymorphism with preeclampsia

Collegium antropologicum, 2008-06, Vol.32 (2), p.339-344

2008

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ATP7B Gene Mutations in Croatian Patients with Wilson Disease

Genetic testing and molecular biomarkers, 2016-03, Vol.20 (3), p.112

2016

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Genetic and Clinical Characterization of Patients with HNF1B-Related MODY in Croatia

Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness

Is there any association of apolipoprotein E gene polymorphisms with metabolic syndrome in a young population of Croatian origin?

Jesu li bubrežne malformacije jedno od obilježja sindroma MEN2B? – prikaz bolesnika i pregled literature

Metabolic syndrome and serum homocysteine in patients with bipolar disorder and schizophrenia treated with second generation antipsychotics

Signal hyperintensities on brain magnetic resonance imaging in patients with primary Sjögren syndrome and frequent episodic tension-type headache: relation to platelet serotonin level and disease activity

Is Apolipoprotein E ε2 Associated with Delayed Onset of Non-Lesional Temporal Lobe Epilepsy?

Adiponectin Level and Gene Variability Are Obesity and Metabolic Syndrome Markers in a Young Population

Angiotensin-Converting Enzyme Genotype Is Not a Significant Genetic Risk Factor for Idiopathic Nephrotic Syndrome in Croatian Children

Estrogen receptor 1 gene (TA)n polymorphism is associated with lone atrial fibrillation in men

Interaction of genetic risk factors confers increased risk for metabolic syndrome: the role of peroxisome proliferator-activated receptor γ

Mutation detection in Croatian patients with Familial Hypercholesterolemia

Effects of lipoprotein lipase and peroxisome proliferator-activated receptor-gamma gene variants on metabolic syndrome traits

Molecular Biomarkers for the Diagnosis, Prognosis, and Pharmacodynamics of Spinal Muscular Atrophy

Total tau in cerebrospinal fluid detects treatment responders among spinal muscular atrophy types 1–3 patients treated with nusinersen

Ethylene glycol poisoning

Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness

CRANIOCERVICAL DYSTONIA INDUCED BY OXYCODONE-ESCITALOPRAM: POSSIBLE ROLE OF GENE POLYMORPHISM AND DRUG-DRUG INTERACTIONS

METOCLOPRAMIDE-INDUCED ACUTE DYSTONIC REACTION IN TWO PATIENTS, CYP2D6 4/4, 10/10 (POOR) AND 1/5 (INTERMEDIATE) METABOLIZERS

FCγRIIIA and FCγRIIA polymorphisms are not associated with response to rituximab and CHOP in patients with diffuse large B-cell lymphoma

Angiotensin-Converting Enzyme Gene Polymorphism and N-Acetyl-β-D-Glucosaminidase Excretion in Endemic Nephropathy

Interactions of MinK and e-NOS gene polymorphisms appear to be inconsistent predictors of atrial fibrillation propensity, but long alleles of ESR1 promoter TA repeat may be a promising marker

Association of angiotensin-converting enzyme insertion-deletion polymorphism with preeclampsia

The Applied Genomics Development Strategy by the Croatian Academy of Sciences and Arts paves the way for the future development of applied genomics in Croatia

ATP7B Gene Mutations in Croatian Patients with Wilson Disease

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