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Analysis of the Association Between Polymorphisms within PAI-1 and ACE genes and Ischemic Stroke Outcome After rt-PA Therapy.
- Published in:
- 2019
- By:
- Publication type:
- journal article
GSTO1*C/ GSTO2*G haplotype is associated with risk of transitional cell carcinoma of urinary bladder.
- Published in:
- International Urology & Nephrology, 2015, v. 47, n. 4, p. 625, doi. 10.1007/s11255-015-0933-0
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- Publication type:
- Article
HPCA-related dystonia: Too rare to be found?
- Published in:
- 2016
- By:
- Publication type:
- letter
De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient.
- Published in:
- Movement Disorders, 2014, v. 29, n. 9, p. 1190, doi. 10.1002/mds.25876
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- Publication type:
- Article
Inter-individual variability in the response of human peripheral blood lymphocytes to ionizing radiation: comparison of the dicentric and micronucleus assays.
- Published in:
- Radiation & Environmental Biophysics, 2015, v. 54, n. 3, p. 317, doi. 10.1007/s00411-015-0596-3
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- Publication type:
- Article
Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia.
- Published in:
- Cells (2073-4409), 2022, v. 11, n. 18, p. N.PAG, doi. 10.3390/cells11182804
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- Publication type:
- Article
Association of PPARG rs3856806 C>T Polymorphism With Body Mass Index, Glycaemia and Lipid Parameters in Serbian Adolescents.
- Published in:
- Scripta Medica, 2021, v. 52, n. 1, p. 15, doi. 10.5937/scriptamed52-29376
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- Publication type:
- Article
INFLUENCE OF MULCHING AND DIRECT PLANT COVERING ON THE NITRATE CONTENT IN LETTUCE.
- Published in:
- Technologica Acta, 2013, v. 6, n. 1, p. 67
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- Publication type:
- Article
Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion.
- Published in:
- PLoS ONE, 2018, v. 13, n. 5, p. 1, doi. 10.1371/journal.pone.0196345
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- Publication type:
- Article
A common polymorphism in the brain-derived neurotrophic factor gene in patients with adult-onset primary focal and segmental dystonia.
- Published in:
- Acta Neurologica Belgica, 2013, v. 113, n. 3, p. 243, doi. 10.1007/s13760-013-0183-9
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- Publication type:
- Article
Multidimensional aspects of pain in myotonic dystrophies.
- Published in:
- Acta Myologica, 2015, v. 34, n. 2/3, p. 126
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- Publication type:
- Article
Clients' Perception of Outcome of Team-Based Prenatal and Reproductive Genetic Counseling in Serbian Service Using the Perceived Personal Control (PPC) Questionnaire.
- Published in:
- Journal of Genetic Counseling, 2016, v. 25, n. 1, p. 189, doi. 10.1007/s10897-015-9857-1
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- Publication type:
- Article
Proximal Dystrophin Gene Deletions and Protein Alterations in Becker Muscular Dystrophy.
- Published in:
- Annals of the New York Academy of Sciences, 2005, v. 1048, n. 1, p. 406, doi. 10.1196/annals.1342.050
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- Publication type:
- Article
Frequency of C9orf72, GRN, and MAPT pathogenic variants in patients recruited at the Belgrade Memory Center.
- Published in:
- Neurogenetics, 2024, v. 25, n. 3, p. 193, doi. 10.1007/s10048-024-00766-8
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- Publication type:
- Article
Whole exome sequencing in Serbian patients with hereditary spastic paraplegia.
- Published in:
- Neurogenetics, 2024, v. 25, n. 3, p. 165, doi. 10.1007/s10048-024-00755-x
- By:
- Publication type:
- Article
NBIA Syndromes: A Step Forward from the Previous Knowledge.
- Published in:
- 2021
- By:
- Publication type:
- Journal Article
C-5 Hydroxyethyl and Hydroxypropyl Acyclonucleosides as Substrates for Thymidine Kinase of Herpes Simplex Virus Type 1 (HSV-1 TK): Syntheses and Biological Evaluation.
- Published in:
- Molecules, 2013, v. 18, n. 5, p. 5104, doi. 10.3390/molecules18055104
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- Publication type:
- Article
Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-45598-x
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- Publication type:
- Article
The Genetic Basis of Strokes in Pediatric Populations and Insight into New Therapeutic Options.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 3, p. 1601, doi. 10.3390/ijms23031601
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- Publication type:
- Article
Current Concepts on Genetic Aspects of Mitochondrial Dysfunction in Amyotrophic Lateral Sclerosis.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 18, p. 9832, doi. 10.3390/ijms22189832
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- Publication type:
- Article
Genetic and Epigenomic Modifiers of Diabetic Neuropathy.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 9, p. 4887, doi. 10.3390/ijms22094887
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- Publication type:
- Article
Genetic Aspects of Inflammation and Immune Response in Stroke.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 19, p. 7409, doi. 10.3390/ijms21197409
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- Publication type:
- Article
Whole Mitochondrial Genome Analysis in Serbian Cases of Leber's Hereditary Optic Neuropathy.
- Published in:
- Genes, 2020, v. 11, n. 9, p. 1037, doi. 10.3390/genes11091037
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- Publication type:
- Article
RADIOTERAPIJSKA OŠTEĆENJA HROMOZOMA KOD KARCINOMA LARINKSA.
- Published in:
- Medical Review / Medicinski Pregled, 2009, v. 62, n. 7-8, p. 314, doi. 10.2298/MPNS0908314S
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- Publication type:
- Article
Analysis of the Association Between Polymorphisms within PAI-1 and ACE genes and Ischemic Stroke Outcome After rt-PA Therapy.
- Published in:
- Journal of Pharmacy & Pharmaceutical Sciences, 2019, v. 22, p. 142, doi. 10.18433/jpps30339
- By:
- Publication type:
- Article
Association of the TYMS 3G/3G genotype with poor response and GGH 354GG genotype with the bone marrow toxicity of the methotrexate in RA patients.
- Published in:
- European Journal of Clinical Pharmacology, 2013, v. 69, n. 3, p. 377, doi. 10.1007/s00228-012-1341-3
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- Publication type:
- Article
Genetic polymorphisms and Methotrexate response in patients with rheumatoid arthritis.
- Published in:
- Journal of Research in Pharmacy, 2024, v. 28, n. 4, p. 1285, doi. 10.29228/jrp.809
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- Publication type:
- Article
KCC2 rs2297201 Gene Polymorphism Might be a Predictive Genetic Marker of Febrile Seizures.
- Published in:
- ASN Neuro (Sage Publications, Ltd.), 2022, p. 1, doi. 10.1177/17590914221093257
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- Publication type:
- Article
KCC2 rs2297201 Gene Polymorphism Might be a Predictive Genetic Marker of Febrile Seizures.
- Published in:
- ASN Neuro (Sage Publications, Ltd.), 2022, v. 14, p. 1, doi. 10.1177/17590914221093257
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- Publication type:
- Article
The emerging role of the FKBP5 gene polymorphisms in vulnerability-stress model of schizophrenia: further evidence from a Serbian population.
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- European Archives of Psychiatry & Clinical Neuroscience, 2017, v. 267, n. 6, p. 527, doi. 10.1007/s00406-016-0720-7
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- Publication type:
- Article
PHYSICAL ACTIVITY AND MENTAL HEALTH OF MEDICAL STUDENTS.
- Published in:
- Central European Journal of Public Health, 2024, v. 32, n. 1, p. 39, doi. 10.21101/cejph.a8097
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- Publication type:
- Article
Screening for gene mutation in early onset Alzheimer's disease and frontotemporal dementia: Report from a Serbian tertiary referral center: Genetics/genetic factors of non‐Alzheimer's tauopathies.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.041807
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- Publication type:
- Article
P2‐292: THE PATTERN OF INHERITANCE IN EARLY ONSET ALZHEIMER'S DISEASE AND FRONTOTEMPORAL DEMENTIA.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P698, doi. 10.1016/j.jalz.2019.06.2699
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- Publication type:
- Article
SCREENING FOR C9ORF72 EXPANSION MUTATION IN SERBIAN PATIENTS WITH EARLY ONSET DEMENTIA.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P337, doi. 10.1016/j.jalz.2017.06.061
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- Publication type:
- Article
Subtelomeric screening in Serbian children with dysmorphic features and unexplained developmental delay/intellectual disabilities.
- Published in:
- Turkish Journal of Pediatrics, 2015, v. 57, n. 2, p. 154, doi. 10.24953/turkjped.2015.1211
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- Publication type:
- Article
Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experience.
- Published in:
- Journal of Neurology, 2022, v. 269, n. 6, p. 3167, doi. 10.1007/s00415-021-10918-7
- By:
- Publication type:
- Article
Yield of the PMP22 deletion analysis in patients with compression neuropathies.
- Published in:
- Journal of Neurology, 2020, v. 267, n. 12, p. 3617, doi. 10.1007/s00415-020-10052-w
- By:
- Publication type:
- Article
Clinical course of patients with pantothenate kinase-associated neurodegeneration (PKAN) before and after DBS surgery.
- Published in:
- Journal of Neurology, 2019, v. 266, n. 12, p. 2962, doi. 10.1007/s00415-019-09499-3
- By:
- Publication type:
- Article
Mutation screening of the DYT6/ THAP1 gene in Serbian patients with primary dystonia.
- Published in:
- Journal of Neurology, 2013, v. 260, n. 4, p. 1037, doi. 10.1007/s00415-012-6753-6
- By:
- Publication type:
- Article
A multicenter study of genetic testing for Parkinson's disease in the clinical setting.
- Published in:
- NPJ Parkinson's Disease, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41531-022-00408-6
- By:
- Publication type:
- Article
Earlier age of symptom onset in younger generation of familial cases of multiple sclerosis.
- Published in:
- Neurological Sciences, 2024, v. 45, n. 9, p. 4463, doi. 10.1007/s10072-024-07512-w
- By:
- Publication type:
- Article
Neuropathic pain in patients with Charcot-Marie-Tooth type 1A.
- Published in:
- 2020
- By:
- Publication type:
- journal article
The Impact of the IKBKG Gene on the Appearance of the Corpus Callosum Abnormalities in Incontinentia Pigmenti.
- Published in:
- Diagnostics (2075-4418), 2023, v. 13, n. 7, p. 1300, doi. 10.3390/diagnostics13071300
- By:
- Publication type:
- Article
miRNAs as a Potential Biomarker in the COVID-19 Infection and Complications Course, Severity, and Outcome.
- Published in:
- Diagnostics (2075-4418), 2023, v. 13, n. 6, p. 1091, doi. 10.3390/diagnostics13061091
- By:
- Publication type:
- Article
Challenges in Rare Diseases Diagnostics: Incontinentia Pigmenti with Heterozygous GBA Mutation.
- Published in:
- Diagnostics (2075-4418), 2022, v. 12, n. 7, p. N.PAG, doi. 10.3390/diagnostics12071711
- By:
- Publication type:
- Article
Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review.
- Published in:
- Diagnostics (2075-4418), 2021, v. 11, n. 11, p. 1969, doi. 10.3390/diagnostics11111969
- By:
- Publication type:
- Article
Genetic Variation in Circadian Rhythm Genes CLOCK and ARNTL as Risk Factor for Male Infertility.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0059220
- By:
- Publication type:
- Article
Mutacioni status gena p53 u oralnim skvamocelularnim karcinomima.
- Published in:
- Serbian Dental Journal / Stomatološki Glasnik Srbije, 2009, v. 56, n. 4, p. 174
- By:
- Publication type:
- Article
Mutation Status of p53 Gene in Oral Squamous Cell Carcinoma.
- Published in:
- Serbian Dental Journal / Stomatološki Glasnik Srbije, 2009, v. 56, n. 4, p. 171, doi. 10.2298/SGS0904171P
- By:
- Publication type:
- Article
Analiza antiapoptotskog proteina bcl-2 u skvamocelularnom karcinomu usne regije.
- Published in:
- Serbian Dental Journal / Stomatološki Glasnik Srbije, 2007, v. 54, n. 3, p. 153, doi. 10.2298/SGS0703153P
- By:
- Publication type:
- Article