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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
- By:
- 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
- By:
- 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
- By:
- 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
- By:
- 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
- By:
- 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
- By:
- 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
- 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
- By:
- 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
- By:
- 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
- By:
- 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:
- 2019
- By:
- Publication type:
- journal 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
- By:
- 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
- By:
- 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
- By:
- 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
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
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
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
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
Current State of Compulsory Basic and Clinical Courses in Genetics for Medical Students at Medical Faculties in Balkan Countries With Slavic Languages.
- Published in:
- Frontiers in Genetics, 2022, v. 12, p. 1, doi. 10.3389/fgene.2021.793834
- By:
- Publication type:
- Article
Population Data on HLA-DQA1, LDLR, GYPA, HBGG, D7S8, and GC PCR-Based Loci in Serbia.
- Published in:
- Journal of Forensic Sciences, 2006, v. 51, n. 3, p. 699, doi. 10.1111/j.1556-4029.2006.00142.x
- By:
- Publication type:
- Article
No Association between Brain-Derived Neurotrophic Factor G196A Polymorphism and Clinical Features of Parkinson's Disease.
- Published in:
- European Neurology, 2013, v. 70, n. 5/6, p. 257, doi. 10.1159/000352033
- By:
- Publication type:
- Article
Associations of Common Variants in HFE and TMPRSS6 Genes with Hepcidin-25 and Iron Status Parameters in Patients with End-Stage Renal Disease.
- Published in:
- Disease Markers, 2019, p. 1, doi. 10.1155/2019/4864370
- By:
- Publication type:
- Article
GALECTIN 3 RS4644 GENE POLYMORPHISM IS ASSOCIATED WITH METABOLIC TRAITS IN SERBIAN ADOLESCENT POPULATION.
- Published in:
- Journal of Medical Biochemistry, 2024, v. 43, n. 3, p. 445, doi. 10.5937/jomb0-47180
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- Publication type:
- Article
INTRODUCTION TO MOLECULAR GENETIC DIAGNOSTICS.
- Published in:
- Journal of Medical Biochemistry, 2014, v. 33, n. 1, p. 3, doi. 10.2478/jomb-2013-0039
- By:
- Publication type:
- Article
GENE POLYMORPHISMS AS MARKERS OF DISEASE SUSCEPTIBILITY.
- Published in:
- Journal of Medical Biochemistry, 2010, v. 29, n. 3, p. 135, doi. 10.2478/v10011-010-0022-y
- By:
- Publication type:
- Article
ANALYSIS OF "CLINICAL EXOME" PANEL IN SERBIAN PATIENTS WITH COGNITIVE DISORDERS.
- Published in:
- Genetika (0534-0012), 2022, v. 54, n. 3, p. 1351, doi. 10.2298/GENSR2203351B
- By:
- Publication type:
- Article
PPARGC1A GENE POLYMORPHISM AND ITS ASSOCIATION WITH OBESITYRELATED METABOLIC TRAITS IN SERBIAN ADOLESCENT POPULATION.
- Published in:
- Genetika (0534-0012), 2022, v. 54, n. 3, p. 1375, doi. 10.2298/GENSR2203375V
- By:
- Publication type:
- Article
C9ORF72 REPEAT EXPANSION IS NOT ASSOCIATED WITH ATYPICAL PARKINSONISM IN THE SERBIAN POPULATION.
- Published in:
- Genetika (0534-0012), 2022, v. 54, n. 3, p. 1313, doi. 10.2298/GENSR2203313M
- By:
- Publication type:
- Article
IMPACT OF THE FETUIN GENE POLYMORPHISMS IN CORONARY ARTERY CALCIFICATION AND MORTALITY OF PATIENTS WITH CHRONIC KIDNEY DISEASE AND RENAL TRANSPLANT.
- Published in:
- Genetika (0534-0012), 2022, v. 54, n. 1, p. 457, doi. 10.2298/GENSR2201457P
- By:
- Publication type:
- Article
CLINICAL EXOME SEQUENCING IN SERBIAN PATIENTS WITH MOVEMENT DISORDERS - SINGLE CENTRE EXPERIENCE.
- Published in:
- Genetika (0534-0012), 2022, v. 54, n. 1, p. 395, doi. 10.2298/GENSR2201395B
- By:
- Publication type:
- Article
ANALYSIS OF T-786C And 4a/b ENDOTHELIAL NITRIC OXIDE SYNTHASE GENE POLYMORPHISMS IN RETINOPATHY OF PREMATURITY.
- Published in:
- Genetika (0534-0012), 2016, v. 48, n. 2, p. 707, doi. 10.2298/GENSR1602707P
- By:
- Publication type:
- Article
GOJAZNOST DECE ŠKOLSKOG UZRASTA I OMLADINE-REZULTATI JUSAD STUDIJE.
- Published in:
- Medical Gazette / Medicinski Glasnik, 2012, v. 17, n. 46S, p. 129
- By:
- Publication type:
- Article
Wilson's disease.
- Published in:
- Srpski Arhiv za Celokupno Lekarstvo, 2024, v. 152, n. 5/6, p. 310, doi. 10.2298/SARH240511046S
- By:
- Publication type:
- Article
Continuous glucose monitoring in pregnancy.
- Published in:
- Srpski Arhiv za Celokupno Lekarstvo, 2024, v. 152, n. 3/4, p. 214, doi. 10.2298/SARH240104028N
- By:
- Publication type:
- Article
Novel PANK2 mutation identified in a patient with pantothenate kinase-associated neurodegeneration.
- Published in:
- Srpski Arhiv za Celokupno Lekarstvo, 2020, v. 148, n. 3/4, p. 203, doi. 10.2298/SARH190812005S
- By:
- Publication type:
- Article
Correlation between leukocyte‐platelet aggregates and thrombosis in myeloproliferative neoplasms.
- Published in:
- International Journal of Laboratory Hematology, 2022, v. 44, n. 2, p. 302, doi. 10.1111/ijlh.13754
- By:
- Publication type:
- Article
Exclusion of linkage to chromosomes 14q, 2q37 and 8p21.1-q11.23 in a Serbian family with idiopathic basal ganglia calcification.
- Published in:
- Journal of Neurology, 2011, v. 258, n. 9, p. 1637, doi. 10.1007/s00415-011-5985-1
- By:
- Publication type:
- Article
ANO10‐Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series.
- Published in:
- Movement Disorders, 2024, v. 39, n. 5, p. 887, doi. 10.1002/mds.29729
- By:
- Publication type:
- Article
Genetic Testing in Parkinson's Disease.
- Published in:
- Movement Disorders, 2023, v. 38, n. 8, p. 1384, doi. 10.1002/mds.29500
- By:
- Publication type:
- Article
Reply to: "Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism".
- Published in:
- Movement Disorders, 2023, v. 38, n. 4, p. 712, doi. 10.1002/mds.29351
- By:
- Publication type:
- Article
Phenotypic expression and founder effect of PANK2 c.1583C>T (p.T528M) mutation in Serbian pantothenate kinase-associated neurodegeneration patients.
- Published in:
- Archives of Biological Sciences, 2019, v. 71, n. 2, p. 275, doi. 10.2298/ABS181227009S
- By:
- Publication type:
- Article
The importance of direct genetic testing for determining female carriers of the mutation in dystrophinopathies.
- Published in:
- Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2023, v. 80, n. 3, p. 201, doi. 10.2298/VSP190208030M
- By:
- Publication type:
- Article
Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies.
- Published in:
- Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2020, v. 77, n. 4, p. 387, doi. 10.2298/VSP180226089M
- By:
- Publication type:
- Article