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Adrenal hypoplasia congenita and hypogonadotropic hypogonadism due to a novel NR0B1 (DAX1) gene mutation associated with common variable immunodeficiency and Hashimoto's thyroiditis.
- Published in:
- Polish Journal of Endocrinology / Endokrynologia Polska, 2024, v. 75, n. 5, p. 560, doi. 10.5603/ep.99536
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- Article
The importance of direct genetic testing for determining female carriers of the mutation in dystrophinopathies.
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- Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2023, v. 80, n. 3, p. 201, doi. 10.2298/VSP190208030M
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- Article
Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies.
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- Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2020, v. 77, n. 4, p. 387, doi. 10.2298/VSP180226089M
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- Article
Significance of KIT and PDGFRA mutations in gastric gastrointestinal stromal tumor imatinib-naive surgically treated patients.
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- Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2019, v. 76, n. 12, p. 1268, doi. 10.2298/VSP180205048E
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- Article
GLUT1 deficiency syndrome: a case report with a novel SLC2A1 mutation.
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- Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2019, v. 76, n. 5, p. 543, doi. 10.2298/VSP170406120I
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- Article
Prospective study of perinatal outcome in pregnancies with primary antiphospholipid syndrome.
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- Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2014, v. 71, n. 8, p. 742, doi. 10.2298/VSP1408742C
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- Article
Mutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilson's disease in Serbia.
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- Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2013, v. 70, n. 5, p. 457, doi. 10.2298/VSP1305457T
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- Publication type:
- Article
Analiza gubitka heterozigotnosti tumor-supresor gena p53 i BRCA1 kod karcinoma ovarijuma.
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- Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2006, v. 63, n. 9, p. 813, doi. 10.2298/VSP0609813P
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- Article
Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients.
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- Human Genomics, 2017, v. 11, p. 1, doi. 10.1186/s40246-017-0126-2
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- Article
A Machine Learning Approach to Gene Expression in Hypertrophic Cardiomyopathy.
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- Pharmaceuticals (14248247), 2024, v. 17, n. 10, p. 1364, doi. 10.3390/ph17101364
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- Publication type:
- Article
Correlation between leukocyte‐platelet aggregates and thrombosis in myeloproliferative neoplasms.
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- International Journal of Laboratory Hematology, 2022, v. 44, n. 2, p. 302, doi. 10.1111/ijlh.13754
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- Publication type:
- Article
RADIOTERAPIJSKA OŠTEĆENJA HROMOZOMA KOD KARCINOMA LARINKSA.
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- Medical Review / Medicinski Pregled, 2009, v. 62, n. 7-8, p. 314, doi. 10.2298/MPNS0908314S
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- Article
Phenotypic expression and founder effect of PANK2 c.1583C>T (p.T528M) mutation in Serbian pantothenate kinase-associated neurodegeneration patients.
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- Archives of Biological Sciences, 2019, v. 71, n. 2, p. 275, doi. 10.2298/ABS181227009S
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- Article
KCC2 rs2297201 Gene Polymorphism Might be a Predictive Genetic Marker of Febrile Seizures.
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- ASN Neuro (Sage Publications, Ltd.), 2022, p. 1, doi. 10.1177/17590914221093257
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- Article
KCC2 rs2297201 Gene Polymorphism Might be a Predictive Genetic Marker of Febrile Seizures.
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- ASN Neuro (Sage Publications, Ltd.), 2022, v. 14, p. 1, doi. 10.1177/17590914221093257
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- Publication type:
- Article
GOJAZNOST DECE ŠKOLSKOG UZRASTA I OMLADINE-REZULTATI JUSAD STUDIJE.
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- Medical Gazette / Medicinski Glasnik, 2012, v. 17, n. 46S, p. 129
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- Publication type:
- Article
Genetic Variation in Circadian Rhythm Genes CLOCK and ARNTL as Risk Factor for Male Infertility.
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- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0059220
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- Publication type:
- Article
Mutacioni status gena p53 u oralnim skvamocelularnim karcinomima.
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- Serbian Dental Journal / Stomatološki Glasnik Srbije, 2009, v. 56, n. 4, p. 174
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- Article
Mutation Status of p53 Gene in Oral Squamous Cell Carcinoma.
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- Serbian Dental Journal / Stomatološki Glasnik Srbije, 2009, v. 56, n. 4, p. 171, doi. 10.2298/SGS0904171P
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- Publication type:
- Article
Analiza antiapoptotskog proteina bcl-2 u skvamocelularnom karcinomu usne regije.
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- Serbian Dental Journal / Stomatološki Glasnik Srbije, 2007, v. 54, n. 3, p. 153, doi. 10.2298/SGS0703153P
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- Publication type:
- Article
Proximal Dystrophin Gene Deletions and Protein Alterations in Becker Muscular Dystrophy.
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- 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
Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-45598-x
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- Article
Association of PPARG rs3856806 C>T Polymorphism With Body Mass Index, Glycaemia and Lipid Parameters in Serbian Adolescents.
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- Scripta Medica, 2021, v. 52, n. 1, p. 15, doi. 10.5937/scriptamed52-29376
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- 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
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- Publication type:
- Article
Continuous glucose monitoring in pregnancy.
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- Srpski Arhiv za Celokupno Lekarstvo, 2024, v. 152, n. 3/4, p. 214, doi. 10.2298/SARH240104028N
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- Publication type:
- Article
Novel PANK2 mutation identified in a patient with pantothenate kinase-associated neurodegeneration.
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- Srpski Arhiv za Celokupno Lekarstvo, 2020, v. 148, n. 3/4, p. 203, doi. 10.2298/SARH190812005S
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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.
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- 2019
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- Publication type:
- journal article
Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experience.
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- Journal of Neurology, 2022, v. 269, n. 6, p. 3167, doi. 10.1007/s00415-021-10918-7
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- Publication type:
- Article
Clinical course of patients with pantothenate kinase-associated neurodegeneration (PKAN) before and after DBS surgery.
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- Journal of Neurology, 2019, v. 266, n. 12, p. 2962, doi. 10.1007/s00415-019-09499-3
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- Article
Mutation screening of the DYT6/ THAP1 gene in Serbian patients with primary dystonia.
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- Journal of Neurology, 2013, v. 260, n. 4, p. 1037, doi. 10.1007/s00415-012-6753-6
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- Publication type:
- Article
Exclusion of linkage to chromosomes 14q, 2q37 and 8p21.1-q11.23 in a Serbian family with idiopathic basal ganglia calcification.
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- Journal of Neurology, 2011, v. 258, n. 9, p. 1637, doi. 10.1007/s00415-011-5985-1
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- Article
PPARGC1A GENE POLYMORPHISM AND ITS ASSOCIATION WITH OBESITYRELATED METABOLIC TRAITS IN SERBIAN ADOLESCENT POPULATION.
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- Genetika (0534-0012), 2022, v. 54, n. 3, p. 1375, doi. 10.2298/GENSR2203375V
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- Publication type:
- Article
ANALYSIS OF "CLINICAL EXOME" PANEL IN SERBIAN PATIENTS WITH COGNITIVE DISORDERS.
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- Genetika (0534-0012), 2022, v. 54, n. 3, p. 1351, doi. 10.2298/GENSR2203351B
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- Publication type:
- Article
C9ORF72 REPEAT EXPANSION IS NOT ASSOCIATED WITH ATYPICAL PARKINSONISM IN THE SERBIAN POPULATION.
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- Genetika (0534-0012), 2022, v. 54, n. 3, p. 1313, doi. 10.2298/GENSR2203313M
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- Publication type:
- Article
IMPACT OF THE FETUIN GENE POLYMORPHISMS IN CORONARY ARTERY CALCIFICATION AND MORTALITY OF PATIENTS WITH CHRONIC KIDNEY DISEASE AND RENAL TRANSPLANT.
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- Genetika (0534-0012), 2022, v. 54, n. 1, p. 457, doi. 10.2298/GENSR2201457P
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- Publication type:
- Article
CLINICAL EXOME SEQUENCING IN SERBIAN PATIENTS WITH MOVEMENT DISORDERS - SINGLE CENTRE EXPERIENCE.
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- Genetika (0534-0012), 2022, v. 54, n. 1, p. 395, doi. 10.2298/GENSR2201395B
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- Publication type:
- Article
ANALYSIS OF T-786C And 4a/b ENDOTHELIAL NITRIC OXIDE SYNTHASE GENE POLYMORPHISMS IN RETINOPATHY OF PREMATURITY.
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- Genetika (0534-0012), 2016, v. 48, n. 2, p. 707, doi. 10.2298/GENSR1602707P
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- Publication type:
- Article
No Association between Brain-Derived Neurotrophic Factor G196A Polymorphism and Clinical Features of Parkinson's Disease.
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- European Neurology, 2013, v. 70, n. 5/6, p. 257, doi. 10.1159/000352033
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- Publication type:
- Article
NBIA Syndromes: A Step Forward from the Previous Knowledge.
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- 2021
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- Publication type:
- Journal Article
ANO10‐Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series.
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- Movement Disorders, 2024, v. 39, n. 5, p. 887, doi. 10.1002/mds.29729
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- Publication type:
- Article
Genetic Testing in Parkinson's Disease.
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- Movement Disorders, 2023, v. 38, n. 8, p. 1384, doi. 10.1002/mds.29500
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- 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
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- Publication type:
- Article
DIABETIC KETOACIDOSIS IN PREGNANCY.
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- Sanamed, 2024, v. 19, n. 2, p. 221, doi. 10.5937/sanamed0-50195
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- Publication type:
- Article
The Impact of the IKBKG Gene on the Appearance of the Corpus Callosum Abnormalities in Incontinentia Pigmenti.
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- Diagnostics (2075-4418), 2023, v. 13, n. 7, p. 1300, doi. 10.3390/diagnostics13071300
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- Publication type:
- Article
Challenges in Rare Diseases Diagnostics: Incontinentia Pigmenti with Heterozygous GBA Mutation.
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- Diagnostics (2075-4418), 2022, v. 12, n. 7, p. N.PAG, doi. 10.3390/diagnostics12071711
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- Publication type:
- Article
Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia.
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- Cells (2073-4409), 2022, v. 11, n. 18, p. N.PAG, doi. 10.3390/cells11182804
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- 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.
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- Frontiers in Genetics, 2022, v. 12, p. 1, doi. 10.3389/fgene.2021.793834
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- Article
PHYSICAL ACTIVITY AND MENTAL HEALTH OF MEDICAL STUDENTS.
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- Central European Journal of Public Health, 2024, v. 32, n. 1, p. 39, doi. 10.21101/cejph.a8097
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- 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
Associations of Common Variants in HFE and TMPRSS6 Genes with Hepcidin-25 and Iron Status Parameters in Patients with End-Stage Renal Disease.
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- Disease Markers, 2019, p. 1, doi. 10.1155/2019/4864370
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- Publication type:
- Article