Found: 40
Select item for more details and to access through your institution.
Antiphospholipid antibodies in patients with upper-extremity deep vein thrombosis.
- Published in:
- Central European Journal of Immunology, 2015, v. 40, n. 3, p. 307, doi. 10.5114/ceji.2015.54592
- By:
- Publication type:
- Article
Arginase deficiency in Bulgaria: first cases and potential endemic region for the disorder.
- Published in:
- Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-022-01399-2
- By:
- Publication type:
- Article
Altered Thermal Behavior of Blood Plasma Proteome Related to Inflammatory Cytokines in Early Pregnancy Loss.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 15, p. 8764, doi. 10.3390/ijms23158764
- By:
- Publication type:
- Article
Morphometric and Nanomechanical Features of Erythrocytes Characteristic of Early Pregnancy Loss.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 9, p. 4512, doi. 10.3390/ijms23094512
- By:
- Publication type:
- Article
Postvaccination SARS‐CoV‐2 Alpha (B.1.1.7) lineage infection among healthcare workers on the background of IgG antibodies.
- Published in:
- Journal of Medical Virology, 2022, v. 94, n. 3, p. 836, doi. 10.1002/jmv.27394
- By:
- Publication type:
- Article
Restriction of the Global IgM Repertoire in Antiphospholipid Syndrome.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.865232
- By:
- Publication type:
- Article
Screening for point mutations in the LDL receptor gene in Bulgarian patients with severe hypercholesterolemia.
- Published in:
- Journal of Human Genetics, 2004, v. 49, n. 4, p. 173, doi. 10.1007/s10038-004-0127-6
- By:
- Publication type:
- Article
Rare Mutations in the PIK3CA Gene Contribute to Aggressive Endometrial Cancer.
- Published in:
- DNA & Cell Biology, 2010, v. 29, n. 2, p. 65, doi. 10.1089/dna.2009.0939
- By:
- Publication type:
- Article
Vitamin D and estrogen receptor gene polymorphisms and the risk of colorectal cancer in Bulgaria.
- Published in:
- International Journal of Colorectal Disease, 2007, v. 22, n. 4, p. 395, doi. 10.1007/s00384-006-0163-0
- By:
- Publication type:
- Article
Association between Estrogen Receptor-α Gene Polymorphisms and Lupus Nephritis in Bulgarian Patients.
- Published in:
- BANTAO Journal, 2012, v. 10, n. 2, p. 59
- By:
- Publication type:
- Article
Positive association between a polymorphic locus near the LBX1 gene and predisposition of idiopathic scoliosis in Southeastern European population.
- Published in:
- Journal of Applied Biomedicine, 2019, v. 17, n. 3, p. 184, doi. 10.32725/jab.2019.011
- By:
- Publication type:
- Article
Positive association between the progression of idiopathic scoliosis and the common variant near the LBX1 gene in Southeast European population.
- Published in:
- Journal of Applied Biomedicine, 2018, v. 16, n. 4, p. 344, doi. 10.1016/j.jab.2018.07.001
- By:
- Publication type:
- Article
Association of vitamin D receptor gene BsmI B/b and FokI F/f polymorphisms with adult dermatomyositis and systemic lupus erythematosus.
- Published in:
- International Journal of Dermatology, 2016, v. 55, n. 8, p. e465, doi. 10.1111/ijd.13263
- By:
- Publication type:
- Article
Association between estrogen receptor-α gene polymorphisms and dermatomyositis in Bulgarian patients.
- Published in:
- International Journal of Dermatology, 2014, v. 53, n. 7, p. e363, doi. 10.1111/ijd.12322
- By:
- Publication type:
- Article
New Territory for an Old Disease: 5-Alpha-Reductase Type 2 Deficiency in Bulgaria.
- Published in:
- Sexual Development, 2017, v. 11, n. 1, p. 21, doi. 10.1159/000454974
- By:
- Publication type:
- Article
A Novel SRY Gene Mutation p.F109L in a 46,XY Female with Complete Gonadal Dysgenesis.
- Published in:
- Sexual Development, 2016, v. 9, n. 6, p. 333, doi. 10.1159/000443807
- By:
- Publication type:
- Article
Role of the IL-6 Gene in the Etiopathogenesis of Idiopathic Scoliosis.
- Published in:
- Analytical Cellular Pathology: Cellular Oncology, 2015, v. 2015, p. 1, doi. 10.1155/2015/621893
- By:
- Publication type:
- Article
Spinal muscular atrophy with congenital bone fractures 2 caused by a rare loss‐of‐function ASCC1 gene mutation in two Bulgarian Roma patients.
- Published in:
- Clinical Genetics, 2022, v. 102, n. 1, p. 78, doi. 10.1111/cge.14130
- By:
- Publication type:
- Article
Genetically Determined TNF-α Secretion Influences the Development of Dermatomyositis and Systemic Lupus Erythematosus.
- Published in:
- Folia Medica, 2018, v. 60, n. 2, p. 216, doi. 10.1515/folmed-2017-0084
- By:
- Publication type:
- Article
IL-1RN VNTR Polymorphism in Adult Dermatomyositis and Systemic Lupus Erythematosus.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
IL-1RN VNTR Polymorphism in Adult Dermatomyositis and Systemic Lupus Erythematosus.
- Published in:
- Dermatology Research & Practice, 2014, p. 1, doi. 10.1155/2014/953597
- By:
- Publication type:
- Article
Blood Plasma Calorimetric Profiles of Women with Preeclampsia: Effect of Oxidative Stress.
- Published in:
- Antioxidants, 2023, v. 12, n. 5, p. 1032, doi. 10.3390/antiox12051032
- By:
- Publication type:
- Article
Identification of 99% of CFTR gene mutations in Bulgarian‐, Bulgarian Turk‐, and Roma cystic fibrosis patients.
- Published in:
- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 8, p. N.PAG, doi. 10.1002/mgg3.696
- By:
- Publication type:
- Article
STK11 GENE MUTATIONS AMONG PATIENTS WITH SPORADIC BREAST CANCER.
- Published in:
- Genetika (0534-0012), 2017, v. 49, n. 2, p. 399, doi. 10.2298/GENSR1702399A
- By:
- Publication type:
- Article
Intragenic Deletions in ATP7B as an Unusual Molecular Genetics Mechanism of Wilson’s Disease Pathogenesis.
- Published in:
- PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0168372
- By:
- Publication type:
- Article
CYP21A2 Intron 2 Genetic Variants Might Be Associated with the Clinical Characteristics of Women with PCOS.
- Published in:
- Biomedicines, 2024, v. 13, n. 7, p. 1528, doi. 10.3390/biomedicines12071528
- By:
- Publication type:
- Article
Epidermal growth factor receptor mutations in East European non-small cell lung cancer patients.
- Published in:
- Cellular Oncology (2211-3428), 2015, v. 38, n. 2, p. 145, doi. 10.1007/s13402-014-0211-7
- By:
- Publication type:
- Article
Investigation of predictive potential of TPH1 common polymorphism in idiopathic scoliosis.
- Published in:
- Journal of Clinical & Experimental Investigations, 2016, v. 7, n. 3, p. 216, doi. 10.5799/jcei.328607
- By:
- Publication type:
- Article
Association Study between Idiopathic Scoliosis and Polymorphic Variants of VDR, IGF-1, and AMPD1 Genes.
- Published in:
- Genetics Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/852196
- By:
- Publication type:
- Article
PNPLA3 I148M Polymorphism in Patients with Nonalcoholic Fatty Liver Disease, Obesity and Prediabetes.
- Published in:
- Journal of Gastrointestinal & Liver Diseases, 2019, v. 28, n. 4, p. 433, doi. 10.15403/jgld-506
- By:
- Publication type:
- Article
The role of IL-17 rs2275913, IL-17RC rs708567 and TGFB1 rs1800469 SNPs and IL-17A serum levels in patients with lupus nephritis.
- Published in:
- Rheumatology International, 2021, v. 41, n. 12, p. 2205, doi. 10.1007/s00296-021-04996-z
- By:
- Publication type:
- Article
Positive Association between TGFB1 Gene and Susceptibility to Idiopathic Scoliosis in Bulgarian Population.
- Published in:
- Analytical Cellular Pathology: Cellular Oncology, 2018, p. 1, doi. 10.1155/2018/6836092
- By:
- Publication type:
- Article
IL-10 A-Allele as a Biomarker for Periodontitis Severity in Bulgarian Patients.
- Published in:
- Genes, 2024, v. 15, n. 9, p. 1221, doi. 10.3390/genes15091221
- By:
- Publication type:
- Article
SSCP analysis: A blind sensitivity trial.
- Published in:
- Human Mutation, 1997, v. 10, n. 1, p. 65, doi. 10.1002/(SICI)1098-1004(1997)10:1<65::AID-HUMU9>3.0.CO;2-L
- By:
- Publication type:
- Article
Pancreatic insufficiency and pulmonary disease in German and Slavic cystic fibrosis patients with the R347P mutation.
- Published in:
- Human Mutation, 1995, v. 6, n. 3, p. 219, doi. 10.1002/humu.1380060304
- By:
- Publication type:
- Article
Androgen receptor (CAG) n polymorphism and androgen levels in women with systemic lupus erythematosus and healthy controls.
- Published in:
- Rheumatology International, 2013, v. 33, n. 8, p. 2031, doi. 10.1007/s00296-013-2687-2
- By:
- Publication type:
- Article
2176insC: A Novel Mutation in Exon 13 of the Cystic Fibrosis Gene.
- Published in:
- Human Heredity, 1996, v. 46, n. 3, p. 166, doi. 10.1159/000154346
- By:
- Publication type:
- Article
Double mutant alleles: are they rare?
- Published in:
- Human Molecular Genetics, 1995, v. 4, n. 7, p. 1169
- By:
- Publication type:
- Article
G1244V: a novel missense mutation in exon 20 of the CFTR gene in a Bulgarian cystic fibrosis patient.
- Published in:
- Human Molecular Genetics, 1994, v. 3, n. 3, p. 513
- By:
- Publication type:
- Article
Antihuman Immunodeficiency Virus Type 1 (HIV-1) Activity of Rare Earth Metal Complexes of 4-Hydroxycoumarins in Cell Culture.
- Published in:
- Bioinorganic Chemistry & Applications, 2006, p. 1, doi. 10.1155/BCA/2006/71938
- By:
- Publication type:
- Article