Каталог "Библиографии" | Списание
Previous cardiac abnormalities in subarachnoid hemorrhage may also have background genetic polymorphisms
P. A. Atanassova
Каталог "Библиографии" | Списание
Outcome of renal transplantation in patients with non-Shiga toxin-associated hemolytic uremic syndrome: prognostic significance of genetic background
E. Bresin; R. Stefanov; et al.
Каталог "Библиографии" | Списание
MLSB genotype is predominant molecular genetic mechanism among erythromycin - resistant Streptococcus pneumoniae for the period: 2006-2008
A. Alexandrova; M. Sredkova; L. Setchanova;
I. Haydoushka;
B. Markova;
U. Proevska;
K. Bojkova;
I. Mitov
и др.
A 512
Каталог "Библиографии" | Списание
On genetic predisposition in rheumatoid arthritis - results from a family study
CD 81
Каталог "Библиографии" | Списание
MLSb genotype in predominant molecular genetic mechanism among Erythromycin - resistatnt Streptococcus pneumoniae for the period: 2006-2008
A. Alexandrova; L. Setchanova; M. Sredkova;
I. Haydoushka;
B. Markova;
U. Proevska;
K. Bojkova;
I. Mitov
и др.
A 512
Каталог "Библиографии" | Списание
Autism spectrum disorder - a complex genetic disorder
Hristo Y. Ivanov; Vili K. Stoyanova; Nikolay T. Popov;
Tihomir I. Vachev
и др.
A 3241
Каталог "Библиографии" | Списание
Rare Case of Heterozygous Microdeletion 9q21.11-q21.2: Clinical and Genetic Characteristics
HY Ivanov; V. Stoyanova; I. Ivanov;
A. Linev;
R. Vazharova;
S. Ivanov;
L. Balabanski;
D. Toncheva
и др.
Каталог "Библиографии" | Списание
International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases
K. M. Boycott; R. Stefanov; et al.
Каталог "Библиографии" | Списание
HIV-1 genetic diversity and demographic characteristics in Bulgaria
E. Billings; N. Popivanova; et al.
Каталог "Библиографии" | Списание
Rare case of a heterozygous microdeletion 9q21.11-q21.2: Clinical and genetic characteristics
A 3330b
Каталог "Библиографии" | Списание
Liquid biopsy - a sensitive tool for detecting genetic variants in solid tumors
Каталог "Библиографии" | Списание
In COVID-19, NLRP3 inflammasome genetic variants are associated with critical disease and these effects are partly mediated by the sickness symptom complex: a nomothetic network approach
Michael Maes; Walton Luiz Del Tedesco Junior; Marcell Alysson Batisti Lozovoy;
et al.
и др.
Каталог "Библиографии" | Списание
Microbiome and Genetic Factors in the Pathogenesis of Liver Diseases
Dimitrina Miteva; Monika Peshevska-Sekulovska; Violeta Snegarova;
Milena Peruhova;
Georgi H. Vasilev;
Georgi V. Vasilev;
Metodija Sekulovski;
Snezhina Lazova;
Milena Gulinac;
Latchezar Tomov;
Antoaneta Mihova;
Tsvetelina Velikova
и др.
Каталог "Библиографии" | Списание
The End or a New Era of Development of SARS-CoV-2 Virus: Genetic Variants Responsible for Severe COVID-19 and Clinical Efficacy of the Most Commonly Used Vaccines in Clinical Practice
Dimitrina Miteva; Meglena Kitanova; Hristiana Batselova;
Snezhina Lazova;
Lyubomir Chervenkov;
Monika Peshevska-Sekulovska;
Metodija Sekulovski;
Milena Gulinac;
Georgi V. Vasilev;
Luchesar Tomov;
Tsvetelina Velikova
и др.
Каталог "Библиографии" | Списание
Editorial: The UN international day of families: neurodegeneration as a result of genetic inheritance
Iliyana Hristova Pacheva; Durga Attili; Stylianos Ravanidis
Каталог "Библиографии" | Списание
A Rare Case of Pulmonary Embolism, Deep Vein Thrombosis, Bilateral Avascular Necrosis of the Femoral Head, and Miscarriage following COVID-19 in a Patient with Multiple Genetic Coagulation Factor Deficiency—A Case Report
Nevena Georgieva Ivanova