Научни изследвания


Научен фонд на Медицински университет - София

Molecular characteristics of autosomal recessive forms of hereditary spastic paraplegy in Bulgaria.M. Иванова2004-2005
Association study for the role of polymorphisms in vitamin D and estrogen receptor type alpha-genes in patients with colorectal carcinom.T. Кадийска2004-2005
Genetic defects in muscular dystrophy type 2A (LGMD2A) in Bulgaria.A. Тодорова2004-2005
Fine mapping of 4p16 locus linked with a bipolar affective disorder in Bulgarian familyР. Кънева2004-2005
Finding the gene for CMT2D neuropathyПроф. И. Кременски2003-2004
550delA CAPN3 gene mutation in Bulgarian patients with LGMD2A.Б. Георгиева2003-2004
Phenotypic characterization and genetic linkage analysis in Bulgarian pedigree with autosoma-dominant proximal spinal muscular atrophyA. Йорданова2002
Molecular diagnostics of autosomal-dominant forms of Hereditary Spastic ParaplegiaПроф. В. Георгиева2002-2003
Linkage analysis on chromosome 21q22 in patients with Bipolar Affective Disorder in Bulgarian FamiliesР. Кънева2001
Limb-girdle muscular dystrophy 2C among Gypsy minority in Bulgaria. Screening for heterozygosity of C283Y mutation in gamma-sarcoglycan gene.A. Тодорова2001-2002
DNA analysis for prenatal and postnatal diagnostics of the two most common human aneuploidies (Down syndrome and Edwards syndrome)Б. Захарова2001
Phenotypic characterisation and genetic analysis of a large Bulgarian pedigree, presenting a rare form of Charcot-Marie-Tooth disease type IIA. Йорданова2001
Microsatellite instability analysis in Bulgarian patients with Colorectal CancerA. Савов2001
Molecular characterisation of patients with Charcot-Marie-Tooth disease in BulgariaA. Йорданова2000
Further investigation of the role of genetic factors on disease progression in HIV-1 infected Bulgarian individualsА. Савов2000
Investigation of the frequency of genetically defined resistance to HIV-1 infection in the Bulgarian populationA Savov1999
Molecular Characteristics of the Wilson diseaseA. Савов1998
Diagnostics of inborn metabolic disorders in the neonatal periodПроф. И. Кременски1997
Clinical and microbiological methods in the diagnostics and treatment of bacterial vaginosesПроф. И. Кременски1996
Molecular Characteristics and genotype-phenotype correlation in patients with cystic fibrosis in BulgariaПроф. T. Симеонова1996
Investigation of allele frequencies of DQB1 gene in patients with Diabetes MellitusПроф. И. Кременски1995