LAMA2 Congenital Muscle Dystrophy: A Novel Pathogenic Mutation in Bulgarian Patient

por Dimova, Ivanka, Kremensky, Ivo
Publicado 2018

Genetic analysis of haemophilia A in Bulgaria

por Petkova, Rumena, Chakarov, Stoian, Kremensky, Ivo
Publicado 2004

Association Study between Promoter Polymorphism of TPH1 and Progression of Idiopathic Scoliosis

por Yablanski, Vasil, Nikolova, Svetla, Vlaev, Evgeni, Savov, Alexey, Kremensky, Ivo
Publicado 2016

Association between Estrogen Receptor Alpha Gene Polymorphisms and Susceptibility to Idiopathic Scoliosis in Bulgarian Patients: A Case-Control Study

por Nikolova, Svetla, Yablanski, Vasil, Vlaev, Evgeni, Stokov, Luben, Savov, Alexey, Kremensky, Ivo
Publicado 2015

Association Study between Idiopathic Scoliosis and Polymorphic Variants of VDR, IGF-1, and AMPD1 Genes

por Nikolova, Svetla, Yablanski, Vasil, Vlaev, Evgeni, Stokov, Luben, Savov, Alexey Slavkov, Kremensky, Ivo Marinov
Publicado 2015

Positive Association between TGFB1 Gene and Susceptibility to Idiopathic Scoliosis in Bulgarian Population

por Nikolova, Svetla, Dikova, Milka, Dikov, Dobrin, Djerov, Assen, Savov, Alexey, Kremensky, Ivo, Loukanov, Alexandre
Publicado 2018

Role of the IL-6 Gene in the Etiopathogenesis of Idiopathic Scoliosis

por Nikolova, Svetla, Dikova, Milka, Dikov, Dobrin, Djerov, Assen, Dzhebir, Gyulnas, Atanasov, Ventseslav, Savov, Alexey, Kremensky, Ivo
Publicado 2015

In Search of Biomarkers for Idiopathic Scoliosis: Leptin and BMP4 Functional Polymorphisms

por Nikolova, Svetla, Yablanski, Vasil, Vlaev, Evgeni, Getova, Gergana, Atanasov, Ventseslav, Stokov, Luben, Savov, Alexey Slavkov, Kremensky, Ivo Marinov
Publicado 2015

Metabolite profile of a mouse model of Charcot–Marie–Tooth type 2D neuropathy: implications for disease mechanisms and interventions

por Bais, Preeti, Beebe, Kirk, Morelli, Kathryn H., Currie, Meagan E., Norberg, Sara N., Evsikov, Alexei V., Miers, Kathy E., Seburn, Kevin L., Guergueltcheva, Velina, Kremensky, Ivo, Jordanova, Albena, Bult, Carol J., Burgess, Robert W.
Publicado 2016

The Slavic NBN Founder Mutation: A Role for Reproductive Fitness?

por Seemanova, Eva, Varon, Raymonda, Vejvalka, Jan, Jarolim, Petr, Seeman, Pavel, Chrzanowska, Krystyna H., Digweed, Martin, Resnick, Igor, Kremensky, Ivo, Saar, Kathrin, Hoffmann, Katrin, Dutrannoy, Véronique, Karbasiyan, Mohsen, Ghani, Mehdi, Barić, Ivo, Tekin, Mustafa, Kovacs, Peter, Krawczak, Michael, Reis, André, Sperling, Karl, Nothnagel, Michael
Publicado 2016

Spectrum and frequencies of BRCA1/2 mutations in Bulgarian high risk breast cancer patients

por Dodova, Rumyana Ivanova, Mitkova, Atanaska Velichkova, Dacheva, Daniela Rosenova, Hadjo, Lina Basam, Vlahova, Alexandrina Ivanova, - Hadjieva, Margarita Stoyanova Taushanova, Valev, Spartak Stoyanov, Caulevska, Marija Mitko, Popova, Stanislava Dimitrova, Popov, Ivan Emilov, Dikov, Tihomir Iliichev, Sedloev, Theophil Angelov, Ionkov, Atanas Stefanov, Timcheva, Konstanta Velinova, Christova, Svetlana Liubomirova, Kremensky, Ivo Marinov, Mitev, Vanio Ivanov, Kaneva, Radka Petrova
Publicado 2015

Erratum to: Spectrum and frequencies of BRCA1/2 mutations in Bulgarian high risk breast cancer patients

por Dodova, Rumyana Ivanova, Mitkova, Atanaska Velichkova, Dacheva, Daniela Rosenova, Hadjo, Lina Basam, Vlahova, Alexandrina Ivanova, Taushanova – Hadjieva, Margarita Stoyanova, Valev, Spartak Stoyanov, Caulevska, Marija Mitko, Popova, Stanislava Dimitrova, Popov, Ivan Emilov, Dikov, Tihomir Iliichev, Sedloev, Theophil Angelov, Ionkov, Atanas Stefanov, Timcheva, Konstanta Velinova, Christova, Svetlana Liubomirova, Kremensky, Ivo Marinov, Mitev, Vanio Ivanov, Kaneva, Radka Petrova
Publicado 2017