Case Report: Difficulties in the Treatment of a 12-Year-Old Patient With Homozygous Familial Hypercholesterolemia, Compound Heterozygous Form - 5 Years Follow-Up von Vladimirova-Kitova, Lyudmila, Kitov, Spas, Ganev, Mihail, Chochkova-Bukova, Lubov

Volltext

Detection of pathogenic variants in Alzheimer's disease related genes in Bulgarian patients by pooled whole-exome sequencing von Karachanak-Yankova, Sena, Serbezov, Dimitar, Mihaylova, Marta, Nikolova, Dragomira, Balabanski, Lubomir, Damyanova, Vera, Antonova, Olga, Staneva, Rada, Ganev, Mihail, Spasova, Victoria, Rukova, Blaga, Nesheva, Desislava, Josifovska, Slavica, Stancheva, Mikaela, Belejanska, Diana, Petrova, Mariya, Mehrabian, Shima, Traykov, Latchezar, Hadjidekova, Savina, Toncheva, Draga

Volltext

Prioritization of genetic variants predisposing to coronary heart disease in the Bulgarian population using centenarian exomes von Ganev, Mihail, Balabanski, Lubomir, Serbezov, Dimitar, Karachanak-Yankova, Sena, Vazharova, Radoslava, Nesheva, Desislava, Hammoudeh, Zora, Nikolova, Dragomira, Antonova, Olga, Staneva, Rada, Mihaylova, Marta, Damyanova, Vera, Hadjidekova, Savina, Toncheva, Draga

Volltext

Clinical impact of copy number variation changes in bladder cancer samples von Spasova, Victoria, Mladenov, Boris, Rangelov, Simeon, Hammoudeh, Zora, Nesheva, Desislava, Serbezov, Dimitar, Staneva, Rada, Hadjidekova, Savina, Ganev, Mihail, Balabanski, Lubomir, Vazharova, Radoslava, Slavov, Chavdar, Toncheva, Draga, Antonova, Olga

Volltext