Výsledky vyhledávání - "Sukarova-Stefanovska E"

Akademický článek

Cystic fibrosis mutation spectrum in north macedonia: A step toward personalized therapy

Autor: Terzic M, Jakimovska M, Fustik S, Jakovska T, Sukarova-Stefanovska E, Plaseska-Karanfilska D

Publikováno v: Balkan Journal of Medical Genetics, Vol 22, Iss 1, Pp 35-40 (2019)

The most prevalent "rare" disease worldwide, cystic fibrosis (CF), is an autosomal recessive multisystem disease, caused by mutations in the CFTR gene. The knowledge of CFTR mutations present in certain population is important for designing a simple,

Externí odkaz: https://doaj.org/article/c5392eab85834d198b8e63ced517a705

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Akademický článek

Rapid and non Invasive Prenatal Diagnosis

Autor: Plaseska-Karanfilska Dijana, Sukarova-Stefanovska E, Kocheva S, Maleva I, Noveski P, Kiprijanovska S, Stankova K, Dimcev P, Madjunkov M, Madjunkova S

Publikováno v: Balkan Journal of Medical Genetics, Vol 15, Iss Supplement, Pp 39-43 (2012)

Externí odkaz: https://doaj.org/article/0f0edd8ebc9744a392b999e5d64cdef1

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Akademický článek

Study of the Hepatitis C Virus in the Republic of Macedonia

Autor: Plaseska-Karanfilska Dijana, Kiprijanovska S, Sukarova-Stefanovska E, Noveski P, Polenakovic M, Chalovska V

Publikováno v: Balkan Journal of Medical Genetics, Vol 15, Iss Supplement, Pp 67-69 (2012)

Hepatitis C virus (HCV) is a major public health problem. It is a leading cause of chronic liver disease and the most common indication for liver transplantation. The therapy for eradication of HCV infection is successful in only 50.0-80.0% of patien

Externí odkaz: https://doaj.org/article/9cc2294eab0749c7b3d4e71180c0a34d

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