The Burden of JAK2V617F Mutated Allele in Turkish Patients With Myeloproliferative Neoplasms

por Yonal-Hindilerden, Ipek, Daglar-Aday, Aynur, Akadam-Teker, Basak, Yilmaz, Ceylan, Nalcaci, Meliha, Yavuz, Akif Selim, Sargin, Deniz
Publicado 2015

Prognostic significance of ASXL1, JAK2V617F mutations and JAK2V617F allele burden in Philadelphia-negative myeloproliferative neoplasms

por Yonal-Hindilerden, Ipek, Daglar-Aday, Aynur, Akadam-Teker, Basak, Yilmaz, Ceylan, Nalcaci, Meliha, Yavuz, Akif Selim, Sargin, Deniz
Publicado 2015

Impact of JAK2V617F Mutational Status on Phenotypic Features in Essential Thrombocythemia and Primary Myelofibrosis

por Yönal, İpek, Dağlar-Aday, Aynur, Akadam-Teker, Başak, Yılmaz, Ceylan, Nalçacı, Meliha, Yavuz, Akif Selim, Sargın, Fatma Deniz
Publicado 2016

The Clinical Significance of IDH Mutations in Essential Thrombocythemia and Primary Myelofibrosis

por Yonal-Hindilerden, Ipek, Daglar-Aday, Aynur, Hindilerden, Fehmi, Akadam-Teker, Basak, Yilmaz, Ceylan, Nalcaci, Meliha, Yavuz, Akif Selim, Sargin, Deniz
Publicado 2016

Glycoprotein Ibα Kozak polymorphism in patients presenting with early-onset acute coronary syndrome

por Golcuk, Ebru, Yalin, Kivanc, Akdeniz, Cansu Selcan, Teker, Erhan, Teker, Başak, Hancer, Veysel Sabri, Altun, Ibrahim, Sezer, Murat, Kucukkaya, Reyhan Diz, Oncul, Aytac
Publicado 2016