Familial Essential Thrombocythemia Associated with MPL W515L Mutation in Father and JAK2 V617F Mutation in Daughter

Por Trifa, Adrian P., Cucuianu, Andrei, Popp, Radu A.
Publicado no Case Rep Hematol (2014)

The role of NOS2A −954G/C and vascular endothelial growth factor +936C/T polymorphisms in type 2 diabetes mellitus and diabetic nonproliferative retinopathy risk management

Por Porojan, Mihai Dumitru, Cătană, Andreea, Popp, Radu A, Dumitrascu, Dan L, Bala, Cornelia
Publicado no Ther Clin Risk Manag (2015)

Combined glutathione S transferase M1/T1 null genotypes is associated with type 2 diabetes mellitus

Por POROJAN, MIHAI D., BALA, CORNELIA, ILIES, ROXANA, CATANA, ANDREEA, POPP, RADU A., DUMITRASCU, DAN L.
Publicado no Clujul Med (2015)

Concomitant Myeloproliferative and Lymphoid Neoplasms in Two Patients Positive for JAK2 V617F Mutation. Case Report and Literature Review

Por Trifa, Adrian P., Cucuianu, Andrei, Popp, Radu A., Paţiu, Mariana, Selicean, Cristina, Militaru, Mariela S., Pop, Ioan V.
Publicado em 2013

The XRCC1 Arg194Trp polymorphism is significantly associated with lung adenocarcinoma: a case-control study in an Eastern European Caucasian group

Por Cătană, Andreea, Pop, Monica, Hincu, Bianca Domokos, Pop, Ioan V, Petrişor, Felicia M, Porojan, Mihai D, Popp, Radu A
Publicado no Onco Targets Ther (2015)

Gene variants of osteoprotegerin, estrogen-, calcitonin- and vitamin D-receptor genes and serum markers of bone metabolism in patients with Gaucher disease type 1

Por Zimmermann, Anca, Popp, Radu A, Rossmann, Heidi, Bucerzan, Simona, Nascu, Ioana, Leucuta, Daniel, Weber, Matthias M, Grigorescu-Sido, Paula
Publicado no Ther Clin Risk Manag (2018)