N. Slavevska

发表

Osteoskeletal Manifestation of Scurvy in a Male Infant (Case Report)

N. Pop-Jordanova, N. Slavevska, S. Fustić, 2008 .

Congenital erythropoietic porphyria with two mutations of the uroporphyrinogen III synthase gene (Cys73Arg, Thr228Met)

Z. Gucev, V. Tasic, N. Pop-Jordanova, 2011, Indian journal of human genetics.

Acute Gallbladder Hydrops and Arthritis: unusual initial manifestations of Wilson's Disease (WD): Case Report.

Z. Gucev, V. Tasic, N. Pop-Jordanova, 2011, Prilozi.