Unraveling the Complexity of Childhood Polycystic Kidney Disease: A Case Study of Three Sisters

por Trutin, Ivana, Oletić, Lea, Nikuševa-Martić, Tamara
Publicado 2023

Genetic and Epigenetic Features of Uveal Melanoma—An Overview and Clinical Implications

por Pašalić, Daria, Nikuševa-Martić, Tamara, Sekovanić, Ankica, Kaštelan, Snježana
Publicado 2023

THE FREQUENCY OF FOLLICLE-STIMULATING HORMONE RECEPTOR 2039A>G GENE POLYMORPHISM AND THE RISK OF MALE INFERTILITY IN ALBANIAN POPULATION

por Shkelzen, Elezaj, Paić, Frane, Stipoljev, Feodora, Gashi, Zafer, Zeqiraj, Afrim, Lila, Albert, Nikuševa Martić, Tamara
Publicado 2020

Letter to the Editor: Characterization of Choriocapillaris and Choroidal Abnormalities in Alport Syndrome

por Bosnar, Damir, Knežić Zagorec, Mira, Bušić, Mladen, Cigić, Valentina, Zagorec, Nikola, Nikuševa Martić, Tamara, Galešić Ljubanović, Danica
Publicado 2023

Frequency of loss of heterozygosity of the NF2 gene in schwannomas from Croatian patients

por Pećina-Šlaus, Nives, Zeljko, Martina, Pećina, Hrvoje Ivan, Nikuševa Martić, Tamara, Bačić, Niko, Tomas, Davor, Hrašćan, Reno
Publicado 2012

Autosomal recessive Alport syndrome caused by a novel COL4A4 splice site mutation: a case report

por Šenjug, Petar, Nikuševa Martić, Tamara, Šenjug Perica, Marija, Oroz, Maja, Horaček, Matija, Ćuk, Martin, Abdović, Slaven, Galešić Ljubanović, Danica
Publicado 2019

Aberrant expression of SFRP1, SFRP3, DVL2 and DVL3 Wnt signaling pathway components in diffuse gastric carcinoma

por Sremac, Maja, Paic, Frane, Grubelic Ravic, Katja, Serman, Ljiljana, Pavicic Dujmovic, Aja, Brcic, Iva, Krznaric, Zeljko, Nikuseva Martic, Tamara
Publicado 2021