Numerical Algorithms for Estimating Probability Density Function Based on the Maximum Entropy Principle and Fup Basis Functions

por Brajčić Kurbaša, Nives, Gotovac, Blaž, Kozulić, Vedrana, Gotovac, Hrvoje
Publicado 2021

Simulation-Based Performance Analysis of the ALICE Mass Storage System

por Vickovic, L, Gotovac, S, Celar, S
Publicado 2016

Software-Defined Storage Optimization of Distributed ALICE Resources

por Lončar, Petra, Gotovac, Sven
Publicado 2020

SNCA 3′ UTR Genetic Variants in Patients with Parkinson’s Disease

por Blažeković, Antonela, Jerčić, Kristina Gotovac, Borovečki, Fran
Publicado 2021

Criteria and Procedures for Breast Conserving Surgery

por Fajdic, Josip, Djurovic, Drazen, Gotovac, Nikola, Hrgovic, Zlatko
Publicado 2013

SUN-LB14 Trans and Non-Binary Youth Accessing Gender Affirming Medical Care in Canada: New Research From the Trans Youth CAN!

por Mokashi, Arati, Lawson, Margaret L, Gotovac, Sandra, Bauer, Greta R
Publicado 2020

A first report of a rare TP53 variant associated with Li-Fraumeni syndrome manifesting as invasive breast cancer and malignant solitary fibrous tumor

por Prejac, Juraj, Dedić Plavetić, Natalija, Gotovac Jerčić, Kristina, Borovečki, Fran
Publicado 2021

Genetic changes observed in a case of adult pilocytic astrocytoma revealed by array CGH analysis

por Pećina-Šlaus, Nives, Gotovac, Kristina, Kafka, Anja, Tomas, Davor, Borovečki, Fran
Publicado 2014

Congenital factor XI deficiency caused by a novel F11 missense variant: a case report

por Gotovac Jerčić, Kristina, Blažeković, Antonela, Hančević, Mirea, Bilić, Ervina, Borovečki, Fran
Publicado 2020

Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex

por Rincic, Martina, Rados, Milan, Krsnik, Zeljka, Gotovac, Kristina, Borovecki, Fran, Liehr, Thomas, Brecevic, Lukrecija
Publicado 2016

Traumatic Optic Neuropathy – Case Report with Discussion on Diagnostic Procedures and Therapy

por Kaštelan, Snježana, Gverović Antunica, Antonela, Salopek Rabatić, Jasminka, Gotovac, Marta, Orešković, Darko, Kasun, Boris
Publicado 2018

Clavicular cortical hyperostosis: new autoinflammatory entity or part of the juvenile spondyloarthropathies clinical picture?

por Lamot, L, Bukovac, LT, Borovecki, F, Vlahovicek, K, Sumic, S, Gotovac, K, Bingula, F, Harjacek, M
Publicado 2011

PReS-FINAL-2151: HLA B27/B7, TLR-4, NLRP3, CXCR4 AND PTPN12: the shared genetic master-key genes leading to development of undifferentiated spondyloarthritis/era in children

por Lamot, L, Vidović, M, Tambić Bukovac, L, Borovečki, F, Gotovac, K, Bingula, F, Harjaček, M
Publicado 2013

Potential biomarkers and therapeutic targets in juvenile spondyloarthritis patients

por Lamot, Lovro, Vidović, Mandica, Perica, Marija, Bukovac, Lana Tambić, Gotovac, Kristina, Borovečki, Fran, Harjaček, Miroslav
Publicado 2014

Aberrant Expression of Shared Master-Key Genes Contributes to the Immunopathogenesis in Patients with Juvenile Spondyloarthritis

por Lamot, Lovro, Borovecki, Fran, Tambic Bukovac, Lana, Vidovic, Mandica, Perica, Marija, Gotovac, Kristina, Harjacek, Miroslav
Publicado 2014

Genome-Wide Expression Profile in People with Optic Neuritis Associated with Multiple Sclerosis

por Habek, Mario, Blazekovic, Antonela, Gotovac Jercic, Kristina, Pivac, Nela, Outero, Tiago Fleming, Borovecki, Fran, Brinar, Vesna
Publicado 2023

Comparable Genomic Copy Number Aberrations Differ across Astrocytoma Malignancy Grades

por Pećina-Šlaus, Nives, Kafka, Anja, Gotovac Jerčić, Kristina, Logara, Monika, Bukovac, Anja, Bakarić, Robert, Borovečki, Fran
Publicado 2019

The prevalence and genotype of 21-hydroxylase deficiency in the Croatian Romani population

por Dumic, Katja K., Grubic, Zorana, Kusec, Vesna, Braovac, Duje, Gotovac, Kristina, Vinkovic, Maja, Vucinic, Maja, Dumic, Miroslav
Publicado 2023

Vagus nerve stimulation in Lafora body disease()

por Hajnsek, Sanja, Petelin Gadze, Zeljka, Borovecki, Fran, Nankovic, Sibila, Mrak, Goran, Gotovac, Kristina, Sulentic, Vlatko, Kovacevic, Ivana, Bujan Kovac, Andreja
Publicado 2013

Clinical and pathohistological characteristics of Alport spectrum disorder caused by COL4A4 mutation c.193-2A>C: a case series

por Šenjug, Petar, Nikuševa, Tamara, Martić, Šenjug Perica, Marija, Oroz, Maja, Horaček, Matija, Gotovac, Kristina, Jerčić, Galešić, Krešimir, Galešić, Danica, Ljubanović
Publicado 2021