Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Goran Krakar"'
Autor:
Ivana Đaković, Ivica Kostović, Katarina Vulin, Iva Prvčić, Goran Tešović, Goran Krakar, Tomislav Gojmerac, Jadranka Sekelj Fureš, Vlatka Mejaški Bošnjak
Publikováno v:
Journal of International Medical Research, Vol 52 (2024)
Objective Congenital cytomegalovirus infection (cCMV) is a common, frequently unrecognized cause of childhood disability. The aim of the present study was to determine the symptoms that raise the suspicion of cCMV, define the neurodevelopmental outco
Externí odkaz:
https://doaj.org/article/7422bbcab720407fb8a1ea26ae10e46e
Autor:
Goran Krakar, M Meštrović, Sanja Delin, Filip Sabol, Z. Sabol, Goran Tešović, Vlasta Đuranović, I Mrkić Kobal, R. Gjergja Juraški, Kovač Šižgorić, Svjetlana Bela Klancir
Publikováno v:
Abstracts.
Autor:
Sanja Delin, Vlasta Đuranović, Goran Krakar, S Bela Klancir, M Meštrović, I Mrkić Kobal, Goran Tešović, R. Gjergja Juraški, Z. Sabol, Filip Sabol, M Kovač Šižgorić
Publikováno v:
Abstracts.
Autor:
Kristina Gotovac Jercic, Fran Borovečki, Goran Krakar, Sanja Delin, Vlasta Duranovic, Tamara Zigman
Publikováno v:
Molecular and Experimental Biology in Medicine
Volume 2
Issue 2
Volume 2
Issue 2
Neurofibromatosis type 1 (NF1) is the most common autosomal dominant neurocutaneous syndrome with the estimated prevalence ranging from 1 in 3000 to 1 in 4000 individuals and wide phenotypical variability. NF1 is caused by autosomal dominant heterozy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b83ed5342e28de8f40b82c0097e44d5
https://doi.org/10.33602/mebm.2.2.4
https://doi.org/10.33602/mebm.2.2.4
Publikováno v:
Paediatria Croatica
Volume 58
Issue 4
Volume 58
Issue 4
Miotonička distrofi ja ili Steinertova bolest druga je po učestalosti mišićna distrofi ja u djetinjstvu, odmah nakon progresivnih mišić- nih distrofi ja (Duchenne i Becker). Incidencija u općoj populaciji iznosi 1:8000 u Europi, 1:30000 u Hrva
Autor:
Goran Krakar, Ozren Polasek, Inga Patarčić, Ivana Kolcic, Andrea Gelemanović, Katie Dobberpuhl
Publikováno v:
Croatian Medical Journal
Volume 57
Issue 4
Volume 57
Issue 4
Aim To summarize available evidence on the role of host genetics in the susceptibility to congenital and childhood cytomegalovirus (CMV) infections by conducting a systematic review of published studies. Methods We searched online databases (PubMed,
Publikováno v:
Braindevelopment. 39(1)
Muscular hypertrophy secondary to denervation is very rare, but well-documented phenomena in adults. This is the first report of a child with neurogenic unilateral hypertrophy due to S1 radiculopathy. A 12-year-old girl presented with left calf hyper
Publikováno v:
Journal of child neurology. 30(1)
Congenital cytomegalovirus infection is the most common infectious cause of congenital brain injury. Type and severity of congenital cytomegalovirus infection–related brain abnormalities depend on the developmental stage of the central nervous syst
Autor:
Maša Malenica, Monika Kukuruzović, Suzana Bitanga, Goran Krakar, Bernardica Valent, Ljerka Cvitanović-Šojat
Publikováno v:
Paediatria Croatica
Volume 58
Issue 4
Volume 58
Issue 4
Friedreich’s ataxia is an autosomal recessive disease and the most frequent inherited ataxia. The disease is characterized by expression of the unstable GAA trinucleotide repeat expansion located in the fi rst intron of the FXN gene on chromosome 9
Autor:
Ljerka Cvitanović-Šojat, Goran Krakar, Monika Kukuruzović, Suzana Bitanga, Maša Malenica, Bernardica Valent
Friedreich’s ataxia is an autosomal recessive disease and the most frequent inherited ataxia. The disease is characterized by expression of the unstable GAA trinucleotide repeat expansion located in the fi rst intron of the FXN gene on chromosome 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95fde7c2d7eaf2ba222042853b1281fa
https://doi.org/10.13112/pc.2014.51
https://doi.org/10.13112/pc.2014.51