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Malčić, Ivan and Belina, Dražen and Slišković, Anamarija and Bartoniček, Dorotea and Jelušić, Marija and Šarić, Dalibor and Petković Ramadža, Danijela and Lehman, Ivan and Jelašić, Dražen and Ferek-Petrić, Božidar and Kifer, Domagoj and Anić, Darko (2019) Kardiomiopatije u djece - Današnja stajališta i naša iskustva Hrvatska retrospektivna epidemiološka studija 1988. - 2016. [Cardiomyopathies in children - Current opinions and our experiences Croatian retrospective epidemiological study 1988-2016]. Liječnički vjesnik, 141 (3-4). pp. 68-80. ISSN 0024-3477
Sakaguchi, Tomohiro and Žigman, Tamara and Petković Ramadža, Danijela and Omerza, Lana and Pušeljić, Silvija and Ereš Hrvaćanin, Zrinka and Miyake, Noriko and Matsumoto, Naomichi and Barić, Ivo (2018) A novel PGAP3 mutation in a Croatian boy with brachytelephalangy and a thin corpus callosum. Human Genome Variation, 5. ISSN 2054-345X
Barić, Ivo and Staufner, Christian and Augoustides-Savvopoulou, Persephone and Chien, Yin-Hsiu and Dobbelaere, Dries and Grünert, Sarah C. and Opladen, Thomas and Petković Ramadža, Danijela and Rakić, Bojana and Wedell, Anna and Blom, Henk J. (2017) Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders. Journal of Inherited Metabolic Disease, 40 (1). pp. 5-20. ISSN 0141-8955
Petković Ramadža, Danijela and Ćuk, Mario and Zibar, Karin and Barić, Marina and Sarnavka, Vladimir and Bilić, Karmen and Fumić, Ksenija and Vuković, Jurica and Pušeljić, Silvija and Ćorić, Marijana and Štern Padovan, Ranka and Kralik, Marko and Barić, Ivo (2015) Manjak lizosomske kisele lipaze u djece: vlastita iskustva i nova mogućnost enzimskoga nadomjesnog liječenja [Lysosomal acid lipase deficiency in children: our experience and a novel possibility of enzyme replacement therapy]. Liječnički vjesnik, 137 (3-4). pp. 81-87. ISSN 0024-3477
Martinac, Iva and Bogović, Marko and Batinica, Stipe and Sarnavka, Vladimir and Huljev Frković, Sanda and Matić, Toni and Jakić-Razumović, Jasminka and Rubin, Otmar and Luetić, Tomislav and Kušec, Vesna and Petković Ramadža, Danijela and Begović, Davor and Benjak, Vesna and Dasović-Buljević, Andrea and Antabak, Anko and Ćavar, Stanko and Kukin, Dijana and Sršen-Medančić, Suzana and Barić, Ivo (2012) Kongenitalni hiperinzulinizam - novosti o nastanku, dijagnosticiranju i liječenju bolesti [Congenital hyperinsulinism - novel insights into etiology, diagnosis and treatment]. Liječnički vjesnik, 134 (9-10). pp. 286-292. ISSN 0024-3477
Petković Ramadža, Danijela and Stipoljev, Feodora and Sarnavka, Vladimir and Begović, Davor and Potočki, Kristina and Fumić, Ksenija and Mornet, Etienne and Barić, Ivo (2009) Hypophosphatasia: phenotypic variability and possible Croatian origin of the c.1402g>A mutation of TNSALP gene [Hipofosfatazija: fenotipska varijabilnost i moguće hrvatsko podrijetlo c.1402g>a mutacije TNSLAP gena]. Collegium Antropologicum, 33 (4). pp. 1255-8. ISSN 0350-6134
Petković Ramadža, Danijela (2018) Nedostatna aktivnost S-adenozilhomocistein hidrolaze i omjer S-adenozilmetionina i S-adenozilhomocisteina u osoba s trajno povišenom aktivnošću kreatin kinaze [S-adenosylhomocysteine hydrolase deficiency and the ratio S-adenosylmethionine/S-adenosylhomocysteine in patients with persistently increased activity of creatine kinase]. PhD thesis, Sveučilište u Zagrebu.
