pid,type,title,authors,mentors,source_title,published_date,url,doi,isbn,issn,eissn
mef:6927,thesis,"Klinička, neuroslikovna i genetička obilježja pacijenata sa sindromom Leigh","Miljanić, Klara",,,,,,,,
mef:6786,thesis,"Metaboličke miopatije","Bukovac, Antonia",,,,,,,,
mef:6762,thesis,"Fenilketonurija i trudnoća","Benčić, Jelena",,,,,,,,
mef:6773,thesis,"Poremećaj metabolizma purina i pirimidina u djece","Bobek, Klara",,,,,,,,
mef:6942,"journal article","Genotype–phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder","D’Onofrio, Gianluca; Accogli, Andrea; Severino, Mariasavina; Caliskan, Haluk; Kokotović, Tomislav; Blažeković, Antonela; Gotovac Jerčić, Kristina; Markovic, Silvana; Žigman, Tamara; Goran, Krnjak; Barišić, Nina; Duranovic, Vlasta; Ban, Ana; Borovečki, Fran; Petković Ramadža, Danijela; Barić, Ivo; Fazeli, Walid; Herkenrath, Peter; Marini, Carla; Vittorini, Roberta; Gowda, Vykuntaraju; Bouman, Arjan; Rocca, Clarissa; Alkhawaja, Issam Azmi; Murtaza, Bibi Nazia; Rehman, Malik Mujaddad Ur; Al Alam, Chadi; Nader, Gisele; Mancardi, Maria Margherita; Giacomini, Thea; Srivastava, Siddharth; Alvi, Javeria Raza; Tomoum, Hoda; Matricardi, Sara; Iacomino, Michele; Riva, Antonella; Scala, Marcello; Madia, Francesca; Pistorio, Angela; Salpietro, Vincenzo; Minetti, Carlo; Rivière, Jean-Baptiste; Srour, Myriam; Efthymiou, Stephanie; Maroofian, Reza; Houlden, Henry; Vernes, Sonja Catherine; Zara, Federico; Striano, Pasquale; Nagy, Vanja",,,,,,,,
mef:5274,thesis,"Prirođeni poremećaji glikozilacije","Pintarić, Martina",,,,,,,,
mef:5141,thesis,"Hipofosfatemični rahitis u djece","Ivanković, Katarina",,,,,,,,
mef:4959,"journal article","Case Report: Advanced Skeletal Muscle Imaging in S-Adenosylhomocysteine Hydrolase Deficiency and Further Insight Into Muscle Pathology","Petković Ramadža, Danijela; Kuhtić, Ivana; Žarković, Kamelija; Lochmüller, Hanns; Čavka, Mislav; Kovač, Ida; Barić, Ivo; Prutki, Maja",,,,,,,,
mef:4348,thesis,"Hipotonično dojenče","Podvorec, Doria",,,,,,,,
mef:3947,thesis,"Kvaliteta života pacijenata s fenilketonurijom u Hrvatskoj","Alaber, Maja",,,,,,,,
mef:4138,thesis,"Porodična hiperkolesterolemija u djece","Jelovčić, Fabijan",,,,,,,,
mef:3803,"journal article","Inborn Errors of Metabolism Associated With Autism Spectrum Disorders: Approaches to Intervention","Žigman, Tamara; Petković Ramadža, Danijela; Šimić, Goran; Barić, Ivo",,,,,,,,
mef:3615,thesis,"Hipofosfatazija u djece","Smajo, Ana",,,,,,,,
mef:8771,"journal article","Kardiomiopatije u djece - Današnja stajališta i naša iskustva Hrvatska retrospektivna epidemiološka studija 1988. - 2016. ","Malčić, Ivan; Belina, Dražen; Slišković, Anamarija; Bartoniček, Dorotea; Jelušić, Marija; Šarić, Dalibor; Petković Ramadža, Danijela; Lehman, Ivan; Jelašić, Dražen; Ferek-Petrić, Božidar; Kifer, Domagoj; Anić, Darko",,,,,,,,
mef:6127,dissertation,"Nedostatna aktivnost S-adenozilhomocistein hidrolaze i omjer S-adenozilmetionina i S-adenozilhomocisteina u osoba s trajno povišenom aktivnošću kreatin kinaze ","Petković Ramadža, Danijela",,,,,,,,
mef:8700,"journal article","A novel PGAP3 mutation in a Croatian boy with brachytelephalangy and a thin corpus callosum","Sakaguchi, Tomohiro; Žigman, Tamara; Petković Ramadža, Danijela; Omerza, Lana; Pušeljić, Silvija; Ereš Hrvaćanin, Zrinka; Miyake, Noriko; Matsumoto, Naomichi; Barić, Ivo",,,,,,,,
kbco:286,"journal article","A Novel PGAP3 Mutation in a Croatian boy with Brachytelephalangy and a Thin Corpus Callosum","Sakaguchi, Tomohiro; Žigman, Tamara; Petković Ramadža, Danijela; Omerza, Lana; Pušeljić, Silvija; Ereš Hrvaćanin, Zrinka; Miyake, Noriko; Matsumoto, Naomichi; Barić, Ivo",,,,,,,,
mef:8197,"journal article","Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders","Barić, Ivo; Staufner, Christian; Augoustides-Savvopoulou, Persephone; Chien, Yin-Hsiu; Dobbelaere, Dries; Grünert, Sarah C.; Opladen, Thomas; Petković Ramadža, Danijela; Rakić, Bojana; Wedell, Anna; Blom, Henk J.",,,,,,,,
mef:8459,"journal article","Manjak lizosomske kisele lipaze u djece: vlastita iskustva i nova mogućnost enzimskoga nadomjesnog liječenja ","Petković Ramadža, Danijela; Ćuk, Mario; Zibar, Karin; Barić, Marina; Sarnavka, Vladimir; Bilić, Karmen; Fumić, Ksenija; Vuković, Jurica; Pušeljić, Silvija; Ćorić, Marijana; Štern Padovan, Ranka; Kralik, Marko; Barić, Ivo",,,,,,,,
kbco:289,"journal article","Manjak lizosomske kisele lipaze u djece: vlastita iskustva i nova mogućnost enzimskoga nadomjesnog liječenja","Ramandža Petković, Danijela; Ćuk, Mario; Zibar, Karin; Barić, Marina; Sarnavka, Vladimir; Bilić, Karmen; Fumić, Ksenija; Vuković, Jurica; Pušeljić, Silvija; Ćorić, Marijana; Padovan Štern, Ranka; Kralik, Marko; Barać, Ivo",,,,,,,,
mef:7763,"journal article","Kongenitalni hiperinzulinizam - novosti o nastanku, dijagnosticiranju i liječenju bolesti ","Martinac, Iva; Bogović, Marko; Batinica, Stipe; Sarnavka, Vladimir; Huljev Frković, Sanda; Matić, Toni; Jakić-Razumović, Jasminka; Rubin, Otmar; Luetić, Tomislav; Kušec, Vesna; Petković Ramadža, Danijela; Begović, Davor; Benjak, Vesna; Dasović-Buljević, Andrea; Antabak, Anko; Ćavar, Stanko; Kukin, Dijana; Sršen-Medančić, Suzana; Barić, Ivo",,,,,,,,
mef:9225,"journal article","Hypophosphatasia: phenotypic variability and possible Croatian origin of the c.1402g>A mutation of TNSALP gene","Petković Ramadža, Danijela; Stipoljev, Feodora; Sarnavka, Vladimir; Begović, Davor; Potočki, Kristina; Fumić, Ksenija; Mornet, Etienne; Barić, Ivo",,,,,,,,