| Inborn errors of metabolism associated with autism spectrum disorders: approaches to intervention T Žigman, D Petković Ramadža, G Šimić, I Barić Frontiers in Neuroscience 15, 673600, 2021 | 45 | 2021 |
| Postnatal evaluation and outcome of infants with antenatal hydronephrosis B Valent-Morić, T Žigman, M Ćuk, O Žaja-Franulović, M Malenica Acta Clin Croat 50 (4), 451-5, 2011 | 23 | 2011 |
| A novel PGAP3 mutation in a Croatian boy with brachytelephalangy and a thin corpus callosum T Sakaguchi, T Žigman, D Petković Ramadža, L Omerza, S Pušeljić, ... Human genome variation 5 (1), 1-4, 2018 | 19 | 2018 |
| The importance of ambulatory blood pressure monitoring in children and adolescents B Valent-Morić, T Žigman, O Žaja-Franulović, M Malenica, M Ćuk Acta clinica Croatica 51 (1), 59-63, 2012 | 15 | 2012 |
| Early initiation of ambroxol treatment diminishes neurological manifestations of type 3 Gaucher disease: A long-term outcome of two siblings DP Ramadža, M Zekušić, T Žigman, A Škaričić, A Bogdanić, G Mustać, ... European journal of paediatric neurology 32, 66-72, 2021 | 13 | 2021 |
| PROGRAM PROŠIRENOG NOVOROĐENAČKOG PROBIRA U REPUBLICI HRVATSKOJ-ZAHTJEVI I IZAZOVI PRAVILNOG UZIMANJA SUHE KAPI KRVI. I Bilandžija, I Barić, A Škaričić, M Zekušić, I Križić, DP RAMADŽA, ... Paediatria Croatica, Supplement 62, 2018 | 12 | 2018 |
| Smjernice za genetičko savjetovanje i testiranje na nasljedni rak dojke i jajnika A Borovečki, M Braš, B Brkljačić, N Canki-Klain, N Dedić Plavetić, ... Liječnički vjesnik 139 (5-6), 0-0, 2017 | 12 | 2017 |
| Bakterijske spolno prenosive bolesti kao čimbenik u nastanku raka vrata maternice: suvremeni terapijski pristupi V Škerk, T Žigman Medicus 15 (2_UG infekcije), 309-316, 2006 | 10 | 2006 |
| Metabolic follow-up of a Croatian patient with gyrate atrophy and a new mutation in the OAT gene: a case report M Zekušić, A Škaričić, K Fumić, D Rogić, T Žigman, D Petković Ramadža, ... Biochemia medica 28 (3), 514-522, 2018 | 8 | 2018 |
| A biallelic loss-of-function variant in MYZAP is associated with a recessive form of severe dilated cardiomyopathy A Maver, T Žigman, AY Rangrez, M Ćorić, J Homolak, D Šarić, I Škifić, ... Molecular Case Studies 8 (5), a006221, 2022 | 5 | 2022 |
| KARDIOMIOPATIJE ZBOG NASLJEDNIH METABOLIČKIH BOLESTI-STARI I NOVI IZAZOVI. IVO BARIĆ, T ŽIGMAN, DP RAMADŽA Paediatria Croatica, Supplement 61, 2017 | 5 | 2017 |
| Defining health-related quality of life in localized and advanced stages of breast cancer–the first step towards hereditary cancer genetic counseling T Žigman, I Lukša, G Mihaljević, M Žarković, I Kirac, DV Vrdoljak, ... Acta Clinica Croatica 59 (2), 209, 2020 | 3 | 2020 |
| Hypogammaglobulinemia and imaging features in a patient with infantile free sialic acid storage disease (ISSD) and a novel mutation in the SLC17A5 gene T Žigman, D Petković Ramadža, M Lušić, M Zekušić, D Ninković, ... Journal of Pediatric Endocrinology and Metabolism 31 (10), 1155-1159, 2018 | 3 | 2018 |
| GPI‐anchoring disorders and the heart: Is cardiomyopathy an overlooked feature? A Bayat, T Lindau, A Aledo‐Serrano, A Gil‐Nagel, I Barić, D Bartoniček, ... Clinical Genetics 104 (5), 598-603, 2023 | 2 | 2023 |
| Abnormal concentrations of acetylated amino acids in cerebrospinal fluid in acetyl‐CoA transporter deficiency K Šikić, TMA Peters, E Marušić, IČ Čagalj, DP Ramadža, T Žigman, ... Journal of inherited metabolic disease 45 (6), 1048-1058, 2022 | 2 | 2022 |
| Definiranje kvalitete života kod bolesnica s lokaliziranim i uznapredovalim stadijem raka dojke-prvi korak prema onkološkom genetskom savjetovanju T Žigman, I Lukša, G Mihaljević, M Žarković, I Kirac, DV Vrdoljak, ... Acta clinica Croatica 59 (2.), 209-215, 2020 | 2 | 2020 |
| Hrvatske smjernice za genetičko savjetovanje i testiranje na nasljedni rak dojke i jajnika B Brkljačić, N Dedić Plavetić, H Haller, S Levanat, P Podolski, L Šerman, ... | 2 | 2016 |
| Niemann-Pick disease type C: mutations of NPC1 gene and the course of disease L Cvitanović-Šojat, M Malenica, K mONIKA, T Žigman, K Kužnik, A Bielen Paediatria Croatica 58 (4), 255-260, 2014 | 2 | 2014 |
| ATP synthase deficiency due to m. 8528T> C mutation–a novel cause of severe neonatal hyperammonemia requiring hemodialysis T Žigman, K Šikić, D Petković Ramadža, J Mayr, S Wortmann, H Prokisch, ... Journal of Pediatric Endocrinology and Metabolism 34 (3), 389-393, 2021 | 1 | 2021 |
| Dihydrolipoamide dehydrogenase deficiency presenting as fulminant hepatic and multi-organ failure with lethal outcome despite successful liver transplantation DP Ramadža, M Mihaljević, T Žigman, I Rako, S Galić, T Matić, F Rubić, ... ICIEM 2021, Sidney, Australia, 2021 | 1 | 2021 |
Ivo BarićProfesor medicine, Medicinski fakultet, Sveučilište u ZagrebuVerified email at kbc-zagreb.hr
