Items where Author is "Barić, Ivo"
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Number of items: 5.
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]. Lijec̆nic̆ki vjesnik, 134 (9-10). pp. 286-92. ISSN 0024-3477
Muačević-Katanec, Diana and Kekez, Tihomir and Fumić, Ksenija and Barić, Ivo and Merkler, Marijan and Jakić-Razumović, Jasminka and Krznarić, Željko and Zadro, Renata and Katanec, Davor and Reiner, Željko (2011) Spontaneous perforation of the small intestine, a novel manifestation of classical homocystinuria in an adult with new cystathionine beta-synthetase gene mutations. Collegium Antropologicum, 35 (1). pp. 181-5. ISSN 0350-6134
Huljev Frković, Sanda and Tonković Đurišević, Ivana and Lasan Trčić, Ružica and Sarnavka, Vladimir and Crkvenac Gornik, Kristina and Mužinić, Dubravka and Letica, Ljiljana and Barić, Ivo and Begović, Davor (2010) Pallister Killian syndrome: unusual significant postnatal overgrowth in a girl with otherwise typical presentation. Collegium Antropologicum, 34 (1). pp. 247-50. ISSN 0350-6134
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. Collegium Antropologicum, 33 (4). pp. 1255-8. ISSN 0350-6134
Maradin, Miljenka and Fumić, Ksenija and Hansikova, H. and Tesarova, M. and Wenchich, L. and Dorner, Sanja and Sarnavka, Vladimir and Zeman, J. and Barić, Ivo (2006) Fumaric aciduria: Mild phenotype in a 8-year-old girl with novel mutations. Journal of Inherited Metabolic Disease, 29 (5). p. 683. ISSN 0141-8955 (Print) 1573-2665 (Electronic)