Items where Author is "Barić, Ivo"

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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

Motzek, Antje and Knežević, Jelena and Switzeny, Olivier J. and Cooper, Alexis and Barić, Ivo and Belužić, Robert and Strauss, Kevin A. and Puffenberger, Erik G. and Mudd, S. Harvey and Vugrek, Oliver and Zechner, Ulrich (2016) Abnormal Hypermethylation at Imprinting Control Regions in Patients with S-Adenosylhomocysteine Hydrolase (AHCY) Deficiency. PLoS ONE, 11 (3). e0151261. ISSN 1932-6203

Cassis, Linda and Cortès-Saladelafont, Elisenda and Molero-Luis, Marta and Yubero, Delia and González, Maria Julieta and Herrero, Aida Ormazabal and Fons, Carme and Jou, Cristina and Sierra, Cristina and Castejon Ponce, Esperanza and Ramos, Federico and Armstrong, Judith and O’Callaghan, M. Mar and Casado, Mercedes and Montero, Raquel and Olivas, Silvia Maria Meavilla and Artuch, Rafael and Barić, Ivo and Bartoloni, Franco and Bellettato, Cinzia Maria and Bonifazi, Fedele and Ceci, Adriana and Cvitanović-Šojat, Ljerka and Dali, Christine I and D’Avanzo, Francesca and Fumić, Ksenija and Giannuzzi, Viviana and Lampe, Christina and Scarpa, Maurizio and Garcia-Cazorla, Ángels (2015) Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disorders. Orphanet Journal of Rare Diseases, 10. p. 164. ISSN 1750-1172

Haack, Tobias B. and Staufner, Christian and Köpke, Marlies G. and Straub, Beate K. and Kölker, Stefan and Thiel, Christian and Freisinger, Peter and Barić, Ivo and McKiernan, Patrick J. and Dikow, Nicola and Harting, Inga and Beisse, Flemming and Burgard, Peter and Kotzaeridou, Urania and Kühr, Joachim and Himbert, Urban and Taylor, Robert W. and Distelmaier, Felix and Vockley, Jerry and Ghaloul-Gonzalez, Lina and Zschocke, Johannes and Kremer, Laura S. and Graf, Elisabeth and Schwarzmayr, Thomas and Bader, Daniel M. and Gagneur, Julien and Wieland, Thomas and Terrile, Caterina and Strom, Tim M. and Meitinger, Thomas and Hoffmann, Georg F. and Prokisch, Holger (2015) Biallelic mutations in NBAS cause recurrent acute liver failure with onset in infancy. American Journal of Human Genetics, 97 (1). pp. 163-9. ISSN 0002-9297

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)

This list was generated on Fri Jun 22 03:29:30 2018 CEST.