Barić I - Search Results

1

[Congenital hyperinsulinism--novel insights into etiology, diagnosis and treatment].

Martinac I, Bogović M, Batinica S, Sarnavka V, Frković SH, Matić T, Jakić-Razumović J, Rubin O, Luetić T, Kusec V, Ramadza DP, Begović D, Benjak V, Dasović-Buljević A, Antabak A, Cavar S, Kukin D, Srsen-Medancić S, Barić I. Martinac I, et al. Among authors: baric i. Lijec Vjesn. 2012 Sep-Oct;134(9-10):286-92. Lijec Vjesn. 2012. PMID: 23297514 Review. Croatian.

2

[Vitamin B12 deficiency in children--underestimated danger in the light of new knowledge].

Juras K, Fumić K, Izaković S, Puseljić S, Culić V, Galić S, Buljević AD, Benjak V, Colić A, Frković SH, Maradin M, Sarnavka V, Bilić K, Baumgartner M, Barić I. Juras K, et al. Among authors: baric i. Lijec Vjesn. 2011 Jan-Feb;133(1-2):39-50. Lijec Vjesn. 2011. PMID: 21644278 Review. Croatian.

3

[Glutaric aciduria type 1: an example of the importance of early detection of so-called cerebral organic aciduria].

Barić I, Baraka K, Maradin M, Bartonicek D, Sarnavka V, Begović D, Fumić K. Barić I, et al. Lijec Vjesn. 2003 Nov-Dec;125(11-12):312-6. Lijec Vjesn. 2003. PMID: 15209027 Croatian.

4

Hyperinsulinism-hyperammonemia syndrome: a de novo mutation of the GLUD1 gene in twins and a review of the literature.

Ninković D, Sarnavka V, Bašnec A, Ćuk M, Ramadža DP, Fumić K, Kušec V, Santer R, Barić I. Ninković D, et al. Among authors: baric i. J Pediatr Endocrinol Metab. 2016 Sep 1;29(9):1083-8. doi: 10.1515/jpem-2016-0086. J Pediatr Endocrinol Metab. 2016. PMID: 27383869 Review.

5

[Lysosomal acid lipase deficiency in children: our experience and a novel possibility of enzyme replacement therapy].

Ramadža DP, Ćuk M, Zibar K, Barić M, Sarnavka V, Bilić K, Fumić K, Vuković J, Pušeljić S, Ćorić M, Padovan RŠ, Kralik M, Barić I. Ramadža DP, et al. Among authors: baric i, baric m. Lijec Vjesn. 2015 Mar-Apr;137(3-4):81-7. Lijec Vjesn. 2015. PMID: 26065284 Croatian.

6

The Therapeutic Hypothermia in Treatment of Hyperammonemic Encephalopathy due to Urea Cycle Disorders and Organic Acidemias.

Ninković D, Mustapić Ž, Bartoniček D, Benjak V, Ćuk M, Buljević AD, Grčić BF, Fumić K, Grizelj R, Lehman I, Ramadža DP, Sarnavka V, Slaviček J, Kastelić JS, Barišić N, Barić I. Ninković D, et al. Among authors: baric i. Klin Padiatr. 2019 Mar;231(2):74-79. doi: 10.1055/a-0855-4001. Epub 2019 Mar 14. Klin Padiatr. 2019. PMID: 30870873 English.

7

Genotype-predicted tetrahydrobiopterin (BH4)-responsiveness and molecular genetics in Croatian patients with phenylalanine hydroxylase (PAH) deficiency.

Karacić I, Meili D, Sarnavka V, Heintz C, Thöny B, Ramadza DP, Fumić K, Mardesić D, Barić I, Blau N. Karacić I, et al. Among authors: baric i. Mol Genet Metab. 2009 Jul;97(3):165-71. doi: 10.1016/j.ymgme.2009.03.009. Epub 2009 Apr 1. Mol Genet Metab. 2009. PMID: 19394257 Clinical Trial.

8

Pallister Killian syndrome: unusual significant postnatal overgrowth in a girl with otherwise typical presentation.

Frković SH, Durisević IT, Trcić RL, Sarnavka V, Gornik KC, Muzinić D, Letica L, Barić I, Begović D. Frković SH, et al. Among authors: baric i. Coll Antropol. 2010 Mar;34(1):247-50. Coll Antropol. 2010. PMID: 20437642

9

Genetic services in Croatia.

Baric I, Barisic I, Begovic D. Baric I, et al. Eur J Hum Genet. 1997;5 Suppl 2:46-50. Eur J Hum Genet. 1997. PMID: 9450195 No abstract available.

10

Molecular basis and clinical presentation of classic galactosemia in a Croatian population.

Ramadža DP, Sarnavka V, Vuković J, Fumić K, Krželj V, Lozić B, Pušeljić S, Pereira H, Silva MJ, Tavares de Almeida I, Barić I, Rivera I. Ramadža DP, et al. Among authors: baric i. J Pediatr Endocrinol Metab. 2018 Jan 26;31(1):71-75. doi: 10.1515/jpem-2017-0302. J Pediatr Endocrinol Metab. 2018. PMID: 29252199

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