Baric I - Search Results

1

Genotype-phenotype correlation in 44 Czech, Slovak, Croatian and Serbian patients with mucopolysaccharidosis type II.

Dvorakova L, Vlaskova H, Sarajlija A, Ramadza DP, Poupetova H, Hruba E, Hlavata A, Bzduch V, Peskova K, Storkanova G, Kecman B, Djordjevic M, Baric I, Fumic K, Barisic I, Reboun M, Kulhanek J, Zeman J, Magner M. Dvorakova L, et al. Among authors: baric i. Clin Genet. 2017 May;91(5):787-796. doi: 10.1111/cge.12927. Epub 2017 Mar 17. Clin Genet. 2017. PMID: 27883178

2

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.

3

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

4

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.

5

Studies of S-adenosylhomocysteine-hydrolase polymorphism in a Croatian population.

Kloor D, Fumic K, Attig S, Tete M, Osswald H, Baric I, Tomiuk J, Kömpf J. Kloor D, et al. Among authors: baric i. J Hum Genet. 2006;51(1):21-24. doi: 10.1007/s10038-005-0315-z. Epub 2005 Nov 5. J Hum Genet. 2006. PMID: 16273424

6

Clinical picture of S-adenosylhomocysteine hydrolase deficiency resembles phosphomannomutase 2 deficiency.

Honzík T, Magner M, Krijt J, Sokolová J, Vugrek O, Belužić R, Barić I, Hansíkova H, Elleder M, Veselá K, Bauerová L, Ondrušková N, Ješina P, Zeman J, Kožich V. Honzík T, et al. Among authors: baric i. Mol Genet Metab. 2012 Nov;107(3):611-3. doi: 10.1016/j.ymgme.2012.08.014. Epub 2012 Aug 23. Mol Genet Metab. 2012. PMID: 22959829

7

Fumaric aciduria: mild phenotype in a 8-year-old girl with novel mutations.

Maradin M, Fumić K, Hansikova H, Tesarova M, Wenchich L, Dorner S, Sarnavka V, Zeman J, Barić I. Maradin M, et al. Among authors: baric i. J Inherit Metab Dis. 2006 Oct;29(5):683. doi: 10.1007/s10545-006-0321-0. Epub 2006 Aug 5. J Inherit Metab Dis. 2006. PMID: 16972175

8

Expand Long PCR for fragile X mutation detection.

Hećimović S, Barisić I, Müller A, Petković I, Barić I, Ligutić I, Pavelić K. Hećimović S, et al. Among authors: baric i. Clin Genet. 1997 Sep;52(3):147-54. doi: 10.1111/j.1399-0004.1997.tb02535.x. Clin Genet. 1997. PMID: 9377803

9

Hypophosphatasia: phenotypic variability and possible Croatian origin of the c.1402g>A mutation of TNSALP gene.

Petković Ramadza D, Stipoljev F, Sarnavka V, Begović D, Potocki K, Fumić K, Mornet E, Barić I. Petković Ramadza D, et al. Among authors: baric i. Coll Antropol. 2009 Dec;33(4):1255-8. Coll Antropol. 2009. PMID: 20102078

10

Metabolic follow-up of a Croatian patient with gyrate atrophy and a new mutation in the OAT gene: a case report.

Zekušić M, Škaričić A, Fumić K, Rogić D, Žigman T, Petković Ramadža D, Vukojević N, Rüfenacht V, Uroić V, Barić I. Zekušić M, et al. Among authors: baric i. Biochem Med (Zagreb). 2018 Oct 15;28(3):030801. doi: 10.11613/BM.2018.030801. Biochem Med (Zagreb). 2018. PMID: 30429681 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

177 results

Search Page

Filters