Fumic K - Search Results

1

Current Status of Newborn Screening in Southeastern Europe.

Koracin V, Mlinaric M, Baric I, Brincat I, Djordjevic M, Drole Torkar A, Fumic K, Kocova M, Milenkovic T, Moldovanu F, Mulliqi Kotori V, Nanu MI, Remec ZI, Repic Lampret B, Platis D, Savov A, Samardzic M, Suzic B, Szatmari I, Toromanovic A, Zerjav Tansek M, Battelino T, Groselj U. Koracin V, et al. Among authors: fumic k. Front Pediatr. 2021 May 7;9:648939. doi: 10.3389/fped.2021.648939. eCollection 2021. Front Pediatr. 2021. PMID: 34026686 Free PMC article.

2

Inborn errors of metabolism at the turn of the millennium.

Barić I, Fumić K, Hoffmann GF. Barić I, et al. Among authors: fumic k. Croat Med J. 2001 Aug;42(4):379-83. Croat Med J. 2001. PMID: 11471189 Free article. Review.

3

Glyceroluria and neonatal hemochromatosis.

Barić I, Zibar K, Ćorić M, Santer R, Bonilla S, Bilić K, Buljević AD, Benjak V, Fumić K, Whitington PF. Barić I, et al. Among authors: fumic k. J Pediatr Gastroenterol Nutr. 2012 Oct;55(4):e126-8. doi: 10.1097/MPG.0b013e3182347a26. J Pediatr Gastroenterol Nutr. 2012. PMID: 21886008 No abstract available.

4

Diagnosis and the importance of early treatment of tyrosinemia type 1: A case report.

Škaričić A, Zekušić M, Fumić K, Rogić D, Uroić V, Petković Ramadža D, Žigman T, Barić I. Škaričić A, et al. Among authors: fumic k. Clin Mass Spectrom. 2019 Feb 2;12:1-6. doi: 10.1016/j.clinms.2019.01.005. eCollection 2019 Apr. Clin Mass Spectrom. 2019. PMID: 34841073 Free PMC article.

5

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: fumic k. 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.

6

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: fumic k. Coll Antropol. 2009 Dec;33(4):1255-8. Coll Antropol. 2009. PMID: 20102078

7

Functional analysis of human S-adenosylhomocysteine hydrolase isoforms SAHH-2 and SAHH-3.

Fumić K, Beluzić R, Cuk M, Pavkov T, Kloor D, Barić I, Mijić I, Vugrek O. Fumić K, et al. Eur J Hum Genet. 2007 Mar;15(3):347-51. doi: 10.1038/sj.ejhg.5201757. Epub 2006 Dec 13. Eur J Hum Genet. 2007. PMID: 17164794

8

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: fumic k. Biochem Med (Zagreb). 2018 Oct 15;28(3):030801. doi: 10.11613/BM.2018.030801. Biochem Med (Zagreb). 2018. PMID: 30429681 Free PMC article.

9

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: fumic k. Clin Genet. 2017 May;91(5):787-796. doi: 10.1111/cge.12927. Epub 2017 Mar 17. Clin Genet. 2017. PMID: 27883178

10

Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?

Barić I, Erdol S, Saglam H, Lovrić M, Belužić R, Vugrek O, Blom HJ, Fumić K. Barić I, et al. Among authors: fumic k. JIMD Rep. 2017;31:101-106. doi: 10.1007/8904_2016_543. Epub 2016 May 21. JIMD Rep. 2017. PMID: 27207470 Free PMC article.

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