Fumić K - Search Results

1

Differential metabolic consequences of fumarate hydratase and respiratory chain defects.

Raimundo N, Ahtinen J, Fumić K, Barić I, Remes AM, Renkonen R, Lapatto R, Suomalainen A. Raimundo N, et al. Among authors: fumic k. Biochim Biophys Acta. 2008 May;1782(5):287-94. doi: 10.1016/j.bbadis.2008.01.008. Epub 2008 Feb 14. Biochim Biophys Acta. 2008. PMID: 18313410 Free article.

2

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: fumic k. 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

3

A single mutation at Tyr143 of human S-adenosylhomocysteine hydrolase renders the enzyme thermosensitive and affects the oxidation state of bound cofactor nicotinamide-adenine dinucleotide.

Beluzić R, Cuk M, Pavkov T, Fumić K, Barić I, Mudd SH, Jurak I, Vugrek O. Beluzić R, et al. Among authors: fumic k. Biochem J. 2006 Dec 1;400(2):245-53. doi: 10.1042/BJ20060749. Biochem J. 2006. PMID: 16872278 Free PMC article.

4

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.

5

[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: fumic k. Lijec Vjesn. 2011 Jan-Feb;133(1-2):39-50. Lijec Vjesn. 2011. PMID: 21644278 Review. Croatian.

6

[Congenital disorders of glycosylation and project "Euroglycanet"].

Petković D, Bilić K, Ninković D, Cuk M, Fumić K, Barić I. Petković D, et al. Among authors: fumic k. Lijec Vjesn. 2007 Aug-Sep;129(8-9):286-92. Lijec Vjesn. 2007. PMID: 18198629 Review. Croatian.

7

Mitochondrial myopathy associated with a novel 5522G>A mutation in the mitochondrial tRNA(Trp) gene.

Barić I, Fumić K, Petković Ramadža D, Sperl W, Zimmermann FA, Muačević-Katanec D, Mitrović Z, Pažanin L, Cvitanović Šojat L, Kekez T, Reiner Z, Mayr JA. Barić I, et al. Among authors: fumic k. Eur J Hum Genet. 2013 Aug;21(8):871-5. doi: 10.1038/ejhg.2012.272. Epub 2012 Dec 12. Eur J Hum Genet. 2013. PMID: 23232693 Free PMC article.

8

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

9

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.

10

The molecular basis of phenylalanine hydroxylase deficiency in Croatia.

Zschocke J, Preusse A, Sarnavka V, Fumic K, Mardesic D, Hoffmann GF, Baric I. Zschocke J, et al. Among authors: fumic k. Hum Mutat. 2003 Apr;21(4):399. doi: 10.1002/humu.9115. Hum Mutat. 2003. PMID: 12655552

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