Peterlin B - Search Results

1

Genetic predisposition to idiopathic recurrent spontaneous abortion: contribution of genetic variations in IGF-2 and H19 imprinted genes.

Ostojić S, Pereza N, Volk M, Kapović M, Peterlin B. Ostojić S, et al. Among authors: peterlin b. Am J Reprod Immunol. 2008 Aug;60(2):111-7. doi: 10.1111/j.1600-0897.2008.00601.x. Am J Reprod Immunol. 2008. PMID: 18573128

2

Human Y-specific STR haplotypes in the Western Croatian population sample.

Lovrecić L, Ristić S, Brajenović B, Kapović M, Peterlin B. Lovrecić L, et al. Among authors: peterlin b. Forensic Sci Int. 2005 May 10;149(2-3):257-61. doi: 10.1016/j.forsciint.2004.06.026. Forensic Sci Int. 2005. PMID: 15749369

3

Mutations in the hemochromatosis gene (HFE) and multiple sclerosis.

Ristić S, Lovrecić L, Brajenović-Milić B, Starcević-Cizmarević N, Jazbec SS, Sepcić J, Kapović M, Peterlin B. Ristić S, et al. Among authors: peterlin b. Neurosci Lett. 2005 Aug 5;383(3):301-4. doi: 10.1016/j.neulet.2005.04.045. Neurosci Lett. 2005. PMID: 15955425

4

No association of CCR5delta32 gene mutation with multiple sclerosis in Croatian and Slovenian patients.

Ristić S, Lovrecić L, Starcević-Cizmarević N, Brajenović-Milić B, Jazbec SS, Barac-Latas V, Vejnović D, Sepcić J, Kapović M, Peterlin B. Ristić S, et al. Among authors: peterlin b. Mult Scler. 2006 Jun;12(3):360-2. doi: 10.1191/135248506ms1305sr. Mult Scler. 2006. PMID: 16764352

5

Region with persistent high frequency of multiple sclerosis in Croatia and Slovenia.

Peterlin B, Ristić S, Sepcić J, Vracko BK, Rako A, Lovrecić L, Brajenović-Milić B, Rudez J, Materljan E, Kapović M. Peterlin B, et al. J Neurol Sci. 2006 Sep 25;247(2):169-72. doi: 10.1016/j.jns.2006.04.002. Epub 2006 Jun 27. J Neurol Sci. 2006. PMID: 16806273

6

Hemochromatosis gene mutations in patients with alcoholic cirrhosis.

Starcevic Cizmarevic N, Stepec S, Ristić S, Milić S, Brajenović-Milić B, Stimac D, Kapović M, Peterlin B. Starcevic Cizmarevic N, et al. Among authors: peterlin b. Clin Genet. 2006 Sep;70(3):257-9. doi: 10.1111/j.1399-0004.2006.00672.x. Clin Genet. 2006. PMID: 16922731 No abstract available.

7

Association between the apolipoprotein B signal peptide gene insertion/deletion polymorphism and male infertility.

Peterlin B, Zorn B, Volk M, Kunej T. Peterlin B, et al. Mol Hum Reprod. 2006 Dec;12(12):777-9. doi: 10.1093/molehr/gal088. Epub 2006 Oct 27. Mol Hum Reprod. 2006. PMID: 17071710

8

Angiotensin-converting enzyme I/D gene polymorphism and risk of multiple sclerosis.

Lovrecić L, Ristić S, Starcević-Cizmarević N, Jazbec SS, Sepcić J, Kapović M, Peterlin B. Lovrecić L, et al. Among authors: peterlin b. Acta Neurol Scand. 2006 Dec;114(6):374-7. doi: 10.1111/j.1600-0404.2006.00711.x. Acta Neurol Scand. 2006. PMID: 17083336

9

Patients with primary cataract as a genetic pool of DMPK protomutation.

Medica I, Teran N, Volk M, Pfeifer V, Ladavac E, Peterlin B. Medica I, et al. Among authors: peterlin b. J Hum Genet. 2007;52(2):123-128. doi: 10.1007/s10038-006-0091-4. Epub 2006 Dec 5. J Hum Genet. 2007. PMID: 17146587

10

Tumor necrosis factor-alpha-308 gene polymorphism in Croatian and Slovenian multiple sclerosis patients.

Ristić S, Lovrecić L, Starcević-Cizmarević N, Brajenović-Milić B, Sega Jazbec S, Sepcić J, Kapović M, Peterlin B. Ristić S, et al. Among authors: peterlin b. Eur Neurol. 2007;57(4):203-7. doi: 10.1159/000099159. Epub 2007 Jan 12. Eur Neurol. 2007. PMID: 17268200

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