Petrovic R - Search Results

1

Atypical Huntington's disease with the clinical presentation of behavioural variant of frontotemporal dementia.

Sutovsky S, Smolek T, Alafuzoff I, Blaho A, Parrak V, Turcani P, Palkovic M, Petrovic R, Novak M, Zilka N. Sutovsky S, et al. Among authors: petrovic r. J Neural Transm (Vienna). 2016 Dec;123(12):1423-1433. doi: 10.1007/s00702-016-1579-5. Epub 2016 Jun 10. J Neural Transm (Vienna). 2016. PMID: 27287334

2

Genetic and clinical characteristics including occurrence of testicular adrenal rest tumors in Slovak and Slovenian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Saho R, Dolzan V, Zerjav Tansek M, Pastorakova A, Petrovic R, Knapkova M, Trebusak Podkrajsek K, Suput Omladic J, Bertok S, Avbelj Stefanija M, Kotnik P, Battelino T, Pribilincova Z, Groselj U. Saho R, et al. Among authors: petrovic r. Front Endocrinol (Lausanne). 2023 Mar 17;14:1134133. doi: 10.3389/fendo.2023.1134133. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37008950 Free PMC article.

3

Adult onset cerebral form of X-linked adrenoleukodystrophy with dementia of frontal lobe type with new L160P mutation in ABCD1 gene.

Sutovský S, Petrovic R, Chandoga J, Turcáni P. Sutovský S, et al. Among authors: petrovic r. J Neurol Sci. 2007 Dec 15;263(1-2):149-53. doi: 10.1016/j.jns.2007.01.082. Epub 2007 Jul 26. J Neurol Sci. 2007. PMID: 17662307

4

Spectrum of DHCR7 mutations in Slovak patients with Smith-Lemli-Opitz syndrome and detection of common mutations by PCR-based assays.

Kolejáková K, Petrovic R, Futas J, Turcáni P, Durovcíková D, Chandoga J. Kolejáková K, et al. Among authors: petrovic r. Gen Physiol Biophys. 2009 Mar;28(1):8-15. Gen Physiol Biophys. 2009. PMID: 19390132

5

Frequency of selected single nucleotide polymorphisms influencing the warfarin pharmacogenetics in Slovak population.

Krajčíová L, Petrovič R, Déžiová L, Chandoga J, Turčáni P. Krajčíová L, et al. Among authors: petrovic r. Eur J Haematol. 2014 Oct;93(4):320-8. doi: 10.1111/ejh.12348. Epub 2014 May 12. Eur J Haematol. 2014. PMID: 24750390

6

Differing clinical presentations of two unrelated cases of X-linked adrenoleukodystrophy with identical mutation Y296C in the ABCD1 gene.

Sutovský S, Kolníková M, Petrovic R, Kollár B, Siarnik P, Chandoga J, Fischerová M, Turcáni P. Sutovský S, et al. Among authors: petrovic r. Neuro Endocrinol Lett. 2014;35(5):411-6. Neuro Endocrinol Lett. 2014. PMID: 25275259

7

Peroxisomal D-bifunctional protein deficiency: First case reports from Slovakia.

Konkoľová J, Petrovič R, Chandoga J, Repiský M, Zelinková H, Kršiaková J, Kolníková M, Kantarská D, Šutovský S, Böhmer D. Konkoľová J, et al. Among authors: petrovic r. Gene. 2015 Aug 15;568(1):61-8. doi: 10.1016/j.gene.2015.05.020. Epub 2015 May 9. Gene. 2015. PMID: 25967389

8

Neuropathology and biochemistry of early onset familial Alzheimer's disease caused by presenilin-1 missense mutation Thr116Asn.

Sutovsky S, Smolek T, Turcani P, Petrovic R, Brandoburova P, Jadhav S, Novak P, Attems J, Zilka N. Sutovsky S, et al. Among authors: petrovic r. J Neural Transm (Vienna). 2018 Jun;125(6):965-976. doi: 10.1007/s00702-018-1850-z. Epub 2018 Feb 5. J Neural Transm (Vienna). 2018. PMID: 29404783

9

Allelic Distribution of Genes for Apolipoprotein E and MTHFR in Patients with Alzheimer's Disease and Their Epistatic Interaction.

Sutovsky S, Petrovic R, Fischerova M, Haverlikova V, Ukropcova B, Ukropec J, Turcani P. Sutovsky S, et al. Among authors: petrovic r. J Alzheimers Dis. 2020;77(3):1095-1105. doi: 10.3233/JAD-200321. J Alzheimers Dis. 2020. PMID: 32804129 Free PMC article.

10

TREM2 coding variants in Slovak Alzheimer's disease patients.

Durmanova V, Javor J, Parnicka Z, Minarik G, Ocenasova A, Vaseckova B, Kiralyova I, Sutovsky S, Petrovic R, Shawkatova I. Durmanova V, et al. Among authors: petrovic r. J Integr Neurosci. 2022 Jun 1;21(4):105. doi: 10.31083/j.jin2104105. J Integr Neurosci. 2022. PMID: 35864757 Free article.

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