Romanowski T - Search Results

1

Association between uridin diphosphate glucuronosylotransferase 1A1 (UGT1A1) gene polymorphism and neonatal hyperbilirubinemia.

Mazur-Kominek K, Romanowski T, Bielawski K, Kiełbratowska B, Preis K, Domżalska-Popadiuk I, Słomińska-Frączek M, Sznurkowska K, Renke J, Plata-Nazar K, Śledzińska K, Sikorska-Wiśniewska G, Góra-Gębka M, Liberek A. Mazur-Kominek K, et al. Among authors: romanowski t. Acta Biochim Pol. 2017;64(2):351-356. doi: 10.18388/abp.2016_1450. Epub 2017 Apr 12. Acta Biochim Pol. 2017. PMID: 28399191 Free article.

2

UGT1A1 gene polymorphism as a potential factor inducing iron overload in the pathogenesis of type 1 hereditary hemochromatosis.

Romanowski T, Sikorska K, Bielawski KP. Romanowski T, et al. Hepatol Res. 2009 May;39(5):469-78. doi: 10.1111/j.1872-034X.2008.00487.x. Epub 2009 Jan 12. Hepatol Res. 2009. PMID: 19207584

3

Diagnosis and treatment difficulties in 18-year-old male patient with hereditary hemochromatosis, chronic hepatitis B, Gilbert syndrome and ulcerative colitis.

Sikorska K, Liberek A, Romanowski T, Szlagatys-Sidorkiewicz A, Landowski P, Bielawski KP. Sikorska K, et al. Among authors: romanowski t. Acta Biochim Pol. 2011;58(2):251-4. Epub 2011 Jun 2. Acta Biochim Pol. 2011. PMID: 21633730 Free article.

4

TNF-α polymorphisms affect persistence and progression of HBV infection.

Woziwodzka A, Rybicka M, Sznarkowska A, Romanowski T, Dręczewski M, Stalke P, Bielawski KP. Woziwodzka A, et al. Among authors: romanowski t. Mol Genet Genomic Med. 2019 Oct;7(10):e00935. doi: 10.1002/mgg3.935. Epub 2019 Aug 23. Mol Genet Genomic Med. 2019. PMID: 31441603 Free PMC article.

5

Liver steatosis correlates with iron overload but not with HFE gene mutations in chronic hepatitis C.

Sikorska K, Stalke P, Romanowski T, Rzepko R, Bielawski KP. Sikorska K, et al. Among authors: romanowski t. Hepatobiliary Pancreat Dis Int. 2013 Aug;12(4):377-84. doi: 10.1016/s1499-3872(13)60059-4. Hepatobiliary Pancreat Dis Int. 2013. PMID: 23924495

6

Coexistence of HFE and rare UGT1A1 genes mutations in patients with iron overload related liver injury.

Sikorska K, Romanowski T, Stalke P, Jaskiewicz K, Bielawski KP. Sikorska K, et al. Among authors: romanowski t. Adv Med Sci. 2010;55(1):108-10. doi: 10.2478/v10039-010-0003-x. Adv Med Sci. 2010. PMID: 20371435

7

HFE gene mutations in Polish patients with disturbances of iron metabolism: an initial assessment.

Sikorska K, Bielawski KP, Stalke P, Lakomy EA, Michalska Z, Witczak-Malinowska K, Romanowski T. Sikorska K, et al. Among authors: romanowski t. Int J Mol Med. 2005 Dec;16(6):1151-6. Int J Mol Med. 2005. PMID: 16273299

8

GUS and PMM1 as suitable reference genes for gene expression analysis in the liver tissue of patients with chronic hepatitis.

Romanowski T, Sikorska K, Bielawski KP. Romanowski T, et al. Med Sci Monit. 2008 Jul;14(7):BR147-52. Med Sci Monit. 2008. PMID: 18591914

9

The role of iron overload and HFE gene mutations in the era of pegylated interferon and ribavirin treatment of chronic hepatitis C.

Sikorska K, Stalke P, Izycka-Swieszewska E, Romanowski T, Bielawski KP. Sikorska K, et al. Among authors: romanowski t. Med Sci Monit. 2010 Mar;16(3):CR137-143. Med Sci Monit. 2010. PMID: 20190684 Clinical Trial.

10

Iron overload and HFE gene mutations in Polish patients with liver cirrhosis.

Sikorska K, Romanowski T, Stalke P, Iżycka-Świeszewska E, Bielawski KP. Sikorska K, et al. Among authors: romanowski t. Hepatobiliary Pancreat Dis Int. 2011 Jun;10(3):270-5. doi: 10.1016/s1499-3872(11)60045-3. Hepatobiliary Pancreat Dis Int. 2011. PMID: 21669570

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