Mlynarski W - Search Results

1

Ancestral mutations may cause a significant proportion of GCK-MODY.

Dusatkova P, Pruhova S, Borowiec M, Vesela K, Antosik K, Lebl J, Mlynarski W, Cinek O. Dusatkova P, et al. Among authors: mlynarski w. Pediatr Diabetes. 2012 Sep;13(6):489-98. doi: 10.1111/j.1399-5448.2011.00845.x. Epub 2012 Feb 15. Pediatr Diabetes. 2012. PMID: 22332836

2

Examination of PPP1R3B as a candidate gene for the type 2 diabetes and MODY loci on chromosome 8p23.

Dunn JS, Mlynarski WM, Pezzolesi MG, Borowiec M, Powers C, Krolewski AS, Doria A. Dunn JS, et al. Among authors: mlynarski wm. Ann Hum Genet. 2006 Sep;70(Pt 5):587-93. doi: 10.1111/j.1469-1809.2005.00248.x. Ann Hum Genet. 2006. PMID: 16907705

3

Mutations at the BLK locus linked to maturity onset diabetes of the young and beta-cell dysfunction.

Borowiec M, Liew CW, Thompson R, Boonyasrisawat W, Hu J, Mlynarski WM, El Khattabi I, Kim SH, Marselli L, Rich SS, Krolewski AS, Bonner-Weir S, Sharma A, Sale M, Mychaleckyj JC, Kulkarni RN, Doria A. Borowiec M, et al. Among authors: mlynarski wm. Proc Natl Acad Sci U S A. 2009 Aug 25;106(34):14460-5. doi: 10.1073/pnas.0906474106. Epub 2009 Aug 10. Proc Natl Acad Sci U S A. 2009. PMID: 19667185 Free PMC article.

4

[Optimization of monogenic diabetes screening programme--initial report on recruitment efficacy of the TEAM project].

Borowiec M, Fendler W, Antosik K, Ciepiela A, Baranowska A, Hogendorf A, Mianowska B, Szadkowska A, Młynarski W. Borowiec M, et al. Among authors: mlynarski w. Pediatr Endocrinol Diabetes Metab. 2010;16(2):73-6. Pediatr Endocrinol Diabetes Metab. 2010. PMID: 20813082 Polish.

5

Paternally inherited proinsulin mutations may result in earlier onset of monogenic diabetes mutation identity effect in monogenic diabetes.

Fendler W, Borowiec M, Antosik K, Jaroszewska-Swiatek B, Szwalkiewicz-Warowicka E, Malecki M, Mysliwiec M, Mlynarski W. Fendler W, et al. Among authors: mlynarski w. Diabetes Care. 2011 Jan;34(1):e9. doi: 10.2337/dc10-1142. Diabetes Care. 2011. PMID: 21193618 No abstract available.

6

Novel glucokinase mutations in patients with monogenic diabetes - clinical outline of GCK-MD and potential for founder effect in Slavic population.

Borowiec M, Antosik K, Fendler W, Deja G, Jarosz-Chobot P, Mysliwiec M, Zmyslowska A, Malecki M, Szadkowska A, Mlynarski W. Borowiec M, et al. Among authors: mlynarski w. Clin Genet. 2012 Mar;81(3):278-83. doi: 10.1111/j.1399-0004.2011.01656.x. Epub 2011 Mar 18. Clin Genet. 2012. PMID: 21348868

7

Phenotype variability and neonatal diabetes in a large family with heterozygous mutation of the glucokinase gene.

Borowiec M, Mysliwiec M, Fendler W, Antosik K, Brandt A, Malecki M, Mlynarski W. Borowiec M, et al. Among authors: mlynarski w. Acta Diabetol. 2011 Sep;48(3):203-8. doi: 10.1007/s00592-011-0279-8. Epub 2011 Mar 25. Acta Diabetol. 2011. PMID: 21437567 Free PMC article.

8

[An evaluation of HLA class 2 alleles and anti-islet antibodies as evidence for non-autoimmune diabetes in Wolfram syndrome].

Zmysłowska A, Borowiec M, Antosik K, Wyka K, Cieślik-Heinrich A, Klich I, Młynarski W. Zmysłowska A, et al. Among authors: mlynarski w. Pediatr Endocrinol Diabetes Metab. 2010;16(4):233-7. Pediatr Endocrinol Diabetes Metab. 2010. PMID: 21447263 Polish.

9

Metabolic syndrome components among children born small for gestational age: analysis of the first decade of life.

Szałapska M, Stawerska R, Borowiec M, Młynarski W, Lewiński A, Hilczer M. Szałapska M, et al. Among authors: mlynarski w. Pediatr Endocrinol Diabetes Metab. 2010;16(4):270-6. Pediatr Endocrinol Diabetes Metab. 2010. PMID: 21447268

10

HDL cholesterol as a diagnostic tool for clinical differentiation of GCK-MODY from HNF1A-MODY and type 1 diabetes in children and young adults.

Fendler W, Borowiec M, Antosik K, Szadkowska A, Deja G, Jarosz-Chobot P, Mysliwiec M, Wyka K, Pietrzak I, Skupien J, Malecki MT, Mlynarski W. Fendler W, et al. Among authors: mlynarski w. Clin Endocrinol (Oxf). 2011 Sep;75(3):321-7. doi: 10.1111/j.1365-2265.2011.04052.x. Clin Endocrinol (Oxf). 2011. PMID: 21521320

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