Borowiec M - Search Results

1

Novel severe hemophilia A and moyamoya (SHAM) syndrome caused by Xq28 deletions encompassing F8 and BRCC3 genes.

Janczar S, Fogtman A, Koblowska M, Baranska D, Pastorczak A, Wegner O, Kostrzewska M, Laguna P, Borowiec M, Mlynarski W. Janczar S, et al. Among authors: borowiec m. Blood. 2014 Jun 19;123(25):4002-4. doi: 10.1182/blood-2014-02-553685. Blood. 2014. PMID: 24948625 Free article. No abstract available.

2

Human leukocyte antigens class II and tumor necrosis factor genetic polymorphisms are independent predictors of non-Hodgkin lymphoma outcome.

Juszczynski P, Kalinka E, Bienvenu J, Woszczek G, Borowiec M, Robak T, Kowalski M, Lech-Maranda E, Baseggio L, Coiffier B, Salles G, Warzocha K. Juszczynski P, et al. Among authors: borowiec m. Blood. 2002 Oct 15;100(8):3037-40. doi: 10.1182/blood-2002-02-0654. Blood. 2002. PMID: 12351419 Free article.

3

FOXP3, IL-10, and TGF-β genes expression in children with IgE-dependent food allergy.

Krogulska A, Borowiec M, Polakowska E, Dynowski J, Młynarski W, Wasowska-Królikowska K. Krogulska A, et al. Among authors: borowiec m. J Clin Immunol. 2011 Apr;31(2):205-15. doi: 10.1007/s10875-010-9487-1. Epub 2010 Nov 24. J Clin Immunol. 2011. PMID: 21107665 Free PMC article.

4

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. 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

5

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. 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.

6

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: borowiec m. Pediatr Endocrinol Diabetes Metab. 2010;16(4):270-6. Pediatr Endocrinol Diabetes Metab. 2010. PMID: 21447268

7

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: borowiec m. Clin Endocrinol (Oxf). 2011 Sep;75(3):321-7. doi: 10.1111/j.1365-2265.2011.04052.x. Clin Endocrinol (Oxf). 2011. PMID: 21521320

8

Wolfram syndrome in the Polish population: novel mutations and genotype-phenotype correlation.

Zmyslowska A, Borowiec M, Antosik K, Szalecki M, Stefanski A, Iwaniszewska B, Jedrzejczyk M, Pietrzak I, Mlynarski W. Zmyslowska A, et al. Among authors: borowiec m. Clin Endocrinol (Oxf). 2011 Nov;75(5):636-41. doi: 10.1111/j.1365-2265.2011.04102.x. Clin Endocrinol (Oxf). 2011. PMID: 21564155

9

Role of 657del5 NBN mutation and 7p12.2 (IKZF1), 9p21 (CDKN2A), 10q21.2 (ARID5B) and 14q11.2 (CEBPE) variation and risk of childhood ALL in the Polish population.

Pastorczak A, Górniak P, Sherborne A, Hosking F, Trelińska J, Lejman M, Szczepański T, Borowiec M, Fendler W, Kowalczyk J, Houlston RS, Młynarski W. Pastorczak A, et al. Among authors: borowiec m. Leuk Res. 2011 Nov;35(11):1534-6. doi: 10.1016/j.leukres.2011.07.034. Epub 2011 Sep 1. Leuk Res. 2011. PMID: 21889209

10

Doubling the referral rate of monogenic diabetes through a nationwide information campaign--update on glucokinase gene mutations in a Polish cohort.

Borowiec M, Fendler W, Antosik K, Baranowska A, Gnys P, Zmyslowska A, Malecki M, Mlynarski W. Borowiec M, et al. Clin Genet. 2012 Dec;82(6):587-90. doi: 10.1111/j.1399-0004.2011.01803.x. Epub 2011 Dec 30. Clin Genet. 2012. PMID: 22035297

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

209 results

Search Page

Filters