Jakóbkiewicz-Banecka J - Search Results

1

Abnormalities in the hair morphology of patients with some but not all types of mucopolysaccharidoses.

Malinowska M, Jakóbkiewicz-Banecka J, Kloska A, Tylki-Szymańska A, Czartoryska B, Piotrowska E, Wegrzyn A, Wegrzyn G. Malinowska M, et al. Eur J Pediatr. 2008 Feb;167(2):203-9. doi: 10.1007/s00431-007-0462-7. Epub 2007 Mar 15. Eur J Pediatr. 2008. PMID: 17361416

2

Atypical microbial infections of digestive tract may contribute to diarrhea in mucopolysaccharidosis patients: a MPS I case study.

Wegrzyn G, Kurlenda J, Liberek A, Tylki-Szymanska A, Czartoryska B, Piotrowska E, Jakóbkiewicz-Banecka J, Wegrzyn A. Wegrzyn G, et al. BMC Pediatr. 2005 May 9;5(1):9. doi: 10.1186/1471-2431-5-9. BMC Pediatr. 2005. PMID: 15882450 Free PMC article.

3

A bacterial model for studying effects of human mutations in vivo: Escherichia coli strains mimicking a common polymorphism in the human MTHFR gene.

Jakóbkiewicz-Banecka J, Kloska A, Stepnowska M, Banecki B, Wegrzyn A, Wegrzyn G. Jakóbkiewicz-Banecka J, et al. Mutat Res. 2005 Oct 15;578(1-2):175-86. doi: 10.1016/j.mrfmmm.2005.05.002. Epub 2005 Jun 14. Mutat Res. 2005. PMID: 15961124

4

A modified procedure for quantitative analysis of mtDNA, detecting mtDNA depletion.

Weglewska A, Jakóbkiewicz-Banecka J, Wegrzyn G. Weglewska A, et al. J Appl Genet. 2005;46(4):423-8. J Appl Genet. 2005. PMID: 16278519

5

Changes in hair morphology of mucopolysaccharidosis I patients treated with recombinant human alpha-L-iduronidase (laronidase, Aldurazyme).

Kloska A, Bohdanowicz J, Konopa G, Tylki-Szymńska A, Jakóbkiewicz-Banecka J, Czartoryska B, Liberek A, Wegrzyn A, Wegrzyn G. Kloska A, et al. Am J Med Genet A. 2005 Dec 15;139(3):199-203. doi: 10.1002/ajmg.a.31021. Am J Med Genet A. 2005. PMID: 16283671

6

Genistein-mediated inhibition of glycosaminoglycan synthesis as a basis for gene expression-targeted isoflavone therapy for mucopolysaccharidoses.

Piotrowska E, Jakóbkiewicz-Banecka J, Barańska S, Tylki-Szymańska A, Czartoryska B, Wegrzyn A, Wegrzyn G. Piotrowska E, et al. Eur J Hum Genet. 2006 Jul;14(7):846-52. doi: 10.1038/sj.ejhg.5201623. Epub 2006 May 3. Eur J Hum Genet. 2006. PMID: 16670689

7

False positive results of mitochondrial DNA depletion/deletion due to single nucleotide substitutions causing appearance of additional PvuII restriction sites.

Weglewska-Jurkiewicz A, Jakóbkiewicz-Banecka J, Pronicka E, Wegrzyn G. Weglewska-Jurkiewicz A, et al. Diagn Mol Pathol. 2007 Jun;16(2):116-20. doi: 10.1097/PDM.0b013e3180336271. Diagn Mol Pathol. 2007. PMID: 17525683

8

Rapid deterioration of a patient with mucopolysaccharidosis type I during interruption of enzyme replacement therapy.

Wegrzyn G, Tylki-Szymańska A, Liberek A, Piotrowska E, Jakóbkiewicz-Banecka J, Marucha J, Czartoryska B, Wegrzyn A. Wegrzyn G, et al. Am J Med Genet A. 2007 Aug 15;143A(16):1925-7. doi: 10.1002/ajmg.a.31831. Am J Med Genet A. 2007. PMID: 17603800 No abstract available.

9

Substrate deprivation therapy: a new hope for patients suffering from neuronopathic forms of inherited lysosomal storage diseases.

Jakóbkiewicz-Banecka J, Wegrzyn A, Wegrzyn G. Jakóbkiewicz-Banecka J, et al. J Appl Genet. 2007;48(4):383-8. doi: 10.1007/BF03195237. J Appl Genet. 2007. PMID: 17998597 Review.

10

Improved HPLC method for total plasma homocysteine detection and quantification.

Sawuła W, Banecka-Majkutewicz Z, Kadziński L, Jakóbkiewicz-Banecka J, Wegrzyn G, Nyka W, Banecki B. Sawuła W, et al. Acta Biochim Pol. 2008;55(1):119-25. Epub 2008 Jan 16. Acta Biochim Pol. 2008. PMID: 18196182

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