Bogdańska A - Search Results

1

Pediatric Liver Disease Patients and Secondary Glycosylation Abnormalities.

Bogdańska A, Lipiński P, Szymańska-Rożek P, Jankowska I, Socha P, Tylki-Szymańska A. Bogdańska A, et al. Front Pediatr. 2021 Jan 13;8:613224. doi: 10.3389/fped.2020.613224. eCollection 2020. Front Pediatr. 2021. PMID: 33520896 Free PMC article.

2

Clinical, biochemical and molecular findings in seven Polish patients with adenylosuccinate lyase deficiency.

Jurecka A, Zikanova M, Tylki-Szymanska A, Krijt J, Bogdanska A, Gradowska W, Mullerova K, Sykut-Cegielska J, Kmoch S, Pronicka E. Jurecka A, et al. Among authors: bogdanska a. Mol Genet Metab. 2008 Aug;94(4):435-442. doi: 10.1016/j.ymgme.2008.04.013. Epub 2008 Jun 3. Mol Genet Metab. 2008. PMID: 18524658

3

Mild phenotype of glutaric aciduria type 1 in polish patients - novel data from a group of 13 cases.

Pokora P, Jezela-Stanek A, Różdżyńska-Świątkowska A, Jurkiewicz E, Bogdańska A, Szymańska E, Rokicki D, Ciara E, Rydzanicz M, Stawiński P, Płoski R, Tylki-Szymańska A. Pokora P, et al. Among authors: bogdanska a. Metab Brain Dis. 2019 Apr;34(2):641-649. doi: 10.1007/s11011-018-0357-5. Epub 2018 Dec 20. Metab Brain Dis. 2019. PMID: 30570710 Free PMC article.

4

NGLY1 deficiency: Novel patient, review of the literature and diagnostic algorithm.

Lipiński P, Bogdańska A, Różdżyńska-Świątkowska A, Wierzbicka-Rucińska A, Tylki-Szymańska A. Lipiński P, et al. Among authors: bogdanska a. JIMD Rep. 2020 Jan 30;51(1):82-88. doi: 10.1002/jmd2.12086. eCollection 2020 Jan. JIMD Rep. 2020. PMID: 32071843 Free PMC article.

5

ATP6AP1-CDG: Follow-up and female phenotype.

Lipiński P, Rokicki D, Bogdańska A, Lesiak J, Lefeber DJ, Tylki-Szymańska A. Lipiński P, et al. Among authors: bogdanska a. JIMD Rep. 2020 Apr 9;53(1):80-82. doi: 10.1002/jmd2.12104. eCollection 2020 May. JIMD Rep. 2020. PMID: 32395412 Free PMC article.

6

Neonatal cholestasis due to citrin deficiency: diagnostic pitfalls.

Lipiński P, Jurkiewicz D, Ciara E, Płoski R, Więcek S, Bogdańska A, Stradomska T, Socha P, Rokicki D, Tylki-Szymańska A, Jankowska I. Lipiński P, et al. Among authors: bogdanska a. Acta Biochim Pol. 2020 May 21;67(2):225-228. doi: 10.18388/abp.2020_5202. Acta Biochim Pol. 2020. PMID: 32436673 Free article.

7

Long Term Follow-Up of Polish Patients with Isovaleric Aciduria. Clinical and Molecular Delineation of Isovaleric Aciduria.

Szymańska E, Jezela-Stanek A, Bogdańska A, Rokicki D, Ehmke Vel Emczyńska-Seliga E, Pajdowska M, Ciara E, Tylki-Szymańska A. Szymańska E, et al. Among authors: bogdanska a. Diagnostics (Basel). 2020 Sep 23;10(10):738. doi: 10.3390/diagnostics10100738. Diagnostics (Basel). 2020. PMID: 32977617 Free PMC article.

8

[Congenital disorders of glycosylation - constantly growing group of metabolic diseases].

Bogdańska A, Tylki-Szymańska A. Bogdańska A, et al. Postepy Biochem. 2020 Oct 29;66(3):213-228. doi: 10.18388/pb.2020_345. Print 2020 Sep 30. Postepy Biochem. 2020. PMID: 33315314 Free article. Review. Polish.

9

Clinical, biochemical and molecular phenotype of congenital disorders of glycosylation: long-term follow-up.

Bogdańska A, Lipiński P, Szymańska-Rożek P, Jezela-Stanek A, Rokicki D, Socha P, Tylki-Szymańska A. Bogdańska A, et al. Orphanet J Rare Dis. 2021 Jan 6;16(1):17. doi: 10.1186/s13023-020-01657-5. Orphanet J Rare Dis. 2021. PMID: 33407696 Free PMC article.

10

Congenital disorders of glycosylation: Prevalence, incidence and mutational spectrum in the Polish population.

Lipiński P, Bogdańska A, Tylki-Szymańska A. Lipiński P, et al. Among authors: bogdanska a. Mol Genet Metab Rep. 2021 Feb 11;27:100726. doi: 10.1016/j.ymgmr.2021.100726. eCollection 2021 Jun. Mol Genet Metab Rep. 2021. PMID: 33643843 Free PMC article.

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