Spychalska J - Search Results

1

Transformation of aplastic anemia with paroxysmal nocturnal hemoglobinuria clone to childhood B-cell precursor acute lymphoblastic leukemia.

Wypyszczak K, Urbanska Z, Miarka-Walczyk K, Kolodrubiec J, Jakubowska J, Spychalska J, Glodkowska-Mrowka E, Ussowicz M, Mlynarski W, Pastorczak A. Wypyszczak K, et al. Among authors: spychalska j. Pediatr Blood Cancer. 2024 Jul;71(7):e30994. doi: 10.1002/pbc.30994. Epub 2024 Apr 11. Pediatr Blood Cancer. 2024. PMID: 38605541 No abstract available.

2

Paroxysmal nocturnal hemoglobinuria: advances in the understanding of pathophysiology, diagnosis, and treatment.

Szlendak U, Budziszewska B, Spychalska J, Drozd-Sokołowska J, Patkowska E, Nowak J. Szlendak U, et al. Among authors: spychalska j. Pol Arch Intern Med. 2022 Jun 29;132(6):16271. doi: 10.20452/pamw.16271. Epub 2022 Jun 6. Pol Arch Intern Med. 2022. PMID: 35699625 Free article. Review.

3

Persistent imbalance, anti-apoptotic, and anti-inflammatory signature of circulating C-C chemokines and cytokines in patients with paroxysmal nocturnal hemoglobinuria.

Szlendak U, Krzymieniewska B, Mendek-Czajkowska E, Rogatko-Koroś M, Witkowska A, Włodarska J, Drozd-Sokołowska J, Spychalska J, Budziszewska B, Patkowska E, Woźniak J, Krzywdzińska A, Jurek S, Juszczyński P, Jaworska M, Rosłon M, Gruber-Bzura B, Wasilewski R, Baran B, Windyga J, Nowak J. Szlendak U, et al. Among authors: spychalska j. Cytokine. 2022 Feb;150:155780. doi: 10.1016/j.cyto.2021.155780. Epub 2021 Dec 10. Cytokine. 2022. PMID: 34896730

4

Congenital disorder of glycosylphosphatidylinositol (GPI)-anchor biosynthesis--The phenotype of two patients with novel mutations in the PIGN and PGAP2 genes.

Jezela-Stanek A, Ciara E, Piekutowska-Abramczuk D, Trubicka J, Jurkiewicz E, Rokicki D, Mierzewska H, Spychalska J, Uhrynowska M, Szwarc-Bronikowska M, Buda P, Said AR, Jamroz E, Rydzanicz M, Płoski R, Krajewska-Walasek M, Pronicka E. Jezela-Stanek A, et al. Among authors: spychalska j. Eur J Paediatr Neurol. 2016 May;20(3):462-73. doi: 10.1016/j.ejpn.2016.01.007. Epub 2016 Feb 4. Eur J Paediatr Neurol. 2016. PMID: 26879448

5

[Standardization of the quantitative flow cytometric test with anti-D antibodies for fetomaternal hemorrhage in RhD negative women].

Spychalska J, Uhrynowska M, Pyl H, Klimczak-Jajor E, Kopeć I, Peciakowska M, Gutowska R, Gawlak M, Słomska S, Dąbkowska S, Szczecina R, Dębska M, Brojer E. Spychalska J, et al. Ginekol Pol. 2015 Jul;86(7):486-93. doi: 10.17772/gp/57854. Ginekol Pol. 2015. PMID: 26376524 Polish.

6

Influence of some cardiovascular risk factors on the expression of platelet glycoprotein IIb/IIIa receptors in patients with myocardial infarction treated with antiplatelet drugs under primary percutaneous coronary intervention.

Konopka A, Spychalska J, Piotrowski W, Stepińska J. Konopka A, et al. Among authors: spychalska j. Mol Diagn Ther. 2009 Dec 1;13(6):375-82. doi: 10.1007/BF03256343. Mol Diagn Ther. 2009. PMID: 19925035

7

[A case of hereditary over-hydrated stomatocytosis with stomatospherocytes and spherocytes in the blood].

Kościelak J, Mendek-Czajkowska E, Spychalska J, Marosz-Rudnicka A, Myślińska A, Adamowicz-Salach A, Gołaszewska E, Witos I. Kościelak J, et al. Among authors: spychalska j. Med Wieku Rozwoj. 2009 Apr-Jun;13(2):131-5. Med Wieku Rozwoj. 2009. PMID: 19837993 Polish.

8

The use of real-time PCR technique in the detection of novel protein 4.2 gene mutations that coexist with thalassaemia alpha in a single patient.

Maciag M, Adamowicz-Salach A, Siwicka A, Spychalska J, Burzynska B. Maciag M, et al. Among authors: spychalska j. Eur J Haematol. 2009 Oct;83(4):373-7. doi: 10.1111/j.1600-0609.2009.01289.x. Epub 2009 Jun 8. Eur J Haematol. 2009. PMID: 19508687 Free PMC article.

9

Expression of platelet surface receptors and early changes in platelet function in patients with STEMI treated with abciximab and clopidogrel versus clopidogrel alone.

Konopka A, Spychalska J, Sitkiewicz D, Zdebska E, Pilichowska I, Piotrowski W, Stepińska J. Konopka A, et al. Among authors: spychalska j. Am J Cardiovasc Drugs. 2007;7(6):433-9. doi: 10.2165/00129784-200707060-00006. Am J Cardiovasc Drugs. 2007. PMID: 18076210

10

Abnormalities of erythrocyte glycoconjugates are identical in two families with congenital dyserythropoietic anemia type II with different chromosomal localizations of the disease gene.

Zdebska E, Iolascon A, Spychalska J, Perrotta S, Lanzara C, Smolenska-Sym G, Koscielak J. Zdebska E, et al. Among authors: spychalska j. Haematologica. 2007 Mar;92(3):427-8. doi: 10.3324/haematol.10803. Haematologica. 2007. PMID: 17339199 Free article.

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