Adamowicz-Salach A[au] - Search Results

Year	Number of Results
1985	2
1987	4
1988	3
1995	1
1999	1
2000	1
2006	3
2008	2
2009	5
2010	1
2012	1
2013	1
2014	1
2015	3
2016	3
2017	5
2018	3
2019	2
2020	3
2024	1

1

Growth hormone deficiency as a complication of haemophilia - a case report and literature data.

Kucharska A, Łaguna P, Adamowicz-Salach A, Witkowska-Sędek E, Klukowska A. Kucharska A, et al. Among authors: adamowicz salach a. Pediatr Endocrinol Diabetes Metab. 2020;26(3):150-154. doi: 10.5114/pedm.2020.95619. Pediatr Endocrinol Diabetes Metab. 2020. PMID: 32729313 Free article. Review. English.

2

A Family Affected by a Life-Threatening Erythrocyte Defect Caused by Pyruvate Kinase Deficiency With Normal Iron Status: A Case Report.

Maciak K, Adamowicz-Salach A, Poznanski J, Gora M, Fronk J, Burzynska B. Maciak K, et al. Among authors: adamowicz salach a. Front Genet. 2020 Oct 28;11:560248. doi: 10.3389/fgene.2020.560248. eCollection 2020. Front Genet. 2020. PMID: 33193643 Free PMC article.

3

Laparoscopic splenectomy for hereditary spherocytosis-preliminary report.

Rogulski R, Adamowicz-Salach A, Matysiak M, Piotrowski D, Gogolewski M, Piotrowska A, Roik D, Kamiński A. Rogulski R, et al. Among authors: adamowicz salach a. Eur J Haematol. 2016 Jun;96(6):637-42. doi: 10.1111/ejh.12649. Epub 2015 Sep 17. Eur J Haematol. 2016. PMID: 26268883

4

Coexistence of Gilbert syndrome with hereditary haemolytic anaemias.

Rawa K, Adamowicz-Salach A, Matysiak M, Trzemecka A, Burzynska B. Rawa K, et al. Among authors: adamowicz salach a. J Clin Pathol. 2012 Jul;65(7):663-5. doi: 10.1136/jclinpath-2011-200580. Epub 2012 May 3. J Clin Pathol. 2012. PMID: 22554963

5

[Beta-Thalassemia in Poland. I. Mediterranean mutations in beta-thalassemia].

Zdebska E, Krawcewicz A, Adamowicz-Salach A, Jackowska T, Tejza B, Strojny W, Kuliszkiewicz-Janus M, Mokras U, Kościelak J. Zdebska E, et al. Among authors: adamowicz salach a. Pol Merkur Lekarski. 2006 Jan;20(115):53-6. Pol Merkur Lekarski. 2006. PMID: 16617736 Polish.

6

Diagnostic difficulties in a patient with paroxysmal cold haemoglobinuria and acute kidney injury.

Daniel M, Adamowicz-Salach A, Szymanik-Grzelak H. Daniel M, et al. Among authors: adamowicz salach a. Cent Eur J Immunol. 2017;42(4):404-406. doi: 10.5114/ceji.2017.72816. Epub 2017 Dec 30. Cent Eur J Immunol. 2017. PMID: 29472820 Free PMC article.

7

PKLR mutations in pyruvate kinase deficient Polish patients: Functional characteristics of c.101-1G > A and c.1058delAAG variants.

Maciak K, Jurkiewicz A, Strojny W, Adamowicz-Salach A, Romiszewska M, Jackowska T, Kwiecinska K, Poznanski J, Gora M, Burzynska B. Maciak K, et al. Among authors: adamowicz salach a. Blood Cells Mol Dis. 2024 Mar 26;107:102841. doi: 10.1016/j.bcmd.2024.102841. Online ahead of print. Blood Cells Mol Dis. 2024. PMID: 38581917

8

Usefulness of Reticulocyte Parameters for Diagnosis of Hereditary Spherocytosis in Children.

Ciepiela O, Adamowicz-Salach A, Radgowska A, Żbikowska K, Kotuła I. Ciepiela O, et al. Among authors: adamowicz salach a. Indian J Hematol Blood Transfus. 2017 Jun;33(2):239-247. doi: 10.1007/s12288-016-0680-0. Epub 2016 May 24. Indian J Hematol Blood Transfus. 2017. PMID: 28596658 Free PMC article.

9

Eosin-5'-maleimide binding test-Do we use appropriate reference values to detect hereditary spherocytosis in neonates?

Ciepiela O, Nowak M, Wrońska M, Adamowicz-Salach A, Kotuła I. Ciepiela O, et al. Among authors: adamowicz salach a. Int J Lab Hematol. 2019 Jun;41(3):e57-e60. doi: 10.1111/ijlh.12958. Epub 2018 Dec 10. Int J Lab Hematol. 2019. PMID: 30548189 No abstract available.

10

Flow cytometric osmotic fragility test: Increased assay sensitivity for clinical application in pediatric hematology.

Ciepiela O, Adamowicz-Salach A, Zgodzińska A, Łazowska M, Kotuła I. Ciepiela O, et al. Among authors: adamowicz salach a. Cytometry B Clin Cytom. 2018 Jan;94(1):189-195. doi: 10.1002/cyto.b.21511. Epub 2017 Feb 1. Cytometry B Clin Cytom. 2018. PMID: 28103644 Free article.

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