List of works - Anna Adamowicz-Salach

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

scientific article published on 28 October 2020

A very rare cause of acute kidney injury: questions and answers

scientific article published on 07 February 2014

Coexistence of Gilbert syndrome with hereditary haemolytic anaemias

scientific article published on 03 May 2012

Delay in the measurement of eosin-5′-maleimide (EMA) binding does not affect the test result for the diagnosis of hereditary spherocytosis

scientific article published in April 2013

Delayed Measurement of Eosin-5'-Maleimide Binding May Affect the Test Results of Highly Hemolyzed Samples In Vivo and In Vitro-A Case Study

scientific article published on 27 July 2016

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

scientific article published on 30 December 2017

Diminished presentation of complement regulatory protein CD55 on red blood cells from patients with hereditary haemolytic anaemias.

scientific article published on 30 September 2017

Diversity of thalassemia variants in Poland - screening by real-time PCR.

scientific article

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

scientific article published on 10 December 2018

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

scientific article published on 19 January 2017

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

scientific article published on 30 July 2020

Haemothorax in children with congenital coagulopathy.

scientific article published on 7 April 2010

Hereditary xerocytosis - spectrum and clinical manifestations of variants in the PIEZO1 gene, including co-occurrence with a novel β-globin mutation

scientific article published on 22 October 2019

Incidence and treatment of hepatitis C virus infection in children with haemophilia in Poland.

scientific article published in November 1999

Laparoscopic splenectomy for hereditary spherocytosis-preliminary report

scientific article

Mean corpuscular volume of control red blood cells determines the interpretation of eosin-5'-maleimide (EMA) test result in infants aged less than 6 months.

scientific article published on 25 April 2015

Molecular and haematological studies of four families with hereditary spherocytosis resulting from band 3 deficiency

scientific article published on 01 January 2006

Novel beta-spectrin mutations in hereditary spherocytosis associated with decreased levels of mRNA.

scientific article published on 15 June 2009

Quantitation of red cell-bound IgG by an enzyme-linked antiglobulin test in the patients with warm-type autoimmune haemolytic anaemia.

scientific article published in August 2006

Short report: erythrocyte membranes from a patient with congenital dyserythropoietic anaemia type I (CDA-I) show identical, although less pronounced, glycoconjugate abnormalities to those from patients with CDA-II (HEMPAS)

scientific article published on 01 September 2000

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.

scientific article published on 08 June 2009

Two novel C-terminal frameshift mutations in the β-globin gene lead to rapid mRNA decay

scientific article

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

scientific article published on 24 May 2016

Zakrzepowa plamica małopłytkowa u 3-letniego chłopca – opis przypadku

scientific article

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

scientific article published on 01 April 2009

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

scientific article published on 01 January 2006

[Danazol - effective second line therapy in idiopathic thrombocytopenic purpura in children. Three case reports]

scientific article published on 01 October 2008

[Erythropoietin treatment of infants with anaemia in the first three months of life]

scientific article published on 01 October 2009

[The C1155G mutation of the red blood cell glucose-6-phosphate dehydrogenase gene in a subject with severe hereditary chronic nonspherocytic anaemia]

scientific article published on 01 April 2009

List of works by Anna Adamowicz-Salach

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

A very rare cause of acute kidney injury: questions and answers

Coexistence of Gilbert syndrome with hereditary haemolytic anaemias

Delay in the measurement of eosin-5′-maleimide (EMA) binding does not affect the test result for the diagnosis of hereditary spherocytosis

Delayed Measurement of Eosin-5'-Maleimide Binding May Affect the Test Results of Highly Hemolyzed Samples In Vivo and In Vitro-A Case Study

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

Diminished presentation of complement regulatory protein CD55 on red blood cells from patients with hereditary haemolytic anaemias.

Diversity of thalassemia variants in Poland - screening by real-time PCR.

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

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

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

Haemothorax in children with congenital coagulopathy.

Hereditary xerocytosis - spectrum and clinical manifestations of variants in the PIEZO1 gene, including co-occurrence with a novel β-globin mutation

Incidence and treatment of hepatitis C virus infection in children with haemophilia in Poland.

Laparoscopic splenectomy for hereditary spherocytosis-preliminary report

Mean corpuscular volume of control red blood cells determines the interpretation of eosin-5'-maleimide (EMA) test result in infants aged less than 6 months.

Molecular and haematological studies of four families with hereditary spherocytosis resulting from band 3 deficiency

Novel beta-spectrin mutations in hereditary spherocytosis associated with decreased levels of mRNA.

Quantitation of red cell-bound IgG by an enzyme-linked antiglobulin test in the patients with warm-type autoimmune haemolytic anaemia.

Short report: erythrocyte membranes from a patient with congenital dyserythropoietic anaemia type I (CDA-I) show identical, although less pronounced, glycoconjugate abnormalities to those from patients with CDA-II (HEMPAS)

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.

Two novel C-terminal frameshift mutations in the β-globin gene lead to rapid mRNA decay

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

Zakrzepowa plamica małopłytkowa u 3-letniego chłopca – opis przypadku

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

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

[Danazol - effective second line therapy in idiopathic thrombocytopenic purpura in children. Three case reports]

[Erythropoietin treatment of infants with anaemia in the first three months of life]

[The C1155G mutation of the red blood cell glucose-6-phosphate dehydrogenase gene in a subject with severe hereditary chronic nonspherocytic anaemia]