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Coheredity of a new silent mutation: c. ‐29G > T, with a severe β‐thal mutation in a patient with β‐thalassemia intermediate
(Source: Clinical and Laboratory Haematology)
Source: Clinical and Laboratory Haematology - February 5, 2018 Category: Hematology Authors: M. Vinciguerra, C. Passarello, F. Cassar à, F. Leto, M. Cannata, G. Calvaruso, D. Renda, A. Maggio, A. Giambona Tags: LETTER TO THE EDITOR Source Type: research

The effect of the acute phase response on routine laboratory markers of folate and vitamin B12 status
(Source: Clinical and Laboratory Haematology)
Source: Clinical and Laboratory Haematology - February 5, 2018 Category: Hematology Authors: J. P. Parkes, L. Wood, A. J. Chadburn, E. Garman, R. Abbas, A. Modupe, S. J. Whitehead, C. Ford, O. L. Thomas, S. Chugh, S. Deshpande, R. Gama Tags: LETTER TO THE EDITOR Source Type: research

State of the art vs biological variability: Comparison on hematology parameters using Spanish EQAS data
ConclusionOur results reflect the feasibility of establishing specifications based on biological variability criteria or the state of the art, which may help to select the proper criteria for each parameter. (Source: Clinical and Laboratory Haematology)
Source: Clinical and Laboratory Haematology - February 5, 2018 Category: Hematology Authors: A. Molina, L. Gui ñon, A. Perez, A. Segurana, J. L. Bedini, J. C. Reverter, A. Merino Tags: ORIGINAL ARTICLE Source Type: research

A KLF1 gene mutation causes β‐thalassemia minor in a Chinese family
International Journal of Laboratory Hematology,Volume 40, Issue 2, Page e35-e37, April 2018. (Source: Clinical and Laboratory Haematology)
Source: Clinical and Laboratory Haematology - February 2, 2018 Category: Hematology Source Type: research

Rare BCR ‐ABL1 transcript in a RUNX1‐RUNX1T1‐positive de novo acute myeloid leukemia: The chicken and egg tale
International Journal of Laboratory Hematology,Volume 40, Issue 2, Page e24-e27, April 2018. (Source: Clinical and Laboratory Haematology)
Source: Clinical and Laboratory Haematology - February 2, 2018 Category: Hematology Source Type: research

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International Journal of Laboratory Hematology,Volume 40, Issue 2, Page e35-e37, April 2018. (Source: Clinical and Laboratory Haematology)
Source: Clinical and Laboratory Haematology - February 2, 2018 Category: Hematology Source Type: research

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International Journal of Laboratory Hematology,Volume 40, Issue 2, Page e24-e27, April 2018. (Source: Clinical and Laboratory Haematology)
Source: Clinical and Laboratory Haematology - February 2, 2018 Category: Hematology Source Type: research

Rare BCR ‐ABL1 transcript in a RUNX1‐RUNX1T1‐positive de novo acute myeloid leukemia: The chicken and egg tale
(Source: Clinical and Laboratory Haematology)
Source: Clinical and Laboratory Haematology - February 2, 2018 Category: Hematology Authors: R. Gupta, N. Mittal, K. Rahman, A. Sharma, P. Singh, S. Kumar, S. Nityanand Tags: LETTER TO THE EDITOR Source Type: research

Thrombopoietin levels in Quebec platelet disorder —Implications for the mechanism of thrombocytopenia
International Journal of Laboratory Hematology,Volume 40, Issue 2, Page e33-e34, April 2018. (Source: Clinical and Laboratory Haematology)
Source: Clinical and Laboratory Haematology - February 1, 2018 Category: Hematology Source Type: research

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International Journal of Laboratory Hematology,Volume 40, Issue 2, Page e33-e34, April 2018. (Source: Clinical and Laboratory Haematology)
Source: Clinical and Laboratory Haematology - February 1, 2018 Category: Hematology Source Type: research

Quantification of NETs ‐associated markers by flow cytometry and serum assays in patients with thrombosis and sepsis
ConclusionFlow cytometry detection of neutrophil NETs markers is feasible in whole blood and correlates with serum markers of NETs. We propose the flow cytometry detection of MPO/H3cit positive neutrophils and serum dsDNA as simple methods to quantify cellular and extracellular NET markers in patients with thrombosis and sepsis. (Source: Clinical and Laboratory Haematology)
Source: Clinical and Laboratory Haematology - February 1, 2018 Category: Hematology Authors: K. H. Lee, L. Cavanaugh, H. Leung, F. Yan, Z. Ahmadi, B. H. Chong, F. Passam Tags: ORIGINAL ARTICLE Source Type: research

Stability of complete blood count in different storage conditions using the ABX PENTRA 60 analyzer
ConclusionThe results demonstrate the importance of the clinical analyst's knowledge about the behavior of the CBC parameters over time under different storage conditions, and mainly the imprecision of the hematological equipment used, for the suitable interpretation of the results. (Source: Clinical and Laboratory Haematology)
Source: Clinical and Laboratory Haematology - February 1, 2018 Category: Hematology Authors: L. R. Oliveira, M. Simionatto, B. R. Cruz, J. I. M. Bittencourt, E. A. Krum, M. F. Moss, D. C. K. Borato Tags: ORIGINAL ARTICLE Source Type: research

Chronic myeloid leukemia, BCR ‐ABL1‐positive with CALR and MPL mutations
(Source: Clinical and Laboratory Haematology)
Source: Clinical and Laboratory Haematology - February 1, 2018 Category: Hematology Authors: M. M. Klairmont, J. Cheng, L. Schwartzberg, H. H. Ho, J. F. Gradowski Tags: LETTER TO THE EDITOR Source Type: research

Role of CD81 and CD58 in minimal residual disease detection in pediatric B lymphoblastic leukemia
ConclusionsOur study highlights importance of using multiple markers to detect MRD in B lymphoblastic leukemia. Our findings indicate that including both CD58 and CD81 markers in addition to CD19, CD34, CD20, CD38, and CD10 are helpful in MRD detection by flow cytometry. (Source: Clinical and Laboratory Haematology)
Source: Clinical and Laboratory Haematology - February 1, 2018 Category: Hematology Authors: E. Tsitsikov, M. H. Harris, L. B. Silverman, S. E. Sallan, O. K. Weinberg Tags: ORIGINAL ARTICLE Source Type: research

Prenatal diagnosis in rare bleeding disorders —An unresolved issue?
Abstract Intracranial haemorrhage (ICH) is the most dreadful complication, and the main cause of death among patients with rare bleeding disorders (RBD) and prenatal diagnosis (PND) is a preventative lifesaving program. A total of 39 PNDs were reported in the literature through a search on PubMed, EMBASE, SCOPUS and Web of Science databases, most often for congenital factor (F) XIII and FVII deficiencies and rarely in FX, FV deficiencies and afibrinogenemia. The main cause to request a PND is ICH and related morbidity and mortality. Different molecular methods including direct sequencing and linkage analysis as well as pol...
Source: Clinical and Laboratory Haematology - February 1, 2018 Category: Hematology Authors: S. Tabibian, M. Shams, M. Naderi, A. Dorgalaleh Tags: REVIEW Source Type: research