ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders.
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The European Hematology Association Roadmap for European Hematology Research: a consensus documentDiagnostic approaches for inherited hemolytic anemia in the genetic eraRepository of Human Blood Derivative Biospecimens in Biobank: Technical ImplicationsPositive predictive value of diagnosis coding for hemolytic anemias in the Danish National Patient Register.Diagnosis and management of congenital dyserythropoietic anemias.Evaluation and optimization of the extended information process unit (E-IPU) validation module integrating the sysmex flag systems and the recommendations of the French-speaking cellular hematology group (GFHC).Advances in understanding the pathogenesis of the red cell volume disorders.Analysis of a cohort of 101 CDAII patients: description of 24 new molecular variants and genotype-phenotype correlations.Detection of new pathogenic mutations in patients with congenital haemolytic anaemia using next-generation sequencing.Flow cytometric analysis of patients with hereditary spherocytosis - an Indian scenario.Erythrocytes from hereditary xerocytosis patients heterozygous for KCNN4 V282M exhibit increased spontaneous Gardos channel-like activity inhibited by senicapoc.Targeted next generation sequencing identifies a novel β-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis.Profound spherocytosis in adulthood: Acquired, hereditary or both?Evaluation of OSMOCELLS, a new semi-automatic device for osmotic fragility assessment.Osmotic gradient ektacytometry: A valuable screening test for hereditary spherocytosis and other red blood cell membrane disorders.CD44 as a potential screening marker for preliminary differentiation between congenital dyserythropoietic anemia type II and hereditary spherocytosis.Usefulness of Reticulocyte Parameters for Diagnosis of Hereditary Spherocytosis in Children.Advances in laboratory diagnosis of hereditary spherocytosis.Novel compound heterozygous SPTA1 mutations in a patient with hereditary elliptocytosis.Use of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) in the Diagnosis of RBC Membrane Disorders, Enzyme Defects, and Congenital Dyserythropoietic Anemias: A Monocentric Study on 202 Patients.Cryohemolysis, erythrocyte osmotic fragility, and supplementary hematimetric indices in the diagnosis of hereditary spherocytosis.Flow Cytometric Eosin-5'-Maleimide Test is a Sensitive Screen for Hereditary SpherocytosisOld and new insights into the diagnosis of hereditary spherocytosisAspects of Modern Biobank Activity - Comprehensive Review
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P2860
ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders.
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name
ICSH guidelines for the labora ...... y red cell membrane disorders.
@en
ICSH guidelines for the labora ...... y red cell membrane disorders.
@nl
type
label
ICSH guidelines for the labora ...... y red cell membrane disorders.
@en
ICSH guidelines for the labora ...... y red cell membrane disorders.
@nl
prefLabel
ICSH guidelines for the labora ...... y red cell membrane disorders.
@en
ICSH guidelines for the labora ...... y red cell membrane disorders.
@nl
P2093
P2860
P356
P1476
ICSH guidelines for the labora ...... y red cell membrane disorders.
@en
P2093
A Iolascon
International Council for Standardization in Haematology
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P304
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10.1111/IJLH.12335
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2015-03-18T00:00:00Z