Old and new insights into the diagnosis of hereditary spherocytosis

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Old and new insights into the diagnosis of hereditary spherocytosis

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wetenschappelijk artikel

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наукова стаття, опублікована у вересні 2018

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Old and new insights into the diagnosis of hereditary spherocytosis

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Old and new insights into the diagnosis of hereditary spherocytosis

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Old and new insights into the diagnosis of hereditary spherocytosis

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Old and new insights into the diagnosis of hereditary spherocytosis

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Old and new insights into the diagnosis of hereditary spherocytosis

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Old and new insights into the diagnosis of hereditary spherocytosis

@nl

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Old and new insights into the diagnosis of hereditary spherocytosis

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Olga Ciepiela

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A pediatrician's practical guide to diagnosing and treating hereditary spherocytosis in neonates

Comparative osmotic gradient ektacytometry data on inter-species differences of experimental animals.

Interpretation of osmotic gradient ektacytometry (osmoscan) data: a comparative study for methodological standards.

Proteomic identification of erythrocyte membrane protein deficiency in hereditary spherocytosis.

Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics.

Comprehensive identification of erythrocyte membrane protein deficiency by 2D gel electrophoresis based proteomic analysis in hereditary elliptocytosis and spherocytosis.

Flow cytometric detection of erythrocyte osmotic fragility.

Identification of a novel p.Q1772X ANK1 mutation in a Korean family with hereditary spherocytosis.

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.

Hereditary spherocytosis: Consequences of delayed diagnosis.

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339

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scholarly article

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10.21037/ATM.2018.07.35

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English

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2018-09-01T00:00:00Z

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30306078

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diagnosis

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6174190

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