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Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders

Blood reviews, 2013-07, Vol.27 (4), p.167-178

2013

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Elevated MCHC reveals a Southeast Asian Ovalocytosis

American journal of hematology, 2024-02, Vol.99 (2), p.331-332

2024

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Molecular characteristics of hereditary red blood cell membrane disorders in Thailand: a multi-center registry

Annals of hematology, 2024-02, Vol.103 (2), p.385-393

2024

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A large family of hereditary spherocytosis and a rare case of hereditary elliptocytosis with a novel SPTA1 mutation underdiagnosed in Taiwan: A case report and literature review

Medicine (Baltimore), 2023-01, Vol.102 (4), p.e32708-e32708

2023

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Homozygous SPTA1‐associated hereditary pyropoikilocytosis presenting as hydrops fetalis

Transfusion (Philadelphia, Pa.), 2024-01, Vol.64 (1), p.189-193

2024

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ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders

International journal of laboratory hematology, 2015-06, Vol.37 (3), p.304-325

2015

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Insane in the membrane: A case of hereditary spherocytic pyropoikilocytosis

American journal of hematology, 2022-10, Vol.97 (10), p.1384-1385

2022

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Characterization of South-East Asian ovalocytosis using osmotic gradient ektacytometry

Medicina clinica, 2024-01, Vol.162 (1), p.43

2024

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Diagnosis and clinical management of red cell membrane disorders

Hematology, 2021-12, Vol.2021 (1), p.331-340

Kalfa, Theodosia A

2021

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Clinical utility of targeted next‐generation sequencing panel in routine diagnosis of hereditary hemolytic anemia: A national reference laboratory experience

European journal of haematology, 2023-06, Vol.110 (6), p.688-695

2023

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Placental Histopathologic Findings in Fetal Hereditary Pyropoikilocytosis after Undergoing Successful Intrauterine Transfusion

Fetal and pediatric pathology, 2024-05, Vol.43 (3), p.273-275

2024

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Whole-exome sequencing for the genetic diagnosis of congenital red blood cell membrane disorders in Taiwan

Clinica chimica acta, 2018-12, Vol.487, p.311-317

2018

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Acquired elliptocytosis in a patient with myelodysplastic syndrome harbouring a novel unbalanced whole‐arm translocation, der(14;20)(q10;p10)

British journal of haematology, 2022-01, Vol.196 (1), p.7-7

2022

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Clinical and gene mutation characteristics of patients with hereditary ellipsocytosis: nine cases report and literature review

Zhōnghuá xuèyèxué zázhì, 2023-04, Vol.44 (4), p.316-320

2023

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Acquired elliptocytosis in a patient with a myelodysplastic syndrome associated with 20q deletion

British journal of haematology, 2019-04, Vol.185 (2), p.206-206

2019

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X-linked elliptocytosis with impaired growth is related to mutated AMMECR1

Gene, 2017-03, Vol.606, p.47-52

2017

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Detection of Southern Asian Ovalocytosis with Sysmex XN‐10: A complement to the decision tree previously described

International Journal of Laboratory Hematology, 2022-04, Vol.44 (2), p.e84-e86

2022

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Hereditary red cell membrane disorders and laboratory diagnostic testing

International journal of laboratory hematology, 2013-06, Vol.35 (3), p.237-243

2013

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Development of a novel test for the identification of hereditary erythrocyte membrane defects by TGA/Chemometrics

Analyst (London), 2020-07, Vol.145 (13), p.4452-4456

2020

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Incidental finding of 3 Southeast Asian ovalocytosis cases by attentive examination of blood smears

Blood, 2017-01, Vol.129 (1), p.133-133

2017

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Acquired elliptocytosis as presenting sign of a myelodysplastic syndrome associated with deletion of chromosome 20 and mutations in TET2, DNMT3A, and U2AF1

Annals of hematology, 2021-08, Vol.100 (8), p.2111-2112

2021

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Laboratory Approach to Hemolytic Anemia

Indian journal of pediatrics, 2020, Vol.87 (1), p.66-74

2020

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Sickle cell trait with β-thalassemia, elliptocytosis, and thrombocytosis

Blood, 2017-09, Vol.130 (10), p.1275-1275

2017

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Accurate light microscopic diagnosis of South‐East Asian ovalocytosis

International journal of laboratory hematology, 2018-12, Vol.40 (6), p.655-662

2018

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Acquired “pyro”-poikilocytosis

Blood, 2017-12, Vol.130 (25), p.2808-2808

2017

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Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders

Elevated MCHC reveals a Southeast Asian Ovalocytosis

Molecular characteristics of hereditary red blood cell membrane disorders in Thailand: a multi-center registry

A large family of hereditary spherocytosis and a rare case of hereditary elliptocytosis with a novel SPTA1 mutation underdiagnosed in Taiwan: A case report and literature review

Homozygous SPTA1‐associated hereditary pyropoikilocytosis presenting as hydrops fetalis

ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders

Insane in the membrane: A case of hereditary spherocytic pyropoikilocytosis

Characterization of South-East Asian ovalocytosis using osmotic gradient ektacytometry

Diagnosis and clinical management of red cell membrane disorders

Clinical utility of targeted next‐generation sequencing panel in routine diagnosis of hereditary hemolytic anemia: A national reference laboratory experience

Placental Histopathologic Findings in Fetal Hereditary Pyropoikilocytosis after Undergoing Successful Intrauterine Transfusion

Whole-exome sequencing for the genetic diagnosis of congenital red blood cell membrane disorders in Taiwan

Acquired elliptocytosis in a patient with myelodysplastic syndrome harbouring a novel unbalanced whole‐arm translocation, der(14;20)(q10;p10)

Clinical and gene mutation characteristics of patients with hereditary ellipsocytosis: nine cases report and literature review

Acquired elliptocytosis in a patient with a myelodysplastic syndrome associated with 20q deletion

X-linked elliptocytosis with impaired growth is related to mutated AMMECR1

Detection of Southern Asian Ovalocytosis with Sysmex XN‐10: A complement to the decision tree previously described

Hereditary red cell membrane disorders and laboratory diagnostic testing

Development of a novel test for the identification of hereditary erythrocyte membrane defects by TGA/Chemometrics

Incidental finding of 3 Southeast Asian ovalocytosis cases by attentive examination of blood smears

Acquired elliptocytosis as presenting sign of a myelodysplastic syndrome associated with deletion of chromosome 20 and mutations in TET2, DNMT3A, and U2AF1

Laboratory Approach to Hemolytic Anemia

Sickle cell trait with β-thalassemia, elliptocytosis, and thrombocytosis

Accurate light microscopic diagnosis of South‐East Asian ovalocytosis

Acquired “pyro”-poikilocytosis

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