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Turning up the heat: heat stress induces markers of programmed cell death in Plasmodium falciparum in vitro

Cell death & disease, 2013-12, Vol.4 (12), p.e971-e971

2013

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Neonatal haemolytic anaemia – a diagnostic approach to red cell membrane disorders

SAJCH : the South African journal of child health, 2018-06, Vol.12 (2), p.81-83

2018

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Automated malaria detection by depolarization of laser light

British journal of haematology, 1999-03, Vol.104 (3), p.499-503

1999

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Thrombocytopenia in patients with malaria: automated analysis of optical platelet counts and platelet clumps with the Cell Dyn CD4000 analyser

Clinical and laboratory haematology, 2002-10, Vol.24 (5), p.295-302

2002

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Real-time quantitative PCR of telomere length

Molecular biotechnology, 2004-06, Vol.27 (2), p.169-172

2004

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Automated detection of malaria-associated intraleucocytic haemozoin by Cell-Dyn CD4000 depolarization analysis

Clinical and laboratory haematology, 2003-04, Vol.25 (2), p.77-86

2003

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Patterns of pseudo-reticulocytosis in malaria: fluorescent analysis with the Cell-Dyn® CD4000

Clinical and laboratory haematology, 2002-02, Vol.24 (1), p.15-20

2002

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Spectrin cagliari. an Ala–>Gly substitution in helix 1 of beta spectrin repeat 17 that severely disrupts the structure and self-association of the erythrocyte spectrin heterodimer

The Journal of biological chemistry, 1993-10, Vol.268 (30), p.22656-22662

1993

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Isolation and Characterization of cDNA Clones for Human Erythrocyte β -spectrin

Proceedings of the National Academy of Sciences - PNAS, 1987-11, Vol.84 (21), p.7468-7472

1987

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Partial Spectrin Deficiency in Hereditary Pyropoikilocytosis

Blood, 1986-04, Vol.67 (4), p.919-924

1986

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A TaqI polymorphism in the human erythroid β spectrin gene

Human genetics, 1995-03, Vol.95 (3), p.365-366

1995

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Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosis

The New England journal of medicine, 1988-01, Vol.318 (4), p.230-234

1988

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Defective binding of spectrin to ankyrin in a kindred with recessively inherited hereditary elliptocytosis

The Journal of clinical investigation, 1984-09, Vol.74 (3), p.753-762

1984

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Development and application of a modified flow cytometric procedure for rapid in vitro quantitation of malaria parasitaemia

South African journal of science, 1997-04, Vol.93 (4), p.156-158

1997

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Real-time quantitative RT-PCR for human telomere elongation reverse transcriptase in chronic myeloid leukemia

Leukemia research, 2004-09, Vol.28 (9), p.969-972

2004

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Band 3 Cape Town (E90K) causes severe hereditary spherocytosis in combination with band 3 Prague III

British journal of haematology, 2001-06, Vol.113 (3), p.689-693

2001

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Pyruvate kinase deficiency protects against malaria in humans

Haematologica (Roma), 2008-06, Vol.93 (6), p.939-940

2008

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Phage display: a useful tool for malaria research?

Trends in parasitology, 2008-01, Vol.24 (1), p.18-23

2008

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Reduced spectrin-ankyrin binding in a South African hereditary elliptocytosis kindred homozygous for spectrin St Claude

Blood, 1998-10, Vol.92 (7), p.2591-2593

1998

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Novel exon 2 spectrin mutation and intragenic crossover: three morphological phenotypes associated with four distinct spectrin defects

Haematologica (Roma), 2013-12, Vol.98 (12), p.1972-1979

2013

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Spectrin-αI/61: A New Structural Variant of α-Spectrin in a Double-Heterozygous Form of Hereditary Pyropoikilocytosis

Blood, 1988-10, Vol.72 (4), p.1412-1415

1988

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Hereditary red cell disorders and malaria resistance

Haematologica (Roma), 2008-07, Vol.93 (7), p.961-963

2008

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Severe hemolysis and red cell fragmentation caused by the combination of a spectrin mutation with a thrombotic microangiopathy

American journal of hematology, 1989-09, Vol.32 (1), p.50-56

1989

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A novel mobile element inserted in the alpha spectrin gene: spectrin dayton. A truncated alpha spectrin associated with hereditary elliptocytosis

The Journal of clinical investigation, 1994-08, Vol.94 (2), p.643-648

1994

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Southeast Asian Ovalocytosis in a South African Kindred With Hemolytic Anemia

Blood, 1996-02, Vol.87 (4), p.1656-1657

1996

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Turning up the heat: heat stress induces markers of programmed cell death in Plasmodium falciparum in vitro

Neonatal haemolytic anaemia – a diagnostic approach to red cell membrane disorders

Automated malaria detection by depolarization of laser light

Thrombocytopenia in patients with malaria: automated analysis of optical platelet counts and platelet clumps with the Cell Dyn CD4000 analyser

Real-time quantitative PCR of telomere length

Automated detection of malaria-associated intraleucocytic haemozoin by Cell-Dyn CD4000 depolarization analysis

Patterns of pseudo-reticulocytosis in malaria: fluorescent analysis with the Cell-Dyn® CD4000

Spectrin cagliari. an Ala–>Gly substitution in helix 1 of beta spectrin repeat 17 that severely disrupts the structure and self-association of the erythrocyte spectrin heterodimer

Isolation and Characterization of cDNA Clones for Human Erythrocyte β -spectrin

Partial Spectrin Deficiency in Hereditary Pyropoikilocytosis

A TaqI polymorphism in the human erythroid β spectrin gene

Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosis

Defective binding of spectrin to ankyrin in a kindred with recessively inherited hereditary elliptocytosis

Development and application of a modified flow cytometric procedure for rapid in vitro quantitation of malaria parasitaemia

Real-time quantitative RT-PCR for human telomere elongation reverse transcriptase in chronic myeloid leukemia

Band 3 Cape Town (E90K) causes severe hereditary spherocytosis in combination with band 3 Prague III

Pyruvate kinase deficiency protects against malaria in humans

Phage display: a useful tool for malaria research?

Reduced spectrin-ankyrin binding in a South African hereditary elliptocytosis kindred homozygous for spectrin St Claude

Novel exon 2 spectrin mutation and intragenic crossover: three morphological phenotypes associated with four distinct spectrin defects

Spectrin-αI/61: A New Structural Variant of α-Spectrin in a Double-Heterozygous Form of Hereditary Pyropoikilocytosis

Hereditary red cell disorders and malaria resistance

Severe hemolysis and red cell fragmentation caused by the combination of a spectrin mutation with a thrombotic microangiopathy

A novel mobile element inserted in the alpha spectrin gene: spectrin dayton. A truncated alpha spectrin associated with hereditary elliptocytosis

Southeast Asian Ovalocytosis in a South African Kindred With Hemolytic Anemia

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