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Kinetic alterations of the red cell membrane phosphatase in α‐ and β‐Thalassemia

American journal of hematology, 1982-12, Vol.13 (4), p.269-282

1982

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The Heterozygous Form of 4.1(-) Hereditary Elliptocytosis [the 4.1(-) Trait]

Blood, 1985-01, Vol.65 (1), p.46-51

1985

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The Screening of α- and β-Globin Chain Variants with Isoelectric Focusing

Hemoglobin, 1982, Vol.6 (5), p.481-491

1982

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Analysis of the red cell membrane in a family with hereditary elliptocytosis--total or partial of protein 4.1

Human genetics, 1981-01, Vol.59 (1), p.68-71

1981

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Homozygous hemoglobin Knossos (α2β227(B9) Ala→Ser): a new variety of β+-thalassemia intermedia associated with δ°-thalassemia

Blood, 1986-04, Vol.67 (4), p.957-961

1986

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Thalassemia‐like abnormalities of the red cell membrane in hemoglobin E trait and disease

American journal of hematology, 1984-04, Vol.16 (3), p.207-217

1984

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Association in cis of β+‐thalassemia and hemoglobin S

American journal of hematology, 1987-11, Vol.26 (3), p.237-245

1987

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A Shortened Variant of Red Cell Membrane Protein 4.1

Blood, 1982-07, Vol.60 (1), p.265-267

1982

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The Association of Hemoglobin Knossos and Hemoglobin Lepore in an Algerian Patient

Hemoglobin, 1984, Vol.8 (3), p.229-238

1984

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Asymptomatic association of hemoglobin Dunn (α6[A4]Asp→Asn) and hemoglobin O‐Arab (β121[GH4]Glu→Lys) in a Moroccan man

American journal of hematology, 1988-04, Vol.27 (4), p.253-256

1988

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Chromatofocusing of human hemoglobins: application to the quantitation of hemoglobin A2

Journal of chromatography, 1982-03, Vol.228, p.177-185

1982

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Microchromatofocusing of hemoglobins. Increased hemoglobin A2 percentage in sickle cell trait

Clinica chimica acta, 1982-05, Vol.121 (2), p.261-264

1982

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A new Case of Hb Little Rock [β143(H21)His → Gln], a high affinity variant. Study during pregnancy

Hemoglobin, 1987, Vol.11 (2), p.113-122

1987

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Homozygous Hemoglobin Knossos (a2ß227(B9) Ala → Ser): A New Variety of ß+ -Thalassemia Intermedia Associated With δ°-Thalassemia

Blood, 1986-04, Vol.67 (4), p.957-961

1986

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Isolation and mapping of a polymorphic DNA sequence (R7) on chromosome 12 (D12S52)

Nucleic acids research, 1991-01, Vol.19 (1), p.193-193

1991

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Effects of fasting on glycemia and plasma levels of nonesterified (FFA) fatty acids in sheep

Journal de physiologie, 1967, Vol.59 (1 Suppl), p.218

1967

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Carrier-ampholyte displacement chromatography (chromatofocusing) on ion-exchange papers : Application to the separation of haemoglobin variants

Journal of Chromatography A, 1981-01, Vol.222 (1), p.116-119

1981

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A shortened variant of red cell membrane protein 4.1

Blood, 1982-07, Vol.60 (1), p.265-267

1982

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Changes in plasma levels of non exterified fatty acids (FFA), of blood sugar and total hepatic lipids during adrenaline and noradrenaline perfusion in sheep

Comptes rendus des seances de la Societe de biologie et de ses filiales, 1967, Vol.161 (7), p.1588-1592

1967

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The Hb F composition in a Moroccan family with beta zero-thalassaemia and Hb O-Arab

Scandinavian journal of haematology, 1984-09, Vol.33 (3), p.281-287

1984

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The genetic abnormalities involving red cell membrane protein 4.1 with or without elliptocytosis

Biomedica biochimica acta, 1983, Vol.42 (11-12), p.S38

1983

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Alterations of globin chain synthesis and of red cell membrane proteins in congenital dyserythropoietic anemia I and II

Pediatric research, 1982-12, Vol.16 (12), p.1016-1021

1982

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Homozygous hemoglobin Knossos (alpha 2 beta 227(B9) Ala----Ser): a new variety of beta+-thalassemia intermedia associated with delta degree- thalassemia

Blood, 1986-04, Vol.67 (4), p.957-961

1986

Volltextzugriff (PDF)

Homozygous hemoglobin Knossos (alpha 2 beta 227(B9) Ala----Ser): a new variety of beta+-thalassemia intermedia associated with delta degree- thalassemia

Blood, 1986-04, Vol.67 (4), p.957-961

1986

Volltextzugriff (PDF)

The Hb F composition in a Moroccan Family with β°-thalassaemia and Hb O-Arab

Scandinavian Journal of Haematology, 1984-09, Vol.33 (3), p.281-287

1984

Volltextzugriff (PDF)

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Kinetic alterations of the red cell membrane phosphatase in α‐ and β‐Thalassemia

The Heterozygous Form of 4.1(-) Hereditary Elliptocytosis [the 4.1(-) Trait]

The Screening of α- and β-Globin Chain Variants with Isoelectric Focusing

Analysis of the red cell membrane in a family with hereditary elliptocytosis--total or partial of protein 4.1

Homozygous hemoglobin Knossos (α2β227(B9) Ala→Ser): a new variety of β+-thalassemia intermedia associated with δ°-thalassemia

Thalassemia‐like abnormalities of the red cell membrane in hemoglobin E trait and disease

Association in cis of β+‐thalassemia and hemoglobin S

A Shortened Variant of Red Cell Membrane Protein 4.1

The Association of Hemoglobin Knossos and Hemoglobin Lepore in an Algerian Patient

Asymptomatic association of hemoglobin Dunn (α6[A4]Asp→Asn) and hemoglobin O‐Arab (β121[GH4]Glu→Lys) in a Moroccan man

Chromatofocusing of human hemoglobins: application to the quantitation of hemoglobin A2

Microchromatofocusing of hemoglobins. Increased hemoglobin A2 percentage in sickle cell trait

A new Case of Hb Little Rock [β143(H21)His → Gln], a high affinity variant. Study during pregnancy

Homozygous Hemoglobin Knossos (a2ß227(B9) Ala → Ser): A New Variety of ß+ -Thalassemia Intermedia Associated With δ°-Thalassemia

Isolation and mapping of a polymorphic DNA sequence (R7) on chromosome 12 (D12S52)

Effects of fasting on glycemia and plasma levels of nonesterified (FFA) fatty acids in sheep

Carrier-ampholyte displacement chromatography (chromatofocusing) on ion-exchange papers : Application to the separation of haemoglobin variants

A shortened variant of red cell membrane protein 4.1

Changes in plasma levels of non exterified fatty acids (FFA), of blood sugar and total hepatic lipids during adrenaline and noradrenaline perfusion in sheep

The Hb F composition in a Moroccan family with beta zero-thalassaemia and Hb O-Arab

The genetic abnormalities involving red cell membrane protein 4.1 with or without elliptocytosis

Alterations of globin chain synthesis and of red cell membrane proteins in congenital dyserythropoietic anemia I and II

Homozygous hemoglobin Knossos (alpha 2 beta 227(B9) Ala----Ser): a new variety of beta+-thalassemia intermedia associated with delta degree- thalassemia

Homozygous hemoglobin Knossos (alpha 2 beta 227(B9) Ala----Ser): a new variety of beta+-thalassemia intermedia associated with delta degree- thalassemia

The Hb F composition in a Moroccan Family with β°-thalassaemia and Hb O-Arab

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