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Hereditary spherocytosis

The Lancet (British edition), 2008-10, Vol.372 (9647), p.1411-1426

2008

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Natural history of hereditary spherocytosis during the first year of life

Blood, 2000-01, Vol.95 (2), p.393-397

2000

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The unusual pathobiology of Hemoglobin Constant Spring red blood cells

Blood, 1997-03, Vol.89 (5), p.1762-1769

1997

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The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia

Nature genetics, 1999-02, Vol.21 (2), p.169-175

1999

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The contribution of endothelial cell P-selectin to the microvascular flow of mouse sickle erythrocytes in vivo

Blood, 2004-11, Vol.104 (10), p.3378-3385

2004

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Static and dynamic rigidities of normal and sickle erythrocytes: major influence of cell hemoglobin concentration

The Journal of clinical investigation, 1984-02, Vol.73 (2), p.477-488

1984

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Mutations in Ribosomal Protein S19 Gene and Diamond Blackfan Anemia: Wide Variations in Phenotypic Expression

Blood, 1999-12, Vol.94 (12), p.4294-4306

1999

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Short survival of phosphatidylserine-exposing red blood cells in murine sickle cell anemia

Blood, 2001-09, Vol.98 (5), p.1577-1584

2001

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Transgenic Knockout Mice with Exclusively Human Sickle Hemoglobin and Sickle Cell Disease

Science (American Association for the Advancement of Science), 1997-10, Vol.278 (5339), p.876-878

1997

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Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis

Blood, 2001-01, Vol.97 (2), p.399-403

2001

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Adherence of Sickle Erythrocytes to Vascular Endothelial Cells: Requirement for Both Cell Membrane Changes and Plasma Factors

Blood, 1984-07, Vol.64 (1), p.282-287

1984

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Identification of new prognosis factors from the clinical and epidemiologic analysis of a registry of 229 diamond-blackfan anemia patients

Pediatric research, 1999-11, Vol.46 (5), p.553-561

1999

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Oxidative red blood cell membrane injury in the pathophysiology of severe mouse β-thalassemia

Blood, 1992-02, Vol.79 (4), p.1064-1067

1992

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Ribosomal protein S19 expression during erythroid differentiation

Blood, 2003-01, Vol.101 (1), p.318-324

2003

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Nucleolar localization of RPS19 protein in normal cells and mislocalization due to mutations in the nucleolar localization signals in 2 Diamond-Blackfan anemia patients: potential insights into pathophysiology

Blood, 2003-06, Vol.101 (12), p.5039-5045

2003

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Study of the effects of proteasome inhibitors on ribosomal protein S19 (RPS19) mutants, identified in patients with Diamond-Blackfan anemia

Haematologica (Roma), 2008-11, Vol.93 (11), p.1627-1634

2008

Volltextzugriff (PDF)

Hydration of red cells in α and β thalassemias differs : a useful approach to distinguish between these red cell phenotypes

American journal of clinical pathology, 1994-08, Vol.102 (2), p.217-222

1994

Volltextzugriff (PDF)

Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis

The Journal of clinical investigation, 1988-08, Vol.82 (2), p.617-623

1988

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Evidence for a protective role of the Gardos channel against hemolysis in murine spherocytosis

Blood, 2005-08, Vol.106 (4), p.1454-1459

2005

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Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia

Blood, 2001-11, Vol.98 (10), p.2894-2899

2001

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The Role of Membrane Skeletal-Associated α-Globin in the Pathophysiology of β-Thalassemia

Blood, 1990-03, Vol.75 (6), p.1333-1336

1990

Volltextzugriff (PDF)

Membrane-Associated Sickle Hemoglobin: A Major Determinant of Sickle Erythrocyte Rigidity

Blood, 1987-11, Vol.70 (5), p.1443-1449

1987

Volltextzugriff (PDF)

Concurrent sickle cell anemia and α-thalassemia: effect on pathological properties of sickle erythrocytes

The Journal of clinical investigation, 1984, Vol.73 (1), p.116-123

1984

Volltextzugriff (PDF)

The Relationship Between in vivo Generated Hemoglobin Skeletal Protein Complex and Increased Red Cell Membrane Rigidity

Blood, 1988-05, Vol.71 (5), p.1427-1431

1988

Volltextzugriff (PDF)

Thrombospondin mediates adherence of CD36+ sickle reticulocytes to endothelial cells

Blood, 1992-11, Vol.80 (10), p.2634-2642

1992

Volltextzugriff (PDF)

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Hereditary spherocytosis

Natural history of hereditary spherocytosis during the first year of life

The unusual pathobiology of Hemoglobin Constant Spring red blood cells

The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia

The contribution of endothelial cell P-selectin to the microvascular flow of mouse sickle erythrocytes in vivo

Static and dynamic rigidities of normal and sickle erythrocytes: major influence of cell hemoglobin concentration

Mutations in Ribosomal Protein S19 Gene and Diamond Blackfan Anemia: Wide Variations in Phenotypic Expression

Short survival of phosphatidylserine-exposing red blood cells in murine sickle cell anemia

Transgenic Knockout Mice with Exclusively Human Sickle Hemoglobin and Sickle Cell Disease

Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis

Adherence of Sickle Erythrocytes to Vascular Endothelial Cells: Requirement for Both Cell Membrane Changes and Plasma Factors

Identification of new prognosis factors from the clinical and epidemiologic analysis of a registry of 229 diamond-blackfan anemia patients

Oxidative red blood cell membrane injury in the pathophysiology of severe mouse β-thalassemia

Ribosomal protein S19 expression during erythroid differentiation

Nucleolar localization of RPS19 protein in normal cells and mislocalization due to mutations in the nucleolar localization signals in 2 Diamond-Blackfan anemia patients: potential insights into pathophysiology

Study of the effects of proteasome inhibitors on ribosomal protein S19 (RPS19) mutants, identified in patients with Diamond-Blackfan anemia

Hydration of red cells in α and β thalassemias differs : a useful approach to distinguish between these red cell phenotypes

Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis

Evidence for a protective role of the Gardos channel against hemolysis in murine spherocytosis

Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia

The Role of Membrane Skeletal-Associated α-Globin in the Pathophysiology of β-Thalassemia

Membrane-Associated Sickle Hemoglobin: A Major Determinant of Sickle Erythrocyte Rigidity

Concurrent sickle cell anemia and α-thalassemia: effect on pathological properties of sickle erythrocytes

The Relationship Between in vivo Generated Hemoglobin Skeletal Protein Complex and Increased Red Cell Membrane Rigidity

Thrombospondin mediates adherence of CD36+ sickle reticulocytes to endothelial cells

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