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The Molecular Basis of Paroxysmal Nocturnal Hemoglobinuria

Blood, 1995-11, Vol.86 (9), p.3277-3286

1995

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Erythrocyte autoantibodies in paediatric patients with sickle cell disease receiving transfusion therapy: frequency, characteristics and significance

British journal of haematology, 1999-01, Vol.104 (1), p.189-194

1999

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(18)F-FDG PET provides high-impact and powerful prognostic stratification in staging newly diagnosed non-small cell lung cancer

The Journal of nuclear medicine (1978), 2001-11, Vol.42 (11), p.1596-1604

2001

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Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly)

Nature genetics, 2002-08, Vol.31 (4), p.410-414

2002

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The utility of (18)F-FDG PET for suspected recurrent non-small cell lung cancer after potentially curative therapy: impact on management and prognostic stratification

The Journal of nuclear medicine (1978), 2001-11, Vol.42 (11), p.1605-1613

2001

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Clinical impact of (18)F fluorodeoxyglucose positron emission tomography in patients with non-small-cell lung cancer: a prospective study

Journal of clinical oncology, 2001-01, Vol.19 (1), p.111-118

2001

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Safety of Hydroxyurea in Children With Sickle Cell Anemia: Results of the HUG-KIDS Study, a Phase I/II Trial

Blood, 1999-09, Vol.94 (5), p.1550-1554

1999

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Molecular Basis of the Heterogeneity of Expression of Glycosyl Phosphatidylinositol Anchored Proteins in Paroxysmal Nocturnal Hemoglobinuria

Blood, 1996-03, Vol.87 (6), p.2546-2557

1996

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Hydroxyurea as an Alternative to Blood Transfusions for the Prevention of Recurrent Stroke in Children With Sickle Cell Disease

Blood, 1999-11, Vol.94 (9), p.3022-3026

1999

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High rate of detection of unsuspected distant metastases by PET in apparent Stage III non–small-cell lung cancer: implications for radical radiation therapy

International journal of radiation oncology, biology, physics, 2001-06, Vol.50 (2), p.287-293

2001

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Circulating PIG-A mutant T lymphocytes in healthy adults and patients with bone marrow failure syndromes

Experimental hematology, 2001-12, Vol.29 (12), p.1403-1409

2001

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Immunophenotypic Analysis of Reticulocytes in Paroxysmal Nocturnal Hemoglobinuria

Blood, 1995-08, Vol.86 (4), p.1586-1589

1995

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Mutations Within the Piga Gene in Patients With Paroxysmal Nocturnal Hemoglobinuria

Blood, 1994-05, Vol.83 (9), p.2418-2422

1994

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A two-year pilot trial of hydroxyurea in very young children with sickle-cell anemia

The Journal of pediatrics, 2001-12, Vol.139 (6), p.790-796

2001

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Effects of inherited thrombophilic mutations in an adolescent with antiphospholipid syndrome and systemic lupus erythematosus

Journal of rheumatology, 2001-02, Vol.28 (2), p.370

2001

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Phenotypic and Clonal Analysis of T Lymphocytes in Childhood Immune Thrombocytopenic Purpura

Blood, 1993-10, Vol.82 (7), p.2137-2142

1993

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Anti-D: mechanisms of action

Seminars in hematology, 1998-01, Vol.35 (1 Suppl 1), p.14-22

1998

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High-dose oral dexamethasone therapy for chronic childhood idiopathic thrombocytopenic purpura

The Journal of pediatrics, 1996-02, Vol.128 (2), p.281-283

1996

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Paroxysmal Nocturnal Hemoglobinuria with Onset in Childhood and Adolescence

The New England journal of medicine, 1991-10, Vol.325 (14), p.991-996

1991

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Enalapril and hydroxyurea therapy for children with sickle nephropathy

Pediatric blood & cancer, 2005-12, Vol.45 (7), p.982-985

2005

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Clinical significance of the antinuclear antibody test in selected children with idiopathic thrombocytopenic purpura

Journal of pediatric hematology/oncology, 1997-07, Vol.19 (4), p.297-303

1997

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The utility of the autohaemolysis test for children with congenital haemolytic anaemia

Clinical and laboratory haematology, 2003-02, Vol.25 (1), p.25-28

2003

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Salmonella infection in sickle cell disease: a clear and present danger

The Journal of pediatrics, 1997-03, Vol.130 (3), p.350-351

Ware, R E

1997

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MR features of soft-tissue abnormalities due to acute marrow infarction in five children with sickle cell disease

American journal of roentgenology (1976), 1999-10, Vol.173 (4), p.989-993

1999

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Palpable splenomegaly in children with haemoglobin SC disease: Haematological and clinical manifestations

Clinical and laboratory haematology, 2000-06, Vol.22 (3), p.145-150

2000

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The Molecular Basis of Paroxysmal Nocturnal Hemoglobinuria

Erythrocyte autoantibodies in paediatric patients with sickle cell disease receiving transfusion therapy: frequency, characteristics and significance

(18)F-FDG PET provides high-impact and powerful prognostic stratification in staging newly diagnosed non-small cell lung cancer

Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly)

The utility of (18)F-FDG PET for suspected recurrent non-small cell lung cancer after potentially curative therapy: impact on management and prognostic stratification

Clinical impact of (18)F fluorodeoxyglucose positron emission tomography in patients with non-small-cell lung cancer: a prospective study

Safety of Hydroxyurea in Children With Sickle Cell Anemia: Results of the HUG-KIDS Study, a Phase I/II Trial

Molecular Basis of the Heterogeneity of Expression of Glycosyl Phosphatidylinositol Anchored Proteins in Paroxysmal Nocturnal Hemoglobinuria

Hydroxyurea as an Alternative to Blood Transfusions for the Prevention of Recurrent Stroke in Children With Sickle Cell Disease

High rate of detection of unsuspected distant metastases by PET in apparent Stage III non–small-cell lung cancer: implications for radical radiation therapy

Circulating PIG-A mutant T lymphocytes in healthy adults and patients with bone marrow failure syndromes

Immunophenotypic Analysis of Reticulocytes in Paroxysmal Nocturnal Hemoglobinuria

Mutations Within the Piga Gene in Patients With Paroxysmal Nocturnal Hemoglobinuria

A two-year pilot trial of hydroxyurea in very young children with sickle-cell anemia

Effects of inherited thrombophilic mutations in an adolescent with antiphospholipid syndrome and systemic lupus erythematosus

Phenotypic and Clonal Analysis of T Lymphocytes in Childhood Immune Thrombocytopenic Purpura

Anti-D: mechanisms of action

High-dose oral dexamethasone therapy for chronic childhood idiopathic thrombocytopenic purpura

Paroxysmal Nocturnal Hemoglobinuria with Onset in Childhood and Adolescence

Enalapril and hydroxyurea therapy for children with sickle nephropathy

Clinical significance of the antinuclear antibody test in selected children with idiopathic thrombocytopenic purpura

The utility of the autohaemolysis test for children with congenital haemolytic anaemia

Salmonella infection in sickle cell disease: a clear and present danger

MR features of soft-tissue abnormalities due to acute marrow infarction in five children with sickle cell disease

Palpable splenomegaly in children with haemoglobin SC disease: Haematological and clinical manifestations

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