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Pain in Sickle Cell Disease: Rates and Risk Factors

The New England journal of medicine, 1991-07, Vol.325 (1), p.11-16

1991

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Role of Child and Maternal Processes in the Psychological Adjustment of Children With Sickle Cell Disease

Journal of consulting and clinical psychology, 1993-06, Vol.61 (3), p.468-474

1993

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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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Erythrocytapheresis can reduce iron overload and prevent the need for chelation therapy in chronically transfused pediatric patients

Journal of pediatric hematology/oncology, 1996-02, Vol.18 (1), p.46-50

1996

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Quantitative analysis of erythrocytes containing fetal hemoglobin (F cells) in children with sickle cell disease

American journal of hematology, 1997-01, Vol.54 (1), p.40-46

1997

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Elective cholecystectomy in children with sickle hemoglobinopathies: successful outcome using a preoperative transfusion regimen

Annals of surgery, 1988-07, Vol.208 (1), p.17-22

1988

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Psychological Adjustment of Children With Sickle Cell Disease: Stability and Change Over a 10-Month Period

Journal of consulting and clinical psychology, 1994-08, Vol.62 (4), p.856-860

1994

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Hydroxyurea: An alternative to transfusion therapy for stroke in sickle cell anemia

American journal of hematology, 1995-10, Vol.50 (2), p.140-143

1995

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Serotype-specific immunoglobulin G antibody responses to pneumococcal polysaccharide vaccine in children with sickle cell anemia: Effects of continued penicillin prophylaxis

The Journal of pediatrics, 1996-12, Vol.129 (6), p.828-835

1996

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Laparoscopic cholecystectomy in young patients with sickle hemoglobinopathies

The Journal of pediatrics, 1992, Vol.120 (1), p.58-61

1992

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Long-term management of splenic sequestration in children with sickle cell disease

The Journal of pediatrics, 1990-08, Vol.117 (2), p.194-199

1990

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Pitfalls in newborn hemoglobinopathy screening: Failure to detect β +-thalassemia

The Journal of pediatrics, 1995-08, Vol.127 (2), p.304-308

1995

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Emergency department visits by children with sickle hemoglobinopathies: Factors associated with hospital admission

Pediatric emergency care, 1995-02, Vol.11 (1), p.9-12

1995

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Skin and nail changes in children with sickle cell anemia receiving hydroxyurea therapy

Journal of the American Academy of Dermatology, 2001-05, Vol.44 (5), p.859-861

2001

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Relationship of clinical severity to packed cell rheology in sickle cell anemia

Blood, 1991-11, Vol.78 (10), p.2735-2739

1991

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Diagnosis and management of common bile duct stones in patients with sickle hemoglobinopathies

Journal of pediatric surgery, 1992-05, Vol.27 (5), p.572-575

1992

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Transient erythroblastopenia in the first year of life

American journal of hematology, 1991-07, Vol.37 (3), p.156-158

1991

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Sickle Cell Disease in Children and Adolescents: The Relation of Child and Parent Pain Coping Strategies to Adjustment

Journal of pediatric psychology, 1991-10, Vol.16 (5), p.643-663

1991

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Psychological Adjustment of Mothers of Children and Adolescents with Sickle Cell Disease: The Role of Stress, Coping Methods, and Family Functioning

Journal of pediatric psychology, 1993-10, Vol.18 (5), p.549-559

1993

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Sickle Cell Disease Pain in Children and Adolescents: Change in Pain Frequency and Coping Strategies Over Time

Journal of pediatric psychology, 1993-10, Vol.18 (5), p.621-637

1993

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Testicle transposition in children who undergo low-pelvic or scrotal irradiation

Urology (Ridgewood, N.J.), 1987-05, p.39-41

1987

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Prolonged use of an implantable central venous access system in a child with severe hemophilia

The Journal of pediatrics, 1989, Vol.114 (1), p.100-101

1989

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Coping strategies and laboratory pain in children with sickle cell disease

Annals of behavioral medicine, 1997-01, Vol.19 (1), p.22-29

1997

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Severe neutropenia caused by copper deficiency in a child receiving continuous ambulatory peritoneal dialysis

The Journal of pediatrics, 1986-05, Vol.108 (5), p.735-737

1986

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Platelet antibody in prolonged remission of childhood idiopathic thrombocytopenic purpura

The Journal of pediatrics, 1985-11, Vol.107 (5), p.708-711

1985

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Pain in Sickle Cell Disease: Rates and Risk Factors

Role of Child and Maternal Processes in the Psychological Adjustment of Children With Sickle Cell Disease

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

Erythrocytapheresis can reduce iron overload and prevent the need for chelation therapy in chronically transfused pediatric patients

Quantitative analysis of erythrocytes containing fetal hemoglobin (F cells) in children with sickle cell disease

Elective cholecystectomy in children with sickle hemoglobinopathies: successful outcome using a preoperative transfusion regimen

Psychological Adjustment of Children With Sickle Cell Disease: Stability and Change Over a 10-Month Period

Hydroxyurea: An alternative to transfusion therapy for stroke in sickle cell anemia

Serotype-specific immunoglobulin G antibody responses to pneumococcal polysaccharide vaccine in children with sickle cell anemia: Effects of continued penicillin prophylaxis

Laparoscopic cholecystectomy in young patients with sickle hemoglobinopathies

Long-term management of splenic sequestration in children with sickle cell disease

Pitfalls in newborn hemoglobinopathy screening: Failure to detect β +-thalassemia

Emergency department visits by children with sickle hemoglobinopathies: Factors associated with hospital admission

Skin and nail changes in children with sickle cell anemia receiving hydroxyurea therapy

Relationship of clinical severity to packed cell rheology in sickle cell anemia

Diagnosis and management of common bile duct stones in patients with sickle hemoglobinopathies

Transient erythroblastopenia in the first year of life

Sickle Cell Disease in Children and Adolescents: The Relation of Child and Parent Pain Coping Strategies to Adjustment

Psychological Adjustment of Mothers of Children and Adolescents with Sickle Cell Disease: The Role of Stress, Coping Methods, and Family Functioning

Sickle Cell Disease Pain in Children and Adolescents: Change in Pain Frequency and Coping Strategies Over Time

Testicle transposition in children who undergo low-pelvic or scrotal irradiation

Prolonged use of an implantable central venous access system in a child with severe hemophilia

Coping strategies and laboratory pain in children with sickle cell disease

Severe neutropenia caused by copper deficiency in a child receiving continuous ambulatory peritoneal dialysis

Platelet antibody in prolonged remission of childhood idiopathic thrombocytopenic purpura

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