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Long-term stroke risk in children with sickle cell disease screened with transcranial doppler

Annals of neurology, 1997-11, Vol.42 (5), p.699-704

1997

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Prevention of a First Stroke by Transfusions in Children with Sickle Cell Anemia and Abnormal Results on Transcranial Doppler Ultrasonography

The New England journal of medicine, 1998-07, Vol.339 (1), p.5-11

1998

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Stroke Prevention Trial in Sickle Cell Anemia

Controlled clinical trials, 1998-02, Vol.19 (1), p.110-129

1998

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Neuropsychologic impairment in children with sickle cell anemia

Pediatrics (Evanston), 1989-12, Vol.84 (6), p.1077-1085

1989

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Identification of the major structural and nonstructural proteins encoded by human parvovirus B19 and mapping of their genes by procaryotic expression of isolated genomic fragments

Journal of Virology, 1986-11, Vol.60 (2), p.548-557

1986

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Clinical and Genetic Heterogeneity in Black Patients With Homozygous β-Thalassemia From the Southeastern United States

Blood, 1988-09, Vol.72 (3), p.1007-1014

1988

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Molecular characterization of Hb S(C) β‐thalassemia in American blacks

American journal of hematology, 1991-09, Vol.38 (1), p.9-14

1991

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Spleen in sickle cell anemia: Comparative studies of Nigerian and U.S. patients

American journal of hematology, 1993-03, Vol.42 (3), p.316-321

1993

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Neuropsychological Impairment in Children With Sickle Cell Anemia and Cerebrovascular Accidents

Clinical pediatrics, 1994-09, Vol.33 (9), p.517-524

1994

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Different ζ globin gene deletions among black Americans

Human genetics, 1986-07, Vol.73 (3), p.221-224

1986

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Haplotypes of βS Chromosomes Among Patients with Sickle Cell Anemia from Georgia

Hemoglobin, 1986, Vol.10 (6), p.623-642

1986

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Biphasic hemolysin hemolytic anemia: Reappraisal of an acute immune hemolytic anemia of infancy and childhood

American journal of hematology, 1992-03, Vol.39 (3), p.220-222

1992

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Effects of α‐thalassemia‐2 on the developmental changes of hematological values in children with sickle cell disease from georgia

American journal of hematology, 1987-08, Vol.25 (4), p.389-400

1987

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Three Sickle Cell Anemia Patients Each with a Different α Chain Variant. Diagnostic Complications

Hemoglobin, 1993, Vol.17 (4), p.295-301

1993

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HB H Disease and Mild Mental Retardation in a Black Girl with a HB S Heterozygosity

Hemoglobin, 1992, Vol.16 (5), p.431-434

1992

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Quantitation of erythropoietin stimulatory activity using [3H]thymidine uptake by K562 cells

Experimental hematology, 1989-02, Vol.17 (2), p.102-105

1989

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Hb Hammersmith [beta 42(CD1) Phe-->Ser]: occurrence as a de novo mutation in black monozygotic twins with multiple congenital anomalies

Journal of pediatric hematology/oncology, 1998-11, Vol.20 (6), p.563-566

1998

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Down's syndrome and acute myelofibrosis. Time study of dna content during the progression to leukemia

Cancer, 1988-06, Vol.61 (11), p.2239-2243

1988

Volltextzugriff (PDF)

Sickle cell anemia in children: practical issues for the pediatrician

Pediatric annals, 1998-08, Vol.27 (8), p.521-524

McKie, V C

1998

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Severe Hb S‐β°‐thalassaemia with a T → C substitution in the donor splice site of the first intron of the β‐globin gene

British journal of haematology, 1989-01, Vol.71 (1), p.113-117

1989

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Cerebral vessel stenosis in sickle cell disease: criteria for detection by transcranial Doppler

The American journal of pediatric hematology/oncology, 1990, Vol.12 (3), p.277

1990

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Hb Evans or α262(E11)Val→Metβ2; an Unstable Hemoglobin Causing a Mild Hemolytic Anemia

Hemoglobin, 1989, Vol.13 (6), p.557-566

1989

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Idiopathic thrombocytopenic purpura in childhood: a current perspective

Journal of the Medical Association of Georgia, 1987-11, Vol.76 (11), p.771

1987

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Unusual encephalopathy after acute chest syndrome in sickle cell disease: acute necrotizing encephalitis

Journal of pediatric hematology/oncology, 2002-10, Vol.24 (7), p.585-588

2002

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Hb Evans or alpha 262(E11)Val----Met beta 2; an unstable hemoglobin causing a mild hemolytic anemia

Hemoglobin, 1989, Vol.13 (6), p.557-566

1989

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Long-term stroke risk in children with sickle cell disease screened with transcranial doppler

Prevention of a First Stroke by Transfusions in Children with Sickle Cell Anemia and Abnormal Results on Transcranial Doppler Ultrasonography

Stroke Prevention Trial in Sickle Cell Anemia

Neuropsychologic impairment in children with sickle cell anemia

Identification of the major structural and nonstructural proteins encoded by human parvovirus B19 and mapping of their genes by procaryotic expression of isolated genomic fragments

Clinical and Genetic Heterogeneity in Black Patients With Homozygous β-Thalassemia From the Southeastern United States

Molecular characterization of Hb S(C) β‐thalassemia in American blacks

Spleen in sickle cell anemia: Comparative studies of Nigerian and U.S. patients

Neuropsychological Impairment in Children With Sickle Cell Anemia and Cerebrovascular Accidents

Different ζ globin gene deletions among black Americans

Haplotypes of βS Chromosomes Among Patients with Sickle Cell Anemia from Georgia

Biphasic hemolysin hemolytic anemia: Reappraisal of an acute immune hemolytic anemia of infancy and childhood

Effects of α‐thalassemia‐2 on the developmental changes of hematological values in children with sickle cell disease from georgia

Three Sickle Cell Anemia Patients Each with a Different α Chain Variant. Diagnostic Complications

HB H Disease and Mild Mental Retardation in a Black Girl with a HB S Heterozygosity

Quantitation of erythropoietin stimulatory activity using [3H]thymidine uptake by K562 cells

Hb Hammersmith [beta 42(CD1) Phe-->Ser]: occurrence as a de novo mutation in black monozygotic twins with multiple congenital anomalies

Down's syndrome and acute myelofibrosis. Time study of dna content during the progression to leukemia

Sickle cell anemia in children: practical issues for the pediatrician

Severe Hb S‐β°‐thalassaemia with a T → C substitution in the donor splice site of the first intron of the β‐globin gene

Cerebral vessel stenosis in sickle cell disease: criteria for detection by transcranial Doppler

Hb Evans or α262(E11)Val→Metβ2; an Unstable Hemoglobin Causing a Mild Hemolytic Anemia

Idiopathic thrombocytopenic purpura in childhood: a current perspective

Unusual encephalopathy after acute chest syndrome in sickle cell disease: acute necrotizing encephalitis

Hb Evans or alpha 262(E11)Val----Met beta 2; an unstable hemoglobin causing a mild hemolytic anemia

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