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Literature DB >> 2817958

Gall stones in homozygous sickle cell disease.

D K Webb, D T Dunn, G R Serjeant.

Abstract

Mesh：

Year: 1989 PMID： 2817958 PMCID： PMC1792710 DOI： 10.1136/adc.64.9.1342

Source DB: PubMed Journal: Arch Dis Child ISSN： 0003-9888 Impact factor: 3.791

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4 in total

1. Cholelithiasis in patients with major sickle hemoglobinopathies.

Authors: M B Rennels; M G Dunne; N J Grossman; A D Schwartz
Journal: Am J Dis Child Date: 1984-01

2. Haematological change in sickle cell-haemoglobin C disease and in sickle cell-beta thalassaemia: a cohort study from birth.

Authors: M C Stevens; G H Maude; M Beckford; Y Grandison; K Mason; B E Serjeant; B Taylor; J M Topley; G R Serjeant
Journal: Br J Haematol Date: 1985-06 Impact factor: 6.998

3. The development of haematological changes in homozygous sickle cell disease: a cohort study from birth to 6 years.

Authors: G R Serjeant; Y Grandison; Y Lowrie; K Mason; J Phillips; B E Serjeant; S Vaidya
Journal: Br J Haematol Date: 1981-08 Impact factor: 6.998

4. Gall stones in Jamaican children with homozygous sickle cell disease.

Authors: D K Webb; J S Darby; D T Dunn; S I Terry; G R Serjeant
Journal: Arch Dis Child Date: 1989-05 Impact factor: 3.791

4 in total

1 in total

1. Influence of UGT1A1 promoter polymorphism, α-thalassemia and β^s haplotype in bilirubin levels and cholelithiasis in a large sickle cell anemia cohort.

Authors: Jéssica V G F Batista; Gabriela S Arcanjo; Thais H C Batista; Marcondes J Sobreira; Rodrigo M Santana; Igor F Domingos; Betânia L Hatzlhofer; Diego A Falcão; Diego A Pereira-Martins; Jéssica M Oliveira; Amanda S Araujo; Luana P M Laranjeira; Fernanda S Medeiros; Flávia P Albuquerque; Dulcinéia M Albuquerque; Magnun N Santos; Manuela F Hazin; Ana C Dos Anjos; Fernando F Costa; Aderson S Araujo; Antonio R Lucena-Araujo; Marcos A Bezerra
Journal: Ann Hematol Date: 2021-02-01 Impact factor: 3.673

1 in total

Gall stones in homozygous sickle cell disease.

1. Cholelithiasis in patients with major sickle hemoglobinopathies.

2. Haematological change in sickle cell-haemoglobin C disease and in sickle cell-beta thalassaemia: a cohort study from birth.

3. The development of haematological changes in homozygous sickle cell disease: a cohort study from birth to 6 years.

4. Gall stones in Jamaican children with homozygous sickle cell disease.

1. Influence of UGT1A1 promoter polymorphism, α-thalassemia and βs haplotype in bilirubin levels and cholelithiasis in a large sickle cell anemia cohort.

1. Influence of UGT1A1 promoter polymorphism, α-thalassemia and β^s haplotype in bilirubin levels and cholelithiasis in a large sickle cell anemia cohort.