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Causes of death and early life determinants of survival in homozygous sickle cell disease: The Jamaican cohort study from birth.
- Published in:
- PLoS ONE, 2018, v. 13, n. 3, p. 1, doi. 10.1371/journal.pone.0192710
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- Article
Comparison of Haematological Features of the β<sup>0</sup> and β<sup>+</sup> Thalassaemia Traits in Jamaican Negroes.
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- British Journal of Haematology, 1977, v. 36, n. 2, p. 161, doi. 10.1111/j.1365-2141.1977.tb00636.x
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- Article
Red cell antibodies in patients with homozygous sickle cell disease: a comparison of patients in Jamaica and the United Kingdom.
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- British Journal of Haematology, 2001, v. 113, n. 3, p. 661, doi. 10.1046/j.1365-2141.2001.02819.x
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- Article
Retained Splenic Function in an Indian Population with Homozygous Sickle Cell Disease May Have Important Clinical Significance.
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- Indian Journal of Community Medicine, 2021, v. 46, n. 4, p. 715, doi. 10.4103/ijcm.IJCM_1054_20
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- Article
Haemoglobin Variant Screening in Jamaica: Meeting Student's Request.
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- British Journal of Haematology, 2016, v. 172, n. 4, p. 634, doi. 10.1111/bjh.13531
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- Article
Newborn screening for abnormal haemoglobins in Jamaica: Practical issues in an island programme.
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- Journal of Medical Screening, 2022, v. 29, n. 4, p. 219, doi. 10.1177/09691413221111209
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- Article
The clinical significance of serum transferrin receptor levels in sickle cell disease.
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- British Journal of Haematology, 1993, v. 84, n. 2, p. 301, doi. 10.1111/j.1365-2141.1993.tb03068.x
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- Article
The haematology of homozygous sickle cell disease after the age of 40 years.
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- British Journal of Haematology, 1991, v. 77, n. 3, p. 382, doi. 10.1111/j.1365-2141.1991.tb08588.x
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- Article
Sickle cell-β<sup>+</sup> thalassaemia in Orissa State, India.
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- British Journal of Haematology, 1991, v. 77, n. 2, p. 215, doi. 10.1111/j.1365-2141.1991.tb07980.x
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- Article
Fetal haemoglobin and pregnancy in homozygous sickle cell disease.
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- British Journal of Haematology, 1989, v. 72, n. 3, p. 434, doi. 10.1111/j.1365-2141.1989.tb07728.x
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- Article
A trial of folate supplementation in children with homozygous sickle cell disease.
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- British Journal of Haematology, 1983, v. 54, n. 4, p. 589, doi. 10.1111/j.1365-2141.1983.tb02138.x
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- Article
Post-natal decline of fetal haemoglobin in homozygous sickle cell disease: relationship to parental Hb F levels.
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- British Journal of Haematology, 1982, v. 52, n. 3, p. 455, doi. 10.1111/j.1365-2141.1982.tb03915.x
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- Article
The Development of Haematological Changes in Homozygous Sickle Cell Disease: a Cohort Study from Birth to 6 Years.
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- British Journal of Haematology, 1981, v. 48, n. 4, p. 533, doi. 10.1111/j.1365-2141.1981.tb02750.x
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- Article
Determinants of Haemoglobin Level in Sickle Cell-Haemoglobin C Disease.
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- British Journal of Haematology, 1979, v. 43, n. 1, p. 49, doi. 10.1111/j.1365-2141.1979.tb03718.x
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- Article
Comparison of Sickle Cell-β° Thalassaemia with Homozygous Sickle Cell Disease.
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- British Journal of Haematology, 1979, v. 41, n. 1, p. 83, doi. 10.1111/j.1365-2141.1979.tb03684.x
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- Article