Ian Hambleton
Ian Hambleton
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"Sickle Cell/*complications/genetics"
Homozygous sickle cell disease in Uganda and Jamaica a comparison of Bantu and Benin haplotypes.
OBJECTIVE: To compare the haematological and clinical features of homozygous sickle cell (SS) disease in Bantu and Benin haplotypes in …
C. Ndugwa
,
D. Higgs
,
C. Fisher
,
I. Hambleton
,
K. Mason
,
B. E. Serjeant
,
G. R. Serjeant
Cite
The changing face of homozygous sickle cell disease: 102 patients over 60 years.
Earlier reports on homozygous sickle cell (SS) disease have been biased by severely affected cases. The Jamaican clinic which seeks to …
G. R. Serjeant
,
B. E. Serjeant
,
K. P. Mason
,
I. R. Hambleton
,
C. Fisher
,
D. R. Higgs
Cite
DOI
Albuminuria and renal function in homozygous sickle cell disease: observations from a cohort study.
BACKGROUND: The glomerular filtration rate (GFR) in homozygous sickle cell (SS) disease is supranormal in childhood but falls steeply …
Joanne Thompson
,
Marvin Reid
,
Ian Hambleton
,
Graham R. Serjeant
Cite
DOI
Significance of fever in Jamaican patients with homozygous sickle cell disease.
OBJECTIVE: To investigate the cause and outcome of high fever in Jamaican children with homozygous sickle cell disease. DESIGN: …
K. J. Wierenga
,
I. R. Hambleton
,
R. M. Wilson
,
H. Alexander
,
B. E. Serjeant
,
G. R. Serjeant
Cite
DOI
Abnormal venous function in patients with homozygous sickle cell (SS) disease and chronic leg ulcers.
Chronic leg ulceration is a major cause of morbidity in homozygous sickle cell (SS) disease in Jamaica. These ulcers have features in …
J. S. Mohan
,
J. E. Vigilance
,
J. M. Marshall
,
I. R. Hambleton
,
H. L. Reid
,
G. R. Serjeant
Cite
Recurrent infections in homozygous sickle cell disease.
The characteristics of 214 episodes of invasive bacterial infection among 176 patients with homozygous sickle cell (SS) disease were …
S. A. Magnus
,
I. R. Hambleton
,
F. Moosdeen
,
G. R. Serjeant
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DOI
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