Ian Hambleton
Ian Hambleton
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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
Postsplenectomy course in homozygous sickle cell disease.
OBJECTIVE: To determine whether children with homozygous sickle cell (SS) disease and splenectomy are at greater risk of death, …
J. G. Wright
,
I. R. Hambleton
,
P. W. Thomas
,
N. D. Duncan
,
S. Venugopal
,
G. R. Serjeant
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DOI
Day-care management of sickle cell painful crisis in Jamaica: a model applicable elsewhere?
In the U.K. and the U.S.A., painful crises account for 80-90% of sickle-related hospital admissions, with average durations of 5-11 d. …
M. A. Ware
,
I. Hambleton
,
I. Ochaya
,
G. R. Serjeant
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DOI
Comparison of responses evoked by mild indirect cooling and by sound in the forearm vasculature in patients with homozygous sickle cell disease and in normal subjects.
In normal individuals, novel or noxious stimuli commonly evoke the pattern of the alerting or defence response which includes cutaneous …
J. S. Mohan
,
J. M. Marshall
,
H. L. Reid
,
P. W. Thomas
,
I. Hambleton
,
G. R. Serjeant
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DOI
Peripheral vascular response to mild indirect cooling in patients with homozygous sickle cell (SS) disease and the frequency of painful crisis.
In homozygous sickle cell (SS) disease, skin cooling is a common precipitating factor of the painful crisis which is associated with …
J. Mohan
,
J. M. Marshall
,
H. L. Reid
,
P. W. Thomas
,
I. Hambleton
,
G. R. Serjeant
Cite
DOI
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