Zobrazeno 1 - 10
of 251
pro vyhledávání: '"Graham R. Serjeant"'
Autor:
Graham R. Serjeant
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
The sickle cell gene in India represents a separate occurrence of the HbS mutation (the Asian haplotype), which has occurred against a genetic background characterised by high levels of fetal haemoglobin and widely varying frequencies of alpha thalas
Externí odkaz:
https://doaj.org/article/6b86d2e6106e4c169c426a2a1d638bb2
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
In 1986, a paper in the Lancet was the first to collate hematology, molecular findings, and clinical features of homozygous sickle cell (SS) disease in India. The paper came from the group organized by Professor Bimal Kar in Burla Medical College, Sa
Externí odkaz:
https://doaj.org/article/865be4b4bd24482ca7564c65522fc71d
Publikováno v:
Indian Journal of Community Medicine, Vol 42, Iss 3, Pp 167-169 (2017)
Background: Sickle cell disease is a common problem across central India, but its clinical features may differ from that in African populations. There is a need to define the features of sickle cell disease in India, and the current study addresses s
Externí odkaz:
https://doaj.org/article/b63fb16225924da9b32d00588c7f2eff
Autor:
Graham R Serjeant, Nicki Chin, Monika R Asnani, Beryl E Serjeant, Karlene P Mason, Ian R Hambleton, Jennifer M Knight-Madden
Publikováno v:
PLoS ONE, Vol 13, Iss 3, p e0192710 (2018)
Globally, the majority of persons born with sickle cell disease do not have access to hydroxyurea or more expensive interventions. The objectives were to estimate the survival in homozygous sickle cell disease, unbiased by symptomatic selection and t
Externí odkaz:
https://doaj.org/article/a3d5b7fa3b904849ab13c0d12123c214
Autor:
Graham R Serjeant, Beryl E Serjeant, Karlene P Mason, Felicea Gibson, Ruth-Ann Gardner, Lansford Warren, Ian R Hambleton, Swee L Thein, Margit Happich, Andreas E Kulozik
Publikováno v:
Journal of medical screening. 29(4)
Objective To report the diagnostic challenges of newborn screening for abnormal haemoglobins. Setting Cord blood samples from 13 hospitals in southwest Jamaica taken in 2008–2019. Methods Blood spots, collected from the umbilical cord, were analyse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec15bcc37b1840fc1fa109c76f2a5e36
https://pubmed.ncbi.nlm.nih.gov/35934992
https://pubmed.ncbi.nlm.nih.gov/35934992
Publikováno v:
Indian Journal of Medical Research, Vol 151, Iss 4, Pp 326-332 (2020)
The Indian Journal of Medical Research
The Indian Journal of Medical Research
Background & objectives: Homozygous sickle cell (SS) disease in Central India runs a more severe clinical course than reports from other areas of India. The current study was undertaken to compare the disease in Central India (Nagpur) with that in Ja
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05e56e14e0e57be8526017bf8a3bb408
http://www.ijmr.org.in/article.asp?issn=0971-5916
http://www.ijmr.org.in/article.asp?issn=0971-5916
Autor:
Graham R Serjeant
Publikováno v:
Expert review of hematology. 15(2)
The hematological and clinical features vary markedly between the different genotypes of sickle cell disease. Even within the single genotype of homozygous sickle cell disease (HbSS), there is marked variability that is presumed to result from intera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7846e9a40bad3a3840bfce4f5d7e0c80
https://pubmed.ncbi.nlm.nih.gov/35143361
https://pubmed.ncbi.nlm.nih.gov/35143361
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
Frontiers in Medicine
Frontiers in Medicine
In 1986, a paper in the Lancet was the first to collate hematology, molecular findings, and clinical features of homozygous sickle cell (SS) disease in India. The paper came from the group organized by Professor Bimal Kar in Burla Medical College, Sa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40e6d84c9c06d3b5b4f637b394bc9848
https://www.frontiersin.org/articles/10.3389/fmed.2021.745337/full
https://www.frontiersin.org/articles/10.3389/fmed.2021.745337/full
Publikováno v:
BJOG : an international journal of obstetrics and gynaecologyReferences. 128(10)
OBJECTIVE To document pregnancy outcome in homozygous sickle cell (SS) disease and in age-matched controls with a normal haemoglobin genotype followed from birth for up to 45 years. METHODS A total of 100 000 consecutive non-operative deliveries scre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd9a804368e7a5786654465376e9c536
https://pubmed.ncbi.nlm.nih.gov/33683802
https://pubmed.ncbi.nlm.nih.gov/33683802
Autor:
J. Christakis, G.S. Lucas, Ronald L. Nagel, K De Ceulaer, Graham R. Serjeant, A.J. Bellingham, H.H. Billett, Dimitris Loukopoulos, John Stuart
Publikováno v:
Clinical Hemorheology and Microcirculation. 10:35-42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ace401ba40397109cf4ca2235b38a2e8
https://doi.org/10.3233/ch-1990-10104
https://doi.org/10.3233/ch-1990-10104