Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 3
1980 2
1981 7
1982 2
1983 1
1984 3
1985 4
1986 5
1987 2
1988 1
1990 4
1991 4
1992 2
1993 3
1994 5
1995 3
1996 4
1997 3
1998 2
1999 3
2000 3
2001 5
2002 2
2004 3
2005 4
2006 1
2007 1
2008 3
2009 1
2011 3
2012 3
2013 3
2015 1
2016 2
2018 1
2019 1
2021 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

97 results

Results by year

Filters applied: . Clear all
Page 1
Folate supplementation in people with sickle cell disease.
Dixit R, Nettem S, Madan SS, Soe HHK, Abas AB, Vance LD, Stover PJ. Dixit R, et al. Cochrane Database Syst Rev. 2018 Mar 16;3(3):CD011130. doi: 10.1002/14651858.CD011130.pub3. Cochrane Database Syst Rev. 2018. PMID: 29546732 Free PMC article. Review.
This was a double-blind placebo-controlled quasi-randomised triaI of supplementation of folic acid in people with SCD. A total of 117 children with homozygous sickle cell (SS) disease aged six months to four years of age participated over a one-year pe …
This was a double-blind placebo-controlled quasi-randomised triaI of supplementation of folic acid in people with SCD. A total of 117 childr …
Folate supplementation in people with sickle cell disease.
Dixit R, Nettem S, Madan SS, Soe HH, Abas AB, Vance LD, Stover PJ. Dixit R, et al. Cochrane Database Syst Rev. 2016 Feb 16;2:CD011130. doi: 10.1002/14651858.CD011130.pub2. Cochrane Database Syst Rev. 2016. PMID: 26880182 Free PMC article. Updated. Review.
This was a double-blind placebo-controlled quasi-randomised triaI of supplementation of folic acid in people with sickle cell disease. A total of 117 children with homozygous sickle cell (SS) disease aged six months to four years of age participated ov …
This was a double-blind placebo-controlled quasi-randomised triaI of supplementation of folic acid in people with sickle cell disease. A tot …
The natural history of sickle cell disease.
Serjeant GR. Serjeant GR. Cold Spring Harb Perspect Med. 2013 Oct 1;3(10):a011783. doi: 10.1101/cshperspect.a011783. Cold Spring Harb Perspect Med. 2013. PMID: 23813607 Free PMC article. Review.
The spectrum of resulting conditions is therefore influenced by the geography of individual hemoglobin genes, but in most populations, the commonest genotype at birth is homozygous sickle cell (SS) disease. Because this genotype generally manifests a g …
The spectrum of resulting conditions is therefore influenced by the geography of individual hemoglobin genes, but in most populations, the c …
Pregnancy outcome in homozygous sickle cell disease: observations from the Jamaican Birth Cohort.
Lewis G, Thame M, Howitt C, Hambleton I, Serjeant GR. Lewis G, et al. BJOG. 2021 Sep;128(10):1703-1710. doi: 10.1111/1471-0528.16696. Epub 2021 Apr 6. BJOG. 2021. PMID: 33683802
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. ...
OBJECTIVE: To document pregnancy outcome in homozygous sickle cell (SS) disease and in age-matched controls with …
Sickle Cell Disease in Central India: A Potentially Severe Syndrome.
Jain D, Warthe V, Dayama P, Sarate D, Colah R, Mehta P, Serjeant G. Jain D, et al. Indian J Pediatr. 2016 Oct;83(10):1071-6. doi: 10.1007/s12098-016-2081-7. Epub 2016 Apr 7. Indian J Pediatr. 2016. PMID: 27053181
OBJECTIVES: To explore clinical, hematological and molecular features of homozygous sickle cell (SS) disease in central India. METHODS: Focusing on the pediatric age group attending a clinic at the Akola Government Medical College, Akola, Maharashtra S …
OBJECTIVES: To explore clinical, hematological and molecular features of homozygous sickle cell (SS) disease in …
UGT1A1 variation and gallstone formation in sickle cell disease.
Haverfield EV, McKenzie CA, Forrester T, Bouzekri N, Harding R, Serjeant G, Walker T, Peto TE, Ward R, Weatherall DJ. Haverfield EV, et al. Blood. 2005 Feb 1;105(3):968-72. doi: 10.1182/blood-2004-02-0521. Epub 2004 Sep 23. Blood. 2005. PMID: 15388579 Free article.
Pigment gallstones are a common clinical complication of sickle cell (SS) disease. Genetic variation in the promoter of uridine diphosphate (UDP)-glucuronosyltransferase 1A1 (UGT1A1) underlies Gilbert syndrome, a chronic form of unconjugated hyperbilir …
Pigment gallstones are a common clinical complication of sickle cell (SS) disease. Genetic variation in the prom …
Albuminuria and renal function in homozygous sickle cell disease: observations from a cohort study.
Thompson J, Reid M, Hambleton I, Serjeant GR. Thompson J, et al. Arch Intern Med. 2007 Apr 9;167(7):701-8. doi: 10.1001/archinte.167.7.701. Arch Intern Med. 2007. PMID: 17420429
BACKGROUND: The glomerular filtration rate (GFR) in homozygous sickle cell (SS) disease is supranormal in childhood but falls steeply with age, often culminating in renal failure. ...
BACKGROUND: The glomerular filtration rate (GFR) in homozygous sickle cell (SS) disease is supranormal in childh …
Homozygous sickle cell disease in Uganda and Jamaica a comparison of Bantu and Benin haplotypes.
Ndugwa C, Higgs D, Fisher C, Hambleton I, Mason K, Serjeant BE, Serjeant GR. Ndugwa C, et al. West Indian Med J. 2012 Oct;61(7):684-91. West Indian Med J. 2012. PMID: 23620965
OBJECTIVE: To compare the haematological and clinical features of homozygous sickle cell (SS) disease in Bantu and Benin haplotypes in a cross-sectional study of 115 Ugandan patients attending the Sickle Cell Clinic at Mulago Hospital, Kampala, Uganda, …
OBJECTIVE: To compare the haematological and clinical features of homozygous sickle cell (SS) disease in Bantu a …
Sickle cell disease and age at menarche in Jamaican girls: observations from a cohort study.
Serjeant GR, Singhal A, Hambleton IR. Serjeant GR, et al. Arch Dis Child. 2001 Nov;85(5):375-8. doi: 10.1136/adc.85.5.375. Arch Dis Child. 2001. PMID: 11668096 Free PMC article.
AIMS: (1) To investigate the distribution of age at menarche in a representative sample of 99 patients with homozygous sickle cell (SS) disease, 69 with sickle cell haemoglobin C (SC) disease, and 100 controls with a normal haemoglobin (AA) genotype fo …
AIMS: (1) To investigate the distribution of age at menarche in a representative sample of 99 patients with homozygous sickle cell …
The changing face of homozygous sickle cell disease: 102 patients over 60 years.
Serjeant GR, Serjeant BE, Mason KP, Hambleton IR, Fisher C, Higgs DR. Serjeant GR, et al. Int J Lab Hematol. 2009 Dec;31(6):585-96. doi: 10.1111/j.1751-553X.2008.01089.x. Epub 2008 Jul 17. Int J Lab Hematol. 2009. PMID: 18644042
Earlier reports on homozygous sickle cell (SS) disease have been biased by severely affected cases. ...
Earlier reports on homozygous sickle cell (SS) disease have been biased by severely affected cases. ...
97 results