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SWEE LAY THEIN, MD

MD

Hematology (Internal Medicine) Physician

NPI: 1992697643Individual

Specialties, Licenses & Credentials

Hematology (Internal Medicine) PhysicianPrimary

Internal Medicine — Hematology

Code: 207RH0000X

D0048419(MD)

Research & Publications (20)

Genetic variation on chromosome 6 influences F cell levels in healthy individuals of African descent and HbF levels in sickle cell patients.
PMID 19148297·PLoS One·2009
8-other
A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function.
PMID 19221038·Blood·2009
4-observational
Quantification of hepcidin using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.
PMID 19399775·Rapid Commun Mass Spectrom·2009
8-other
Association of sickle avascular necrosis with bone morphogenic protein 6.
PMID 19093115·Ann Hematol·2009
8-other
A randomized, double-blind, placebo-controlled, crossover study of XP13512/GSK1838262 in the treatment of patients with primary restless legs syndrome.
PMID 19238802·Sleep·2009
4-observational
Genetic architecture of hemoglobin F control.
PMID 19475730·Curr Opin Hematol·2009
6-review
Glucose 6 phosphate dehydrogenase deficiency is not associated with cerebrovascular disease in children with sickle cell anemia.
PMID 19608759·Blood·2009
8-other
Ethnic differences in F cell levels in Jamaica: a potential tool for identifying new genetic loci controlling fetal haemoglobin.
PMID 19120354·Br J Haematol·2009
4-observational
The HBS1L-MYB intergenic interval associated with elevated HbF levels shows characteristics of a distal regulatory region in erythroid cells.
PMID 19528534·Blood·2009
8-other
Discovering the genetics underlying foetal haemoglobin production in adults.
PMID 19344402·Br J Haematol·2009
6-review
Quantitation of hepcidin in human urine by liquid chromatography-mass spectrometry.
PMID 18951868·Anal Biochem·2009
4-observational
The effects of air quality on haematological and clinical parameters in children with sickle cell anaemia.
PMID 18769920·Ann Hematol·2009
8-other
Hydroxyurea therapy lowers circulating DNA levels in sickle cell anemia.
PMID 18615556·Am J Hematol·2008
8-other
The presence of alpha-thalassaemia trait blunts the response to hydroxycarbamide in patients with sickle cell disease.
PMID 18764867·Br J Haematol·2008
4-observational
Genetic modifiers of the beta-haemoglobinopathies.
PMID 18410570·Br J Haematol·2008
6-review
Sickle cell disease in a carrier with pyruvate kinase deficiency.
PMID 19055867·Hematology·2008
5-case
Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and function.
PMID 17874450·Am J Hematol·2008
8-other
A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.
PMID 17767159·Nat Genet·2007
8-other
Circulating DNA: a potential marker of sickle cell crisis.
PMID 17897311·Br J Haematol·2007
4-observational
Hepatic dysfunction in sickle cell disease: a new system of classification based on global assessment.
PMID 17900995·Clin Gastroenterol Hepatol·2007
8-other

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
10 CENTER DR RM 6S241
BETHESDA, MD 20892

Location

Practice Location

10 CENTER DR RM 6S241, BETHESDA, MD
(301) 648-0178

Quick Facts

NPI
1992697643
Entity Type
Individual
Gender
Female
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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