Sumalee Jindadamrongwech
Overview
Explore the profile of Sumalee Jindadamrongwech including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
15
Citations
74
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Banyatsuppasin W, Jindadamrongwech S, Limrungsikul A, Butthep P
Hemoglobin
. 2017 Dec;
41(4-6):260-266.
PMID: 29251006
Thalassemias and glucose-6-phosphate dehydrogenase (G6PD) deficiency are the most common inherited blood disorders. They are distributed among populations living in malaria endemic regions resulting in survival advantage from severe malaria...
2.
Kamseng P, Trakulsrichai S, Trachoo O, Yimniam W, Panthan B, Jittorntam P, et al.
Hematology
. 2016 Sep;
22(2):114-118.
PMID: 27670359
Objective: To investigate the cause(s) of a Thai male proband presenting low oxygen saturation by pulse oximetry (SpO) and severe anemia. Methods: As Hb variant was suspected, Hb typing was...
3.
Pongjantharasatien K, Banyatsuppasin W, Pounsawat S, Jindadamrongwech S
Hemoglobin
. 2016 Aug;
40(4):283-4.
PMID: 27492767
α-Thalassemia (α-thal) is one of the most common genetic diseases in Thailand. Homozygosity of α-thal-1 (- -/- -) and compound heterozygosity of α-thal-1/α-thal-2 (- -/-α) leads to Hb Bart's (γ4)...
4.
Ruangrai W, Jindadamrongwech S
Southeast Asian J Trop Med Public Health
. 2016 Apr;
47(1):84-91.
PMID: 27086429
Genetic factors influencing Hb F content in adult red blood cells include β-thalassemia genotypes, co-inheritance of α-thalassemia traits and single nucleotide polymorphisms (SNPs). Genotyping of α- and β-thalassemia and five...
5.
Yimniam W, Jindadamrongwech S
J Clin Lab Anal
. 2016 Feb;
30(5):633-40.
PMID: 26892340
Background: Definitive detection of hemoglobin (Hb) variants requires DNA sequencing. High-resolution melting (HRM) analysis of polymerase chain reaction (PCR) amplicons was applied to detect and discriminate among uncommon α-Hb variants...
6.
Wisedpanichkij R, Jindadamrongwech S, Butthep P
Hemoglobin
. 2015 May;
39(3):190-5.
PMID: 26016900
Laboratory investigation of hemoglobinopathies includes complete blood count (CBC), hemoglobin (Hb) typing by high performance liquid chromatography (HPLC) and DNA analysis. DNA analysis is the most reliable method but requires...
7.
Butthep P, Wisedpanichkij R, Jindadamrongwech S, Fucharoen S
Blood Cells Mol Dis
. 2014 Dec;
54(2):170-6.
PMID: 25477265
Serum EPO concentration is related primarily to the rate of erythrocyte production and, under the stimulation of hypoxia, increases exponentially as hemoglobin (Hb) decreased. The level of EPO was determined...
8.
Siriworadechkul S, Jindadamrongwech S, Chuncharunee S, Aupparakkitanon S
Ann Clin Lab Sci
. 2014 Nov;
44(4):437-42.
PMID: 25361929
One of the factors affecting the degree of severity in β-thalassemia disease is the presence of unmatched α-hemoglobin chains. Thus, the expression levels of globin genes in reticulocytes of β-thalassemia...
9.
Nillakupt K, Nathalang O, Arnutti P, Jindadamrongwech S, Boonsiri T, Panichkul S, et al.
J Med Assoc Thai
. 2012 Sep;
95 Suppl 5:S124-32.
PMID: 22934458
Objective: To determine the prevalence, molecular characteristics and hematological study of thalassemia in Tha Kradarn Subdistrict Chachoengsao Province. Material And Method: The present study population consisted of266 participants from Moo...
10.
Sroymora S, Jindadamrongwech S, Butthep P, Chuncharunee S
Hemoglobin
. 2012 Mar;
36(3):293-8.
PMID: 22384838
A rare nondeletional α-thalassemia-2 (α-thal-2) allele was identified in a Thai boy with Hb H (β4) disease. The proband has α-thal-1 (- -(SEA) type) together with a non productive Hb...