A Mobile App, KhunLook, to Support Thai Parents and Caregivers With Child Health Supervision: Development, Validation, and Acceptability Study

Authors: Areemit, Rosawan, Lumbiganon, Pagakrong, Suphakunpinyo, Chanyut, Jetsrisuparb, Arunee, Sutra, Sumitr, Sripanidkulchai, Kunwadee

Source: JMIR mHealth and uHealth, Vol 8, Iss 10, p e15116 (2020)

Subject Terms: Information technology, T58.5-58.64, Public aspects of medicine, RA1-1270

File Description: electronic resource

Relation: http://mhealth.jmir.org/2020/10/e15116/; https://doaj.org/toc/2291-5222

Access URL: https://doaj.org/article/e982ece732ab4b13975e03c6900d3bf3

Abnormalities of teeth and jaws in thalassemia pediatric patients.

Authors: Lertsirivorakul, Jinda, Sukanindr, Parichamon, Jetsrisuparb, Arunee, Pitiphat, Waranuch, Sutthiprapaporn, Pipop

Source: Special Care in Dentistry; Jan/Feb2025, Vol. 45 Issue 1, p1-9, 9p

Subject Terms: MAXILLARY sinus, CHILD patients, FISHER exact test, PEDIATRIC clinics, DENTAL caries

Hematopoietic Stem Cell Transplantation for Severe Thalassemia Patients from Haploidentical Donors Using a Novel Conditioning Regimen

Authors: Anurathapan, Usanarat, Hongeng, Suradej, Pakakasama, Samart, Songdej, Duantida, Sirachainan, Nongnuch, Pongphitcha, Pongpak, Chuansumrit, Ampaiwan, Charoenkwan, Pimlak, Jetsrisuparb, Arunee, Sanpakit, Kleebsabai, Rujkijyanont, Piya, Meekaewkunchorn, Arunotai, Lektrakul, Yujinda, Iamsirirak, Pornchanok, Surapolchai, Pacharapan, Sirireung, Somtawin, Sruamsiri, Rosarin, Wahidiyat, Pustika Amalia, Andersson, Borje S.

Source: In Biology of Blood and Marrow Transplantation June 2020 26(6):1106-1112

Prevalence and predictors of cardiac and liver iron overload in patients with thalassemia: A multicenter study based on real-world data

Authors: Krittayaphong, Rungroj, Viprakasit, Vip, Saiviroonporn, Pairash, Siritanaratkul, Noppadol, Siripornpitak, Suvipaporn, Meekaewkunchorn, Arunotai, Kirawittaya, Thawatchai, Sripornsawan, Pornpun, Jetsrisuparb, Arunee, Srinakarin, Jiraporn, Wong, Peerapon, Phalakornkul, Nuttaporntira, Sinlapamongkolkul, Phakatip, Wood, John

Source: In Blood Cells, Molecules and Diseases July 2017 66:24-30

Frataxin expression in reticulocytes of non-splenectomized and splenectomized patients with HbE-β-thalassaemia

Authors: Suebpeng, Yollada, Jetsrisuparb, Arunee, Fucharoen, Supan, Tripatara, Amporn

Source: In Clinical Biochemistry April 2016 49(6):463-466

Severe bacterial infections in patients with non-transfusion-dependent thalassemia: prevalence and clinical risk factors

Authors: Teawtrakul, Nattiya, Jetsrisuparb, Arunee, Sirijerachai, Chittima, Chansung, Kanchana, Wanitpongpun, Chinadol

Source: In International Journal of Infectious Diseases October 2015 39:53-56

Molecular and hematological characteristics of a novel form of α-globin gene triplication: The hemoglobin St.Luke's-Thailand [α95(G2)Pro→Arg] or Hb St. Luke's [A2] HBA2

Authors: Singha, Kritsada, Fucharoen, Goonnapa, Jetsrisuparb, Arunee, Fucharoen, Supan

Source: In Clinical Biochemistry May 2013 46(7-8):675-680

Molecular, hematological and clinical aspects of thalassemia major and thalassemia intermedia associated with Hb E-β-thalassemia in Northeast Thailand

Authors: Nuntakarn, Lalana, Fucharoen, Supan, Fucharoen, Goonnapa, Sanchaisuriya, Kanokwan, Jetsrisuparb, Arunee, Wiangnon, Surapon

Source: In Blood Cells, Molecules and Diseases 2009 42(1):32-35

Mitochondrial ferritin expression in erythroid cells from patients with alpha-thalassaemia.

Authors: Putburee, Rungtip¹, Jetsrisuparb, Arunee^1,2, Fucharoen, Supan¹, Tripatara, Amporn¹ amptri@kku.ac.th

Source: Hematology. Dec2018, Vol. 23 Issue 10, p844-848. 5p.

Subject Terms: *FERRITIN, *BETA-Thalassemia, *OXIDATIVE stress, *IRON deficiency, *HEMOGLOBINS, *GENE expression

Hemostatic alterations in splenectomized and non-splenectomized patients with β-thalassemia/hemoglobin E disease

Authors: Tripatara, Amporn, Jetsrisuparb, Arunee, Teeratakulpisarn, Jamaree, Kuaha, Kunnika

Source: In Thrombosis Research 2007 120(6):805-810

α/β-Globin mRNA ratio determination by multiplex quantitative real-time reverse transcription-polymerase chain reaction as an indicator of globin gene function

Authors: Chaisue, Chulaporn, Kitcharoen, Suttiphan, Wilairat, Prapon, Jetsrisuparb, Arunee, Fucharoen, Goonnapa, Fucharoen, Supan

Source: In Clinical Biochemistry 2007 40(18):1373-1377

Epidemiologic study of major complications in adolescent and adult patients with thalassemia in Northeastern Thailand: the E-SAAN study phase I.

Authors: Teawtrakul, Nattiya¹ (AUTHOR) nattiya@kku.ac.th, Jetsrisuparb, Arunee² (AUTHOR), Pongudom, Saranya³ (AUTHOR), Sirijerachai, Chittima¹ (AUTHOR), Chansung, Kanchana¹ (AUTHOR), Wanitpongpun, Chinadol¹ (AUTHOR), Fucharoen, Supan⁴ (AUTHOR)

Source: Hematology. Jan2018, Vol. 23 Issue 1, p55-60. 6p.

Subject Terms: *THALASSEMIA diagnosis, *EPIDEMIOLOGY, *DISEASE complications, DISEASES in adults

Geographic Terms: NORTHEASTERN Thailand

Intestinal obstruction from calcium polystyrene sulfonate in pediatric cancer patients

Authors: Getsuwan, Songpon, Komwilaisak, Patcharee, Laoaroon, Napat, Tanming, Patchareeporn, Suwannaying, Kunanya, Wiangnon, Surapon, Jetsrisuparb, Arunee

Source: In Pediatric Hematology Oncology Journal December 2022 7(4):122-125

The serum ferritin levels and liver iron concentrations in patients with alpha-thalassemia: is there a good correlation?

Authors: Teawtrakul, Nattiya, Sirijerachai, Chittima, Chansung, Kanchana, Jetsrisuparb, Arunee

Source: Hematology; Dec 2021, Vol. 26 Issue 1, p473-477, 5p

Subject Terms: ALPHA-Thalassemia, FERRITIN, OLDER patients, LOGISTIC regression analysis, IRON

Geographic Terms: THAILAND

Hepcidin expression from monocyte of splenectomized and non-splenectomized patients with HbE-β-thalassemia.

Authors: Pratummo, Kanita¹ (AUTHOR), Jetsrisuparb, Arunee^1,2 (AUTHOR), Fucharoen, Supan¹ (AUTHOR), Tripatara, Amporn¹ (AUTHOR) amptri@kku.ac.th

Source: Hematology. Apr2014, Vol. 19 Issue 3, p175-180. 6p.

Subject Terms: *HEMATOLOGY, *HEPCIDIN, *SPLENECTOMY, *THALASSEMIA, *HEMOGLOBINOPATHY, *HEMOLYTIC anemia, *BETA-Thalassemia, *INTERLEUKIN-6, *PATIENTS

Severe thalassemia syndrome caused by Hemoglobin Pak Num Po AEBart's disease: A hematological, molecular, and diagnostic aspects.

Authors: Singha, Kritsada, Wiangnon, Surapon, Fucharoen, Goonnapa, Jetsrisuparb, Arunee, Komwilaisak, Patcharee, Fucharoen, Supan

Source: International Journal of Laboratory Hematology; Aug2020, Vol. 42 Issue 4, pe173-e176, 4p

Subject Terms: THALASSEMIA diagnosis, GENETIC mutation, MOLECULAR pathology, THAI people, ALPHA-Thalassemia, BETA-Thalassemia

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