Search Results - "Siritanaratkul, Noppadol"

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  1. 1

    A systematic review and meta-analysis of the prevalence of thrombosis and bleeding at diagnosis of Philadelphia-negative myeloproliferative neoplasms by Rungjirajittranon, Tarinee, Owattanapanich, Weerapat, Ungprasert, Patompong, Siritanaratkul, Noppadol, Ruchutrakool, Theera

    Published in BMC cancer (28-02-2019)
    “…Philadelphia (Ph) chromosome-negative myeloproliferative neoplasms (MPNs) are a heterogeneous group of hematopoietic stem cell clonal diseases. Most patients…”
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    Journal Article
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    Review of disease-related complications and management in adult patients with thalassemia: A multi-center study in Thailand by Chuncharunee, Suporn, Teawtrakul, Nattiya, Siritanaratkul, Noppadol, Chueamuangphan, Nonlawan

    Published in PloS one (20-03-2019)
    “…Disease-related complications and management are different among patients with thalassemia. This study was aimed to review the prevalence, clinical risk…”
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    An urgent need for improving thalassemia care due to the wide gap in current real-life practice and clinical practice guidelines by Ekwattanakit, Supachai, Hantaweepant, Chattree, Khuhapinant, Archrob, Siritanaratkul, Noppadol, Viprakasit, Vip

    Published in Scientific reports (24-06-2021)
    “…Based on Thalassemia International Federation clinical practice guidelines (CPG) for non-transfusion dependent and transfusion dependent thalassemia, several…”
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    Exploring health-related quality of life among non-Hodgkin’s lymphoma survivors after completion of primary treatment: a cross-sectional study in Thailand by Lekdamrongkul, Pichitra, Pongthavornkamol, Kanaungnit, Molassiotis, Alex, Sriyuktasuth, Aurawamon, Siritanaratkul, Noppadol, Chansatitporn, Natkamol

    Published in Supportive care in cancer (01-11-2021)
    “…Purposes To investigate health-related quality of life (HR-QoL) and its influencing factors among non-Hodgkin’s lymphoma (NHL) survivors after completion of…”
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    High proportion of TAFRO syndrome in Thai adult Castleman’s disease patients: a 10-year experience by Owattanapanich, Weerapat, Pholmoo, Wikanda, Pongpruttipan, Tawatchai, Siritanaratkul, Noppadol

    Published in Annals of hematology (01-06-2018)
    “…Castleman’s disease (CD) is a rare lymphoproliferative disorder, and its prevalence in Thailand is not known. This 10-year period study investigated the…”
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    Quantitative proteomics of plasma vesicles identify novel biomarkers for hemoglobin E/β-thalassemic patients by Kittivorapart, Janejira, Crew, Vanja Karamatic, Wilson, Marieangela C., Heesom, Kate J., Siritanaratkul, Noppadol, Toye, Ashley M.

    Published in Blood advances (23-01-2018)
    “…Hemoglobin E (HbE)/β-thalassemia has a wide spectrum of clinical manifestations that cannot be explained purely by its genetic background. Circulating…”
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    Journal Article
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    Glutathione Redox System in β-Thalassemia/Hb E Patients by Siritanaratkul, Noppadol, Panichkul, Narumol, Charoensakdi, Ratiya, Hatairaktham, Suneerat, Tangjaidee, Thongchai, Kalpravidh, Ruchaneekorn W., Fucharoen, Suthat

    Published in TheScientificWorld (01-01-2013)
    “…β-thalassemia/Hb E is known to cause oxidative stress induced by iron overload. The glutathione system is the major endogenous antioxidant that protects animal…”
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    Efficacy of Lenalidomide plus Low-Dose Dexamethasone in Thai Patients with Relapsed and/or Refractory Multiple Myeloma by Chutima Kunacheewa, Noppadol Siritanaratkul

    Published in Siriraj Medical Journal (19-04-2021)
    “…Objective: Lenalidomide is an immunomodulatory agent with proven efficacy in the treatment of multiple myeloma. In large global clinical studies, lenalidomide…”
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    A prospective analysis for prevalence of complications in Thai nontransfusion‐dependent Hb E/β‐thalassemia and α‐thalassemia (Hb H disease) by Ekwattanakit, Supachai, Siritanaratkul, Noppadol, Viprakasit, Vip

    Published in American journal of hematology (01-05-2018)
    “…Recently, complications in patients with nontransfusion‐dependent thalassemia (NTDT), in particular those with β‐thalassemia intermedia (β‐TI), were found to…”
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    Clofazimine-induced crystal-storing histiocytosis producing chronic abdominal pain in a leprosy patient by SUKPANICHNANT, S, NARUMOL SRISUTHAPAN HARGROVE, KACHINTORN, U, MANATSATHIT, S, CHANCHAIRUJIRA, T, SIRITANARATKUL, N, AKARAVIPUTH, T, THAKERNGPOL, K

    “…Clofazimine-induced crystal-storing histiocytosis is a rare but well-recognized condition in the literature. Besides the common reddish discoloration of the…”
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