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Journal Abstract Search


232 related items for PubMed ID: 30006733

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Strong Linkage of the Single Nucleotide Polymorphism rs77308790 with an α0-Thalassemia (- -SEA deletion) Allele and Application for Double-Check Diagnosis of Hb Bart's Hydrops Fetalis Syndrome in Thailand.
    Jomoui W, Tepakhan W, Karnpean R.
    Hemoglobin; 2019; 43(4-5):236-240. PubMed ID: 31635494
    [Abstract] [Full Text] [Related]

  • 3. Characterization of Hb Bart's Hydrops Fetalis Caused by - -SEA and a Large Novel α0-Thalassemia Deletion.
    He S, Li J, Huang P, Zhang S, Lin L, Zuo Y, Tian X, Zheng C, Qiu X, Chen B.
    Hemoglobin; 2018 Jan; 42(1):61-64. PubMed ID: 29493331
    [Abstract] [Full Text] [Related]

  • 4. Analysis of Deletional Hb H Diseases in Samples with Hb A2-Hb H and Hb A2-Hb Bart's on Capillary Electrophoresis.
    Khongthai K, Ruengdit C, Panyasai S, Pornprasert S.
    Hemoglobin; 2019 Jan; 43(4-5):245-248. PubMed ID: 31687860
    [Abstract] [Full Text] [Related]

  • 5. Hb Bart's Hydrops Fetalis Syndrome and Hb H Disease Caused by Deletional Chiang Rai (- -CR) α0-Thalassemia in Two Unrelated Thai Families.
    Ruengdit C, Khamphikham P, Jinorose N, Pornprasert S.
    Hemoglobin; 2021 Mar; 45(2):75-79. PubMed ID: 33821735
    [Abstract] [Full Text] [Related]

  • 6. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different alpha-thalassemia determinants.
    Siriratmanawong N, Pinmuang-Ngam C, Fucharoen G, Fucharoen S.
    Fetal Diagn Ther; 2007 Mar; 22(4):264-8. PubMed ID: 17369692
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  • 7. Prevention of Hb Bart's (γ4) Disease Associated with the - -(THAI) α(0)-Thalassemia Deletion in Mainland China.
    Li DZ, Li Y, Li J, Li SC, Li R.
    Hemoglobin; 2015 Mar; 39(6):412-4. PubMed ID: 26212676
    [Abstract] [Full Text] [Related]

  • 8. Diagnostic value of fetal hemoglobin Bart's for evaluation of fetal α-thalassemia syndromes: application to prenatal characterization of fetal anemia caused by undiagnosed α-hemoglobinopathy.
    Singha K, Yamsri S, Chaibunruang A, Srivorakun H, Sanchaisuriya K, Fucharoen G, Fucharoen S.
    Orphanet J Rare Dis; 2022 Feb 10; 17(1):45. PubMed ID: 35144630
    [Abstract] [Full Text] [Related]

  • 9. Molecular and clinical features of Hb H disease in northern Thailand.
    Charoenkwan P, Taweephon R, Sae-Tung R, Thanarattanakorn P, Sanguansermsri T.
    Hemoglobin; 2005 Feb 10; 29(2):133-40. PubMed ID: 15921165
    [Abstract] [Full Text] [Related]

  • 10. Hb Constant Spring [alpha 142, Term-->Gln (TAA>CAA in alpha2)] in the alpha-thalassemia of anemic patients in Myanmar.
    Ne-Win, Harano K, Harano T, Kyaw-Shwe, Aye-Aye-Myint, Khin-Thander-Aye, Okada S.
    Hemoglobin; 2008 Feb 10; 32(5):454-61. PubMed ID: 18932070
    [Abstract] [Full Text] [Related]

  • 11. Identification of nondeletional α-thalassemia in a prenatal screening program by reverse dot-blot in southern China.
    Li J, Li R, Li DZ.
    Hemoglobin; 2015 Feb 10; 39(1):42-5. PubMed ID: 25523870
    [Abstract] [Full Text] [Related]

  • 12. Simplified PGD of common determinants of haemoglobin Bart's hydrops fetalis syndrome using multiplex-microsatellite PCR.
    Wang W, Yap CH, Loh SF, Tan AS, Lim MN, Prasath EB, Chan ML, Tan WC, Jiang B, Yeo GH, Mathew J, Ho A, Ho SS, Wong PC, Choolani MA, Chong SS.
    Reprod Biomed Online; 2010 Nov 10; 21(5):642-8. PubMed ID: 20864413
    [Abstract] [Full Text] [Related]

  • 13. Hb H Hydrops Fetalis Syndrome Caused by Association of the - -(SEA) Deletion and Hb Constant Spring (HBA2: c.427T > C) Mutation in a Chinese Family.
    He S, Zheng C, Meng D, Chen R, Zhang Q, Tian X, Chen S.
    Hemoglobin; 2015 Nov 10; 39(3):216-9. PubMed ID: 25897478
    [Abstract] [Full Text] [Related]

  • 14. Molecular analysis and clinical significance of hemoglobin Quong Sze in Huizhou city, Southern China.
    Zhong Z, Guan Z, Chen D, Zhong G, He H, Yang K, Chen J.
    Taiwan J Obstet Gynecol; 2023 Sep 10; 62(5):709-712. PubMed ID: 37678999
    [Abstract] [Full Text] [Related]

  • 15. Occurrence of the - -(SEA), - -(THAI) and - -(FIL) α-Thalassemia-1 Carriers from a 7-Year Study at Ramathibodi Hospital, Bangkok, Thailand.
    Pongjantharasatien K, Banyatsuppasin W, Pounsawat S, Jindadamrongwech S.
    Hemoglobin; 2016 Aug 10; 40(4):283-4. PubMed ID: 27492767
    [Abstract] [Full Text] [Related]

  • 16. Early onset of fetal hydrops associated with the α-thalassemia - -(THAI) deletion.
    Yang Y, Li DZ.
    Hemoglobin; 2014 Aug 10; 38(6):431-4. PubMed ID: 25370866
    [Abstract] [Full Text] [Related]

  • 17. [Prenatal diagnosis of Thailand deletion of α-thalassemia 1 families].
    Lin N, Lin Y, Huang HL, Lin XL, He DQ, He SQ, Guo DH, Li Y, Xu LP.
    Zhonghua Yi Xue Za Zhi; 2016 Jun 28; 96(24):1919-22. PubMed ID: 27373361
    [Abstract] [Full Text] [Related]

  • 18. Prenatal diagnosis of hemoglobin Bart's hydrops fetalis by HPLC analysis of hemoglobin in fetal blood samples.
    Sanguansermsri T, Thanaratanakorn P, Steger HF, Tongsong T, Sirivatanapa P, Wanapirak C, Sirichotiyakul S, Chanprapas P, Flatz G.
    Southeast Asian J Trop Med Public Health; 2001 Mar 28; 32(1):180-5. PubMed ID: 11485083
    [Abstract] [Full Text] [Related]

  • 19. Unmasking Hb Paksé (codon 142, TAA>TAT, α2) and its combinations in patients also carrying Hb Constant Spring (codon 142, TAA>CAA, α2) in northern Thailand.
    Pornprasert S, Panyasai S, Treesuwan K.
    Hemoglobin; 2012 Mar 28; 36(5):491-6. PubMed ID: 22881835
    [Abstract] [Full Text] [Related]

  • 20. Accurate prenatal diagnosis of Hb Bart's hydrops fetalis in daily practice with a double-check PCR system.
    Karnpean R, Fucharoen G, Fucharoen S, Sae-ung N, Sanchaisuriya K, Ratanasiri T.
    Acta Haematol; 2009 Mar 28; 121(4):227-33. PubMed ID: 19546525
    [Abstract] [Full Text] [Related]


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