These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

138 related items for PubMed ID: 12144063

  • 1. Compound heterozygosity for Hb Spanish town [alpha27(B8)Glu-->Val], Hb S [beta6(A3)Glu-->Val] and the -alpha(3.7kb) thalassemia deletion.
    Faustino P, Picanço I, Miranda A, Seixas T, Ferrão A, Morais A, Lavinha J, Romão L.
    Hemoglobin; 2002 May; 26(2):185-9. PubMed ID: 12144063
    [No Abstract] [Full Text] [Related]

  • 2. Complex interaction of Hb Hekinan [alpha27(B8) Glu-Asp] and Hb E [beta26(B8) Glu-Lys] with a deletional alpha-thalassemia 1 in a Thai family.
    Fucharoen S, Changtrakun Y, Ratanasiri T, Fucharoen G, Sanchaisuriya K.
    Eur J Haematol; 2003 May; 70(5):304-9. PubMed ID: 12694166
    [Abstract] [Full Text] [Related]

  • 3. Laboratory diagnosis of a compound heterozygosity for Hb Hekinan [alpha27(B8) Glu-Asp] and a deletional alpha-thalassaemia 2 in Thailand.
    Chunpanich S, Ayukarn K, Sanchaisuriya K, Fucharoen G, Fucharoen S.
    Clin Lab Haematol; 2004 Oct; 26(5):355-8. PubMed ID: 15485467
    [Abstract] [Full Text] [Related]

  • 4. Complex interaction of Hb E [beta26(B8)Glu-->Lys], Hb Korle-Bu [beta73(E17)Asp-->Asn] and a deletional alpha-thalassemia-1 in pregnancy.
    Siriratmanawong N, Chansri W, Singsanan S, Fucharoen G, Fucharoen S.
    Hemoglobin; 2009 Oct; 33(6):507-14. PubMed ID: 19958198
    [Abstract] [Full Text] [Related]

  • 5. Complex interaction of hemoglobin (Hb) Nakhon Ratchasima [α63(E12)Ala→Val], a novel α2-globin chain variant with Hb E [β26(B8)Glu→Lys] and a deletional α(+)-thalassemia.
    Srivorakun H, Fucharoen G, Puangplruk R, Kheawon N, Fucharoen S.
    Eur J Haematol; 2011 Jul; 87(1):68-72. PubMed ID: 21447006
    [Abstract] [Full Text] [Related]

  • 6. Novel interactions of two α-Hb variants with SEA deletion α0-thalassemia: hematological and molecular analyses.
    Srivorakun H, Singha K, Fucharoen G, Fucharoen S.
    Hematology; 2018 Apr; 23(3):187-191. PubMed ID: 28945175
    [Abstract] [Full Text] [Related]

  • 7. Two cases of compound heterozygosity for Hb Hekinan [alpha27(B8)Glu-->Asp (alpha1)] and alpha-thalassemia in Thailand.
    Ngiwsara L, Srisomsap C, Winichagoon P, Fucharoen S, Svasti J.
    Hemoglobin; 2004 May; 28(2):145-50. PubMed ID: 15182057
    [Abstract] [Full Text] [Related]

  • 8. Compound heterozygosity for Hb S [β6(A3)Glu→Val] and Hb Kenya (Aγ81Leu-β86Ala) in a Ugandan woman.
    Han ZJ, Lapuz C, Rovenger JF, Dreyfus PA, Vispo BG, Ou CN, Luo HY, Chui DH, Gallivan MV.
    Hemoglobin; 2012 May; 36(3):270-5. PubMed ID: 22384817
    [Abstract] [Full Text] [Related]

  • 9. Hemoglobinopathies in the Çukurova Region and Neighboring Provinces.
    Yuzbasioglu Ariyurek S, Yildiz SM, Yalin AE, Guzelgul F, Aksoy K.
    Hemoglobin; 2016 Jun; 40(3):168-72. PubMed ID: 26984585
    [Abstract] [Full Text] [Related]

  • 10. Compound heterozygosity of Hb D(Iran) (beta(22) Glu-->Gln) and beta(0)-thalassemia (619 bp-deletion) in India.
    Agrawal MG, Bhanushali AA, Dedhia P, Jeswani KD, Dayanand S, Dasgupta A, Das BR.
    Eur J Haematol; 2007 Sep; 79(3):248-50. PubMed ID: 17655708
    [Abstract] [Full Text] [Related]

  • 11. Hb Westmead [alpha 122(H5)His----Gln], Hb E [beta 26(B8)Glu----Lys], and alpha-thalassemia-2 (3.7 Kb deletion) in a Laotian family.
    Gu YC, Gu LH, Wilson JB, Cepreganova B, Ramachandran M, Walker EL, Huisman TH, Potitong P.
    Hemoglobin; 1991 Sep; 15(4):297-302. PubMed ID: 1787098
    [No Abstract] [Full Text] [Related]

  • 12. The clinical and laboratory spectrum of Hb C [β6(A3)Glu→Lys, GAG>AAG] disease.
    Cook CM, Smeltzer MP, Mortier NA, Kirk SE, Despotovic JM, Ware RE, Hankins JS.
    Hemoglobin; 2013 Sep; 37(1):16-25. PubMed ID: 23297836
    [Abstract] [Full Text] [Related]

  • 13. Double heterozygosity for Hb Pyrgos [beta83(EF7)Gly-->Asp] and Hb E [beta26(B8)Glu-->Lys] found in association with alpha-thalassemia.
    Sawangareetrakul P, Svasti S, Yodsowon B, Winichagoon P, Srisomsap C, Svasti J, Fucharoen S.
    Hemoglobin; 2002 May; 26(2):191-6. PubMed ID: 12144064
    [No Abstract] [Full Text] [Related]

  • 14. A new δ chain variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], observed in a Tunisian family in association with a compound heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A].
    Moumni I, Zorai A, Mahjoub S, Mosbahi I, Chaouechi D, Benromdhane N, Abbes S.
    Hemoglobin; 2014 May; 38(2):88-90. PubMed ID: 24471655
    [Abstract] [Full Text] [Related]

  • 15. Hb Oegstgeest [alpha104(G11)Cys-->Ser (alpha1)]. A new hemoglobin variant associated with a mild alpha-thalassemia phenotype.
    Harteveld CL, Rozendaal L, Blom NA, Lo-A-Njoe S, Akkerman N, Arkestijn S, Van Delft P, Giordano PC.
    Hemoglobin; 2005 May; 29(3):165-9. PubMed ID: 16114179
    [Abstract] [Full Text] [Related]

  • 16. Evaluation of Alpha-Thalassemia Mutations in Cases with Hypochromic Microcytic Anemia: The İstanbul Perspective.
    Karakaş Z, Koç B, Temurhan S, Elgün T, Karaman S, Asker G, Gençay G, Timur Ç, Yıldırmak ZY, Celkan T, Devecioğlu Ö, Aydın F.
    Turk J Haematol; 2015 Dec; 32(4):344-50. PubMed ID: 26377141
    [Abstract] [Full Text] [Related]

  • 17. Molecular characterization of Hb D-Ibadan [beta87(F3)Thr-->Lys] in combination with Hb S [beta6(A3)Glu-->Val] and with beta+-Thalassemia: report of two cases.
    Redding-Lallinger R, Tankut G, Holley L, Wright F, Kutlar A, Kutlar F.
    Hemoglobin; 2002 May; 26(2):129-34. PubMed ID: 12144055
    [Abstract] [Full Text] [Related]

  • 18. Association of Hb Thailand [α56(E5)Lys→Thr] and Hb Phnom Penh [α117(GH5)-Ile-α118(H1)] with α(0)-thalassemia: molecular and hematological features and differential diagnosis.
    Singha K, Srivorakun H, Fucharoen G, Changtrakul Y, Komwilaisak P, Jetsrisuparb A, Puangplruk R, Fucharoen S.
    Hemoglobin; 2013 May; 37(1):37-47. PubMed ID: 23215800
    [Abstract] [Full Text] [Related]

  • 19. Hb G-Makassar [beta6(A3)Glu-->Ala; codon 6 (GAG-->GCG)]: molecular characterization, clinical, and hematological effects.
    Viprakasit V, Wiriyasateinkul A, Sattayasevana B, Miles KL, Laosombat V.
    Hemoglobin; 2002 Aug; 26(3):245-53. PubMed ID: 12403489
    [Abstract] [Full Text] [Related]

  • 20. Molecular and hematological characterization of hemoglobin Hope/hemoglobin E and hemoglobin Hope/alpha-thalassemia 2 in Thai patients.
    Chunpanich S, Fucharoen S, Sanchaisuriya K, Fucharoen G, Kam-itsara K.
    Lab Hematol; 2004 Aug; 10(4):215-20. PubMed ID: 15697092
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.