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Journal Abstract Search

130 related items for PubMed ID: 25342395

  • 1. Homozygosity for HBA1: c.179G > A: Hb Adana in an infant.
    Aksu T, Yarali N, Bayram C, Fettah A, Avci Z, Tunç B.
    Hemoglobin; 2014; 38(6):449-50. PubMed ID: 25342395
    [Abstract] [Full Text] [Related]

  • 2. A Unique Interaction of IVS-I-1 (G>A) (HBA2: c.95+1G>A) with Hb Adana (HBA2: c.179G>A) Presenting as Transfusion-Dependent α-Thalassemia.
    Alauddin H, Kamarudin K, Loong TY, Azma RZ, Ithnin A, Jalil N, Razak NF, Koh-Xuan-Rong D, Ismail E, C-Khai L, Abdul Latiff Z, Alias H, Othman A.
    Hemoglobin; 2018 Jul; 42(4):247-251. PubMed ID: 30623696
    [Abstract] [Full Text] [Related]

  • 3. Hb Milano [α109(G16)Leu→Pro (CTG>CCG); HBA1: c.329T>C]: A Novel Variant on the α1-Globin Gene in an Italian Family.
    Curcio C, Giannone V, Benzoni E, Cesaretti C, Ivaldi G.
    Hemoglobin; 2019 Jan; 43(1):4-6. PubMed ID: 31084368
    [Abstract] [Full Text] [Related]

  • 4. Hb G-Waimanalo [A1] [α64(E13)Asp→Asn; HBA1: c.193 G > A] with Decreased Oxygen Affinity.
    Karow A, Eekels JJ, Zurbriggen K, Schmid M, Schmugge M, Speer O.
    Hemoglobin; 2015 Jan; 39(6):432-4. PubMed ID: 26291968
    [Abstract] [Full Text] [Related]

  • 5. Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype-phenotype correlation.
    Singh SA, Sarangi S, Appiah-Kubi A, Hsu P, Smith WB, Gallagher PG, Glader B, Chui DHK.
    Pediatr Blood Cancer; 2018 Sep; 65(9):e27220. PubMed ID: 29749692
    [Abstract] [Full Text] [Related]

  • 6. Hb G-Waimanalo [A1] or α64(E13)Asp→Asn (α1) (HBA1: c.193G>A) Observed in a Bulgarian Family.
    Petkov G, Dimishkovska M, Tsoneva Ivanova V, Yordanov G, Zdraveski A, Plaseska-Karanfilska D.
    Hemoglobin; 2015 Sep; 39(6):430-1. PubMed ID: 26212674
    [Abstract] [Full Text] [Related]

  • 7. Severe α-thalassemia intermedia due to a compound heterozygosity for the highly unstable Hb Adana (HBA2: c.179G>A) and a novel codon 24 (HBA2: c.75T>A) mutation.
    Megawati D, Nainggolan IM, Swastika M, Susanah S, Mose JC, Harahap AR, Setianingsih I.
    Hemoglobin; 2014 Sep; 38(2):149-51. PubMed ID: 24351118
    [Abstract] [Full Text] [Related]

  • 8. Analysis of α1 and α2 globin genes among patients with hemoglobin Adana in Malaysia.
    Lee TY, Lai MI, Ismail P, Ramachandran V, Tan JA, Teh LK, Othman R, Hussein NH, George E.
    Genet Mol Res; 2016 Apr 07; 15(2):. PubMed ID: 27173219
    [Abstract] [Full Text] [Related]

  • 9. A case series of α-thalassemia intermedia due to compound heterozygosity for Hb Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] with other α-thalassemias in Malay families.
    Alauddin H, Jaapar NA, Azma RZ, Ithnin A, Razak NF, Loh CK, Alias H, Abdul-Latiff Z, Othman A.
    Hemoglobin; 2014 Apr 07; 38(4):277-81. PubMed ID: 24829075
    [Abstract] [Full Text] [Related]

  • 10. An alpha-thalassemic hemoglobinopathy: homozygosity for the HB Agrinio alpha 2-globin chain variant.
    Traeger-Synodinos J, Metaxotou-Mavromati A, Kanavakis E, Vrettou C, Papassotiriou I, Michael T, Kattamis C.
    Hemoglobin; 1998 May 07; 22(3):209-15. PubMed ID: 9629496
    [Abstract] [Full Text] [Related]

  • 11. 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 07; 32(4):344-50. PubMed ID: 26377141
    [Abstract] [Full Text] [Related]

  • 12. Screening and diagnosis of Hb Quong Sze [HBA2: c.377T > C (or HBA1)] in a prenatal control program for thalassemia.
    Yang Y, Lou JW, Liu YH, He Y, Li DZ.
    Hemoglobin; 2014 Dec 07; 38(3):158-60. PubMed ID: 24826791
    [Abstract] [Full Text] [Related]

  • 13. Hb Fulton-Georgia [α20(B1)His→Pro; HBA1: c.62A>C]: a new α-globin variant coinherited with α-thalassemia-2 (3.7 kb deletion) and Hb SC disease.
    Zhuang L, Patel N, Bryant S, Kutlar A, Kutlar F, Young AN.
    Hemoglobin; 2013 Dec 07; 37(5):481-5. PubMed ID: 24006930
    [Abstract] [Full Text] [Related]

  • 14. Clinical presentation and molecular identification of four uncommon alpha globin variants in Thailand. Initiation codon mutation of α2-globin Gene (HBA2:c.1delA), donor splice site mutation of α1-globin gene (IVSI-1, HBA1:c.95 + 1G>A), hemoglobin Queens Park/Chao Pra Ya (HBA1:c.98T>A) and hemoglobin Westmead (HBA2:c.369C>G).
    Viprakasit V, Ekwattanakit S, Chalaow N, Riolueang S, Wijit S, Tanyut P, Chat-Uthai N, Tachavanich K.
    Acta Haematol; 2014 Dec 07; 131(2):88-94. PubMed ID: 24081251
    [Abstract] [Full Text] [Related]

  • 15. α-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [α31(B12)Arg→Ser (HBA1 or HBA2 c.96G>T or C)] with the α-Thalassemia-1 [- -SEA (Southeast Asian)] Deletion in Thailand.
    Panyasai S, Phasit A.
    Hemoglobin; 2020 Jul 07; 44(4):264-271. PubMed ID: 32727229
    [Abstract] [Full Text] [Related]

  • 16. A 21 Nucleotide Duplication on the α1- and α2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease.
    Farashi S, Faramarzi Garous N, Zeinali F, Vakili S, Ashki M, Imanian H, Najmabadi H, Azarkeivan A, Tamaddoni A.
    Hemoglobin; 2015 Jul 07; 39(3):196-200. PubMed ID: 25976776
    [Abstract] [Full Text] [Related]

  • 17. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
    Traeger-Synodinos J, Papassotiriou I, Metaxotou-Mavrommati A, Vrettou C, Stamoulakatou A, Kanavakis E.
    Blood Cells Mol Dis; 2000 Aug 07; 26(4):276-84. PubMed ID: 11042028
    [Abstract] [Full Text] [Related]

  • 18. Uncommon Combination of Hemoglobin Jax and Hemoglobin Constant Spring Leading to Microcytic Anemia.
    Srichairatanakool S, Chai-Adisaksopha C, Tantiworawit A, Phusua A, Charoenkwan P.
    Am J Case Rep; 2024 May 10; 25():e943560. PubMed ID: 38725231
    [Abstract] [Full Text] [Related]

  • 19. Two α1-Globin Gene Point Mutations Causing Severe Hb H Disease.
    Jiang H, Huang LY, Zhen L, Jiang F, Li DZ.
    Hemoglobin; 2017 May 10; 41(4-6):293-296. PubMed ID: 29115167
    [Abstract] [Full Text] [Related]

  • 20. Compound Heterozygosity for Hb Adana (HBA2: c.179G>A) and the -α3.7/αα Thalassemia Deletion in Greece: Clinical Phenotype and Genetic Counseling.
    Theodoridou S, Teli A, Yfanti E, Vyzantiadis TA, Theodoridis T, Economou M.
    Hemoglobin; 2018 Mar 10; 42(2):129-131. PubMed ID: 30025477
    [Abstract] [Full Text] [Related]

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