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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 1486044)

  • 1. Polycythaemia and microcytosis arising from the combination of a new high oxygen affinity haemoglobin (Hb luton, alpha 89 His-->Leu) and alpha thalassaemia trait.
    Williamson D; Langdown JV; Myles T; Mason C; Henthorn JS; Davies SC
    Br J Haematol; 1992 Nov; 82(3):621-2. PubMed ID: 1486044
    [No Abstract]   [Full Text] [Related]  

  • 2. Hb Angers: A new α2-globin variant [α2 (140)(HC2) Tyr → Ser; HBA2: C.422 A>C] with increased oxygen affinity leading to erythrocytosis.
    Orvain C; Kiger L; Peronet I; Peron A; Galacteros F; Wajcman H; Pissard S
    Int J Lab Hematol; 2021 Jun; 43(3):e114-e117. PubMed ID: 33217156
    [No Abstract]   [Full Text] [Related]  

  • 3. A new highly unstable alpha chain variant causing alpha(+)-thalassemia: Hb Zurich Albisrieden [alpha59(E8)Gly-->Arg (alpha2)].
    Dutly F; Fehr J; Goede JS; Morf M; Troxler H; Frischknecht H
    Hemoglobin; 2004; 28(4):347-51. PubMed ID: 15658192
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Erythrocytosis due to a combination of the high oxygen affinity hemoglobin variant, Hb Olympia [beta20(B2)Val-->Met] with beta- and alpha-thalassemia mutations: first case in the literature.
    Kalotychou V; Tzanetea R; Konstantopoulos K; Papassotiriou I; Rombos I
    Hemoglobin; 2010; 34(4):383-8. PubMed ID: 20642336
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Secondary erythrocytosis due to compound homozygosity, but not compound heterozygosity, for Hb Luton and α-thalassemia: a family study.
    El-Sharkawi D; Fisher C; Khambadkone S; Stephens AD; Porter JB
    Hemoglobin; 2012; 36(1):7-17. PubMed ID: 22217338
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Symptomatic Erythrocytosis Due to Homozygosity for Hb Luton [HBA2: c.269A>T (or HBA1)] and α-Thalassemia: A Clinical Update.
    Oliveira A; Warcel D; Huntley N; Eleftheriou P; Porter JB
    Hemoglobin; 2016; 40(2):127-9. PubMed ID: 26852627
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Polycythaemia associated with homozygosity for the abnormal haemoglobin Sherwood Forest (beta 104 (G6)Arg-->Thr).
    Williamson D; Beresford CH; Langdown JV; Anderson CC; Green AR
    Br J Haematol; 1994 Apr; 86(4):890-2. PubMed ID: 7918091
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Coexistence of Hb Lepore-Boston-Washington (delta 87Gln-beta-IVS-II-8) with alpha-thalassemia [alpha(-5NT)alpha/alpha alpha].
    Oner C; Oner R; Balkan H; Gümrük F; Gürgey A
    Hemoglobin; 1998 May; 22(3):273-6. PubMed ID: 9629502
    [No Abstract]   [Full Text] [Related]  

  • 9. A new alpha-thalassemia-2 deletion resulting in microcytosis and hypochromia and in vitro chain imbalance in the heterozygote.
    Indrak K; Gu YC; Novotny J; Huisman TH
    Am J Hematol; 1993 Jun; 43(2):144-5. PubMed ID: 8342542
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Haemoglobin Tunis-Bizerte: a new alpha 1 globin 129 Leu-->Pro unstable variant with thalassaemic phenotype.
    Darbellay R; Mach-Pascual S; Rose K; Graf J; Beris P
    Br J Haematol; 1995 May; 90(1):71-6. PubMed ID: 7786798
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hb Trollhättan [beta 20(B2)Val-->Glu]--a new haemoglobin variant with increased oxygen affinity causing erythrocytosis.
    Landin B; Berglund S; Lindoff B
    Eur J Haematol; 1994 Jul; 53(1):21-5. PubMed ID: 7914875
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hb Questembert is due to a base substitution (T-->C) in codon 131 of the alpha 2-globin gene and has an alpha-thalassemia biosynthetic ratio.
    Rochette J; Barnetson R; Thein SL; Varet B; Valensi F
    Am J Hematol; 1995 Apr; 48(4):289-90. PubMed ID: 7717382
    [No Abstract]   [Full Text] [Related]  

  • 13. A third instance of the high oxygen affinity variant, Hb Heathrow [beta 103(G5)Phe- greater than Leu]: identification of the mutation by mass spectrometry and by DNA analysis.
    Marsh G; Marino G; Pucci P; Ferranti P; Malorni A; Kaeda J; Marsh J; Luzzatto L
    Hemoglobin; 1991; 15(1-2):43-51. PubMed ID: 1917536
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association of a novel high oxygen affinity haemoglobin variant with delta beta thalassaemia.
    Rochette J; Barnetson R; Kiger L; Kister J; Littlewood TJ; Webster R; Poyart C; Thein SL
    Br J Haematol; 1994 Jan; 86(1):118-24. PubMed ID: 8011519
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Erythrocytosis in a child due to Hb Andrew-Minneapolis [β144(HC1)Lys→Asn (AAG>AAT or AAC)] associated with a Spanish (δβ)(0)-thalassemia.
    Ropero P; González FA; Cela E; Beléndez C; Pérez B; Seri C; Fontanes E; Villegas A; Díaz-Mediavilla J
    Hemoglobin; 2013; 37(1):48-55. PubMed ID: 23215953
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Diagnostic applications of newborn screening for α-thalassaemias, haemoglobins E and H disorders using isoelectric focusing on dry blood spots.
    Jindatanmanusan P; Riolueang S; Glomglao W; Sukontharangsri Y; Chamnanvanakij S; Torcharus K; Viprakasit V
    Ann Clin Biochem; 2014 Mar; 51(Pt 2):237-47. PubMed ID: 23901141
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hb Bronovo, a new globin gene mutation at alpha2 103 (His->Leu) associated with an alpha thalassemia phenotype.
    Harteveld CL; Steen G; Vlasveld LT; van Delft P; Giordano PC
    Haematologica; 2006 Apr; 91(4):570-1. PubMed ID: 16533721
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel mutation of the alpha2-globin causing alpha(+)-thalassemia: Hb Plasencia [alpha125(H8)Leu--Arg (alpha2).
    Martin G; Villegas A; González FA; Ropero P; Hojas R; Polo M; Mateo M; Salvador M; Benavente C
    Hemoglobin; 2005; 29(2):113-7. PubMed ID: 15921163
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial relative polycythaemia due to haemoglobin Heathrow.
    Beard ME; Hamer JW; Brennan SO; Jones JN; Sheat JM; Maclaurin JS
    Aust N Z J Med; 1979 Jun; 9(3):297-301. PubMed ID: 288399
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hb Tsurumai [beta 82(EF6)Lys-->Gln]: a new Hb variant with high oxygen affinity and erythrocytosis.
    Ohba Y; Yamada H; Takamatsu S; Imai K
    Hemoglobin; 1996 May; 20(2):141-6. PubMed ID: 8811318
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.