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Journal Abstract Search

194 related items for PubMed ID: 32657857

  • 1. Hemoglobin S/Hemoglobin Quebec-Chori Presenting as Sickle Cell Disease: A Case Report.
    Goode E, Boruchov D, Oliveira JL, Lau CC.
    J Pediatr Hematol Oncol; 2020 Nov; 42(8):e775-e777. PubMed ID: 32657857
    [Abstract] [Full Text] [Related]

  • 2. Sickle cell disease caused by Hb S/Québec-CHORI: treatment with hydroxyurea and response.
    Tubman VN, Bennett CM, Luo HY, Chui DH, Heeney MM.
    Pediatr Blood Cancer; 2007 Aug; 49(2):207-10. PubMed ID: 17551985
    [Abstract] [Full Text] [Related]

  • 3. A rare case of a compound heterozygote hemoglobin S/hemoglobin Fannin-Lubbock-I individual. Is it a sickling disorder?
    Burns NK, Risin SA.
    Lab Hematol; 2010 Jun; 16(2):26-7. PubMed ID: 20534428
    [No Abstract] [Full Text] [Related]

  • 4. A novel sickling hemoglobinopathy.
    McFarlane A, Warkentin TE, Cartín W.
    N Engl J Med; 2011 Oct 20; 365(16):1548-9. PubMed ID: 22010933
    [No Abstract] [Full Text] [Related]

  • 5. Compound heterozygosity for hemoglobins S and D.
    Lund K, Chakravorty S, Toma S, Bain BJ.
    Am J Hematol; 2015 Sep 20; 90(9):842. PubMed ID: 26103542
    [No Abstract] [Full Text] [Related]

  • 6. Compound Heterozygosity of β-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India.
    Jha AN, Mishra H, Verma HK, Pandey I, Lakkakula BVKS.
    Hemoglobin; 2018 Mar 20; 42(2):84-90. PubMed ID: 30200838
    [Abstract] [Full Text] [Related]

  • 7. HbS-oman heterozygote: a new dominant sickle syndrome.
    Nagel RL, Daar S, Romero JR, Suzuka SM, Gravell D, Bouhassira E, Schwartz RS, Fabry ME, Krishnamoorthy R.
    Blood; 1998 Dec 01; 92(11):4375-82. PubMed ID: 9834244
    [Abstract] [Full Text] [Related]

  • 8. Bone marrow necrosis and sickle cell crisis associated with double heterozygosity for HbS and HbOARAB.
    Rossi P, Curiel M, Demoux AL, Bagneres D, Costello R, Chaumoitre K, Bernard F, Frances Y, Granel B.
    Am J Hematol; 2011 Mar 01; 86(3):309-10. PubMed ID: 20954261
    [No Abstract] [Full Text] [Related]

  • 9. Sickle cell disease in a patient with sickle cell trait and compound heterozygosity for hemoglobin S and hemoglobin Quebec-Chori.
    Witkowska HE, Lubin BH, Beuzard Y, Baruchel S, Esseltine DW, Vichinsky EP, Kleman KM, Bardakdjian-Michau J, Pinkoski L, Cahn S.
    N Engl J Med; 1991 Oct 17; 325(16):1150-4. PubMed ID: 1891024
    [No Abstract] [Full Text] [Related]

  • 10. Hemoglobin SO-Arab and α-thalassemia diagnosed in an adult: A case-based review of the hemoglobinopathies.
    Zacharia G, Maronge GF, Brazda FW, Boulmay BC.
    Am J Med Sci; 2013 Oct 17; 346(4):325-7. PubMed ID: 23221516
    [Abstract] [Full Text] [Related]

  • 11. First report of successful stem cell transplantation in a patient with sickle cell hemoglobin D disease.
    Hamidieh AA, Jalili M, Khojasteh O, Ghavamzadeh A.
    J Pediatr Hematol Oncol; 2010 Jul 17; 32(5):397-9. PubMed ID: 20502357
    [Abstract] [Full Text] [Related]

  • 12. Strategy for identification by mass spectrometry of a new human hemoglobin variant with two mutations in Cis in the beta-globin chain: Hb S-Clichy [beta6(A3)Glu-->Val; beta8(A5)Lys-->Thr].
    Zanella-Cleon I, Préhu C, Joly P, Riou J, Becchi M, Wajcman H, Francina A.
    Hemoglobin; 2009 Jul 17; 33(3):177-87. PubMed ID: 19657831
    [Abstract] [Full Text] [Related]

  • 13. Hemoglobin sickle-Lepore: report of two siblings and review of the literature.
    Seward DP, Ware RE, Kinney TR.
    Am J Hematol; 1993 Nov 17; 44(3):192-5. PubMed ID: 8213769
    [Abstract] [Full Text] [Related]

  • 14. First case of Hb Fontainebleau with sickle haemoglobin and other non-deletional α gene variants identified in neonates during newborn screening for sickle cell disorders.
    Upadhye DS, Jain D, Nair SB, Nadkarni AH, Ghosh K, Colah RB.
    J Clin Pathol; 2012 Jul 17; 65(7):654-9. PubMed ID: 22461654
    [Abstract] [Full Text] [Related]

  • 15. Homozygous hemoglobin S with concomitant hemoglobin G-Philadelphia: a diagnostic challenge.
    Racsa L, Mitui M, Park JY, Timmons CF, Luu HS, Rogers ZR, Park JY.
    Pediatr Blood Cancer; 2014 Oct 17; 61(10):1899-900. PubMed ID: 24777785
    [No Abstract] [Full Text] [Related]

  • 16. Abnormal hemoglobins; clinical disorders resulting from various combinations.
    LAWRENCE JS, VALENTINE WN.
    Calif Med; 1955 Jan 17; 82(1):1-5. PubMed ID: 13230906
    [Abstract] [Full Text] [Related]

  • 17. An unusual case of heterozygous hemoglobin S/hemoglobin Fannin-Lubbock misidentified by capillary hemoglobin electrophoresis.
    Welsh KJ, Bai Y.
    Ann Clin Lab Sci; 2015 Jan 17; 45(2):199-201. PubMed ID: 25887875
    [Abstract] [Full Text] [Related]

  • 18. De novo heterozygous Hb G-Waimanalo (α64(E13)Asp>Asn, CTG>CCG; HBA1:c.193G>A) variant in a sickle cell disease patient of an Indian tribe.
    Kumar R, Mishra S, Uikey RS, Gwal A, Mun A, Bharti PK, Shanmugam R.
    J Clin Pathol; 2021 May 17; 74(5):336-338. PubMed ID: 32817264
    [No Abstract] [Full Text] [Related]

  • 19.
    Ashorobi D, Ramsey A, Killeen RB, Bhatt R.
    ; 2024 01 17. PubMed ID: 30725815
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
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