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 *

104 related articles for article (PubMed ID: 2301375)

  • 1. Sickle hemoglobinopathies in Sicily.
    Schilirò G; Spena M; Giambelluca E; Maggio A
    Am J Hematol; 1990 Feb; 33(2):81-5. PubMed ID: 2301375
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical, hematological, and molecular features in Sicilians with sickle cell disease.
    Schilirò G; Samperi P; Consalvo C; Gangarossa S; Testa R; Miraglia V; Lo Nigro L
    Hemoglobin; 1992; 16(6):469-80. PubMed ID: 1487418
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical and laboratory features of sickle cell disease in The Netherlands.
    Aluoch JR; De Geus A; Goudsmit R
    Trop Geogr Med; 1988 Jan; 40(1):7-12. PubMed ID: 3381319
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Funduscopic alterations in SS and SC hemoglobinopathies. Study of a Brazilian population.
    Bonanomi MT; Cunha SL; de Araújo JT
    Ophthalmologica; 1988; 197(1):26-33. PubMed ID: 3186205
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cholelithiasis in patients with major sickle hemoglobinopathies.
    Rennels MB; Dunne MG; Grossman NJ; Schwartz AD
    Am J Dis Child; 1984 Jan; 138(1):66-7. PubMed ID: 6691315
    [TBL] [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; 42(2):84-90. PubMed ID: 30200838
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Comparison of clinical, hematological and molecular findings of Jamaican and Sicilian patients with sickle cell disease.
    Schiliro G; Russo Mancuso G; Kulozik AE; Serjeant BE; Serjeant GR
    Haematologica; 1990; 75 Suppl 5():42-56. PubMed ID: 2086381
    [No Abstract]   [Full Text] [Related]  

  • 8. Hematological findings in 375 Sicilians with Hb S trait.
    Schilirò G; Comisi FF; Testa R; Dibenedetto SP; Samperi P; Marino S
    Haematologica; 1990; 75(2):113-6. PubMed ID: 2358201
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A case of Hb-SC disease presenting as priapism.
    Noor NA; Qazi AW; Mohyuddin ; Masood ; Ali Z
    J Pak Med Assoc; 1987 Nov; 37(11):302-3. PubMed ID: 3126318
    [No Abstract]   [Full Text] [Related]  

  • 10. Sickle cell disease in Sicily.
    Roth EF; Schiliro G; Russo A; Musumeci S; Rachmilewitz E; Neske V; Nagel R
    J Med Genet; 1980 Feb; 17(1):34-8. PubMed ID: 7365760
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interaction of the alpha alpha alpha globin gene haplotype and sickle haemoglobin.
    Higgs DR; Clegg JB; Weatherall DJ; Serjeant BE; Serjeant GR
    Br J Haematol; 1984 Aug; 57(4):671-8. PubMed ID: 6331494
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sickle cell syndromes: misdiagnosis can affect treatment.
    Golden WE; Moore G
    J Ark Med Soc; 2004 Nov; 101(5):144-5. PubMed ID: 15554178
    [No Abstract]   [Full Text] [Related]  

  • 13. Beta S gene in Sicily is in linkage disequilibrium with the Benin haplotype: implications for gene flow.
    Ragusa A; Lombardo M; Sortino G; Lombardo T; Nagel RL; Labie D
    Am J Hematol; 1988 Feb; 27(2):139-41. PubMed ID: 2893541
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pediatric sickle cell retinopathy: correlation with clinical factors.
    Rosenberg JB; Hutcheson KA
    J AAPOS; 2011 Feb; 15(1):49-53. PubMed ID: 21397806
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sickle cell disease in the Kurdish population of northern Iraq.
    Al-Allawi NA; Jalal SD; Nerwey FF; Al-Sayan GO; Al-Zebari SS; Alshingaly AA; Markous RD; Jubrael JM; Hamamy H
    Hemoglobin; 2012; 36(4):333-42. PubMed ID: 22686351
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Hemoglobin Boumerdès alpha 2(37) (C2) Pro----Arg beta 2: a new variant of the alpha chain associated with hemoglobin S in an Algerian family].
    Dahmane-Arbane M; Blouquit Y; Arous N; Bardakdjian J; Benamani M; Riou J; Benabadji M; Rosa J; Galacteros F
    Nouv Rev Fr Hematol (1978); 1987; 29(5):317-20. PubMed ID: 3438164
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The clinical pathophysiology of sickle cell disease.
    Embury SH
    Annu Rev Med; 1986; 37():361-76. PubMed ID: 2423018
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical, hematological, and molecular features in Sicilians with Hb S-beta-thalassemia.
    Schiliro G; Samperi P; Testa R; Gupta RB; Gu LH; Huisman TH
    Am J Hematol; 1992 Dec; 41(4):264-9. PubMed ID: 1283809
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Predicting changes in hemoglobin S after simple transfusion using complete blood counts.
    Mathur G; Ten Eyck P; Knudson CM
    Transfusion; 2018 Jan; 58(1):138-144. PubMed ID: 29023896
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Blood group phenotypes and the origin of sickle cell hemoglobin in Sicilians.
    Sandler SG; Schilirò G; Russo A; Musumeci S; Rachmilewitz EA
    Acta Haematol; 1978; 60(6):350-7. PubMed ID: 103355
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.