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2. Sickle haemoglobin and haemoglobin Stanleyville II: possible confusion with sickle cell-haemoglobin C disease. Serjeant GR; Wild B; Tebasulwa S; Mason KP; Serjeant BE; Ndugwa CM East Afr Med J; 2005 Jul; 82(7):367-70. PubMed ID: 16167711 [TBL] [Abstract][Full Text] [Related]
3. Haemoglobin sickle D disease: A presentation with ischaemic stroke. Afzal H; Umair SF J Pak Med Assoc; 2016 Mar; 66(3):348-50. PubMed ID: 26968293 [TBL] [Abstract][Full Text] [Related]
4. Haemoglobin SD disease--rare case of jaundice. Ghosh UC; Sen K; Narayan A; Banik KK; Saha PK J Indian Med Assoc; 2012 Jul; 110(7):501-2. PubMed ID: 23520682 [TBL] [Abstract][Full Text] [Related]
5. Sickle-cell anaemia, sickle-cell thalassaemia, sickle-cell haemoglobin C disease, and asymptomatic haemoglobin C thalassaemia in one Ghanaian family. Konotey-Ahulu FI; Ringelhann B Br Med J; 1969 Mar; 1(5644):607-12. PubMed ID: 5766126 [TBL] [Abstract][Full Text] [Related]
7. [Cardiac manifestations of sickle cell anemia]. Gacon PH; Donatien Y Presse Med; 2001 May 5-12; 30(17):841-5. PubMed ID: 11402936 [TBL] [Abstract][Full Text] [Related]
8. Compound heterozygosity for hemoglobins S and D. Lund K; Chakravorty S; Toma S; Bain BJ Am J Hematol; 2015 Sep; 90(9):842. PubMed ID: 26103542 [No Abstract] [Full Text] [Related]
9. Genetic disorders of hemoglobin synthesis. Bank A Hosp Pract (Off Ed); 1985 Sep; 20(9):109-11, 115-9, 123-4. PubMed ID: 2411743 [No Abstract] [Full Text] [Related]
10. 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; 65(7):654-9. PubMed ID: 22461654 [TBL] [Abstract][Full Text] [Related]
11. Evaluation of eight and a half years of neonatal screening for haemoglobinopathies in Birmingham. Griffiths PD; Mann JR; Darbyshire PJ; Green A Br Med J (Clin Res Ed); 1988 Jun; 296(6636):1583-5. PubMed ID: 3135019 [TBL] [Abstract][Full Text] [Related]
12. Review: the sickle hemoglobinopathies--genetic analyses of common phenocopies and new molecular approaches to treatment. Steinberg MH Am J Med Sci; 1984 Nov; 288(4):169-74. PubMed ID: 6208780 [TBL] [Abstract][Full Text] [Related]
13. Molecular exclusion of haemoglobin SD disease by prenatal diagnosis. Fodor FH; Eng CM Prenat Diagn; 1999 Jan; 19(1):58-60. PubMed ID: 10073909 [TBL] [Abstract][Full Text] [Related]
14. 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 [TBL] [Abstract][Full Text] [Related]
15. The intrauterine diagnosis of hemoglobin disorders. Wong SC; Ali MA; Benzie R Clin Perinatol; 1984 Jun; 11(2):283-308. PubMed ID: 6086205 [TBL] [Abstract][Full Text] [Related]
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18. The association of Hb Stanleyville II with alpha thalassemia and Hb S. Costa FF; Zago MA; Sonati MF; Bottura C Nouv Rev Fr Hematol (1978); 1987; 29(6):387-90. PubMed ID: 3452204 [TBL] [Abstract][Full Text] [Related]
19. Accuracy of neurologic examination and history in detecting evidence of MRI-diagnosed cerebral infarctions in children with sickle cell hemoglobinopathy. Glauser TA; Siegel MJ; Lee BC; DeBaun MR J Child Neurol; 1995 Mar; 10(2):88-92. PubMed ID: 7782614 [TBL] [Abstract][Full Text] [Related]
20. 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; 86(3):309-10. PubMed ID: 20954261 [No Abstract] [Full Text] [Related] [Next] [New Search]