175 related articles for article (PubMed ID: 20954261)
1. 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]
2. 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]
3. A novel sickling hemoglobinopathy.
McFarlane A; Warkentin TE; Cartín W
N Engl J Med; 2011 Oct; 365(16):1548-9. PubMed ID: 22010933
[No Abstract] [Full Text] [Related]
4. [Hemoglobinopathies and related syndromes. General introduction. Personal experience in Africa and Europe].
Lambotte C
J Genet Hum; 1986 Nov; 34(5):375-92. PubMed ID: 3540208
[No Abstract] [Full Text] [Related]
5. 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]
6. 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]
7. Genetic epidemiology of the three predominant abnormal hemoglobins in India.
Balgir RS
J Assoc Physicians India; 1996 Jan; 44(1):25-8. PubMed ID: 8773089
[TBL] [Abstract][Full Text] [Related]
8. 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; 92(11):4375-82. PubMed ID: 9834244
[TBL] [Abstract][Full Text] [Related]
9. Sickle cell-like crisis and bone marrow necrosis associated with parvovirus B19 infection and heterozygosity for haemoglobins S and E.
Eichhorn RF; Buurke EJ; Blok P; Berends MJ; Jansen CL
J Intern Med; 1999 Jan; 245(1):103-6. PubMed ID: 10095824
[TBL] [Abstract][Full Text] [Related]
10. HbHope/HbS and HbS/beta-thal double compound heterozygosity in a Mauritanian family: clinical and biochemical studies.
Deyde VM; Lo BB; Aw T; Fattoum S
Ann Hematol; 2003 Jul; 82(7):423-6. PubMed ID: 12764548
[TBL] [Abstract][Full Text] [Related]
11. Mitral valve reconstruction in a compound heterozygote for sickle cell anemia and hemoglobin Lepore.
Tziomalos K; Garipidou V; Houmpouridou E; Pitsis AA; Basayannis E
J Thorac Cardiovasc Surg; 2005 Sep; 130(3):932-3. PubMed ID: 16153972
[No Abstract] [Full Text] [Related]
12. Clinical and molecular characterization of Hb Hofu in eastern India.
Purohit P; Mashon RS; Patel S; Dehury S; Pattanayak C; Das K; Nair S; Italia K; Bag S; Colah R; Patel DK
Int J Lab Hematol; 2014 Feb; 36(1):71-6. PubMed ID: 23889802
[TBL] [Abstract][Full Text] [Related]
13. Potential pitfalls in the diagnosis of Hb Handsworth in areas with high prevalence of HbS.
Al Zadjali S; Al-Riyami AZ; Gravell D; Al Haddabi H; Al Rawahi M; Al Falahi K; Daar S
Int J Lab Hematol; 2014 Aug; 36(4):488-92. PubMed ID: 24165563
[TBL] [Abstract][Full Text] [Related]
14. Double heterozygous hemoglobinopathies--diagnostic importance of parent studies.
Patra SB; Giri DD; Patel RZ; Modi UJ; Amin NS
Indian Pediatr; 1983 Jul; 20(7):485-8. PubMed ID: 6654480
[No Abstract] [Full Text] [Related]
15. [Hemoglobinopathy S with an interaction of HbS and Hb G-Ferrara].
Cañizares ME; Martínez G; Hernández S; Raymond P; Colombo B
Sangre (Barc); 1983; 28(6):770-4. PubMed ID: 6673168
[No Abstract] [Full Text] [Related]
16. 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
[TBL] [Abstract][Full Text] [Related]
17. Diagnosis of a novel hemoglobinopathy of compound heterozygosity of hemoglobin S/hemoglobin Q India.
Parab S; Sakhare S; Sengupta C; Velumani A
Clin Chim Acta; 2015 Mar; 442():33-5. PubMed ID: 25576799
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Unusual sickle cell disease observed for the first time in Italy: Hb S-Hb D Los Angeles.
Samperi P; Dibenedetto SP; di Cataldo A; Mancuso GR; Schilirò G
Haematologica; 1990; 75(5):464-6. PubMed ID: 2097263
[TBL] [Abstract][Full Text] [Related]
20. Homozygous HbE and HbSE disease in a Saudi family.
Hardy MJ; Ragbeer MS
Hemoglobin; 1985; 9(1):47-52. PubMed ID: 3997540
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
