224 related articles for article (PubMed ID: 17007653)
21. Using the fluorescence spot test for neonatal screening of G6PD deficiency.
Jiang J; Ma X; Song C; Lin B; Cao W; Wu S; Hsiao KJ
Southeast Asian J Trop Med Public Health; 2003; 34 Suppl 3():140-2. PubMed ID: 15906719
[TBL] [Abstract][Full Text] [Related]
22. Screening for sickle cell disease on dried blood: a new approach evaluated on 27,000 Belgian newborns.
Boemer F; Vanbellinghen JF; Bours V; Schoos R
J Med Screen; 2006; 13(3):132-6. PubMed ID: 17007654
[TBL] [Abstract][Full Text] [Related]
23. Sickle cell haemoglobin, thalassaemia and G-6-PD enzyme deficiency genes in Garasiya tribe inhabited malaria endemic areas of Sirohi District, Rajasthan (India).
Choubisa SL
J Commun Dis; 2009 Mar; 41(1):13-8. PubMed ID: 19886170
[TBL] [Abstract][Full Text] [Related]
24. Neonatal haemoglobinopathy screening in Belgium.
Gulbis B; Cotton F; Ferster A; Ketelslegers O; Dresse MF; Rongé-Collard E; Minon JM; Lé PQ; Vertongen F
J Clin Pathol; 2009 Jan; 62(1):49-52. PubMed ID: 19103861
[TBL] [Abstract][Full Text] [Related]
25. Chromatographic analysis of Hb S for the diagnosis of various sickle cell disorders in Pakistan.
Hashmi NK; Moiz B; Nusrat M; Hashmi MR
Ann Hematol; 2008 Aug; 87(8):639-45. PubMed ID: 18465131
[TBL] [Abstract][Full Text] [Related]
26. Haematological study in Cabo Delgado province, Mozambique; sickle cell trait and G6PD deficiency.
Nieuwenhuis F; Wolf B; Bomba A; De Graaf P
Trop Geogr Med; 1986 Jun; 38(2):183-7. PubMed ID: 3488609
[TBL] [Abstract][Full Text] [Related]
27. A comprehensive study on the major mutations in glucose-6-phosphate dehydrogenase-deficient polymorphic variants identified in the coastal provinces of Caspian Sea in the north of Iran.
Noori-Daloii MR; Hajebrahimi Z; Najafi L; Mesbah-Namin SA; Mowjoodi A; Mohammad Ganji S; Yekaninejad MS; Sanati MH
Clin Biochem; 2007 Jun; 40(9-10):699-704. PubMed ID: 17499234
[TBL] [Abstract][Full Text] [Related]
28. Neonatal haemoglobinopathy screening in Burkina Faso.
Kafando E; Nacoulma E; Ouattara Y; Ayéroué J; Cotton F; Sawadogo M; Gulbis B
J Clin Pathol; 2009 Jan; 62(1):39-41. PubMed ID: 19103858
[TBL] [Abstract][Full Text] [Related]
29. G6PD enzyme activity in normal term Malaysian neonates and adults using a OSMMR2000-D kit with Hb normalization.
Azma RZ; Hidayati N; Farisah NR; Hamidah NH; Ainoon O
Southeast Asian J Trop Med Public Health; 2010 Jul; 41(4):982-8. PubMed ID: 21073074
[TBL] [Abstract][Full Text] [Related]
30. Prevalence of classic erythrocyte polymorphisms among 749 children in southern highland Rwanda.
Gahutu JB; Musemakweri A; Harms G; Mockenhaupt FP
Trans R Soc Trop Med Hyg; 2012 Jan; 106(1):63-5. PubMed ID: 22018599
[TBL] [Abstract][Full Text] [Related]
31. Prevalence of sickle cell disease in a northeastern region of the Democratic Republic of Congo: what impact on transfusion policy?
Agasa B; Bosunga K; Opara A; Tshilumba K; Dupont E; Vertongen F; Cotton F; Gulbis B
Transfus Med; 2010 Feb; 20(1):62-5. PubMed ID: 19712051
[TBL] [Abstract][Full Text] [Related]
32. Incidence of haemoglobinopathies detected through neonatal screening in the United Arab Emirates.
Al Hosani H; Salah M; Osman HM; Farag HM; Anvery SM
East Mediterr Health J; 2005 May; 11(3):300-7. PubMed ID: 16602448
[TBL] [Abstract][Full Text] [Related]
33. The potential of electrospray ionization mass spectrometry for the diagnosis of hemoglobin variants found in newborn screening.
Wild BJ; Green BN; Stephens AD
Blood Cells Mol Dis; 2004; 33(3):308-17. PubMed ID: 15528150
[TBL] [Abstract][Full Text] [Related]
34. A community-based study of common hereditary blood disorders in Oman.
Al-Riyami AA; Suleiman AJ; Afifi M; Al-Lamki ZM; Daar S
East Mediterr Health J; 2001 Nov; 7(6):1004-11. PubMed ID: 15332742
[TBL] [Abstract][Full Text] [Related]
35. Campaign to control genetic blood diseases in Bahrain.
Al Arrayed S
Community Genet; 2005; 8(1):52-5. PubMed ID: 15767757
[TBL] [Abstract][Full Text] [Related]
36. Glucose-6-phosphate dehydrogenase deficiency neonatal screening: preliminary evidence that a high percentage of partially deficient female neonates are missed during routine screening.
Reclos GJ; Hatzidakis CJ; Schulpis KH
J Med Screen; 2000; 7(1):46-51. PubMed ID: 10807147
[TBL] [Abstract][Full Text] [Related]
37. Newborn screening shows a high incidence of sickle cell anemia in Central India.
Jain DL; Sarathi V; Upadhye D; Gulhane R; Nadkarni AH; Ghosh K; Colah RB
Hemoglobin; 2012; 36(4):316-22. PubMed ID: 22712682
[TBL] [Abstract][Full Text] [Related]
38. [Neonatal screening for sickle cell disease in the Consorci Sanitari de Mataro. Rationale and first results].
Cabot Dalmau A; Casado Toda M; Barberán Pérez J; Roqueta Sureda M; Martorell Aymerich Q; Bosch Llobet A; Rovira Fernández JM
An Esp Pediatr; 1998 Aug; 49(2):157-60. PubMed ID: 9773551
[TBL] [Abstract][Full Text] [Related]
39. Quality assurance program for neonatal screening of glucose-6-phosphate dehydrogenase deficiency.
Chiang SH; Wu KF; Liu TT; Wu SJ; Hsiao KJ
Southeast Asian J Trop Med Public Health; 2003; 34 Suppl 3():130-4. PubMed ID: 15906716
[TBL] [Abstract][Full Text] [Related]
40. Sickle cell anemia in Garasia tribals of Rajasthan.
Mandot S; Khurana VL; Sonesh JK
Indian Pediatr; 2009 Mar; 46(3):239-40. PubMed ID: 19179738
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
