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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
121 related items for PubMed ID: 38980121
21. Newborn screening by tandem mass spectrometry confirms the high prevalence of sickle cell disease among German newborns. Lobitz S, Klein J, Brose A, Blankenstein O, Frömmel C. Ann Hematol; 2019 Jan; 98(1):47-53. PubMed ID: 30132072 [Abstract] [Full Text] [Related]
22. Diagnostic accuracy in field conditions of the sickle SCAN® rapid test for sickle cell disease among children and adults in two West African settings: the DREPATEST study. Segbena AY, Guindo A, Buono R, Kueviakoe I, Diallo DA, Guernec G, Yerima M, Guindo P, Lauressergues E, Mondeilh A, Picot V, Leroy V. BMC Hematol; 2018 Jan; 18():26. PubMed ID: 30237894 [Abstract] [Full Text] [Related]
23. Fifteen years of newborn sickle cell disease screening in Madrid, Spain: an emerging disease in a European country. García-Morín M, Bardón-Cancho EJ, Beléndez C, Zamarro R, Béliz-Mendiola C, González-Rivera M, Vecilla C, Llorente-Otones L, Pérez-Alonso V, Román SS, Sebastián E, Dulín E, Cela E. Ann Hematol; 2020 Jul; 99(7):1465-1474. PubMed ID: 32451712 [Abstract] [Full Text] [Related]
28. New approach to accurate interpretation of sickle cell disease newborn screening by applying multiple of median cutoffs and ratios. Allaf B, Patin F, Elion J, Couque N. Pediatr Blood Cancer; 2018 Sep; 65(9):e27230. PubMed ID: 29781571 [Abstract] [Full Text] [Related]
30. HemoTypeSC point-of-care testing shows high sensitivity with alkaline cellulose acetate hemoglobin electrophoresis for screening hemoglobin SS and SC genotypes. Adegoke SA, Oladimeji OI, Akinlosotu MA, Akinwumi AI, Matthew KA. Hematol Transfus Cell Ther; 2022 Sep; 44(3):341-345. PubMed ID: 33531281 [Abstract] [Full Text] [Related]
31. Newborn Screening and Clinical Profile of Children With Sickle Cell Disease in a Tribal Area of Gujarat. Dave K, Desai S, Italia Y, Mukherjee MB, Mehta P, Desai G. Indian Pediatr; 2022 Mar 15; 59(3):230-233. PubMed ID: 35014619 [Abstract] [Full Text] [Related]
33. Characteristics of a rapid, point-of-care lateral flow immunoassay for the diagnosis of sickle cell disease. McGann PT, Schaefer BA, Paniagua M, Howard TA, Ware RE. Am J Hematol; 2016 Feb 15; 91(2):205-10. PubMed ID: 26537622 [Abstract] [Full Text] [Related]
34. Overview of current progress and challenges in diagnosis, and management of pediatric sickle cell disease in Democratic Republic of the Congo. Kasai ET, Alworong'a Opara JP, Ntokamunda Kadima J, Kalenga M, Batina Agasa S, Marini Djang'eing'a R, Boemer F. Hematology; 2022 Dec 15; 27(1):132-140. PubMed ID: 35068390 [Abstract] [Full Text] [Related]
38. Feasibility of a newborn screening and follow-up programme for sickle cell disease among South Gujarat (India) tribal populations. Italia Y, Krishnamurti L, Mehta V, Raicha B, Italia K, Mehta P, Ghosh K, Colah R. J Med Screen; 2015 Mar 15; 22(1):1-7. PubMed ID: 25341880 [Abstract] [Full Text] [Related]
39. Neonatal Screening and the Clinical Outcome in Children with Sickle Cell Disease in Central India. Upadhye DS, Jain DL, Trivedi YL, Nadkarni AH, Ghosh K, Colah RB. PLoS One; 2016 Mar 15; 11(1):e0147081. PubMed ID: 26785407 [Abstract] [Full Text] [Related]