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Items: 1 to 20 of 402

1.

Care for Haemoglobinopathy Patients in Slovakia.

Fábryová V, Božek P, Drakulová M, Kollárová A, Striežencová ZL, Macichová M, Sakalová A.

Cent Eur J Public Health. 2017 Mar;25(1):67-71. doi: 10.21101/cejph.a4471.

PMID:
28399358
2.

Inheritance of the Bantu/Benin haplotype causes less severe hemolytic and oxidative stress in sickle cell anemia patients treated with hydroxycarbamide.

Okumura JV, Silva DG, Torres LS, Belini-Junior E, Barberino WM, Oliveira RG, Carrocini GC, Gelaleti GB, Lobo CL, Bonini-Domingos CR.

J Hum Genet. 2016 Jul;61(7):605-11. doi: 10.1038/jhg.2016.16. Epub 2016 Mar 10.

PMID:
26961071
3.

Minireview: Genetic basis of heterogeneity and severity in sickle cell disease.

Habara A, Steinberg MH.

Exp Biol Med (Maywood). 2016 Apr;241(7):689-96. doi: 10.1177/1535370216636726. Epub 2016 Mar 1. Review.

5.

Sickle cell trait diagnosis: clinical and social implications.

Naik RP, Haywood C Jr.

Hematology Am Soc Hematol Educ Program. 2015;2015:160-7. doi: 10.1182/asheducation-2015.1.160. Review.

6.

Youth with Sickle Cell Disease: Genetic and Sexual Health Education Needs.

Housten AJ, Abel RA, Dadekian J, Schwieterman K, Jason D, King AA.

Am J Health Behav. 2015 Nov;39(6):856-65. doi: 10.5993/AJHB.39.6.13.

7.

Reproductive Health CHOICES for Young Adults with Sickle Cell Disease or Trait: Randomized Controlled Trial Outcomes over Two Years.

Gallo AM, Wilkie DJ, Yao Y, Molokie RE, Stahl C, Hershberger PE, Zhao Z, Suarez ML, Johnson B, Angulo R, Carrasco J, Angulo V, Thompson AA.

J Genet Couns. 2016 Apr;25(2):325-36. doi: 10.1007/s10897-015-9874-0. Epub 2015 Aug 28.

8.

Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease.

Hussein N, Weng SF, Kai J, Kleijnen J, Qureshi N.

Cochrane Database Syst Rev. 2015 Aug 12;(8):CD010849. doi: 10.1002/14651858.CD010849.pub2. Review.

PMID:
26264938
9.

Haemoglobinopathies in tribal populations of India.

Ghosh K, Colah RB, Mukherjee MB.

Indian J Med Res. 2015 May;141(5):505-8.

10.

Perspectives in Genetics and Sickle Cell Disease Prevention in Africa: Beyond the Preliminary Data from Cameroon.

Wonkam A, Ngo Bitoungui VJ, Ngogang J.

Public Health Genomics. 2015;18(4):237-41. doi: 10.1159/000431020. Epub 2015 Jun 4.

11.

Sickle Cell Trait Screening of Collegiate Athletes: Ethical Reasons for Program Reform.

Ferrari R, Parker LS, Grubs RE, Krishnamurti L.

J Genet Couns. 2015 Dec;24(6):873-7. doi: 10.1007/s10897-015-9849-1. Epub 2015 Jun 5.

PMID:
26040250
12.

Assessing Parental Knowledge About Thalassemia in a Thalassemia Center of Karachi, Pakistan.

Maheen H, Malik F, Siddique B, Qidwai A.

J Genet Couns. 2015 Dec;24(6):945-51. doi: 10.1007/s10897-015-9830-z. Epub 2015 Apr 7.

PMID:
25843562
13.

[Information for parents of children with sickle cell trait detected by neonatal screening: A 10-year experience].

Joly P, Badens C, Fekih S, Philippe N, Merono F, Thuret I, Pondarré C.

Arch Pediatr. 2015 May;22(5):562-3. doi: 10.1016/j.arcped.2015.02.020. Epub 2015 Apr 1. French. No abstract available.

PMID:
25842198
14.

Recent trends in the gene therapy of β-thalassemia.

Finotti A, Breda L, Lederer CW, Bianchi N, Zuccato C, Kleanthous M, Rivella S, Gambari R.

J Blood Med. 2015 Feb 19;6:69-85. doi: 10.2147/JBM.S46256. eCollection 2015. Review.

15.

Incidence of haemoglobinopathies in Sicily: the impact of screening and prenatal diagnosis.

Giambona A, Damiani G, Vinciguerra M, Jakil C, Cannata M, Cassarà F, Picciotto F, Schillaci G, Cigna V, Renda D, Leto F, Passarello C, Maggio A.

Int J Clin Pract. 2015 Oct;69(10):1129-38. doi: 10.1111/ijcp.12628. Epub 2015 Feb 27.

PMID:
25727926
16.

Evaluation of high performance liquid chromatography (HPLC) pattern and prevalence of beta-thalassaemia trait among sickle cell disease patients in Lagos, Nigeria.

Adeyemo T, Ojewunmi O, Oyetunji A.

Pan Afr Med J. 2014 May 22;18:71. doi: 10.11604/pamj.2014.18.71.4239. eCollection 2014.

17.

Q&A: healthy progress.

Serjeant G, Mallapaty S.

Nature. 2014 Nov 13;515(7526):S6-7. doi: 10.1038/515S6a. No abstract available.

PMID:
25390144
18.

An easy test but a hard decision: ethical issues concerning non-invasive prenatal testing for autosomal recessive disorders.

Skirton H, Goldsmith L, Chitty LS.

Eur J Hum Genet. 2015 Aug;23(8):1004-9. doi: 10.1038/ejhg.2014.238. Epub 2014 Nov 5.

19.

Improving the quality of physician communication with rapid-throughput analysis and report cards.

Farrell MH, Christopher SA, La Pean Kirschner A, Roedl SJ, O'Tool FO, Ahmad NY, Farrell PM.

Patient Educ Couns. 2014 Nov;97(2):248-55. doi: 10.1016/j.pec.2014.07.028. Epub 2014 Aug 28.

20.

Using formative research to develop a counselor training program for newborn screening in Ghana.

Treadwell MJ, Anie KA, Grant AM, Ofori-Acquah SF, Ohene-Frempong K.

J Genet Couns. 2015 Apr;24(2):267-77. doi: 10.1007/s10897-014-9759-7. Epub 2014 Sep 7.

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