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Items: 1 to 20 of 420

1.

Prevalence and Genetic Analysis of α- and β-Thalassemia and Sickle Cell Anemia in Southwest Iran.

Nezhad FH, Nezhad KH, Choghakabodi PM, Keikhaei B.

J Epidemiol Glob Health. 2018 Dec;8(3-4):189-195. doi: 10.2991/j.jegh.2018.04.103.

PMID:
30864762
2.

Awareness and Attitude of University Students About Screening and Testing for Hemoglobinopathies: Case Study of the Aseer Region, Saudi Arabia.

Eissa M, Patel AA, Farag S, Babiker NH, Al-Shahrani MS, Al-Nahari AM, Al Sahmaa AM, Al-Shraim M.

Hemoglobin. 2018 Jul;42(4):264-268. doi: 10.1080/03630269.2018.1541802. Epub 2019 Jan 3.

PMID:
30821195
3.

Premarital Screening and Genetic Counseling Program: Studies from an Endogamous Population.

Bener A, Al-Mulla M, Clarke A.

Int J Appl Basic Med Res. 2019 Jan-Mar;9(1):20-26. doi: 10.4103/ijabmr.IJABMR_42_18.

4.

Knowledge Deficit of Sickle Cell Trait Status: Can Nurses Help?

Arhin AO.

Crit Care Nurs Q. 2019 Apr/Jun;42(2):198-201. doi: 10.1097/CNQ.0000000000000254.

PMID:
30807345
5.

The current state of sickle cell trait: implications for reproductive and genetic counseling.

Pecker LH, Naik RP.

Hematology Am Soc Hematol Educ Program. 2018 Nov 30;2018(1):474-481. doi: 10.1182/asheducation-2018.1.474. Review.

PMID:
30504348
6.

Efficacy of the National Thalassaemia and Sickle Cell Disease Prevention Programme in Northern Greece: 15-Year Experience, Practice and Policy Gaps for Natives and Migrants.

Theodoridou S, Prapas N, Balassopoulou A, Boutou E, Vyzantiadis TA, Adamidou D, Delaki EE, Yfanti E, Economou M, Teli Α, Karakasidou O, Skatharoudi E, Theodoridis T, Voskaridou E.

Hemoglobin. 2018 Jul;42(4):257-263. doi: 10.1080/03630269.2018.1528986. Epub 2018 Dec 3.

PMID:
30501529
7.

Distribution of hemoglobinopathy disorders in Saudi Arabia based on data from the premarital screening and genetic counseling program, 2011-2015.

Alsaeed ES, Farhat GN, Assiri AM, Memish Z, Ahmed EM, Saeedi MY, Al-Dossary MF, Bashawri H.

J Epidemiol Glob Health. 2018 Mar;7 Suppl 1:S41-S47. doi: 10.1016/j.jegh.2017.12.001. Epub 2017 Dec 15.

8.

Identifying Factors Underlying the Decision for Sickle Cell Carrier Screening Among African Americans Within Middle Reproductive Age.

Mayo-Gamble TL, Middlestadt SE, Lin HC, Cunningham-Erves J, Barnes P, Jackson PB.

J Genet Couns. 2018 Sep;27(5):1302-1311. doi: 10.1007/s10897-018-0255-3. Epub 2018 Mar 24.

PMID:
29574538
9.

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. 2018 Mar 14;3:CD010849. doi: 10.1002/14651858.CD010849.pub3. Review.

10.

Perinatal and Neonatal Implications of Sickle Cell Disease.

Phillips C, Boyd MP.

Nurs Womens Health. 2017 Dec;21(6):474-487. doi: 10.1016/j.nwh.2017.10.007.

PMID:
29223211
11.

Variability of homozygous sickle cell disease: The role of alpha and beta globin chain variation and other factors.

Serjeant GR, Vichinsky E.

Blood Cells Mol Dis. 2018 May;70:66-77. doi: 10.1016/j.bcmd.2017.06.004. Epub 2017 Jun 21. Review.

PMID:
28689691
12.

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.

13.

Sickle Cell Trait and the Risk of ESRD in Blacks.

Naik RP, Irvin MR, Judd S, Gutiérrez OM, Zakai NA, Derebail VK, Peralta C, Lewis MR, Zhi D, Arnett D, McClellan W, Wilson JG, Reiner AP, Kopp JB, Winkler CA, Cushman M.

J Am Soc Nephrol. 2017 Jul;28(7):2180-2187. doi: 10.1681/ASN.2016101086. Epub 2017 Mar 9.

14.

'It means everyone should know their status': exploring lay conceptions of sickle cell trait and sickle cell trait screening among African Americans within middle reproductive age.

Mayo-Gamble TL, Barnes PA, Cunningham Erves J, Middlestadt SE, Lin HC.

Ethn Health. 2018 Oct;23(7):813-829. doi: 10.1080/13557858.2017.1295135. Epub 2017 Feb 21.

PMID:
28277026
15.

[Sickle cell syndrome. Association between hemoglobin S and β thalassemia].

Gasparini NP, Agriello EE, Zanella MJ, Iommi MP, Maradei J, Sandoval MJ.

Medicina (B Aires). 2016;76(6):369-372. Spanish.

16.

Is the Game Over or Starting Again? The Role of the Transplant Team in Genetic Counseling for Adult Sickle Cell Disease Recipients.

Aytan P, Gereklioğlu Ç, Yeral M, Korur A, Asma S, Kozanoğlu İ, Özdoğu H, Boğa C.

Turk J Haematol. 2017 Jun 5;34(2):196-197. doi: 10.4274/tjh.2016.0355. Epub 2016 Dec 12. No abstract available.

17.

Non-invasive prenatal diagnosis (NIPD) for single gene disorders: cost analysis of NIPD and invasive testing pathways.

Verhoef TI, Hill M, Drury S, Mason S, Jenkins L, Morris S, Chitty LS.

Prenat Diagn. 2016 Jul;36(7):636-42. doi: 10.1002/pd.4832. Epub 2016 May 22.

18.

Parents' Experiences of Receiving the Initial Positive Newborn Screening (NBS) Result for Cystic Fibrosis and Sickle Cell Disease.

Chudleigh J, Buckingham S, Dignan J, O'Driscoll S, Johnson K, Rees D, Wyatt H, Metcalfe A.

J Genet Couns. 2016 Dec;25(6):1215-1226. Epub 2016 Apr 20.

19.

Prevalence of sickle cell gene among apparently healthy under-two south-east Nigerian children: what is the role of parental premarital counselling and socio-demographic characteristics? A pilot study.

Okocha C, Onubogu CU, Aneke J, Onah C, Ajuba I, Ibeh N, Egbuonu I.

Niger J Med. 2016 Apr-Jun;25(2):176-181. No abstract available.

PMID:
29944316
20.

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

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