Pulè G - Search Results

1

Distribution of HbS Allele and Haplotypes in a Multi-Ethnic Population of Guinea Bissau, West Africa: Implications for Public Health Screening.

Martella M, Campeggio M, Pulè G, Wonkam A, Menzato F, Munaretto V, Viola G, Da Costa SP, Reggiani G, Araujo A, Cumbà D, Liotta G, Sainati L, Riccardi F, Colombatti R. Martella M, et al. Among authors: pule g. Front Pediatr. 2022 Apr 7;10:826262. doi: 10.3389/fped.2022.826262. eCollection 2022. Front Pediatr. 2022. PMID: 35463879 Free PMC article.

2

Treatment for sickle cell disease in Africa: should we invest in haematopoietic stem cell transplantation?

Pule G, Wonkam A. Pule G, et al. Pan Afr Med J. 2014 May 13;18:46. doi: 10.11604/pamj.2014.18.46.3923. eCollection 2014. Pan Afr Med J. 2014. PMID: 25368735 Free PMC article. No abstract available.

3

Hydroxyurea-Induced miRNA Expression in Sickle Cell Disease Patients in Africa.

Mnika K, Mazandu GK, Jonas M, Pule GD, Chimusa ER, Hanchard NA, Wonkam A. Mnika K, et al. Among authors: pule gd. Front Genet. 2019 May 28;10:509. doi: 10.3389/fgene.2019.00509. eCollection 2019. Front Genet. 2019. PMID: 31231425 Free PMC article.

4

An Expert Review of Pharmacogenomics of Sickle Cell Disease Therapeutics: Not Yet Ready for Global Precision Medicine.

Mnika K, Pule GD, Dandara C, Wonkam A. Mnika K, et al. Among authors: pule gd. OMICS. 2016 Oct;20(10):565-574. doi: 10.1089/omi.2016.0105. Epub 2016 Sep 16. OMICS. 2016. PMID: 27636225 Free PMC article. Review.

5

Beta-globin gene haplotypes among cameroonians and review of the global distribution: is there a case for a single sickle mutation origin in Africa?

Bitoungui VJ, Pule GD, Hanchard N, Ngogang J, Wonkam A. Bitoungui VJ, et al. OMICS. 2015 Mar;19(3):171-9. doi: 10.1089/omi.2014.0134. OMICS. 2015. PMID: 25748438 Free PMC article. Review.

6

Hydroxyurea down-regulates BCL11A, KLF-1 and MYB through miRNA-mediated actions to induce γ-globin expression: implications for new therapeutic approaches of sickle cell disease.

Pule GD, Mowla S, Novitzky N, Wonkam A. Pule GD, et al. Clin Transl Med. 2016 Mar;5(1):15. doi: 10.1186/s40169-016-0092-7. Epub 2016 Apr 7. Clin Transl Med. 2016. PMID: 27056246 Free PMC article.

7

A systematic review of known mechanisms of hydroxyurea-induced fetal hemoglobin for treatment of sickle cell disease.

Pule GD, Mowla S, Novitzky N, Wiysonge CS, Wonkam A. Pule GD, et al. Expert Rev Hematol. 2015 Oct;8(5):669-79. doi: 10.1586/17474086.2015.1078235. Epub 2015 Sep 1. Expert Rev Hematol. 2015. PMID: 26327494 Free PMC article. Review.

8

Genetics of Sickle Cell-Associated Cardiovascular Disease: An Expert Review with Lessons Learned in Africa.

Geard A, Pule GD, Chelo D, Bitoungui VJ, Wonkam A. Geard A, et al. Among authors: pule gd. OMICS. 2016 Oct;20(10):581-592. doi: 10.1089/omi.2016.0125. OMICS. 2016. PMID: 27726639 Free PMC article. Review.

9

Burden, genotype and phenotype profiles of adult patients with sickle cell disease in Cape Town, South Africa.

Pule GD, Mnica K, Joubert M, Mowla S, Novitsky N, Wonkam A. Pule GD, et al. S Afr Med J. 2017 Jan 30;107(2):149-155. doi: 10.7196/SAMJ.2017.v107i2.10849. S Afr Med J. 2017. PMID: 28220744

10

Association between Variants at BCL11A Erythroid-Specific Enhancer and Fetal Hemoglobin Levels among Sickle Cell Disease Patients in Cameroon: Implications for Future Therapeutic Interventions.

Pule GD, Ngo Bitoungui VJ, Chetcha Chemegni B, Kengne AP, Antonarakis S, Wonkam A. Pule GD, et al. OMICS. 2015 Oct;19(10):627-31. doi: 10.1089/omi.2015.0124. Epub 2015 Sep 22. OMICS. 2015. PMID: 26393293 Free PMC article.

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