Twumasi Aboagye E - Search Results

Save citations to file

Email citations

Your saved search

Your RSS Feed

Page 1

Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden.

Adadey SM, Wonkam-Tingang E, Twumasi Aboagye E, Nayo-Gyan DW, Boatemaa Ansong M, Quaye O, Awandare GA, Wonkam A. Adadey SM, et al. Among authors: twumasi aboagye e. Life (Basel). 2020 Oct 28;10(11):258. doi: 10.3390/life10110258. Life (Basel). 2020. PMID: 33126609 Free PMC article. Review.

Enhancing Genetic Medicine: Rapid and Cost-Effective Molecular Diagnosis for a GJB2 Founder Mutation for Hearing Impairment in Ghana.

Adadey SM, Tingang Wonkam E, Twumasi Aboagye E, Quansah D, Asante-Poku A, Quaye O, Amedofu GK, Awandare GA, Wonkam A. Adadey SM, et al. Among authors: twumasi aboagye e. Genes (Basel). 2020 Jan 27;11(2):132. doi: 10.3390/genes11020132. Genes (Basel). 2020. PMID: 32012697 Free PMC article.

A cross-sectional comparative study of perceived stigma between patients with epilepsy and patients living with HIV/AIDS in Accra, Ghana.

Adjei P, Nkromah K, Akpalu A, Laryea R, Osei Poku F, Ohene S, Puplampu P, Twumasi Aboagye E. Adjei P, et al. Among authors: twumasi aboagye e. Epilepsy Behav. 2018 Dec;89:1-7. doi: 10.1016/j.yebeh.2018.10.015. Epub 2018 Oct 25. Epilepsy Behav. 2018. PMID: 30384093

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

3 results

Search Page

Filters