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Barriers to biomedical care for people with epilepsy in Uganda: A cross-sectional study.
Kaddumukasa MN, Kaddumukasa M, Kajumba M, Smith PJ, Bobholz S, Kakooza-Mwesige A, Sinha DD, Almojuela A, Chakraborty P, Nakasujja N, Nakku J, Gualtieri A, Onuoha E, Kolls BJ, Muhumuza C, Smith CE, Sanchez N, Fuller AT, Haglund MM, Koltai DC. Kaddumukasa MN, et al. Among authors: smith ce, smith pj. Epilepsy Behav. 2021 Jan;114(Pt B):107349. doi: 10.1016/j.yebeh.2020.107349. Epub 2020 Sep 20. Epilepsy Behav. 2021. PMID: 32962922
Healthcare provider perspectives regarding epilepsy care in Uganda.
Koltai DC, Smith CE, Cai GY, Ratliff O, Kakooza-Mwesige A, Najjuma JN, Muhindo R, Rukundo GZ, Teuwen DE, Kayanja A, Kalubi P, Haglund MM, Fuller AT. Koltai DC, et al. Among authors: smith ce. Epilepsy Behav. 2021 Jan;114(Pt B):107294. doi: 10.1016/j.yebeh.2020.107294. Epub 2020 Aug 3. Epilepsy Behav. 2021. PMID: 32763023
Sociocultural determinants and patterns of healthcare utilization for epilepsy care in Uganda.
Koltai DC, Dunn TW, Smith PJ, Sinha DD, Bobholz S, Kaddumukasa M, Kakooza-Mwesige A, Kajumba M, Smith CE, Kaddumukasa MN, Teuwen DE, Nakasujja N, Chakraborty P, Kolls BJ, Nakku J, Haglund MM, Fuller AT. Koltai DC, et al. Among authors: smith ce, smith pj. Epilepsy Behav. 2021 Jan;114(Pt B):107304. doi: 10.1016/j.yebeh.2020.107304. Epub 2020 Aug 4. Epilepsy Behav. 2021. PMID: 32768344
Pluralistic and singular causal attributions for epilepsy in Uganda.
Smith CE, Kajumba M, Bobholz S, Smith PJ, Kaddumukasa M, Kakooza-Mwesige A, Chakraborty P, Sinha DD, Kaddumukasa MN, Gualtieri A, Nakasujja N, Onuoha E, Nakku J, Muhumuza C, Sanchez N, Fuller AT, Haglund MM, Koltai DC. Smith CE, et al. Among authors: smith pj. Epilepsy Behav. 2021 Jan;114(Pt B):107334. doi: 10.1016/j.yebeh.2020.107334. Epub 2020 Aug 22. Epilepsy Behav. 2021. PMID: 32839144
Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability.
Smith CEL, Laugel-Haushalter V, Hany U, Best S, Taylor RL, Poulter JA, Wortmann SB, Feichtinger RG, Mayr JA, Al Bahlani S, Nikolopoulos G, Rigby A, Black GC, Watson CM, Mansour S, Inglehearn CF, Mighell AJ, Bloch-Zupan A; UK Inherited Retinal Disease Consortium, Genomics England Research Consortium. Smith CEL, et al. J Med Genet. 2024 Apr 8:jmg-2023-109728. doi: 10.1136/jmg-2023-109728. Online ahead of print. J Med Genet. 2024. PMID: 38458752 Free article.
1,104 results