Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Carmen de Kock"'
Autor:
Samuel Mawuli Adadey, Edmond Wonkam-Tingang, Leonardo Alves de Souza Rios, Elvis Twumasi Aboagye, Kevin Esoh, Noluthando Manyisa, Carmen De Kock, Gordon A. Awandare, Shaheen Mowla, Ambroise Wonkam
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
We have previously reported CLIC5A and SLC12A2 variants in two families from Cameroon and Ghana, segregating non-syndromic hearing impairment (NSHI). In this study, biological assays were performed to further functionally investigate the pathogenicit
Externí odkaz:
https://doaj.org/article/c30eeef92166471a8d715fdaa6992a3d
Autor:
Edmond Wonkam-Tingang, Karen Kengne Kamga, Samuel Mawuli Adadey, Seraphin Nguefack, Carmen De Kock, Nchangwi Syntia Munung, Ambroise Wonkam
Publikováno v:
Frontiers in Rehabilitation Sciences, Vol 2 (2021)
Background: This study aimed to gain an understanding of the challenges faced by people with hearing impairment (HI) in Cameroon, their understanding of the causes of HI, and how challenges could be remedied to improve the quality of life of persons
Externí odkaz:
https://doaj.org/article/23e2dae17c264b6c8e4e9b5b1b727664
Autor:
Yacouba Dia, Samuel Mawuli Adadey, Jean Pascal Demba Diop, Elvis Twumasi Aboagye, Seydi Abdoul Ba, Carmen De Kock, Cheikh Ahmed Tidjane Ly, Oluwafemi Gabriel Oluwale, Andrea Regina Gnilane Sène, Pierre Diaga Sarr, Bay Karim Diallo, Rokhaya Ndiaye Diallo, Ambroise Wonkam
Publikováno v:
Biology, Vol 11, Iss 5, p 795 (2022)
This study aimed to investigate GJB2 (MIM: 121011) and GJB6 (MIM: 604418) variants associated with familial non-syndromic hearing impairment (HI) in Senegal. We investigated a total of 129 affected and 143 unaffected individuals from 44 multiplex fam
Externí odkaz:
https://doaj.org/article/2d1c2feb18454af69a407c83b21b5b7b
Autor:
Elvis Twumasi Aboagye, Samuel Mawuli Adadey, Kevin Esoh, Mario Jonas, Carmen de Kock, Lucas Amenga-Etego, Gordon A. Awandare, Ambroise Wonkam
Publikováno v:
Biology, Vol 11, Iss 3, p 476 (2022)
Gap junction protein beta 2 (GJB2) (connexin 26) variants are commonly implicated in non-syndromic hearing impairment (NSHI). In Ghana, the GJB2 variant p.(Arg143Trp) is the largest contributor to NSHI and has a reported prevalence of 25.9% in affect
Externí odkaz:
https://doaj.org/article/48277725a2b240b086e2f01f96c1e1dd
Autor:
Samuel M. Adadey, Noluthando Manyisa, Khuthala Mnika, Carmen de Kock, Victoria Nembaware, Osbourne Quaye, Geoffrey K. Amedofu, Gordon A. Awandare, Ambroise Wonkam
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Our study aimed to investigate GJB2 (connexin 26) and GJB6 (connexin 30) mutations associated with non-syndromic childhood hearing impairment (HI) as well as the environmental causes of HI in Ghana. Medical reports of 1,104 students attending schools
Externí odkaz:
https://doaj.org/article/855234770c8e43139389a56257fde263
Autor:
Yacouba Dia, Birame Loum, Yaay Joor Koddu Biigé Dieng, Jean Pascal Demba Diop, Samuel Mawuli Adadey, Elvis Twumasi Aboagye, Seydi Abdoul Ba, Abdoul Aziz Touré, Fallou Niang, Pierre Diaga Sarr, Cheikh Ahmed Tidiane Ly, Andrea Regina Gnilane Sène, Carmen De Kock, Rhiyana Bassier, Kalinka Popel, Rokhaya Ndiaye Diallo, Ambroise Wonkam, Bay Karim Diallo
Publikováno v:
Genes
Volume 14
Issue 3
Pages: 562
Volume 14
Issue 3
Pages: 562
We recently showed that variants in GJB2 explained Hearing Impairment (HI) in 34.1% (n = 15/44) of multiplex families in Senegal. The present study aimed to use community-based nationwide recruitment to determine the etiologies and the clinical profi
Autor:
Celestine Raidron, Audrey Jordaan, Ronnett Seldon, Digby F. Warner, Carmen de Kock, Dale Taylor, Stefan Louw, Suthananda Sunassee, Renate Hazel Hans
Publikováno v:
Journal of ethnopharmacology. 295
Eight indigenous medicinal plants which are used traditionally for the treatment of tuberculosis (TB), malaria, and associated symptoms, were selected for this study.The aim of this study was to evaluate the antiplasmodial and antimycobacterial activ
Autor:
Elvis Twumasi, Aboagye, Samuel Mawuli, Adadey, Kevin, Esoh, Mario, Jonas, Carmen, de Kock, Lucas, Amenga-Etego, Gordon A, Awandare, Ambroise, Wonkam
Publikováno v:
Biology. 11(3)
Gap junction protein beta 2 (
Autor:
Noluthando, Manyisa, Isabelle, Schrauwen, Leonardo Alves, de Souza Rios, Shaheen, Mowla, Cedrik, Tekendo-Ngongang, Kalinka, Popel, Kevin, Esoh, Thashi, Bharadwaj, Liz M, Nouel-Saied, Anushree, Acharya, Abdul, Nasir, Edmond, Wonkam-Tingang, Carmen de, Kock, Collet, Dandara, Suzanne M, Leal, Ambroise, Wonkam
Publikováno v:
Genes
Hearing impairment (HI) is a sensory disorder with a prevalence of 0.0055 live births in South Africa. DNA samples from a South African family presenting with progressive, autosomal dominant non-syndromic HI were subjected to whole-exome sequencing,
Autor:
Karen Kengne Kamga, Carmen de Kock, Edmond Wonkam-Tingang, Séraphin Nguefack, Samuel Mawuli Adadey, Nchangwi Syntia Munung, Ambroise Wonkam
Publikováno v:
Frontiers in Rehabilitation Sciences, Vol 2 (2021)
Background: This study aimed to gain an understanding of the challenges faced by people with hearing impairment (HI) in Cameroon, their understanding of the causes of HI, and how challenges could be remedied to improve the quality of life of persons