Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Zamzam Mrad"'
Autor:
Lama Jaffal, Hawraa Joumaa, Jinane Noureldine, Malak Banjak, Mariam Ibrahim, Zamzam Mrad, Ali Salami, Said El Shamieh
Publikováno v:
BMC Medical Genomics, Vol 16, Iss 1, Pp 1-9 (2023)
Abstract Inherited retinal dystrophies (IRDs) are a major cause of vision loss. Altogether are highly heterogeneous genotypically and phenotypically, exhibiting substantial differences worldwide. To shed more light on these conditions, we investigate
Externí odkaz:
https://doaj.org/article/b0843a79bd91497c91545f3f7b03c4e1
Autor:
Lama Jaffal, Zamzam Mrad, Mariam Ibrahim, Ali Salami, Isabelle Audo, Christina Zeitz, Said El Shamieh
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-12 (2022)
Abstract Non-syndromic rod-cone dystrophy (RCD) is the most common condition in inherited retinal diseases. The aim of this study was to evaluate the research output and productivity related to RCD genetics per countries as classified by the human de
Externí odkaz:
https://doaj.org/article/ef5259803b554c239ed519d52d50e673
Publikováno v:
Eur J Hum Genet
Since a substantial difference in the prevalence of genetic causes of rod-cone dystrophy (RCD) was found among different populations, we conducted a systematic review of the genetic findings associated with RCD in Arab countries. Of the 816 articles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f43eebcedf935f018ec50569a8f6847
https://pubmed.ncbi.nlm.nih.gov/33188265
https://pubmed.ncbi.nlm.nih.gov/33188265
Autor:
Jaffal, Lama1 (AUTHOR), Joumaa, Hawraa2 (AUTHOR), Noureldine, Jinane2 (AUTHOR), Banjak, Malak2 (AUTHOR), Ibrahim, Mariam2 (AUTHOR), Mrad, Zamzam2 (AUTHOR), Salami, Ali3 (AUTHOR), Shamieh, Said El4 (AUTHOR) s.elshamieh@bau.edu.lb
Publikováno v:
BMC Medical Genomics. 5/1/2023, Vol. 16 Issue 1, p1-9. 9p.
Autor:
Jaffal, Lama1,2 (AUTHOR), Mrad, Zamzam1 (AUTHOR), Ibrahim, Mariam1 (AUTHOR), Salami, Ali3 (AUTHOR), Audo, Isabelle4,5,6 (AUTHOR), Zeitz, Christina4 (AUTHOR), El Shamieh, Said7 (AUTHOR) s.elshamieh@bau.edu.lb
Publikováno v:
Orphanet Journal of Rare Diseases. 4/23/2022, Vol. 17 Issue 1, p1-12. 12p.
Publikováno v:
Pain & Central Nervous System Week; 5/26/2023, p1025-1025, 1p