Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Khaled Ben Helel"'
Autor:
Meriam Hadj Amor, Sarra Dimassi, Amel Taj, Wafa Slimani, Hanene Hannachi, Adnene Mlika, Khaled Ben Helel, Ali Saad, Soumaya Mougou-Zerelli
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-11 (2020)
Abstract Background While Miller-Dieker syndrome critical region deletions are well known delineated anomalies, submicroscopic duplications in this region have recently emerged as a new distinctive syndrome. So far, only few cases have been described
Externí odkaz:
https://doaj.org/article/6e8d2af9d0624869a30bede1b6354a49
Autor:
Khaled Ben Helel, Mohamed Ben Rejeb, Zakia Habboul, Nizar Khattat, Houssain Mejaouel, Houyem Said-Latiri, Belhassen Kaabi, Elyes Zhioua
Publikováno v:
PLoS ONE, Vol 12, Iss 12, p e0189725 (2017)
Zoonotic visceral leishmaniasis (ZVL) caused by Leishmania infantum is endemic with an epidemiological profile of a paediatric disease in Tunisia. In the context of a high fatality rate, identifying risk factors for in-hospital mortality in children
Externí odkaz:
https://doaj.org/article/cde6f6bd471c4cdf8db7f1333113d63f
Autism in patients with Williams-Beuren syndrome: A re-evaluation of 31 Tunisian patients’ phenotype
Autor:
Soumaya Mougou-Zerelli, Rim Khelifi, Afef Jelloul, Houda Ajmi, Sarra Dimassi, Wafa Slimani, Najla Soyeh, Khouloud Rjiba, Manel Dardour, Hamza Hadj Abdallah, Hend Dridi, Asma Guedria, Molka Kammoun, Hela Ben Khelifa, Hayet Mkadem, Ines Hssairi Guidara, Hayet Ben Hamida, Khaled Ben Helel, Habib Kharrat, Essia Sboui, Elies Naffeti, Naoufel Gaddour, Faouzi Maatouk, Hatem El Ghezal, Ali Saad, Ons Nouira, Afif Zouari
Background Williams Beuren Syndrome is a multisystemic disorder manifested by congenital heart defects associated with dysmorphic features, intellectual delay, and a particular behavioural profile due to a microdeletion in 7q11.2. Methods To establis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9c293816195e7d860f1a839aadd47cd
https://doi.org/10.21203/rs.3.rs-2139963/v1
https://doi.org/10.21203/rs.3.rs-2139963/v1
Autor:
Mohamed Soltani, Lamia Sfaihi, Rafiaa Mustapha, Jihen Bouguila, Khaled Ben Helel, Chebil Ben Meriem, Manel Ben Fredj, Mohamed Sfar, Sana El Mhamdi, Arwa Ben Salah
Publikováno v:
Eastern Mediterranean Health Journal. 25:861-871
Background Pneumococcal infections are an important cause of morbidity and mortality in the world and in Tunisia. Data on the economic burden of these infections are needed to inform decision-making to include pneumococcal vaccinations in routine chi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6a8d36b96dd4fcdcba25128fc1514a5
https://doi.org/10.26719/emhj.19.036
https://doi.org/10.26719/emhj.19.036
Autor:
Abdellatif Gargouri, I. Turki, Moncef Feki, Hassen Seboui, Myriam Cheour, Kamel Monastiri, Manel Charfi, Wiem Zidi, Neji Tebib, Sana Ben Massoued, Naziha Kaabachi, Awatef Jelassi, Houssain Mejaoual, Khaled Ben Helel, Nabiha Mahdhaoui, Amel Ben Chehida, Fahmi Nasrallah, Sameh Hadj-Taieb, F. Amri, Haifa Sanhaji
Publikováno v:
Neuropediatrics. 51(5)
Aim The aim of the study is to report on epidemiological, clinical, and biochemical characteristics of nonketotic hyperglycinemia (NKH) in Tunisia. Methods Patients diagnosed with NKH in Laboratory of Biochemistry at Rabta hospital (Tunis, Tunisia) b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33d2bef22b0086eea2fa0238f6471b94
https://pubmed.ncbi.nlm.nih.gov/32818969
https://pubmed.ncbi.nlm.nih.gov/32818969
Autor:
Amel Taj, Khaled Ben Helel, Ali Saad, Wafa Slimani, Meriam Hadj Amor, Hanene Hannachi, Soumaya Mougou-Zerelli, Adnene Mlika, Sarra Dimassi
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-11 (2020)
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-11 (2020)
Background While Miller-Dieker syndrome critical region deletions are well known delineated anomalies, submicroscopic duplications in this region have recently emerged as a new distinctive syndrome. So far, only few cases have been described overlapp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21910608b540b9605a61d07ba8b4fe59
https://pubmed.ncbi.nlm.nih.gov/32028920
https://pubmed.ncbi.nlm.nih.gov/32028920
Autor:
Elyes Zhioua, Belhassen Kaabi, Houssain Mejaouel, H. Said-Latiri, Nizar Khattat, Mohamed Ben Rejeb, Zakia Habboul, Khaled Ben Helel
Publikováno v:
PLoS ONE, Vol 12, Iss 12, p e0189725 (2017)
PLoS ONE
PLoS ONE
Background Zoonotic visceral leishmaniasis (ZVL) caused by Leishmania infantum is endemic with an epidemiological profile of a paediatric disease in Tunisia. In the context of a high fatality rate, identifying risk factors for in-hospital mortality i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d27f784757a8adaea6105a1119b2a47
https://doi.org/10.1371/journal.pone.0189725
https://doi.org/10.1371/journal.pone.0189725