Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Awatef, Jelassi"'
Autor:
Awatef Jelassi, Fahmi Nasrallah, Emna Talbi, Mohamed Bassem Hammami, Rihab Ghodbane, Haifa Sanhaji, Moncef Feki, Naziha Kaabachi, Sameh Hadj-Taieb
Publikováno v:
Saudi Journal of Medicine and Medical Sciences, Vol 12, Iss 1, Pp 27-34 (2024)
Background: Organic aciduria diseases (OADs) occur worldwide, with differences in prevalence and patterns between populations. Objectives: To describe the spectrum of OADs identified in Tunisia over a 35-years period. Materials and Methods: Thi
Externí odkaz:
https://doaj.org/article/e45b7e156cec42b184a3e546a168adc5
Autor:
Rim Jbeli, Awatef Jelassi
Publikováno v:
Euro-Mediterranean Journal for Environmental Integration
The novel coronavirus disease 2019 (COVID-19) that emerged in China has spread to more than 212 countries to date. COVID-19 can cause serious acute respiratory syndrome (SARS). Therefore, research advances on the associated SARS-coronavirus-2 (CoV-2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::796e933386ee7e702c48c6d365fcaf47
https://doi.org/10.1007/s41207-021-00263-6
https://doi.org/10.1007/s41207-021-00263-6
Autor:
Najah, Mohamed, Di Leo, Enza, Awatef, Jelassi, Magnolo, Lucia, Imene, Jgurim, Pinotti, Elisa, Bahri, Mahjoub, Barsaoui, Sihem, Brini, Ines, Fekih, Moncef, Slimane, Mohamed Naceur, Tarugi, Patrizia
Publikováno v:
In Clinica Chimica Acta 2009 401(1):51-56
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:
Awatef Jelassi, Mohamed Najah, Imen Jguirim, Mohamed Naceur Slimane, Mathilde Varret, Afef Slimani
Publikováno v:
Current Genomics
Autosomal dominant hypercholesterolemia (ADH) is characterized by an isolated elevation of plasmatic low-density lipoprotein (LDL), which predisposes to premature coronary artery disease (CAD) and early death. ADH is largely due to mutations in the l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c999b27bdc992cf61fd45e4fa4589912
http://europepmc.org/articles/PMC3580777
http://europepmc.org/articles/PMC3580777
Autor:
Mohamed Naceur Slimane, Mathilde Varret, F. Addad, Mohsen Hassine, Faouzi Maatouk, Awatef Jelassi, Afef Slimani, Mohamed Najah, K. B. Hamda, Imen Jguirim
Publikováno v:
Pathologie Biologie. 60:180-184
Resume Objectifs Les variations du gene de la lipoproteine lipase peuvent contribuer a l’atherosclerose et aux maladies coronariennes. Le but de ce travail est d’examiner les frequences des trois variations du gene de la lipoproteine lipase (p.As
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d6996e93359cd8fb772bb63642463df
https://doi.org/10.1016/j.patbio.2011.04.003
https://doi.org/10.1016/j.patbio.2011.04.003
Autor:
Mohamed Najah, Afef Slimani, F. Addad, Mohamed Naceur Slimane, M. Rouis, Y. Hrira, F. Maatouk, M. Hassine, K. B. Hamda, Awatef Jelassi, I. Jguirim-Souissi
Publikováno v:
Genetics and Molecular Research. 9:1326-1333
Peroxisome proliferator-activated receptor delta (PPAR-delta) is a transcription factor implicated in metabolism and inflammation. The +294T/C polymorphism in the PPAR-delta gene is associated with risk of coronary artery disease (CAD) in dyslipidemi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a11dd00d9f53b3f4ef555f435a314f2
https://doi.org/10.4238/vol9-3gmr831
https://doi.org/10.4238/vol9-3gmr831
Autor:
K. Ben Hamda, Faouzi Maatouk, Mohamed Naceur Slimane, Mohamed Najah, Awatef Jelassi, Imen Jguirim
Publikováno v:
Pathologie Biologie. 57:444-450
Familial hypercholesterolemia or autosomal dominant hypercholesterolemia is characterized by raised serum LDL (low density lipoproteins)-cholesterol levels, which result in excess deposition of cholesterol in tissues, leading to accelerated atheroscl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1224b5f27f66fbf11bd65bf2227dd690
https://doi.org/10.1016/j.patbio.2008.09.015
https://doi.org/10.1016/j.patbio.2008.09.015
Autor:
A.M. Abid, Mathilde Varret, Imen Jguirim, Awatef Jelassi, L. Boughamoura, Mohamed Najah, Jean-Pierre Rabès, Mohamed Naceur Slimane, F. Maatouk, Catherine Boileau, M. Rouis
Publikováno v:
Atherosclerosis. 203:449-453
Familial hypercholesterolemia (FH) is an autosomal dominant disease caused by mutations in the low-density lipoprotein receptor ( LDLR ), apolipoprotein B ( APOB ), and proprotein convertase subtilisin/kexin type 9 ( PCSK9 ) genes. In previous studie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62b8ac7bf14410138bcb45e98321a6a6
https://doi.org/10.1016/j.atherosclerosis.2008.07.011
https://doi.org/10.1016/j.atherosclerosis.2008.07.011
Autor:
Khaldoun Ben Hamda, Faouzi Maatouk, Imen Jguirim-Souissi, Afef Slimani, Awatef Jelassi, Mustapha Rouis, Mohamed Najah, Majed Hassine, Faouzi Addad, Mohamed Naceur Slimane
Publikováno v:
Coronary artery disease. 22(6)
OBJECTIVES In this study, we investigated the association between matrix metalloproteinase-1 (MMP-1) G-1607GG, MMP-12 A-82G and MMP-12 A1082G genotypes and haplotypes and the prognosis of coronary artery disease (CAD). METHODS A total of 129 Tunisian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ba7d820cb611c43e354891228e21e96
https://pubmed.ncbi.nlm.nih.gov/21606841
https://pubmed.ncbi.nlm.nih.gov/21606841