Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Taheni Ben Lazreg"'
Autor:
Najla Soyah, Abdelbasset Amara, Faïza Zbidi, Ilhem Charfeddine, Abdelkarim Ayedi, Ahlem M'sakni, Saoussen Abroug, Jihene Bouguila, Hechmi Ben Hamouda, Adnène Mlika, Khalid Hlel, Taheni Ben Lazreg, Ali Saad, N. Zouari, Anouar Chaieb, Lamia Boughamoura, Moez Gribaa
Publikováno v:
Hemoglobin. 39:251-255
The β hemoglobinopathies [β-thalassemia (β-thal) and structural hemoglobin (Hb) variants such as Hb S (HBB: c.20A T) and Hb E (HBB: c.79G A)] are among the most common inherited diseases worldwide. In Tunisia, due to the high prevalence of consang
Autor:
Moez Gribaa, Oualid Naiija, Amira Mili, Taheni Ben Lazreg, Ali Saad, Abdelbacet Amara, Ons Mammai, Ilhem Charfeddine, Mohamed Dogui
Publikováno v:
Biological Rhythm Research. 45:285-292
Blood pressure (BP) and heart rate (HR) profiles follow circadian rhythm and day-to-day variations. It has been established that cardiovascular parameters decreased in sleep with the lowering of physical and mental activity. Sleeping has a profound e
Publikováno v:
Biological Rhythm Research. 44:435-443
Many physiological functions exhibit circadian rhythmicity. These functional rhythms are driven in part by the circadian clock, which plays an important role in maintaining stability of internal conditions. The present study was designed to evaluate
Autor:
Zouhaier Tabka, Abdelkarim Zbidi, Larbi Chaieb, Nada Dallel, Molka Chaieb, Monia Zaouali, Taheni Ben Lazreg
Publikováno v:
Biological Rhythm Research. 38:9-17
The recent discovery of leptin, the product of the “ob” gene has greatly advanced the understanding of body adiposity and energy balance regulation. Serum leptin levels follow a circadian rhythm, which seems to be regulated predominantly by insul
Autor:
Narjes Ben Rayana, Ahlem M'sakni, L. Knani, Ilhem Charfeddine, Taheni Ben Lazreg, Ali Saad, Ons Mamaï, Fafani Ben Hadj Hamida, Amira Mili, Moez Gribaa, Abdelbasset Amara
Publikováno v:
Annales de biologie clinique. 73(4)
Choroideremia is a rare X-linked recessive, hereditary retinal pigment epithelial dystrophy, characterized by night blindness and progressive constriction of the visual fields leading to blindness in young adulthood. In this study, we reported three
Autor:
Lamia Boughammura, Abdelbasset Amara, Ilhem Charfeddine, Fathi Amri, D. Hmida, Najla Salem, Ons Mamaï, Moez Gribaa, Labiba Adala, Taheni Ben Lazreg, Ali Saad, Amira Mili
Publikováno v:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 16(2)
Objectives Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder which is characterized by a high clinical variability with severe, intermediate, mild and adult forms. These forms are caused, in 95% of cases, by a homozygous
Publikováno v:
La Tunisie medicale [Tunis Med] 2014 Jul; Vol. 92 (7), pp. 452-7.