Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Ksibi, Imen"'
Autor:
Maaoui Rim, Rouached Leila, Ben Tekaya Aicha, Saidane Olfa, Hfaiedh Meriem, Lajnef Ines, Mouhli Najla, Rahali Hajer, Ksibi Imen
Publikováno v:
Korean Journal of Family Medicine. 43:367-373
Background: This study aimed to assess the benefits of associating rehabilitation with therapeutic patient education (TPE) to decrease fear-avoidance belief and pain and improve function in adults with chronic low back pain (CLBP).Methods: This rando
Autor:
Fares, Samira, Sethom, Mohamed Marouane, Kacem, Samia, Ksibi, Imen, Feki, Moncef, Jebnoun, Sami, Kaabachi, Naziha
Publikováno v:
In Pediatrics & Neonatology April 2016 57(2):120-126
Akademický článek
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Autor:
Achour Radhouane, Ben Jemaa Nadia, Ksibi Imen, Meriem Cheour, Bouriel Ines, Ayari Feirouz, Samia Kacem, Neji Khaled
Publikováno v:
Australasian Medical Journal, Vol 10, Iss 8, Pp 647-655 (2017)
Background Preterm birth is a leading cause of perinatal morbidity and mortality and represents a major public health problem. It is associated with a 15–20 per cent mortality rate and remains responsible for 75 per cent of perinatal deaths in foet
Publikováno v:
Journal of the Textile Institute; Feb2021, Vol. 112 Issue 2, p200-206, 7p
Autor:
Ksibi Imen, Bouriel Ines, Ayari Feirouz, Samia Kacem, Achour Radhouane, Meriem Cheour, Neji Khaled, Ben Jemaa Nadia
Publikováno v:
Australasian Medical Journal. 10
Autor:
Kacem Samia, Cheour Meriem, Ben Amara Moez, Jammeli Nadia, Ksibi Imen, Neji Khaled, Achour Radhouane, Ayari Feirouz, H Hafsi, Ben Ameur Nadia, Aloui Nadia
Publikováno v:
Journal of Neonatal Biology. 5
Introduction: Cutis marmorata telangiectatica congenita (CMTC) is a sporadic congenital skin vascular abnormality, present at birth or shortly thereafter. The prognosis is generally good. Case report: we report the case of a preterm female newborn wi
Autor:
Yacoubi Mohamed Tahar, Achour Radhouane, Nadia Ben Jamaa, Delesoide Anne Lise, Ksibi Imen, Mokni Moncef
Publikováno v:
Journal of Pregnancy and Child Health.
Objective: Dyssegmental dysplasia, Silverman-Handmaker Type, is an autosomal recessive lethal disorder, originally considered as a Kniest-like skeletal dysplasia with camptomelia. It is linked to functional null mutations of the perlecan gene (HSPG2)
Autor:
Neji Khaled, Ben Amara Moez, Masmoudi Aida, Ben Ameur N, Ben Jamaa Nadia, Bennour Wafa, Achour Radhouane, Aloui Nadia, Ksibi Imen, Kacem Samia, Ayari Fayrouz, Cheour Meriem
Publikováno v:
Journal of Neonatal Biology.
McKusick-Kaufman syndrome (MKKS) is a rare autosomal recessive disorder. We report the case of McKusick-Kaufman syndrome in a term female neonate. Antenatal ultrasound found a large cystic abdominal mass corresponding to hydrometrocolpos with bilater
Akademický článek
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