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Hela Hajji

Showing results (1-10 of 5) with videos related to

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La Tunisie Medicale|November 16, 2019
Role play for genetic counseling learning: Value and students perceptionsRim Ben Abdelaziz, Hela Boudabous, Hela Hajji, et al.
La Tunisie Medicale|October 17, 2018
Patient-management Problem (PMP) for paediatrics learning: Value and students perceptionsRim Ben Abdelaziz, Hela Hajji, Hela Boudabous, et al.
BMC Pediatrics|December 21, 2017
Peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort studyRim Ben Abdelaziz, Habiba Hafsi, Hela Hajji, et al.
BMC Pediatrics|September 26, 2018
Correction to: Full title: peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort studyRim Ben Abdelaziz, Habiba Hafsi, Hela Hajji, et al.
Molecular Genetics and Metabolism Reports|November 17, 2022
Initial presentation, management and follow-up data of 33 treated patients with hereditary tyrosinemia type 1 in the absence of newborn screeningHela Hajji, Apolline Imbard, Anne Spraul, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
La Tunisie Medicale|November 16, 2019
Role play for genetic counseling learning: Value and students perceptionsRim Ben Abdelaziz, Hela Boudabous, Hela Hajji, et al.
La Tunisie Medicale|October 17, 2018
Patient-management Problem (PMP) for paediatrics learning: Value and students perceptionsRim Ben Abdelaziz, Hela Hajji, Hela Boudabous, et al.
BMC Pediatrics|December 21, 2017
Peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort studyRim Ben Abdelaziz, Habiba Hafsi, Hela Hajji, et al.
BMC Pediatrics|September 26, 2018
Correction to: Full title: peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort studyRim Ben Abdelaziz, Habiba Hafsi, Hela Hajji, et al.
Molecular Genetics and Metabolism Reports|November 17, 2022
Initial presentation, management and follow-up data of 33 treated patients with hereditary tyrosinemia type 1 in the absence of newborn screeningHela Hajji, Apolline Imbard, Anne Spraul, et al.
Pageof 1