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La Tunisie Medicale
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November 16, 2019
Role play for genetic counseling learning: Value and students perceptions
Rim Ben Abdelaziz, Hela Boudabous, Hela Hajji, et al.
La Tunisie Medicale
|
October 17, 2018
Patient-management Problem (PMP) for paediatrics learning: Value and students perceptions
Rim 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 study
Rim 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 study
Rim 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 screening
Hela Hajji, Apolline Imbard, Anne Spraul, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
La Tunisie Medicale
|
November 16, 2019
Role play for genetic counseling learning: Value and students perceptions
Rim Ben Abdelaziz, Hela Boudabous, Hela Hajji, et al.
La Tunisie Medicale
|
October 17, 2018
Patient-management Problem (PMP) for paediatrics learning: Value and students perceptions
Rim 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 study
Rim 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 study
Rim 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 screening
Hela Hajji, Apolline Imbard, Anne Spraul, et al.
Page
of 1