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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
January 23, 2024
Single-center experience of congenital disorders of glycosylation syndrome screening in Tunisia: A retrospective study over a 15-year period (2007-2021)
Wiem Zidi, Sameh Hadj-Taieb, Ichraf Kraoua, et al.
La Tunisie Medicale
|
March 10, 2010
Incidence of mucopolysaccharidoses in Tunisia
Hadhami Ben Turkia, Néji Tebib, Hatem Azzouz, et al.
Clinical Genetics
|
March 19, 2026
Using Exome Sequencing to Identify the Causes of Neurodevelopmental Disorders: Experience of a North African Genetic Center
Myriam Chaabouni, Najoua Miladi, Kamel Monastiri, et al.
La Tunisie Medicale
|
November 16, 2018
Extremely preterm infants in Tunisia: Where are we now?
Fatma Zohra Chioukh, Karim Ben Ameur, Nédia Kasdallah, et al.
BMC Pediatrics
|
August 31, 2018
Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome
Nehla Ghedira, Arnaud Lagarde, Karim Ben Ameur, et al.
La Tunisie Medicale
|
May 28, 2019
Transported neonates in Tunisia
Fatma Zohra Chioukh, Karim Ben Ameur, Kamel Monastiri, et al.
Neuropediatrics
|
August 21, 2020
Nonketotic Hyperglycinemia in Tunisia. Report upon a Series of 69 Patients
Fahmi Nasrallah, Sameh Hadj-Taieb, Amel Ben Chehida, et al.
Journal of Dermatological Science
|
January 12, 2010
Mutational survey of recessive dystrophic epidermolysis bullosa in Tunisian families unveils a spectrum of private, ethnic specific and world wide recurrent mutations
Houyem Ouragini, Faïka Cherif, Sabrine Ahlem Ben Brick, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
April 21, 2023
Turner syndrome: results of the first Tunisian study group on Turner syndrome (TuSGOT)
Leila Essaddam, Ons Zitouni, Lilia Kraoua, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 24, 2022
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease
Elisa Calì, Sheng-Jia Lin, Clarissa Rocca, et al.
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Showing results (21-30 of 30) with videos related to
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This site can display upto 30 results.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
January 23, 2024
Single-center experience of congenital disorders of glycosylation syndrome screening in Tunisia: A retrospective study over a 15-year period (2007-2021)
Wiem Zidi, Sameh Hadj-Taieb, Ichraf Kraoua, et al.
La Tunisie Medicale
|
March 10, 2010
Incidence of mucopolysaccharidoses in Tunisia
Hadhami Ben Turkia, Néji Tebib, Hatem Azzouz, et al.
Clinical Genetics
|
March 19, 2026
Using Exome Sequencing to Identify the Causes of Neurodevelopmental Disorders: Experience of a North African Genetic Center
Myriam Chaabouni, Najoua Miladi, Kamel Monastiri, et al.
La Tunisie Medicale
|
November 16, 2018
Extremely preterm infants in Tunisia: Where are we now?
Fatma Zohra Chioukh, Karim Ben Ameur, Nédia Kasdallah, et al.
BMC Pediatrics
|
August 31, 2018
Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome
Nehla Ghedira, Arnaud Lagarde, Karim Ben Ameur, et al.
La Tunisie Medicale
|
May 28, 2019
Transported neonates in Tunisia
Fatma Zohra Chioukh, Karim Ben Ameur, Kamel Monastiri, et al.
Neuropediatrics
|
August 21, 2020
Nonketotic Hyperglycinemia in Tunisia. Report upon a Series of 69 Patients
Fahmi Nasrallah, Sameh Hadj-Taieb, Amel Ben Chehida, et al.
Journal of Dermatological Science
|
January 12, 2010
Mutational survey of recessive dystrophic epidermolysis bullosa in Tunisian families unveils a spectrum of private, ethnic specific and world wide recurrent mutations
Houyem Ouragini, Faïka Cherif, Sabrine Ahlem Ben Brick, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
April 21, 2023
Turner syndrome: results of the first Tunisian study group on Turner syndrome (TuSGOT)
Leila Essaddam, Ons Zitouni, Lilia Kraoua, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 24, 2022
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease
Elisa Calì, Sheng-Jia Lin, Clarissa Rocca, et al.
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of 3