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Fatma Kamoun

Showing results (1-10 of 33) with videos related to

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La Tunisie Medicale|November 16, 2018
What is the interest of the electroencephalogram in the syndromic diagnosis?Ines Kammoun, Héla Mnif, Fatma Kamoun Feki, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|October 17, 2023
Complex genotypes in family with metachromatic leukodystrophy: Effect of trans and cis mutations distribution on the phenotype variabilityAbir Ben Issa, Fatma Kamoun, Wafa Bouchaala, et al.
Journal of Human Genetics|October 29, 2024
First description of novel compound heterozygous mutations in HYCC1: clinical evaluations and molecular analysis in patient with hypomyelinating leukodystrophy-5 with retrospective viewAbir Ben Issa, Fatma Kamoun, Boudour Khabou, et al.
Molecular Biology Reports|February 28, 2012
Impact of single-nucleotide polymorphisms at the TP53-binding and responsive promoter region of BCL2 gene in modulating the phenotypic variability of LGMD2C patientsIkhlass Hadj Salem, Fatma Kamoun, Nacim Louhichi, et al.
Journal of Pediatric Hematology/Oncology|January 7, 2017
Frequent Infections, Hypotonia, and Anemia in a Breastfed InfantFatma Kamoun, Rime Guirat, Fatma Megdich, et al.
La Tunisie Medicale|June 19, 2014
[Bacterial meningitis in children: epidemiological data and outcome]Lamia Sfaihi, Fatma Kamoun, Thouraya Kamoun, et al.
Multiple Sclerosis and Related Disorders|October 8, 2021
Acute Demyelinating Syndromes: A report of child neurology department of Sfax University HospitalSalma Zouari Mallouli, Sihem Ben Nsir, Wafa Bouchaala, et al.
Genetic Testing and Molecular Biomarkers|March 25, 2009
A novel MECP2 gene mutation in a Tunisian patient with Rett syndromeNourhène Fendri-Kriaa, Zaineb Abdelkafi, Imen Ben Rebeh, et al.
La Tunisie Medicale|November 16, 2019
Clinical and genetic aspect of 30 tunisian families with febrile seizuresFatma Kamoun Feki, Norhene Fendri Kriaa, Dalinda Kolsi, et al.
La Tunisie Medicale|November 6, 2002
[Cimetidine therapy for multiple warts in children]Monia Kharfi, Olfa Chtourou, Fatma Kamoun, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
La Tunisie Medicale|November 16, 2018
What is the interest of the electroencephalogram in the syndromic diagnosis?Ines Kammoun, Héla Mnif, Fatma Kamoun Feki, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|October 17, 2023
Complex genotypes in family with metachromatic leukodystrophy: Effect of trans and cis mutations distribution on the phenotype variabilityAbir Ben Issa, Fatma Kamoun, Wafa Bouchaala, et al.
Journal of Human Genetics|October 29, 2024
First description of novel compound heterozygous mutations in HYCC1: clinical evaluations and molecular analysis in patient with hypomyelinating leukodystrophy-5 with retrospective viewAbir Ben Issa, Fatma Kamoun, Boudour Khabou, et al.
Molecular Biology Reports|February 28, 2012
Impact of single-nucleotide polymorphisms at the TP53-binding and responsive promoter region of BCL2 gene in modulating the phenotypic variability of LGMD2C patientsIkhlass Hadj Salem, Fatma Kamoun, Nacim Louhichi, et al.
Journal of Pediatric Hematology/Oncology|January 7, 2017
Frequent Infections, Hypotonia, and Anemia in a Breastfed InfantFatma Kamoun, Rime Guirat, Fatma Megdich, et al.
La Tunisie Medicale|June 19, 2014
[Bacterial meningitis in children: epidemiological data and outcome]Lamia Sfaihi, Fatma Kamoun, Thouraya Kamoun, et al.
Multiple Sclerosis and Related Disorders|October 8, 2021
Acute Demyelinating Syndromes: A report of child neurology department of Sfax University HospitalSalma Zouari Mallouli, Sihem Ben Nsir, Wafa Bouchaala, et al.
Genetic Testing and Molecular Biomarkers|March 25, 2009
A novel MECP2 gene mutation in a Tunisian patient with Rett syndromeNourhène Fendri-Kriaa, Zaineb Abdelkafi, Imen Ben Rebeh, et al.
La Tunisie Medicale|November 16, 2019
Clinical and genetic aspect of 30 tunisian families with febrile seizuresFatma Kamoun Feki, Norhene Fendri Kriaa, Dalinda Kolsi, et al.
La Tunisie Medicale|November 6, 2002
[Cimetidine therapy for multiple warts in children]Monia Kharfi, Olfa Chtourou, Fatma Kamoun, et al.
Pageof 4