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Imen Chabchoub

Showing results (31-40 of 55) with videos related to

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European Journal of Trauma and Emergency Surgery : Official Publication of the European Trauma Society|December 14, 2017
Clinical characteristics and prognosis of traumatic head injury following road traffic accidents admitted in ICU "analysis of 694 cases"Hedi Chelly, Mabrouk Bahloul, Rania Ammar, et al.
La Tunisie Medicale|June 24, 2014
[Primary immune thrombocytopenia in childhood: a regional study in the south of Tunisia]Lamia Sfaihi, Olfa Kassar, Moez Medhaffar, et al.
The American Journal of Tropical Medicine and Hygiene|November 2, 2010
Scorpion envenomation among children: clinical manifestations and outcome (analysis of 685 cases)Mabrouk Bahloul, Imen Chabchoub, Anis Chaari, et al.
The Journal of Infection|July 10, 2012
Management of severe rubella encephalitis requiring intensive care unit admissionMabrouk Bahloul, Anis Chaari, Rania Ammar, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|March 30, 2005
Neurological complications secondary to severe scorpion envenomationMabrouk Bahloul, Noureddine Rekik, Imen Chabchoub, et al.
Intensive Care Medicine|May 13, 2017
Pulmonary embolism following severe traumatic brain injury: incidence, risk factors and impact outcomeMabrouk Bahloul, Hedi Chelly, Kais Regaieg, et al.
Molecular Genetics & Genomic Medicine|January 8, 2022
Custom Next-Generation Sequencing Identifies Novel Mutations Expanding the Molecular and clinical spectrum of isolated Hearing Impairment or along with defects of the retina, the thyroid, and the kidneysMariem Ben Said, Ikhlas Ben Ayed, Ines Elloumi, et al.
Biochemical and Biophysical Research Communications|May 8, 2016
Mutational screening in patients with profound sensorineural hearing loss and neurodevelopmental delay: Description of a novel m.3861A > C mitochondrial mutation in the MT-ND1 geneMarwa Ammar, Mouna Tabebi, Lamia Sfaihi, et al.
Journal of Pediatric Hematology/Oncology|July 19, 2019
Hemophagocytic Lymphohistiocytosis: A Rare Complication of an Ultrarare Lysosomal Storage DiseaseImen Chabchoub, Hela Boudabbous, Ines Maaloul, et al.
Molecular Biology Reports|April 25, 2026
A novel homozygous MICOS13 frameshift mutation causing mitochondrial hepatoencephalopathy and mtDNA depletion: clinical characterization and dynamic structural simulationMarwa Ammar, Fakher Frikha, Imen Chabchoub, et al.
Pageof 6

Showing results (31-40 of 55) with videos related to

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European Journal of Trauma and Emergency Surgery : Official Publication of the European Trauma Society|December 14, 2017
Clinical characteristics and prognosis of traumatic head injury following road traffic accidents admitted in ICU "analysis of 694 cases"Hedi Chelly, Mabrouk Bahloul, Rania Ammar, et al.
La Tunisie Medicale|June 24, 2014
[Primary immune thrombocytopenia in childhood: a regional study in the south of Tunisia]Lamia Sfaihi, Olfa Kassar, Moez Medhaffar, et al.
The American Journal of Tropical Medicine and Hygiene|November 2, 2010
Scorpion envenomation among children: clinical manifestations and outcome (analysis of 685 cases)Mabrouk Bahloul, Imen Chabchoub, Anis Chaari, et al.
The Journal of Infection|July 10, 2012
Management of severe rubella encephalitis requiring intensive care unit admissionMabrouk Bahloul, Anis Chaari, Rania Ammar, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|March 30, 2005
Neurological complications secondary to severe scorpion envenomationMabrouk Bahloul, Noureddine Rekik, Imen Chabchoub, et al.
Intensive Care Medicine|May 13, 2017
Pulmonary embolism following severe traumatic brain injury: incidence, risk factors and impact outcomeMabrouk Bahloul, Hedi Chelly, Kais Regaieg, et al.
Molecular Genetics & Genomic Medicine|January 8, 2022
Custom Next-Generation Sequencing Identifies Novel Mutations Expanding the Molecular and clinical spectrum of isolated Hearing Impairment or along with defects of the retina, the thyroid, and the kidneysMariem Ben Said, Ikhlas Ben Ayed, Ines Elloumi, et al.
Biochemical and Biophysical Research Communications|May 8, 2016
Mutational screening in patients with profound sensorineural hearing loss and neurodevelopmental delay: Description of a novel m.3861A > C mitochondrial mutation in the MT-ND1 geneMarwa Ammar, Mouna Tabebi, Lamia Sfaihi, et al.
Journal of Pediatric Hematology/Oncology|July 19, 2019
Hemophagocytic Lymphohistiocytosis: A Rare Complication of an Ultrarare Lysosomal Storage DiseaseImen Chabchoub, Hela Boudabbous, Ines Maaloul, et al.
Molecular Biology Reports|April 25, 2026
A novel homozygous MICOS13 frameshift mutation causing mitochondrial hepatoencephalopathy and mtDNA depletion: clinical characterization and dynamic structural simulationMarwa Ammar, Fakher Frikha, Imen Chabchoub, et al.
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