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Zemmouri

Showing results (41-50 of 48) with videos related to

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Brain : a Journal of Neurology|November 11, 2003
Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/CM Tazir, H Azzedine, S Assami, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Charcot-Marie-Tooth 2-like presentation of an Algerian family with giant axonal neuropathyR Zemmouri, H Azzedine, S Assami, et al.
Neurology|March 15, 2006
Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegiaN Elleuch, C Depienne, A Benomar, et al.
The Pan African Medical Journal|July 14, 2020
Solid pseudopapillary tumor of the pancreas: a rare entity in childrenGhita Berrada, Soukaina Belaaroussi, Kamilia Chbani, et al.
Life (Basel, Switzerland)|November 27, 2024
Contribution of an Artificial Intelligence Tool in the Detection of Incidental Pulmonary Embolism on Oncology Assessment ScansSamy Ammari, Astrid Orfali Camez, Angela Ayobi, et al.
Archives of Neurology|August 17, 1999
Clinical heterogeneity of autosomal recessive spastic paraplegias: analysis of 106 patients in 46 familiesP Coutinho, J Barros, R Zemmouri, et al.
La Radiologia Medica|August 2, 2025
Deep learning-driven incidental detection of vertebral fractures in cancer patients: advancing diagnostic precision and clinical managementEl Mehdi Mniai, Vladimir Laletin, Lambros Tselikas, et al.
Swiss Medical Weekly|October 24, 2025
Paediatric bed capacity in Swiss hospitals: a comprehensive analysisJuliane Wurm, Christoph Berger, Vera Bernet, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Brain : a Journal of Neurology|November 11, 2003
Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/CM Tazir, H Azzedine, S Assami, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Charcot-Marie-Tooth 2-like presentation of an Algerian family with giant axonal neuropathyR Zemmouri, H Azzedine, S Assami, et al.
Neurology|March 15, 2006
Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegiaN Elleuch, C Depienne, A Benomar, et al.
The Pan African Medical Journal|July 14, 2020
Solid pseudopapillary tumor of the pancreas: a rare entity in childrenGhita Berrada, Soukaina Belaaroussi, Kamilia Chbani, et al.
Life (Basel, Switzerland)|November 27, 2024
Contribution of an Artificial Intelligence Tool in the Detection of Incidental Pulmonary Embolism on Oncology Assessment ScansSamy Ammari, Astrid Orfali Camez, Angela Ayobi, et al.
Archives of Neurology|August 17, 1999
Clinical heterogeneity of autosomal recessive spastic paraplegias: analysis of 106 patients in 46 familiesP Coutinho, J Barros, R Zemmouri, et al.
La Radiologia Medica|August 2, 2025
Deep learning-driven incidental detection of vertebral fractures in cancer patients: advancing diagnostic precision and clinical managementEl Mehdi Mniai, Vladimir Laletin, Lambros Tselikas, et al.
Swiss Medical Weekly|October 24, 2025
Paediatric bed capacity in Swiss hospitals: a comprehensive analysisJuliane Wurm, Christoph Berger, Vera Bernet, et al.
Pageof 5