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Rim Amouri

Showing results (11-20 of 42) with videos related to

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The International Journal of Neuroscience|November 5, 2010
Spinal muscular atrophy due to double gene conversion eventWiéme Maamouri, Monia Benhamed Hammer, Yosr Bouhlel, et al.
Journal of Molecular Neuroscience : MN|March 19, 2011
Computational analysis of a novel SACS gene mutation with BioExtract serverYosr Bouhlal, Douglas M Jennewein, Brent Anderson, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|October 22, 2013
Clinical features and molecular genetics of two Tunisian families with abetalipoproteinemiaMonia Benhamed Hammer, Ghada El Euch-Fayache, Houda Nehdi, et al.
Clinical Case Reports|December 30, 2022
A Tunisian patient with CLCN2-related leukoencephalopathyDina Ben Mohamed, Zacharia Saied, Samia Ben Sassi, et al.
Archives of Neurology|July 23, 2003
Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in TunisiaGhada El Euch-Fayache, Irfan Lalani, Rim Amouri, et al.
Neuromuscular Disorders : NMD|October 17, 2003
Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth diseaseNadia Ammar, Eva Nelis, Luciano Merlini, et al.
Parkinsonism & Related Disorders|June 5, 2003
Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological studyNeziha Gouider-Khouja, Abdelmajid Larnaout, Rim Amouri, et al.
Journal of Neurogenetics|December 18, 2023
Genetic heterogeneity within a consanguineous family involving <i>TTPA</i> and <i>SETX</i> genesCyrine Jeridi, Amine Rachdi, Fatma Nabli, et al.
Cytokine|March 11, 2020
Discriminative expression of CD39 and CD73 in Cerebrospinal fluid of patients with Multiple Sclerosis and Neuro-Behçet's diseaseKhadija Bahrini, Meriam Belghith, Olfa Maghrebi, et al.
Parkinsonism & Related Disorders|November 8, 2011
Cognitive dysfunction in Tunisian LRRK2 associated Parkinson's diseaseSamia Ben Sassi, Fatma Nabli, Emna Hentati, et al.
Pageof 5

Showing results (11-20 of 42) with videos related to

Sort By:
Pageof 5
The International Journal of Neuroscience|November 5, 2010
Spinal muscular atrophy due to double gene conversion eventWiéme Maamouri, Monia Benhamed Hammer, Yosr Bouhlel, et al.
Journal of Molecular Neuroscience : MN|March 19, 2011
Computational analysis of a novel SACS gene mutation with BioExtract serverYosr Bouhlal, Douglas M Jennewein, Brent Anderson, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|October 22, 2013
Clinical features and molecular genetics of two Tunisian families with abetalipoproteinemiaMonia Benhamed Hammer, Ghada El Euch-Fayache, Houda Nehdi, et al.
Clinical Case Reports|December 30, 2022
A Tunisian patient with CLCN2-related leukoencephalopathyDina Ben Mohamed, Zacharia Saied, Samia Ben Sassi, et al.
Archives of Neurology|July 23, 2003
Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in TunisiaGhada El Euch-Fayache, Irfan Lalani, Rim Amouri, et al.
Neuromuscular Disorders : NMD|October 17, 2003
Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth diseaseNadia Ammar, Eva Nelis, Luciano Merlini, et al.
Parkinsonism & Related Disorders|June 5, 2003
Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological studyNeziha Gouider-Khouja, Abdelmajid Larnaout, Rim Amouri, et al.
Journal of Neurogenetics|December 18, 2023
Genetic heterogeneity within a consanguineous family involving <i>TTPA</i> and <i>SETX</i> genesCyrine Jeridi, Amine Rachdi, Fatma Nabli, et al.
Cytokine|March 11, 2020
Discriminative expression of CD39 and CD73 in Cerebrospinal fluid of patients with Multiple Sclerosis and Neuro-Behçet's diseaseKhadija Bahrini, Meriam Belghith, Olfa Maghrebi, et al.
Parkinsonism & Related Disorders|November 8, 2011
Cognitive dysfunction in Tunisian LRRK2 associated Parkinson's diseaseSamia Ben Sassi, Fatma Nabli, Emna Hentati, et al.
Pageof 5