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Marina Frontali

Showing results (1-10 of 32) with videos related to

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International Journal of Molecular Sciences|September 9, 2020
Episodic Ataxias: Faux or Real?Paola Giunti, Elide Mantuano, Marina Frontali
Frontiers in Cellular Neuroscience|March 13, 2015
Molecular mechanism of Spinocerebellar Ataxia type 6: glutamine repeat disorder, channelopathy and transcriptional dysregulation. The multifaceted aspects of a single mutationPaola Giunti, Elide Mantuano, Marina Frontali, et al.
Journal of the Neurological Sciences|September 4, 2007
Functional characterization of a novel mutation in TITF-1 in a patient with benign hereditary choreaClaudia Provenzano, Liana Veneziano, Richard Appleton, et al.
Plos One|May 11, 2011
Fractal analysis reveals reduced complexity of retinal vessels in CADASILMichele Cavallari, Teresa Falco, Marina Frontali, et al.
Journal of the Neurological Sciences|March 29, 2011
Dramatically different levels of Cacna1a gene expression between pre-weaning wild type and leaner miceLiana Veneziano, Serena Albertosi, Daniela Pesci, et al.
Familial Cancer|September 7, 2015
Rhabdoid tumor predisposition syndrome caused by SMARCB1 constitutional deletion: prenatal detection of new case of recurrence in siblings due to gonadal mosaicismLaura Gigante, Irene Paganini, Marina Frontali, et al.
Journal of the Neurological Sciences|November 6, 2018
Leukocyte telomere shortening in Huntington's diseaseDaniela Scarabino, Liana Veneziano, Martina Peconi, et al.
Cerebellum (London, England)|June 16, 2014
A novel de novo mutation of the TITF1/NKX2-1 gene causing ataxia, benign hereditary chorea, hypothyroidism and a pituitary mass in a UK family and review of the literatureLiana Veneziano, Michael H Parkinson, Elide Mantuano, et al.
International Journal of Molecular Sciences|November 11, 2022
Leukocyte Telomere Length as Potential Biomarker of HD Progression: A Follow-Up StudyDaniela Scarabino, Liana Veneziano, Elide Mantuano, et al.
Frontiers in Molecular Neuroscience|December 5, 2015
Analyzing the Effects of a G137V Mutation in the FXN GeneNathalie Faggianelli, Rita Puglisi, Liana Veneziano, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
International Journal of Molecular Sciences|September 9, 2020
Episodic Ataxias: Faux or Real?Paola Giunti, Elide Mantuano, Marina Frontali
Frontiers in Cellular Neuroscience|March 13, 2015
Molecular mechanism of Spinocerebellar Ataxia type 6: glutamine repeat disorder, channelopathy and transcriptional dysregulation. The multifaceted aspects of a single mutationPaola Giunti, Elide Mantuano, Marina Frontali, et al.
Journal of the Neurological Sciences|September 4, 2007
Functional characterization of a novel mutation in TITF-1 in a patient with benign hereditary choreaClaudia Provenzano, Liana Veneziano, Richard Appleton, et al.
Plos One|May 11, 2011
Fractal analysis reveals reduced complexity of retinal vessels in CADASILMichele Cavallari, Teresa Falco, Marina Frontali, et al.
Journal of the Neurological Sciences|March 29, 2011
Dramatically different levels of Cacna1a gene expression between pre-weaning wild type and leaner miceLiana Veneziano, Serena Albertosi, Daniela Pesci, et al.
Familial Cancer|September 7, 2015
Rhabdoid tumor predisposition syndrome caused by SMARCB1 constitutional deletion: prenatal detection of new case of recurrence in siblings due to gonadal mosaicismLaura Gigante, Irene Paganini, Marina Frontali, et al.
Journal of the Neurological Sciences|November 6, 2018
Leukocyte telomere shortening in Huntington's diseaseDaniela Scarabino, Liana Veneziano, Martina Peconi, et al.
Cerebellum (London, England)|June 16, 2014
A novel de novo mutation of the TITF1/NKX2-1 gene causing ataxia, benign hereditary chorea, hypothyroidism and a pituitary mass in a UK family and review of the literatureLiana Veneziano, Michael H Parkinson, Elide Mantuano, et al.
International Journal of Molecular Sciences|November 11, 2022
Leukocyte Telomere Length as Potential Biomarker of HD Progression: A Follow-Up StudyDaniela Scarabino, Liana Veneziano, Elide Mantuano, et al.
Frontiers in Molecular Neuroscience|December 5, 2015
Analyzing the Effects of a G137V Mutation in the FXN GeneNathalie Faggianelli, Rita Puglisi, Liana Veneziano, et al.
Pageof 4