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Lorena Travaglini

Showing results (1-10 of 74) with videos related to

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Cell Research|October 11, 2005
Dynamic and reversibility of heterochromatic gene silencing in human diseaseGiuseppe Zardo, Francesco Fazi, Lorena Travaglini, et al.
The International Journal of Biochemistry & Cell Biology|September 16, 2008
Epigenetic reprogramming of breast cancer cells by valproic acid occurs regardless of estrogen receptor statusLorena Travaglini, Laura Vian, Monia Billi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 9, 2019
SLC2A1 mutations are a rare cause of pediatric-onset hereditary spastic paraplegiaFrancesco Nicita, Tommaso Schirinzi, Fabrizia Stregapede, et al.
Clinical Neurology and Neurosurgery|January 5, 2023
Leukoencephalopathy with spot-like calcifications caused by recessive COL4A2 variantsFrancesco Nicita, Chiara Aiello, Alessia Carboni, et al.
The Journal of Headache and Pain|July 29, 2021
CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family reportMarina Romozzi, Guido Primiano, Eleonora Rollo, et al.
Neurology. Genetics|March 7, 2022
Novel <i>SEPSECS</i> Pathogenic Variants Featuring Unusual Phenotype of Complex Movement Disorder With Thin Corpus Callosum: A Case ReportFrancesco Nicita, Lorena Travaglini, Francesco Bombelli, et al.
International Journal of Cancer|March 28, 2008
Targeting of the N-terminal coiled coil oligomerization interface by a helix-2 peptide inhibits unmutated and imatinib-resistant BCR/ABLTim Beissert, Alena Hundertmark, Velina Kaburova, et al.
Movement Disorders Clinical Practice|January 27, 2023
Mild Neurological Phenotype Associated with Hypomorphic Variants in the Ataxia-Telangiectasia Mutated GeneCaterina Caputi, Giulia Federici, Silvia Soddu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 7, 2025
Biallelic Variants in SLC27A3 Cause a Complex Form of Neurodegeneration with Brain Iron AccumulationLorena Travaglini, Cherim Jeon, Teresa Rizza, et al.
Frontiers in Genetics|November 19, 2019
Diagnostic Yield of a Targeted Next-Generation Sequencing Gene Panel for Pediatric-Onset Movement Disorders: A 3-Year Cohort StudyFederica Graziola, Giacomo Garone, Fabrizia Stregapede, et al.
Pageof 8

Showing results (1-10 of 74) with videos related to

Sort By:
Pageof 8
Cell Research|October 11, 2005
Dynamic and reversibility of heterochromatic gene silencing in human diseaseGiuseppe Zardo, Francesco Fazi, Lorena Travaglini, et al.
The International Journal of Biochemistry & Cell Biology|September 16, 2008
Epigenetic reprogramming of breast cancer cells by valproic acid occurs regardless of estrogen receptor statusLorena Travaglini, Laura Vian, Monia Billi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 9, 2019
SLC2A1 mutations are a rare cause of pediatric-onset hereditary spastic paraplegiaFrancesco Nicita, Tommaso Schirinzi, Fabrizia Stregapede, et al.
Clinical Neurology and Neurosurgery|January 5, 2023
Leukoencephalopathy with spot-like calcifications caused by recessive COL4A2 variantsFrancesco Nicita, Chiara Aiello, Alessia Carboni, et al.
The Journal of Headache and Pain|July 29, 2021
CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family reportMarina Romozzi, Guido Primiano, Eleonora Rollo, et al.
Neurology. Genetics|March 7, 2022
Novel <i>SEPSECS</i> Pathogenic Variants Featuring Unusual Phenotype of Complex Movement Disorder With Thin Corpus Callosum: A Case ReportFrancesco Nicita, Lorena Travaglini, Francesco Bombelli, et al.
International Journal of Cancer|March 28, 2008
Targeting of the N-terminal coiled coil oligomerization interface by a helix-2 peptide inhibits unmutated and imatinib-resistant BCR/ABLTim Beissert, Alena Hundertmark, Velina Kaburova, et al.
Movement Disorders Clinical Practice|January 27, 2023
Mild Neurological Phenotype Associated with Hypomorphic Variants in the Ataxia-Telangiectasia Mutated GeneCaterina Caputi, Giulia Federici, Silvia Soddu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 7, 2025
Biallelic Variants in SLC27A3 Cause a Complex Form of Neurodegeneration with Brain Iron AccumulationLorena Travaglini, Cherim Jeon, Teresa Rizza, et al.
Frontiers in Genetics|November 19, 2019
Diagnostic Yield of a Targeted Next-Generation Sequencing Gene Panel for Pediatric-Onset Movement Disorders: A 3-Year Cohort StudyFederica Graziola, Giacomo Garone, Fabrizia Stregapede, et al.
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