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Francesca Gualandi

Showing results (21-30 of 169) with videos related to

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Heliyon|January 3, 2023
Severe hypertrophic cardiomyopathy in a patient with a homozygous MYH7 gene variantWalter Serra, Giulia Vitetta, Vera Uliana, et al.
Muscle & Nerve|April 14, 2011
Macrophages: a minimally invasive tool for monitoring collagen VI myopathiesFrancesca Gualandi, Rosa Curci, Patrizia Sabatelli, et al.
American Journal of Medical Genetics. Part A|April 12, 2011
LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutationsAlberto Sensi, Stefano Ceruti, Patrizia Trevisi, et al.
American Journal of Medical Genetics. Part A|January 11, 2005
Genomic and transcription studies as diagnostic tools for a prenatal detection of X-linked dilated cardiomyopathy due to a dystrophin gene mutationPaola Rimessi, Francesca Gualandi, Laurence Duprez, et al.
Placenta|January 9, 2023
Pregnancy complications after allogeneic hematopoietic stem cells transplantation: Focus on the placentaIrene Gazzo, Claudia Massarotti, Sandra Chiodi, et al.
Journal of Cardiovascular Development and Disease|April 25, 2025
Dilated Cardiomyopathy: A Novel <i>BAG3</i> Mutation Associated with Aggressive Disease Progression and Ventricular ArrhythmiasPaolo Pastori, Cristina Balla, Marta Rasia, et al.
Gene|July 11, 2003
Genomic definition of a pure intronic dystrophin deletion responsible for an XLDC splicing mutation: in vitro mimicking and antisense modulation of the splicing abnormalityFrancesca Gualandi, Paola Rimessi, Barbara Cardazzo, et al.
Parkinsonism & Related Disorders|October 28, 2021
Parkinson's disease-dementia in trans LRP10 and GBA variants: Response to deep brain stimulationMarcella Neri, Arianna Braccia, Celeste Panteghini, et al.
The American Journal of Emergency Medicine|July 21, 2022
Cardiac Arrest in a Young Woman: A Near Miss DiagnosisValeria Carinci, Laura Sofia Cardelli, Lorenzo Gamberini, et al.
BMC Medical Genetics|April 30, 2010
Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosisAlessandra Ferlini, Matteo Bovolenta, Marcella Neri, et al.
Pageof 17

Showing results (21-30 of 169) with videos related to

Sort By:
Pageof 17
Heliyon|January 3, 2023
Severe hypertrophic cardiomyopathy in a patient with a homozygous MYH7 gene variantWalter Serra, Giulia Vitetta, Vera Uliana, et al.
Muscle & Nerve|April 14, 2011
Macrophages: a minimally invasive tool for monitoring collagen VI myopathiesFrancesca Gualandi, Rosa Curci, Patrizia Sabatelli, et al.
American Journal of Medical Genetics. Part A|April 12, 2011
LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutationsAlberto Sensi, Stefano Ceruti, Patrizia Trevisi, et al.
American Journal of Medical Genetics. Part A|January 11, 2005
Genomic and transcription studies as diagnostic tools for a prenatal detection of X-linked dilated cardiomyopathy due to a dystrophin gene mutationPaola Rimessi, Francesca Gualandi, Laurence Duprez, et al.
Placenta|January 9, 2023
Pregnancy complications after allogeneic hematopoietic stem cells transplantation: Focus on the placentaIrene Gazzo, Claudia Massarotti, Sandra Chiodi, et al.
Journal of Cardiovascular Development and Disease|April 25, 2025
Dilated Cardiomyopathy: A Novel <i>BAG3</i> Mutation Associated with Aggressive Disease Progression and Ventricular ArrhythmiasPaolo Pastori, Cristina Balla, Marta Rasia, et al.
Gene|July 11, 2003
Genomic definition of a pure intronic dystrophin deletion responsible for an XLDC splicing mutation: in vitro mimicking and antisense modulation of the splicing abnormalityFrancesca Gualandi, Paola Rimessi, Barbara Cardazzo, et al.
Parkinsonism & Related Disorders|October 28, 2021
Parkinson's disease-dementia in trans LRP10 and GBA variants: Response to deep brain stimulationMarcella Neri, Arianna Braccia, Celeste Panteghini, et al.
The American Journal of Emergency Medicine|July 21, 2022
Cardiac Arrest in a Young Woman: A Near Miss DiagnosisValeria Carinci, Laura Sofia Cardelli, Lorenzo Gamberini, et al.
BMC Medical Genetics|April 30, 2010
Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosisAlessandra Ferlini, Matteo Bovolenta, Marcella Neri, et al.
Pageof 17