Fabrizio Rinaldi - Concepedia

Author

Fabrizio Rinaldi

Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia ORCID

Also Known As

F Rinaldi, F. Rinaldi, FABRIZIO RINALDI, Fabrizio Rinaldi, Kacey Marra, Rinaldi, Fabrizio

Publications

2.1K

Citations

H-Index

Concepts

All Affiliations

Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia University of Rome Tor Vergata University of Brescia Vita-Salute San Raffaele University University of Minnesota

About

Fabrizio Rinaldi is an author at Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia specializing in medicine, cell biology, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	18	760
2	Health Sciences	2	2	111
3	Social Sciences	2	2	52
4	Engineering	1	1	65
5	Biology	1	1	16

Fabrizio Rinaldi

Publications

1.2K

Citations

H-Index

Page 1

	Year	Citations
Validation study of the Italian version of the Insomnia Severity Index (ISI) Vincenza Castronovo, Andrea Galbiati, Sara Marelli, Neurological Sciences ReliabilityQuality Of LifeSleepInsomnia Severity IndexItalian Version	2016	207
Overexpression of microRNA-206 in the skeletal muscle from myotonic dystrophy type 1 patients Stefano Gambardella, Fabrizio Rinaldi, Saverio Massimo Lepore, Journal of Translational Medicine	2010	111
Normal myogenesis and increased apoptosis in myotonic dystrophy type-1 muscle cells Emanuele Loro, Fabrizio Rinaldi, Adriana Malena, Cell Death and Differentiation Muscle FunctionDevelopmental BiologySkeletal MuscleNormal MyogenesisPhysiology	2010	86
PAX7 Targets, CD54, Integrin α9β1, and SDC2, Allow Isolation of Human ESC/iPSC-Derived Myogenic Progenitors Alessandro Magli, Tania Incitti, James P. Kiley, Cell Reports	2017	83
Screening identifies small molecules that enhance the maturation of human pluripotent stem cell-derived myotubes Sridhar Selvaraj, Ricardo Mondragón-González, Bin Xu, eLife Skeletal Muscle DiseasesEngineeringMechanotransductionCell SpecializationCellular Physiology	2019	65
The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic dystrophy type 1 patients Annalisa Botta, Fabrizio Rinaldi, Claudio Catalli, Journal of Medical Genetics	2008	57
Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2 Rosanna Cardani, Marzia Giagnacovo, Annalisa Botta, Journal of Neurology Rare DiseasesMendelian DisorderGenetic DisorderGeneticsRecessive Clcn1 Mutation	2012	49
Gene Expression Analysis in Myotonic Dystrophy: Indications for a Common Molecular Pathogenic Pathway in DM1 and DM2 Annalisa Botta, Laura Vallo, Fabrizio Rinaldi, Gene Expression Muscle FunctionPathologyInsulin ReceptorCellular PhysiologyExpanded Transcripts	2006	47
Novel mutations of TCOF1 gene in European patients with treacher Collins syndrome Chiara Conte, Maria Rosaria D’Apice, Fabrizio Rinaldi, BMC Medical Genetics	2011	47
A follow-up 18F-FDG brain PET study in a case of Hashimoto's encephalopathy causing drug-resistant status epilepticus treated with plasmapheresis Elisa Pari, Fabrizio Rinaldi, Enrico Premi, Journal of Neurology Neurobiology Of DiseaseNeurological DisorderNeuropharmacologyDrug-resistant Status EpilepticusNeuroscience	2014	34

Page 1