Giuliana Galluzzi - Concepedia

Concepedia

Author

Giuliana Galluzzi

Università Cattolica del Sacro Cuore

Also Known As

G Galluzzi, G. Galluzzi, Giuliana Galluzzi, Giuliana Galluzzi (578454)

48

Publications

2.8K

Citations

24

H-Index

66

Concepts

All Affiliations

Università Cattolica del Sacro Cuore Institute of Cell Biology and Neurobiology University of Padua University of Verona Fondazione Santa Lucia

GG

About

Giuliana Galluzzi is an author at Università Cattolica del Sacro Cuore specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	14	1.7K
2	Public Health	4	4	640
3	Health Sciences	3	3	260
4	Engineering	1	1	244
5	Applied Physiology	1	1	151

Giuliana Galluzzi

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27

Publications

2.8K

Citations

24

H-Index

	Year	Citations
Different Mutations in the LMNA Gene Cause Autosomal Dominant and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy Marina Raffaele di Barletta, Enzo Ricci, Giuliana Galluzzi, The American Journal of Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsDegenerative Disease	2000	411
Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number ofKpnI repeats at the 4q35 locus and clinical phenotype Enzo Ricci, Giuliana Galluzzi, Giancarlo Deidda, Annals of Neurology Ecori Fragment SizeRare DiseasesFacioscapulohumeral Muscular DystrophyEcori FragmentMendelian Disorder	1999	296
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression Mario Pescatori, Aldobrando Broccolini, Carlo Minetti, The FASEB Journal Muscle FunctionEngineeringGeneticsGene CharacterizationDisease Gene Identification	2007	244
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north‐east Italian population sample ML Mostacciuolo, Ebe Pastorello, Giovanni Vazza, Clinical Genetics Facioscapulohumeral Muscular DystrophyMendelian DisorderFshd PatientsGenetic DisorderGenetics	2009	156
A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score Costanza Lamperti, Greta Fabbri, Liliana Vercelli, Muscle & Nerve Muscle FunctionDiagnosisOrthopaedic SurgeryKinesiologyMuscle Weakness	2010	151
Phenotypic clustering of lamin A/C mutations in neuromuscular patients Sara Benedetti, I. Menditto, Massimo Degano, Neurology	2007	128
Chimeric snRNA molecules carrying antisense sequences against the splice junctions of exon 51 of the dystrophin pre-mRNA induce exon skipping and restoration of a dystrophin synthesis in Δ48-50 DMD cells Fernanda Gabriella De Angelis, Olga Sthandier, Barbara Berarducci, Proceedings of the National Academy of Sciences	2002	128
Large-Scale Population Analysis Challenges the Current Criteria for the Molecular Diagnosis of Fascioscapulohumeral Muscular Dystrophy Isabella Scionti, Francesca Gabriella Greco, Giulia Ricci, The American Journal of Human Genetics Genetic AnalysisMolecular DiagnosisMendelian DisorderMedicineGenetic Epidemiology	2012	123
Large scale genotype–phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy Giulia Ricci, Isabella Scionti, Francesco Sera, Brain	2013	119
Mutation analysis of the lamin A/C gene (<i>LMNA</i>) among patients with different cardiomuscular phenotypes Michal Vytopil, Sara Benedetti, Enzo Ricci, Journal of Medical Genetics	2003	113

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