المؤلفون: Volpi, L., Ricci, G., Passino, C., Di Pierri, E., Alì, G., Maccherini, M., Benedetti, S., Lattanzi, G., Columbaro, M., Ferrari, M., Caramella, D., Tanganelli, P., Emdin, M., Siciliano, G.

المصدر: In Neuromuscular Disorders 2010 20(8):512-516

المؤلفون: Volpi, L., Ricci, G., Pasquali, L., Calsolaro, V., Emdin, M., Passino, C., Benedetti, S., Di Pierri, E., Ferrari, M., Gabriele Siciliano

المصدر: ResearcherID

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4194f3b426061c832bea2e3225346aeb
http://hdl.handle.net/11382/370034

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المؤلفون: Luigi M.E. Grimaldi, Elisabetta Munerati, Sara Benedetti, Maurizio Ferrari, Angelo Quattrini, Lara Piantoni, Maria Chiara Malaguti, Nilo Riva, Silvia Coviello, Marina Scarlato, Ivana Spiga, Federica Cerri, Maurizio De Pellegrin, Alessandra Bolino, Maria Giovanna Marrosu, Patrizia Dacci, Raffaella Fazio, Emanuela Di Pierri, Giancarlo Comi, Maria Grazia Natali Sora, Stefano C. Previtali

المساهمون: Benedetti, S, Previtali, Sc, Coviello, S, Scarlato, M, Cerri, F, DI PIERRI, E, Piantoni, L, Spiga, I, Fazio, R, Riva, N, NATALI SORA, Mg, Dacci, P, Malaguti, Mc, Munerati, E, Grimaldi, Lm, Marrosu, Mg, DE PELLEGRIN, M, Ferrari, Maurizio, Comi, Giancarlo, Quattrini, A, Bolino, A.

المصدر: Archives of neurology. 67(12)

مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, Pathology, medicine.medical_specialty, Adolescent, DNA Mutational Analysis, MFN2, HSP27 Heat-Shock Proteins, Sural nerve, medicine.disease_cause, Connexins, GTP Phosphohydrolases, Central nervous system disease, Pathogenesis, Cohort Studies, Mitochondrial Proteins, Young Adult, Degenerative disease, Arts and Humanities (miscellaneous), Sural Nerve, Charcot-Marie-Tooth Disease, Biopsy, medicine, Humans, Child, Pathological, Heat-Shock Proteins, Aged, Retrospective Studies, Aged, 80 and over, Mutation, medicine.diagnostic_test, business.industry, Intracellular Signaling Peptides and Proteins, Membrane Proteins, Middle Aged, medicine.disease, Phosphoproteins, Ether-A-Go-Go Potassium Channels, nervous system diseases, Female, Neurology (clinical), business, Demyelinating Diseases, Molecular Chaperones, Transcription Factors

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e4f2da39b0ef6d3844ebc1c2921c54f
https://pubmed.ncbi.nlm.nih.gov/21149811

المؤلفون: Sara Benedetti, Maurizio Ferrari, Marta Columbaro, Piero Tanganelli, Massimo Maccherini, E Di Pierri, Gabriele Siciliano, Davide Caramella, Giulia Ricci, Claudio Passino, Leda Volpi, Michele Emdin, Giovanna Lattanzi, Greta Alì

المساهمون: Volpi, L, Ricci, G, Passino, C, Di Pierri, E, Alì, G, Maccherini, M, Benedetti, S, Lattanzi, G, Columbaro, M, Ferrari, Maurizio, Caramella, D, Tanganelli, P, Emdin, M, Siciliano, G.

مصطلحات موضوعية: Proband, medicine.medical_treatment, Cardiomyopathy, Bioinformatics, LMNA, Electrocardiography, Lamin A/C, Limb-girdle muscular dystrophy, Gene Duplication, Gene duplication, Medicine, Muscular dystrophy, Genetics (clinical), Heart transplantation, Muscle Weakness, Nuclear Proteins, Dilated cardiomyopathy, Heart, Middle Aged, Lamin Type A, LMNA GENE, Immunohistochemistry, Pedigree, Phenotype, Neurology, Cardiology, HEART, Female, Adult, Cardiomyopathy, Dilated, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Heart Diseases, Molecular Sequence Data, Internal medicine, Humans, Amino Acid Sequence, Muscle, Skeletal, business.industry, Membrane Proteins, Stroke Volume, medicine.disease, Muscular Dystrophies, Limb-Girdle, Pediatrics, Perinatology and Child Health, Heart Transplantation, Neurology (clinical), business, Tomography, X-Ray Computed

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d12ee6d03689ddf46be72706c6c9933b
http://hdl.handle.net/11382/304703