BUGIARDINI, ENRICO

BUGIARDINI, ENRICO  

Universita' degli Studi di MILANO  

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Risultati 1 - 10 di 10 (tempo di esecuzione: 0.012 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
SCN4A mutation as modifying factor of myotonic dystrophy type 2 phenotype 2015 E. BugiardiniG. Meola + Article (author) -
Gonadal failure is associated with visceral adiposity in myotonic dystrophies 2015 E. PasseriE. BugiardiniV.A. SansoneA. PizzocaroR. ValapertaE. CostaF. BanderaB. AmbrosiG. MeolaL. PersaniS. Corbetta + Article (author) -
Genome wide identification of aberrant alternative splicing events in myotonic dystrophy type 2 2014 A. PerfettiE. BugiardiniR. CardaniG. Meola + Article (author) -
Plasma microRNAs as biomarkers for myotonic dystrophy type 1 2014 A. PerfettiE. BugiardiniR. CardaniP. GaiaG. Meola + Article (author) -
RNA transcription and maturation in skeletal muscle cells are similarly impaired in myotonic dystrophy and sarcopenia : the ultrastructural evidence 2014 L.V. RennaE. BugiardiniA. BottaG. Meola + Article (author) -
Progression of muscle histopathology but not of spliceopathy in myotonic dystrophy type 2 2014 R. CardaniG. RossiL.V. RennaE. BugiardiniG. Meola + Article (author) -
Overexpression of CUGBP1 in Skeletal Muscle from Adult Classic Myotonic Dystrophy Type 1 but Not from Myotonic Dystrophy Type 2 2013 R. CardaniE. BugiardiniL.V. RennaG. ColomboR. ValapertaG. Meola + Article (author) -
Vitamin D, parathyroid hormone and muscle impairment in myotonic dystrophies 2013 E. PasseriE. BugiardiniV. SansoneR. ValapertaB. AmbrosiG. MeolaS. Corbetta + Article (author) -
Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2 2012 R. CardaniL.V. RennaV. SansoneE. BugiardiniG. Meola + Article (author) -
High prevalence of vitamin D deficiency in myotonic dystrophies 2012 E. BugiardiniE. PasseriV. SansoneB. AmbrosiS. CorbettaL. RennaG. Meola + Article (author) -