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Preview	Issue Date	Title	Contributor(s)
	1-Jun-2019	Cardiac diseases as a predictor warning of hereditary muscle diseases. The case of laminopathies	D’AMBROSIO, PAOLA; PETILLO, ROBERTA; TORELLA, ANNALAURA; PAPA, ANDREA ANTONIO; PALLADINO, ALBERTO; ORSINI, CHIARA; ERGOLI, MANUELA; PASSAMANO, LUIGIA; NOVELLI, ANTONIO; NIGRO, VINCENZO; POLITANO, LUISA
	1-Jun-2019	An unusual presentation of scleromyxedema as inflammatory myopathy	VYSAKHA, KAVADISSERIL VIVEKANANDAN; POYURAN, RAJALAKSHMI; NAIR, SRUTHI S; NAIR, MURALIDHARAN
	1-Jun-2019	Are there real benefits to implanting cardiac devices in patients with end-stage dilated dystrophinopathic cardiomyopathy? Review of literature and personal results	PALLADINO, ALBERTO; PAPA, ANDREA A.; MORRA, SALVATORE; RUSSO, VINCENZO; ERGOLI, MANUELA; RAGO, ANNA; ORSINI, CHIARA; NIGRO, GERARDO; POLITANO, LUISA
	1-Jun-2019	Rare variant in LAMA2 gene causing congenital muscular dystrophy in a Sudanese family. A case report	AMIN, MUTAZ; BAKHIT, YOUSUF; KOKO, MAHMOUD; IBRAHIM, MOHAMED OSAMA MIRGAHNI; SALIH, MA; IBRAHIM, MUNTASER; SEIDI, OSHEIK A
	1-Jun-2019	Clinicopathologic features in a case of intermuscular myopericitoma of thigh	HODZIC, RENATA; HODZIC, MIRSAD; PIRIC, NERMINA; KARASALIHOVIC, ZINAIDA
	1-Jun-2019	Facio-scapulo-humeral muscular dystrophy with early joint contractures and rigid spine	PAPADOPOULOS, CONSTANTINOS; ZOUVELOU, VASILIKI; PAPADIMAS, GEORGE KONSTANTINOS
	1-Dec-2018	Immune-mediated necrotizing myopathy due to statins exposure	VILLA, LUISA; LERARIO, ALBERTO; CALLONI, SONIA; PEVERELLI, LORENZO; MATINATO, CATERINA; DE LISO, FEDERICA; CERIOTTI, FERRUCCIO; TIRONI, ROBERTO; SCIACCO, MONICA; MOGGIO, MAURIZIO; TRIULZI, FABIO; CINNANTE, CLAUDIA
	1-Dec-2018	Therapeutic approach with Ataluren in Duchenne symptomatic carriers with nonsense mutations in dystrophin gene. Results of a 9-month follow-up in a case report	D’AMBROSIO, PAOLA; ORSINI, CHIARA; NIGRO, VINCENZO; POLITANO, LUISA
	1-Jun-2019	Modified Atkins ketogenic diet improves heart and skeletal muscle function in glycogen storage disease type III	FRANCINI-PESENTI, FRANCESCO; TRESSO, SILVIA; VITTURI, NICOLA
	1-Jun-2019	Subacute inflammatory myopathy associated with papillary cancer of the thyroid gland	MARTINS, ANA INÊS; LAGES, ADRIANA; REBELO, OLINDA; NEGRÃO, LUÍS
	1-Jun-2019	PROCEEDINGS OF THE XIX CONGRESS OF THE ITALIAN SOCIETY OF MYOLOGY: Bergamo, Italy June 05-08, 2019	-
	1-Jun-2019	Novel TRIM32 mutation in sarcotubular myopathy	PANICUCCI, CHIARA; TRAVERSO, MONICA; BARATTO, SERENA; ROMEO, CHIARA; IACOMINO, MICHELE; GEMELLI, CHIARA; TAGLIAFICO, ALBERTO; BRODA, PAOLO; ZARA, FEDERICO; BRUNO, CLAUDIO; MINETTI, CARLO; FIORILLO, CHIARA
	1-Dec-2018	Metabolic impairments in patients with myotonic dystrophy type 2	VUJNIC, MILORAD; PERIC, STOJAN; CALIC, ZELJKA; BENOVIC, NATASA; NISIC, TANJA; PESOVIC, JOVAN; SAVIC-PAVICEVIC, DUSANKA; RAKOCEVIC-STOJANOVIC, VIDOSAVA
	1-Sep-2018	Prevalence of metabolic syndrome and non-alcoholic fatty liver disease in a cohort of italian patients with spinal-bulbar muscular atrophy	FRANCINI-PESENTI, FRANCESCO; QUERIN, GIORGIA; MARTINI, CRISTINA; MARESO, SARA; SACERDOTI, DAVID
	1-Dec-2018	The role of rehabilitation in the management of late-onset Pompe disease: a narrative review of the level of evidence	IOLASCON, GIOVANNI; VITACCA, MICHELE; CARRARO, ELENA; CHISARI, CARMELO; FIORE, PIETRO; MESSINA, SONIA; MONGINI, TIZIANA ENRICA GIOVANNA; SANSONE, VALERIA A.; TOSCANO, ANTONIO; SICILIANO, GABRIELE
	1-Sep-2018	LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation	BOHLEGA, SAEED A.; ALFAWAZ, SARAH; ABOU-AL-SHAAR, HUSSAM; AL-HINDI, HINDI N.; MURAD, HATEM N.; BOHLEGA, MOHAMED S.; MEYER, BRIAN F.; MONIES, DOROTA
	1-Dec-2018	Heart transplantation in a patient with Myotonic Dystrophy type 1 and end-stage dilated cardiomyopathy: a short term follow-up	PAPA, ANDREA ANTONIO; VERRILLO, FEDERICA; SCUTIFERO, MARIANNA; RAGO, ANNA; MORRA, SALVATORE; CASSESE, ANTONIO; CIOPPA, NADIA DELLA; MAGLIOCCA, MARIA CRISTINA GIADA; GALANTE, DARIO; PALLADINO, ALBERTO; GOLINO, PAOLO; POLITANO, LUISA
	1-Dec-2018	Novel desmoplakin mutations in familial Carvajal syndrome	YERMAKOVICH, DANAT; SIVITSKAYA, LARYSA; VAIKHANSKAYA, TATIYANA; DANILENKO, NINA; MOTUK, IRYNA
	1-Sep-2018	Kir2.2 p.Thr140Met: a genetic susceptibility to sporadic periodic paralysis	FAN, CHUNXIANG; KUHN, MARIUS; MBIOL, ALEXANDER PEPLER; GROOME, JAMES; WINSTON, VERN; BISKUP, SASKIA; LEHMANN-HORN, FRANK; JURKAT-ROTT, KARIN
	1-May-2018	PROCEEDINGS OF THE XVIII CONGRESS OF THE ITALIAN ASSOCIATION OF MYOLOGY: Genoa, Italy June 6-9, 2018	-