MEOLA, GIOVANNI

MEOLA, GIOVANNI  

Dipartimento di Scienze Biomediche per la Salute  

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Titolo Data di pubblicazione Autori Tipo File Abstract
Case report: Sodium and chloride muscle channelopathy coexistence: A complicated phenotype and a challenging diagnosis 2022 Pagliarani, SerenaMeola, GiovanniComi, Giacomo PietroLucchiari, Sabrina + Article (author) -
Co-occurrence of DMPK expansion and CLCN1 mutation in a patient with myotonia 2021 Cardani R.Lucchiari S.Comi G. P.Meola G. + Article (author) -
Guidelines on clinical presentation and management of nondystrophic myotonias 2020 Giovanni MeolaValeria A. Sansone + Article (author) -
Rare Disease : Cardiac Risk Assessment With MRI in Patients With Myotonic Dystrophy Type 1 2020 Ali M.Monti C. B.Melazzini L.Secchi F.Meola G.Sardanelli F. + Article (author) -
Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4 2020 Pagliarani S.Lucchiari S.Redaelli E.Magri F.Fossati B.Sansone V. A.Meola G.Comi G. P. + Article (author) -
Fragility fractures and bone mineral density in male patients affected by type 1 and type 2 myotonic dystrophy 2020 Passeri, ESansone, VASconfienza, MMessina, CMeola, GCorbetta, S Article (author) -
Neuropsychological and psychological functioning aspects in myotonic dystrophy type 1 patients in Italy 2018 Callus, EdwardBeretta, MariaCardani, RosannaFossati, BarbaraBrigonzi, ElisaMeola, Giovanni + Article (author) -
Report of the third outcome measures in myotonic dystrophy type 1 (OMMYD-3) international workshop Paris, France, June 8, 2015 2018 Meola GSansone V + Article (author) -
The role of clinical and neuroimaging features in the diagnosis of CADASIL 2018 Vitali, PaoloSasanelli, FrancescoComi, GiancarloSilani, VincenzoMeola, GiovanniComi, Giacomo PietroCorti, StefaniaRonchi, DarioBassi, Maria Teresa + Article (author) -
The analysis of myotonia congenita mutations discloses functional clusters of amino acids within the CBS2 domain and the C-terminal peptide of the ClC-1 channel 2018 Lucchiari, SabrinaUlzi, GiannaComi, Giacomo P.Cardani, RosannaMeola, Giovanni + Article (author) -
Consensus-based care recommendations for adults with myotonic dystrophy type 1. 2018 Meola GBozzali MSansone V + Article (author) -
Myotonic dystrophy type 2 and modifier genes : an update on clinical and pathomolecular aspects 2017 G. MeolaR. Cardani Article (author) -
A novel Ile1455Thr variant in the skeletal muscle sodium channel alpha-subunit in a patient with a severe adult-onset proximal myopathy with electrical myotonia and a patient with mild paramyotonia phenotype 2017 G. Meola + Article (author) -
Circulating irisn is reduced in male patients with type 1 and type 2 Myotonic Dystrophies 2017 E. DozioE. PasseriR. CardaniS. BenediniC. ArestaR. ValapertaM. Corsi RomanelliG. MeolaV. SansoneS. Corbetta Article (author) -
Myotonic dystrophies : state of the art of new therapeutic developments for the CNS 2017 G. Meola + Article (author) -
Posterior reversible encephalopathy syndrome after long-term treatment with low-dose sunitinib : a case report 2017 L. SaracenoV.A..G. RiciglianoM. CavalliG. Meola Article (author) -
Clinical Reasoning : a 35-year-old woman with hyperstartling, stiffness, and accidental falls : a startling diagnosis 2017 RUSSO, SILVIA PAOLAB. FossatiTOFFETTI, MAUROR. CardaniG. Meola + Article (author) -
Clusters of cognitive impairment among different phenotypes of myotonic dystrophy type 1 and type 2 2017 G. Meola + Article (author) -
Biomolecular diagnosis of myotonic dystrophy type 2 : a challenging approach 2017 G. MeolaR. ValapertaE. CostaR. Cardani + Article (author) -
Receptor and post-receptor abnormalities contribute to insulin resistance in myotonic dystrophy type 1 and type 2 skeletal muscle 2017 RENNA, LAURA VALENTINABOSE', FRANCESCAB. FossatiL. SaracenoG. MeolaR. Cardani + Article (author) -