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MEOLA, GIOVANNI

MEOLA, GIOVANNI  

Dipartimento di Scienze Biomediche per la Salute  

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Titolo Data di pubblicazione Autori Tipo File Abstract
"I know that you know that I know" : Neural substrates associated with social cognition deficits in DM1 patients 1-gen-2016 G. Meola + Article (author) -
140th ENMC International Workshop : Myotonic Dystrophy DM2/PROMM and other myotonic dystrophies with guidelines on management 1-gen-2006 G. Meola + Article (author) -
[Expression of a defect in the respiratory chain in cultured human cells] 1-gen-1991 G. MeolaV. SansoneN. BresolinG. Comi + Article (author) -
A CASE OF MITOCHONDRIAL MYOPATHY, LACTIC-ACIDOSIS AND COMPLEX-I DEFICIENCY 1-gen-1990 L. BETN. BRESOLING. MEOLAF. FORTUNATO + Article (author) -
A clinical, genetic and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegia 1-apr-2008 G. MeolaG.P. ComiN. Bresolin + Article (author) -
A comparative analysis of collagen III, IV, laminin and fibronectin in Duchenne muscular dystrophy biopsies and cell cultures 1-ott-1986 G. MeolaA. M. ContiL. Larizza + Article (author) -
A family with an unusual myotonic and myopathic phenotype and no CTG expansion (proximal myotonic myopathy syndrome): a challenge for future molecular studies 1-mag-1996 G. MeolaV. Sansone + Article (author) -
A multidisciplinary approach improves quality of life perception in patients with amyotrophic lateral sclerosis 21-giu-2009 V. SansoneG. Meola + Conference Object -
A newly-described myotonic disorder (proximal myotonic myopathy--PROMM): personal experience and review of the literature 1-ott-1996 G. MeolaV. Sansone 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 1-feb-2017 G. Meola + Article (author) -
A putative role of ribonuclear inclusions and MBNL1 in the impairment of gallbladder smooth muscle contractility with cholelithiasis in myotonic dystrophy type 1 1-gen-2008 R. CardaniE. MancinelliL. BonavinaG. Meola + Article (author) -
Aberrant expression of microRNA in myotonia dystrophies 10-set-2009 G. Meola + Conference Object -
Abnormalities of proliferative and differentiative properties in DM1 and DM2 senescence myoblasts -in vitro- 1-mag-2011 V. RennaG. Meola + Conference Object -
Acetazolamide prevents vacuolar myopathy in skeletal muascle of K+ -depleted rats 1-gen-2008 MANCINELLI, ENZOG. Meola + Article (author) -
Acute disseminated encephalomyelitis and multiple sclerosis 1-gen-2004 G. Meola Article (author) -
Advanced microscopic and histochemical techniques : diagnostic tools in the molecular era of myology 1-gen-2005 G. Meola Article (author) -
Alterazioni proteine tau liquorali e quoziente intellettivo (QI) nelle Distrofie Miotonichew di tipo 1 (DM1) e di tipo 2 (DM2). 1-gen-2008 V. SansoneE. ScarpiniG. Meola + Article (author) -
Altered pre-mRNA processing in myotonic dystrophy type 2 (DM2) myoblasts 1-gen-2010 L.V. RennaG. Meola + Article (author) -
Altered Pre-mRNA processing is a common feature of muscle cells in senescence and myotonic dystrophy type 2 (DM2) 15-apr-2010 G. Meola + Conference Object -
Amyotrophic lateral sclerosis in pregnancy is associated with a vascular endothelial growth factor promoter genotype 1-apr-2014 V.A. SansoneC. TarlariniF. AvemariaG. Meola + Article (author) -