LA PREVENZIONE DELLA DISTROFIA MUSCOLARE DI DUCHENNE: PROBLEMI METODOLOGICI IN TEMA DI DIAGNOSI DELLA CONDIZIONE DI "PORTATRICE". = LA PREVENTION DE LA DYSTROPHIE MUSCULAIRE DE DUCHENNE: PROBLEMES DE METHODOLOGIE POUR LE DIAGNOSTIC DE L'ETAT DE "TRANSMETTRICE"SCARLATO G; VALLI G; MEOLA G et al.1977; RIV. PATOL. NERV. MENTALE; ITA; DA. 1977 PUBL. 1978; VOL. 98; NO 3; PP. 133-150; ABS. ENG; BIBL. 2 P.Article

AMYOTROPHY AND KLUEVER-BUCY SYNDROME. A CASE REPORTCAPITANI E; MEOLA G; SPINNLER H et al.1977; EUROP. NEUROL.; CHE; DA. 1977; VOL. 16; NO 1-6; PP. 99-105; BIBL. 2 P.Article

LA PATOLOGIA MUSCOLARE NELL'IPERPIRESSIA MALIGNA DELL'NOMO E DEL SUINO. STUDIO COMPARATIVO = LA PATHOLOGIE MUSCULAIRE DANS L'HYPERTHERMIE MALIGNE CHEZ L'HOMME ET LE PORC. ETUDE COMPARATIVESCARLATO G; MEOLA G; PELLEGRINI G et al.1976; ACTA NEUROL.; ITAL.; DA. 1976; VOL. 31; NO 1; PP. 58-61; BIBL. 8 REF.Article

STUDIO ISTOLOGICO DELLA MUSCOLATURA EXTRAOCULARE NELLE COSIDETTE OFTALMOPLEGIE NUCLEARI PROGRESSIVE = ETUDE HISTOLOGIQUE DE LA MUSCULATURE EXTRINSEQUE DE L'OEIL DANS LA DITE OPHTALMOPLEGIE NUCLEAIRE PROGRESSIVESCARLATO G; PELLEGRINI G; MEOLA G et al.1976; ACTA NEUROL.; ITAL.; DA. 1976; VOL. 31; NO 1; PP. 93-99; ABS. ANGL.; BIBL. 10 REF.Article

PHOSPHOFRUCTOKINASE (PFK) DEFICIENCY DUE TO A CATALYTICALLY INACTIVE MUTANT M-TYPE SUBUNITZANELLA A; MARIANI M; MEOLA G et al.1982; AM. J. HEMATOL.; ISSN 0361-8609; USA; DA. 1982; VOL. 12; NO 3; PP. 215-225; BIBL. 36 REF.Article

MUSCULAR CARNITINE SYNTHESIS AND PALMITATE METABOLISM IN VITRO.SCARLATO G; MEOLA G; SCARPINI E et al.1978; J. NEUROL.; DEU; DA. 1978; VOL. 218; NO 3; PP. 149-156; ABS. ALLEM.; BIBL. 25 REF.Article

QUANTITATIVE EMG AND HISTOLOGICAL CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY.SCARLATO G; VALLI G; MEOLA G et al.1977; J. NEUROL.; GERM.; DA. 1977; VOL. 216; NO 4; PP. 235-249; ABS. ALLEM.; BIBL. 2 P. 1/2Article

Treatment in myotonia and periodic paralysisMEOLA, G; SANSONE, V.Revue neurologique (Paris). 2004, Vol 160, Num 5, pp 4S55-4S69, issn 0035-3787, CAH2Conference Paper

MYOPATHY WITH PAROXYSMAL MYOGLOBINURIA AND FOCAL MUSCLE NECROSIS FOLLOWING ENFLUORANE ANAESTHESIACACCIA MR; CERRI C; GRAVAME V et al.1978; J. NEUROL. SCI.; NLD; DA. 1978; VOL. 39; NO 1; PP. 61-69; BIBL. 26 REF.Article

FAMILIAL NEMALINE MYOPATHYSCARLATO G; PELLEGRINI G; MOGGIO M et al.1982; NEUROPEDIATRICS; ISSN 0174-304X; DEU; DA. 1982; VOL. 13; NO 4; PP. 211-215; BIBL. 35 REF.Article

ERYTHROCYTE SPECTROFLUOROMETRIC ABNORMALITIES IN DUCHENNE PATIENTS AND CARRIERS. A NEW APPROACH TO CARRIER DETECTIONSCARLATO G; MEOLA G; SILANI V et al.1979; ACTA NEUROL. SCAND.; DNK; DA. 1979; VOL. 59; NO 5; PP. 262-269; BIBL. 3 P.Article

METABOLIC IMPAIRMENT AND MEMBRANE ABNORMALITY IN RED CELLS FROM HUNTINGTON'S DISEASEZANELLA A; IZZO C; MEOLA G et al.1980; J. NEUROL. SCI.; NLD; DA. 1980; VOL. 47; NO 1; PP. 93-103; BIBL. 32 REF.Article

Danazol and internal carotid artery thrombosisCORNO, M; VALLAR, G; SCARIATO, G et al.European neurology. 1989, Vol 29, Num 4, pp 235-237, issn 0014-3022Article

Recessive carnitine palmityl transferase deficiency: biochemical studies in tissue cultures and plateletsMEOLA, G; BRESOLIN, N; RIMOLDI, M et al.Journal of neurology. 1987, Vol 235, Num 2, pp 74-79, issn 0340-5354Article

Muscle surface mechanical and electrical activities in myotonic dystrophyORIZIO, C; ESPOSITO, F; SANSONE, V et al.Electromyography and clinical neurophysiology. 1997, Vol 37, Num 4, pp 231-239, issn 0301-150XArticle

In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondriaCHOMYN, A; MEOLA, G; BRESOLIN, N et al.Molecular and cellular biology (Print). 1991, Vol 11, Num 4, pp 2236-2244, issn 0270-7306, 9 p.Article

De novo 14484 mitochondrial DNA mutation in monozygotic twins discordant for Leber's hereditary optic neuropathyBIOUSSE, V; BROWN, M. D; NEWMAN, N. J et al.Neurology. 1997, Vol 49, Num 4, pp 1136-1138, issn 0028-3878Article

Muscle phosphoglycerate mutase (PGAM) deficiency in the first Caucasian patient : biochemistry, muscle culture and ³¹P-MR spectroscopyVITA, G; TOSCANO, A; BRESOLIN, N et al.Journal of neurology. 1994, Vol 241, Num 5, pp 289-294, issn 0340-5354Article

Neural regulation of acide maltase in an unusual adult onset deficiencyMEOLA, G; SANSONE, V; ROTONDO, G et al.Clinical neuropathology. 1994, Vol 13, Num 5, pp 286-291, issn 0722-5091Conference Paper

Proximal myotonic myopathy: a syndrome with a favourable prognosis?MEOLA, G; SANSONE, V; MARINOU, K et al.Journal of the neurological sciences. 2002, Vol 193, Num 2, pp 89-96, issn 0022-510XArticle

Muscle glucose-6 phosphate dehydrogenase deficiencyBRESOLIN, N; BET, L; MEOLA, G et al.Journal of neurology. 1989, Vol 236, Num 4, pp 193-198, issn 0340-5354, 6 p.Article

Reduced cerebral blood flow and impaired visual-spatial function in proximal myotonic myopathyMEOLA, G; SANSONE, V; PERANI, D et al.Neurology. 1999, Vol 53, Num 5, pp 1042-1050, issn 0028-3878Article

A case of mitochondrial myopathy, lactic acidosis and complex I deficiencyBET, L; BRESOLIN, N; SCARLATO, G et al.Journal of neurology. 1990, Vol 237, Num 7, pp 399-404, issn 0340-5354, 6 p.Article

Cultures of human Schwann cells isolated from fetal nervesSCARPINI, E; KREIDER, B. Q; LISAK, R. P et al.Brain research. 1988, Vol 440, Num 2, pp 261-266, issn 0006-8993Article

Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysisMATTHEWS, E; LABRUM, R; HANNA, M. G et al.Neurology. 2009, Vol 72, Num 18, pp 1544-1547, issn 0028-3878, 4 p.Article