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LA MIOPATIA IPOTIROIDEA: ASPETTI ISTOCHIMICI, ULTRASTRUTTURALI E CORRELAZIONI FISIOPATOLOGICHE = LA MYOPATHIE HYPOTHYROIDIENNE. ASPECTS HISTOCHIMIQUES, D'ULTRASTRUCTURE ET CORRELATIONS PHYSIOPATHOLOGIQUESPELLEGRINI G; MOGGIO M.1979; RIV. PATOL. NERV. MENTALE; ITA; DA. 1979; VOL. 99; NO 5; PP. 275-288; ABS. ENG; BIBL. 2 P.Article

A HEREDITARY CASE OF LIPID STORAGE MYOPATHY WITH CARNITINE DEFICIENCY: ULTRASTRUCTURAL OBSERVATION OF MUSCLE TISSUE IN PARENTSPELLEGRINI G; SCARLATO G; MOGGIO M et al.1980; J. NEUROL.; DEU; DA. 1980; VOL. 223; NO 2; PP. 73-84; ABS. GER; BIBL. 27 REF.Article

Electron cytochemical study of the muscle cell surfaceBONILLA, E; MOGGIO, M.Histochemistry (Berlin). 1987, Vol 86, Num 5, pp 503-507, issn 0301-5564Article

METABOLIC EFFECTS OF PYRIDOXINE ALPHA-KETOGLUTARATE IN OPHTHALMOPLEGIA PLUSSCARLATO G; PELLEGRINI G; MOGGIO M et al.1982; ACTA NEUROL.; ISSN 0001-6276; ITA; DA. 1982; VOL. 4; NO 2; PP. 92-97; ABS. ITA; BIBL. 28 REF.Article

Ultrastructural localization of anionic phospholipids in skeletal muscle plasma membraneMOGGIO, M; BONILLA, E.Histochemistry (Berlin). 1985, Vol 83, Num 6, pp 519-523, issn 0301-5564Article

PRACTICAL VALUE OF CSF CYTOLOGICAL EXAMINATION IN THE DIAGNOSTICS OF INTRACRANIAL NEOPLASM: A PRELIMINARY REPORTRAVETTO C; SCARLATO G; MOGGIO M et al.1980; J. NEUROSURG. SCI.; ISSN 0390-5616; ITA; DA. 1980; VOL. 24; NO 2; PP. 53-56; BIBL. 36 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

FAMILIAL MEGACONIAL MYOPATHY: A REAL NOSOLOGIC ENTITY. CLINICAL AND HISTOPATHOLOGIC STUDIES IN TWO SIBLINGSPELLEGRINI G; MOGGIO M; CHELDI A et al.1983; ACTA NEUROPATHOLOGICA; ISSN 0001-6322; DEU; DA. 1983; VOL. 59; NO 1; PP. 70-74; BIBL. 14 REF.Article

High-dose intravenous human immunoglobulin in polymyositis resitant to treatmentJANN, S; BERETTA, S; MOGGIO, M et al.Journal of neurology, neurosurgery and psychiatry. 1992, Vol 55, Num 1, pp 60-62, issn 0022-3050Article

Fatal infantile mitochondrial myopathy and renal dysfunction caused by cytochrome c oxidase deficiency: immunological studies in a new patientZEVIANI, M; NONAKA, I; BONILLA, E et al.Annals of neurology. 1985, Vol 17, Num 4, pp 414-417, issn 0364-5134Article

Immunogenicity of Haemophilus B conjugate vaccine (meningococcal protein conjugate) in children with prior invasive hamophilus influenzae type b diseaseWALTER, E. B; MOGGIO, M. V; DRUCKER, R. P et al.The Pediatric infectious disease journal. 1990, Vol 9, Num 9, pp 632-635, issn 0891-3668Article

Lack of anionic phospholipid calcium binding sites in Duchene muscular dystrophyMOGGIO, M; FAGIOLARI, G; PRELLE, A et al.Muscle & nerve. 1992, Vol 15, Num 3, pp 325-331, issn 0148-639XArticle

A case of congenital neuromuscular disease with uniform type I fibers, abnormal mitochondrial network and jagged Z-linePELLEGRINI, G; BARBIERI, S; MOGGIO, M et al.Neuropediatrics. 1985, Vol 16, Num 3, pp 162-166, issn 0174-304XArticle

Neurogenic muscular atrophy in myasthenia gravis : possible motor neuron involvementVALLI, G; CAPPELLARI, A; MINZI, G. L et al.Nuova rivista di neurologia. 1992, Vol 2, Num 5, pp 198-202, issn 1122-035XArticle

Anionic phospholipids calcium binding sites in Duchenne and murine X-linked muscular dystrophyMOGGIO, M; PRELLE, A; FAGIOLARI, G et al.Muscle & nerve. 1994, Vol 17, Num 5, pp 485-488, issn 0148-639XArticle

Decrease of nerve Na+, K+-ATPase activity in the pathogenesis of human diabetic neuropathySCARPINI, E; BIANCHI, R; MOGGIO, M et al.Journal of the neurological sciences. 1993, Vol 120, Num 2, pp 159-167, issn 0022-510XArticle

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

Desmin and vimentin as markers of regeneration in muscle diseasesGALLANTI, A; PRELLE, A; MOGGIO, M et al.Acta neuropathologica. 1992, Vol 85, Num 1, pp 88-92, issn 0001-6322Article

Biochemical and immunologic studies in a case of congenital myopathy with unusual morphologic featuresBIRAL, D; DAMIANI, E; SCARPINI, E et al.Neurology. 1987, Vol 37, Num 10, pp 1658-1662, issn 0028-3878Article

Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathyCHECCARELLI, N; PRELLE, A; MOGGIO, M et al.Journal of the neurological sciences. 1994, Vol 123, Num 1-2, pp 74-79, issn 0022-510XArticle

Multiple deletions of mitochondrial DNA in a patient with periode attacks of paralysisPRELLE, A; MOGGIO, M; CHECCARELLI, N et al.Journal of the neurological sciences. 1993, Vol 117, Num 1-2, pp 24-27, issn 0022-510XArticle

Dystrophin deficiency in a case of congenital myopathyPRELLE, A; MEDORI, R; MOGGIO, M et al.Journal of neurology. 1992, Vol 239, Num 2, pp 76-78, issn 0340-5354Article

Peripheral neuropathy in macroglobulinemia: incidence and antigen-specificity of M proteinsNOBILE-ORAZIO, E; MARMIROLI, P; BALDINI, L et al.Neurology. 1987, Vol 37, Num 9, pp 1506-1514, issn 0028-3878Article

Phenotypic and proliferative properties of Schwann cells from nerves of diabetic patientsSCARPINI, E; DORONZO, R; BARON, P et al.International journal of clinical pharmacology research. 1992, Vol 12, Num 5-6, pp 211-215, issn 0251-1649Article

Cytochrome C oxidase during human fetal developmentMOGGIO, M; BRESOLIN, N; SCARPINI, E et al.International journal of developmental neuroscience. 1989, Vol 7, Num 1, pp 5-14, issn 0736-5748Article

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