MOTOR NEURON DISEASE FOLLOWING POLIOMYELITIS. BIOPTIC STUDY OF FIVE CASESPALMUCCI L; BERTOLOTTO A; DORIGUZZI C et al.1980; EUR. NEUROL.; ISSN 0014-3022; CHE; DA. 1980; VOL. 19; NO 6; PP. 414-418; BIBL. 28 REF.Article

OSTEOMALACIC MYOPATHY IN A CASE OF DIFFUSE NODULAR LIPOMATOSIS OF THE SMALL BOWELPALMUCCI L; BERTOLOTTO A; DORIGUZZI C et al.1982; ACTA NEUROL. BELG.; ISSN 0300-9009; BEL; DA. 1982; VOL. 82; NO 2; PP. 65-71; BIBL. 20 REF.Article

Early sarcolemmal dysfunction in skeletal muscle amyloidosisDORIGUZZI, C; MONGINI, T; TRONI, W et al.Journal of neurology. 1987, Vol 234, Num 1, pp 52-54, issn 0340-5354Article

Interictal conduction slowing in muscle fibers in hypokalemic periodic paralysisTRONI, W; DORIGUZZI, C; MONGINI, T et al.Neurology. 1983, Vol 33, Num 11, pp 1522-1525, issn 0028-3878Article

Familial autosomal recessive rigid spine syndrome with neurogenic facio-scapulo-peroneal muscle atrophyPALMUCCI, L; MONGINI, T; DORIGUZZI, C et al.Journal of neurology, neurosurgery and psychiatry. 1991, Vol 54, Num 1, pp 42-45, issn 0022-3050, 4 p.Article

Sporadic distal myopathy with early adult onset: study of muscle biopsies and muscle cell culturesMONGINI, T; DORIGUZZI, C; PALMUCCI, L et al.European neurology. 1989, Vol 39, Num 5, pp 287-290, issn 0014-3022Article

Human myopathies in muscle culture: morphological, cytochemical, and biochemical studiesMIRANDA, A. F; MONGINI, T; DI MAURO, S et al.Advances in cell culture. 1985, Vol 4, pp 1-45Article

A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiencySILVESTRI, G; MONGINI, T; ODOARDI, F et al.Neurology. 2000, Vol 54, Num 8, pp 1693-1696, issn 0028-3878Article

Unusual clinical expression of dystrophinopathy in a female, mimicking a congenital myopathyPALMUCCI, L; DORIGUZZI, C; MONGINI, T et al.European neurology. 1999, Vol 42, Num 4, pp 221-224, issn 0014-3022Article

Systematic use of dystrophin testing in muscle biopsies: results in 201 casesDORIGUZZI, C; PALMUCCI, L; MONGINI, T et al.European journal of clinical investigation. 1997, Vol 27, Num 4, pp 352-358, issn 0014-2972Article

Analysis of dystrophin expression after activation of myogenesis in amniocytes, chorionic-villus cells, and fibroblastsSANCHO, S; MONGINI, T; TANJI, K et al.The New England journal of medicine. 1993, Vol 329, Num 13, pp 915-920, issn 0028-4793Article

Cytochrome c oxidase and coenzyme Q in neuromuscular diseases : a histochemical studyDORIGUZZI, C; PALMUCCI, L; POLLO, B et al.Acta neuropathologica. 1990, Vol 81, Num 1, pp 25-29, issn 0001-6322, 5 p.Article

Quantitative analysis of quadriceps muscle biopsy: results in 30 healthy femalesDORIGUZZI, C; MONGINI, T; PALMUCCI, L et al.Journal of the neurological sciences. 1984, Vol 66, Num 2-3, pp 319-326, issn 0022-510XArticle

Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophyMERCURI, E; BERTINI, E; CINI, C et al.Neurology. 2007, Vol 68, Num 1, pp 51-55, issn 0028-3878, 5 p.Article

Alpha-sarcoglycan deficiency featuring exercise intolerance and myoglobinuriaMONGINI, T; DORIGUZZI, C; BOSONE, I et al.Neuropediatrics. 2002, Vol 33, Num 2, pp 109-111, issn 0174-304XArticle

Carrier detection of Duchenne muscular dystrophy through analysis of DNA from deciduous teeth of a dead affected childRESTAGNO, G; FERRONE, M; DORIGUZZI, C et al.Prenatal diagnosis. 1995, Vol 15, Num 7, pp 672-674, issn 0197-3851Article

Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophyPALMUCCI, L; DORIGUZZI, C; MONGINI, T et al.Journal of the neurological sciences. 1992, Vol 111, Num 2, pp 218-221, issn 0022-510XArticle

Myoglobinuria and carnitine palmityl transferase deficiency in father and sonMONGINI, T; DORIGUZZI, C; PALMUCCI, L et al.Journal of neurology. 1991, Vol 238, Num 6, pp 323-324, issn 0340-5354Article

Free cytoplasmic Ca⁺⁺ at rest and after cholinergic stimulus is increased in cultured muscle cells from Duchenne muscular dystrophy patientsMONGINI, T; GHIGO, D; DORIGUZZI, C et al.Neurology. 1988, Vol 38, Num 3, pp 476-480, issn 0028-3878Article

Functional changes in Duchenne muscular dystrophy: A 12-month longitudinal cohort studyMAZZONE, E; VASCO, G; FROSINI, S et al.Neurology. 2011, Vol 77, Num 3, pp 250-256, issn 0028-3878, 7 p.Article

Outcome and length of stay in psychiatric hospitalization, the experience of the University Clinic of TurinROCCA, Paola; MINGRONE, C; MONGINI, T et al.Social psychiatry and psychiatric epidemiology (Print). 2010, Vol 45, Num 6, pp 603-610, issn 0933-7954, 8 p.Article

MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutationMONGINI, T; DORIGUZZI, C; CHIADO-PIAT, L et al.Clinical neuropathology. 2002, Vol 21, Num 2, pp 72-76, issn 0722-5091Article

Late onset and very mild course of Xp21 Becker type muscular dystrophyBOSONE, I; BORTOLOTTO, S; MONGINI, T et al.Clinical neuropathology. 2001, Vol 20, Num 5, pp 196-199, issn 0722-5091Article

Variable histological expression of dystrophinopathy in two femalesDORIGUZZI, C; PALMUCCI, L; MONGINI, T et al.Acta neuropathologica. 1999, Vol 97, Num 6, pp 657-660, issn 0001-6322Article

Quantitative and qualitative alterations of dystrophin are expressed in muscle cell cultures of Xp21 muscular dystrophy patients (Duchenne and Becker type)MONGINI, T; DORIGUZZI, C; PALMUCCI, L et al.European journal of clinical investigation. 1996, Vol 26, Num 4, pp 322-324, issn 0014-2972Article