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 method for myofibrillar Ca⁺⁺-ATPase reaction based on the use of metachromatic dyes: its advantages in muscle fibre typingDORIGUZZI, C; MONGINI, T; PALMUCCI, L et al.Histochemistry (Berlin). 1983, Vol 79, Num 3, pp 289-294, issn 0301-5564Article

LA DISTROFIA MUSCOLARE PROGRESSIVA TIPO DUCHENNE. EPIDEMIOLOGIA E STRATEGIA DI PREVENTIONE = LA DYSTROPHIE MUSCULAIRE PROGRESSIVE DE TYPE DUCHENNE. EPIDEMIOLOGIE ET STRATEGIE DE PREVENTIONDORIGUZZI C; BERTOLOTTO A; MONGINI T et al.1980; MINERVA MED.; ISSN 0026-4806; ITA; DA. 1980; VOL. 71; NO 33; PP. 2337-2344; BIBL. 127 REF.Article

Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 yearsANGELINI, C; SEMPLICINI, C; TONIN, P et al.Journal of neurology. 2012, Vol 259, Num 5, pp 952-958, issn 0340-5354, 7 p.Article

Clinical spectrum of McArdle disease : three cases with unusual expressionCHIADO-PIAT, L; MONGINI, T; DORIGUZZI, C et al.European neurology. 1993, Vol 33, Num 3, pp 208-211, issn 0014-3022Article

Congenital muscular dystrophy associated with familial junctional epidermolysis bullosa letalisDORIGUZZI, C; PALMUCCI, L; MONGINI, T et al.European neurology. 1993, Vol 33, Num 6, pp 454-460, issn 0014-3022Article

Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiencyDORIGUZZI, C; PALMUCCI, L; MONGINI, T et al.Journal of neurology, neurosurgery and psychiatry. 1989, Vol 52, Num 1, pp 122-125, issn 0022-3050Article

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

Congenital muscular dystrophies with cognitive impairment: A population studyMESSINA, S; BRUNO, C; MINETTI, C et al.Neurology. 2010, Vol 75, Num 10, pp 898-903, issn 0028-3878, 6 p.Article

Congenital muscular dystrophies with defective glycosylation of dystroglycan: A population studyMERCURI, E; MESSINA, S; BOFFI, P et al.Neurology. 2009, Vol 72, Num 21, pp 1802-1809, issn 0028-3878, 8 p.Article

Dystrophinopathy expressing as either cardiomyopathy or Becker dystrophy in the same familyPALMUCCI, L; MONGINI, T; CHIADO-PIAT, L et al.Neurology. 2000, Vol 54, Num 2, pp 529-530, issn 0028-3878Article

Unusual expression and very mild course of Xp21 muscular dystrophy (Becker type) in a 60-year-old man with 26 percent deletion at the dystrophin genePALMUCCI, L; DORIGUZZI, C; MONGINI, T et al.Neurology. 1994, Vol 44, Num 3, pp 541-543, issn 0028-3878, 1Article

Malformation cérébrale associée à des défauts de fermeture du tube neural. 3 cas d'agénésie partielle du corps calleux avec myélémeningocèle = Brain malformation associated with neural tube effects. Report of 3 cases of partial agenesie of the corpus callosum and myelomeningoceleRUGGIERO, R; MONGINI, T; COLANGELO, M et al.Journal of neuroradiology. 1987, Vol 14, Num 3, pp 287-292, issn 0150-9861Article

Immunohistochemical localization of chondroitin sulfate in normal and pathological human muscleBERTOLOTTO, A; PALMUCCI, L; GAGLIANO, A et al.Journal of the neurological sciences. 1986, Vol 73, Num 3, pp 233-244, issn 0022-510XArticle