Repetitive nerve stimulation and muscle membrane excitability: case report and reviewSCAIOLI, V; MORANDI, L.Electromyography and clinical neurophysiology. 2002, Vol 42, Num 6, pp 333-336, issn 0301-150X, 4 p.Article

Low bone density and bone metabolism alterations in Duchenne muscular dystrophy: response to calcium and vitamin D treatmentBIANCHI, M. L; MORANDI, L; ANDREUCCI, E et al.Osteoporosis international. 2011, Vol 22, Num 2, pp 529-539, issn 0937-941X, 11 p.Article

Atypical cutaneous mycobacteriosis diagnosed by polymerase chain reactionCOLLINA, G; MORANDI, L; LANZONI, A et al.British journal of dermatology (1951). 2002, Vol 147, Num 4, pp 781-784, issn 0007-0963, 4 p.Article

X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sampleMORA, M; CARTEGNI, L; DONATI, M. A et al.Annals of neurology. 1997, Vol 42, Num 2, pp 249-253, issn 0364-5134Article

Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the diseaseBIONE, S; SMALL, K; TONIOLO, D et al.Human molecular genetics (Print). 1995, Vol 4, Num 10, pp 1859-1863, issn 0964-6906Article

Dystrophin analysis in Duchenne and Becker muscular dystrophy carriers : correlation with intracellular calcium and albuminMORANDI, L; MORA, M; GUSSONI, E et al.Annals of neurology. 1990, Vol 28, Num 5, pp 674-679, issn 0364-5134, 6 p.Article

The neurotrophin receptor p75NTR is induced on mature myofibres in inflammatory myopathies and promotes myotube survival to inflammatory stressCOLOMBO, E; ROMAGGI, S; BLASEVICH, F et al.Neuropathology and applied neurobiology (Print). 2012, Vol 38, Num 4, pp 367-378, issn 0305-1846, 12 p.Article

Clinical correlations in 16 patients with total or partial laminin α2 deficiency characterized using antibodies against 2 fragments of the proteinMORANDI, L; DI BLASI, C; CORNELIO, F et al.Archives of neurology (Chicago). 1999, Vol 56, Num 2, pp 209-215, issn 0003-9942Article

A new non-radioactive method for the screening and prenatal diagnosis of myotonic dystrophy patientsBRUGNONI, R; MORANDI, L; BRAMBATI, B et al.Journal of neurology. 1998, Vol 245, Num 5, pp 289-293, issn 0340-5354Article

Fetus-like dystrophin expression and other cytoskeletal protein abnormalities in centronuclear myopathiesMORA, M; MORANDI, L; CORNELIO, F et al.Muscle & nerve. 1994, Vol 17, Num 10, pp 1176-1184, issn 0148-639XArticle

Content of methylhistidines in normal and pathological human skeletal musclesMUSSINI, E; CORNELIO, F; DWORZAK, F et al.Muscle & nerve. 1983, Vol 6, Num 6, pp 423-429, issn 0148-639XArticle

Novel POMGNT1 point mutations and intragenic rearrangements associated with muscle-eye-brain diseaseSAREDI, S; ARDISSONE, A; MORANDI, L et al.Journal of the neurological sciences. 2012, Vol 318, Num 1-2, pp 45-50, issn 0022-510X, 6 p.Article

Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV)BRUNO, C; VAN DIGGELEN, O. P; MORA, M et al.Neurology. 2004, Vol 63, Num 6, pp 1053-1058, issn 0028-3878, 6 p.Article

Fibrinogen storage disease without hypofibrinogenaemia associated with acute infectionMARUCCI, G; MORANDI, L; MACCHIA, S et al.Histopathology. 2003, Vol 42, Num 1, pp 22-25, issn 0309-0167, 4 p.Article

Dystrophin characterization in BMD patients : correlation of abnormal protein with clinical phenotypeMORANDI, L; MORA, M; BALESTRINI, M. R et al.Journal of the neurological sciences. 1995, Vol 132, Num 2, pp 146-155, issn 0022-510XArticle

Late-onset riboflavin-responsive myopathy with combined multiple acyl coenzyme A dehydrogenase and respiratory chain deficiencyANTOZZI, C; GARAVAGLIA, B; MORA, M et al.Neurology. 1994, Vol 44, Num 11, pp 2153-2158, issn 0028-3878Article

Dystrophin abnormalities in Duchenne and Becker dystrophy carriers : correlation with cytoskeletal proteins and myosinsMORA, M; MORANDI, L; PICCINELLI, A et al.Journal of neurology. 1993, Vol 240, Num 8, pp 455-461, issn 0340-5354Article

Neurogenic muscle hypertrophyPAREYSON, D; MORANDI, L; SCAIOLI, V et al.Journal of neurology. 1989, Vol 236, Num 5, pp 292-295, issn 0340-5354Article

Cardiac transplantation in Becker muscular dystrophyCASAZZA, F; BRAMBILLA, G; SALVATO, A et al.Journal of neurology. 1988, Vol 235, Num 8, pp 496-498, issn 0340-5354Article

Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybridsRONCUZZI, L; FADDA, S; ROMEO, G et al.American journal of human genetics. 1985, Vol 37, Num 2, pp 407-417, issn 0002-9297Article

Risk of arrhythmia in type I myotonic dystrophy: the role of clinical and genetic variablesCUDIA, P; BERNASCONI, P; PALLADINO, A et al.Journal of neurology, neurosurgery and psychiatry. 2009, Vol 80, Num 7, pp 790-793, issn 0022-3050, 4 p.Article

Management and treatment of glycogenosis type IIBEMBI, B; CERINI, E; TOSCANO, A et al.Neurology. 2008, Vol 71, Num 23, issn 0028-3878, S12-S36, SUP2Conference Paper

Phenotypic clustering of lamin A/C mutations in neuromuscular patientsBENEDETTI, S; MENDITTO, I; MORANDI, L et al.Neurology. 2007, Vol 69, Num 12, pp 1285-1292, issn 0028-3878, 8 p.Article

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

Severe neonatal onset of glycogenosis type IV: Clinical and laboratory findings leading to diagnosis in two siblingsGIUFFRE, B; PARINI, R; RIZZWI, T et al.Journal of inherited metabolic disease. 2004, Vol 27, Num 5, pp 609-619, issn 0141-8955, 11 p.Article