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Angelini C Documents (Authors) Articles : A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy : The FSHD clinical score / Lamperti C ; Fabbri G ; Vercelli L ; d'Amico R ; Frusciante R ; Bonifazi E ; Fiorillo C ; Borsato C ; Cao M ; Servida M ; Greco F ; Di Leo R ; Volpi L ; Manzoli C ; Cudia P ; Pastorello E ; Ricciardi L ; Siciliano G ; Galluzzi G ; Rodolico C ; Santoro L ; Tomelleri G ; Angelini C ; Ricci E ; Palmucci L ; Moggio M ; Tupler R. Muscle and nerve, 2010. - 42, 2, p. 213-217 Articles : Italian validation of INQoL, a quality of life questionnaire for adults with muscle diseases / Sansone VA ; Panzeri M ; Montanari M ; Apolone G ; Gandossini S ; Rose MR ; Politano L ; Solimene C ; Siciliano G ; Volpi L ; Angelini C ; Palmieri A ; Toscano A ; Musumeci O ; Mongini T ; Vercelli L ; Massa R ; Panico MB ; Grandi M ; Meola G. European journal of neurology, 2010. - 17, 9, p. 1178-1187 Articles : Normal myogenesis and increased apoptosis in myotonic dystrophy type-1 muscle cells / Loro E ; Rinaldi F ; Malena A ; Masiero E ; Novelli G ; Angelini C ; Romeo V ; Sandri M ; Botta A ; Vergani L. Cell death and differentiation, 2010. - 17, 8, p. 1315-1324 Articles : EFNS guidelines on the diagnostic approach to pauci- or asymptomatic hyperCKemia / Kyriakides T ; Angelini C ; Schaefer J ; Sacconi S ; Siciliano G ; Vilchez JJ ; Hilton-Jones D. European journal of neurology, 2010. - 17, 6, p. 767-773 Articles : Metabolic myopathies : the challenge of new treatments / Angelini C ; Semplicini C. Current opinion in pharmacology, 2010. - 10, 3, p. 338-345 Articles : Brain involvement in myotonic dystrophies : neuroimaging and neuropsychological comparative study in DM1 and DM2 / Romeo V ; Pegoraro E ; Ferrati C ; Squarzanti F ; Soraru G ; Palmieri A ; Zucchetta P ; Antunovic L ; Bonifazi E ; Novelli G ; Trevisan CP ; Ermani M ; Manara R ; Angelini C. Journal of neurology, 2010. - 257, 8, p. 1246-1255 Articles : The clinical course of calpainopathy (LGMD2A) and dysferlinopathy (LGMD2B) / Angelini C ; Nardetto L ; Borsato C ; Padoan R ; Fanin M ; Nascimbeni AC ; Tasca E. Neurological research, 2010. - 32, 1, p. 41-46 Articles : Muscular Dystrophy / Angelini C. Handbook of clinical neurology, 2009. - 95, 3rd series, chap 31, p. 477-488 Articles : Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathy / Sacconi S ; Trevisson E ; Salviati L ; Aymé S ; Rigal O ; Redondo AG ; Mancuso M ; Siciliano G ; Tonin P ; Angelini C ; Auré K ; Lombès A ; Desnuelle C. Neuromuscular disorders, 2009. - 20, 1, p. 44-48 Articles : Mitochondrial disorders of the nuclear genome / Angelini C ; Bello L ; Spinazzi M ; Ferrati C. Acta myologica, 2009. - XXVIII, 1, p. 16-23 Articles : Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes / Fanin M ; Nascimbeni AC ; Aurino S ; Tasca E ; Pegoraro E ; Nigro V ; Angelini C. Neurology, 2009. - 72, 16, p. 1432-1435 Articles : Facioscapulohumeral muscular dystrophy : epidemiological and molecular study in a north-east Italian population sample / Mostacciuolo ML ; Pastorello E ; Vazza G ; Miorin M ; Angelini C ; Tomelleri G ; Galluzzi G ; Trevisan CP. Clinical genetics, 2009. - Epub ahead of print 2009 Mar 23, p. 1-6 Articles : Risk of arrhythmia in type I myotonic dystrophy : the role of clinical and genetic variables / Cudia P ; Bernasconi P ; Chiodelli R ; Mangiola F ; Bellocci F ; Dello Russo A ; Angelini C ; Romeo V ; Melancini P ; Politano L ; Palladino A ; Nigro G ; Siciliano G ; Falorni M ; Bongiorni MG ; Falcone C ; Mantegazza R ; Morandi LO. Journal of neurology, neurosurgery and psychiatry, 2009. - 80, 7, p. 790-793 Articles : Muscle histopathology in myasthenia gravis with antibodies against MuSK and AChR / Martignago S ; Fanin M ; Albertini E ; Pegoraro E ; Angelini C. Neuropathology and applied neurobiology, 2009. - 35, 1, p. 103-110 Articles : How to tackle the diagnosis of limb-girdle muscular dystrophy 2A / Fanin M ; Nascimbeni AC ; Tasca E ; Angelini C. European journal of human genetics, 2009. - 17, 5, p. 598-603 Conferences : In vitro study of DM1 primary myotubes (Poster) / Loro E ; Botta A ; Catalli C ; Romeo V ; Rinaldi F ; Angelini C ; Vergani L. Neuromuscular disorders, 2008. - 18, 9-10, p. 798 Conferences : Nutritional recommendations for patients with glycogen storage disease Type II / Angelini C. Clinical Therapeutics, 2008. - 30, Suppl 1, p. S21 Articles : Preferential central nucleation of type 2 myofibers is an invariable feature of myotonic dystrophy type 2 / Pisani V ; Panico MB ; Terracciano C ; Bonifazi E ; Meola G ; Novelli G ; Bernardi G ; Angelini C ; Massa R. Muscle and nerve, 2008. - 38, 5, p. 1405-1411 Conferences : Inhibition of proteasome activity promotes the correct localization of disease-causing alpha-sarcoglycan mutants in a heterologous cell system expressing beta-, gamma-, and delta-sarcoglycan / Sandona D ; Gastaldello S ; Franzoso S ; Fanin M ; Angelini C ; Vidal J ; Basse N ; Reboud-Ravaux M ; Betto R. 2008. - p. 409 Conferences : Size and number of D4Z4 alleles play a role in FSHD phenotype (Poster) / Fabbri G ; Fiorillo C ; Borsato C ; Greco F ; Bonifazi E ; Vercelli L ; Palmucci L ; Tomelleri G ; Angelini C ; Santoro L ; Tupler R. Neuromuscular disorders, 2008. - 18, 9-10, p. 727 Conferences : A robust tool to quantify disability in patients affected by facioscapulohumeral muscular dystrophy (Poster) / Lamperti C ; Fabbri G ; Greco F ; Servida M ; Vercelli L ; Fiorillo C ; Borsato C ; Cao M ; Cudia P ; Frusciante R ; Di Leo R ; Volpi L ; d'Amico R ; Pastorello RE ; Ricciardi L ; Galluzzi G ; Siciliano G ; A. Muzio A ; D'Angelo G ; Rodolico C ; Morandi L ; Tomelleri G ; Trevisan C ; Angelini C ; Santoro L ; Ricci E ; Palmucci L ; Moggio M ; Tupler RG. Neuromuscular disorders, 2008. - 18, 9-10, p. 726 Articles : The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic dystrophy type 1 patients / Botta A ; Rinaldi F ; Catalli C ; Vergani L ; Bonifazi E ; Romeo V ; Loro E ; Viola A ; Angelini C ; Novelli G. Journal of medical genetics, 2008. - 45, 10, p. 639-646 Articles : Molecular pathology and enzyme processing in various phenotypes of acid maltase deficiency / Nascimbeni AC ; Fanin M ; Tasca E ; Angelini C. Neurology, 2008. - 70, 8, p. 617-626 Articles : Spinal and bulbar muscular atrophy : skeletal muscle pathology in male patients and heterozygous females / Soraru G ; D'Ascenzo C ; Polo A ; Palmieri A ; Baggio L ; Vergani L ; Gellera C ; Moretto G ; Pegoraro E ; Angelini C. Journal of the neurological sciences, 2008. - 264, 1-2, p. 100-105 Articles : Disorders of lipid metabolism / Mastaglia FL ; Hilton-Jones D ; Angelini C. Handbook of Clinical Neurology (Myopathie), 2007. - 86, 3rd series, chap. 8, p. 183-191 Articles : Facioscapulohumeral muscular dystrophy : a multicenter study on hearing function / Trevisan CP ; Pastorello E ; Ermani M ; Angelini C ; Tomelleri G ; Tonin P ; Mongini T ; Palmucci L ; Galluzzi G ; Tupler RG ; Marioni G ; Rimini A. Audiology and neuro-otology, 2007. - 13, p. 1-6 Articles : The role of corticosteroids in muscular dystrophy : a critical appraisal / Angelini C. Muscle and nerve, 2007. - 36, 4, p. 424-435 Articles : Risk prediction for clinical phenotype in myotonic dystrophy type 1 : data from 2,650 patients / Salehi LB ; Bonifazi E ; DI Stasio E ; Gennarelli M ; Botta A ; Vallo L ; Iraci R ; Massa R ; Antonini G ; Angelini C ; Novelli G. Genetic testing, 2007. - 11, 1, p. 84-90 Articles : Correlations between clinical severity, genotype and muscle pathology in LGMD2A / Fanin M ; Nardetto L ; Nascimbeni AC ; Tasca E ; Spinazzi M ; Padoan R ; Angelini C. Journal of medical genetics, 2007. - 44, 10, p. 609-614 Articles : MYH7 gene mutation in myosin storage myopathy and scapulo-peroneal myopathy / Pegoraro E ; Gavassini BF ; Borsato C ; Melacini P ; Vianello A ; Stramare R ; Cenacchi G ; Angelini C. Neuromuscular disorders, 2007. - 17, 4, p. 321-329 Articles : Screening of calpain-3 autolytic activity in LGMD muscle : a functional map of CAPN3 gene mutations / Fanin M ; Nascimbeni AC ; Angelini C. Journal of medical genetics, 2007. - 44, p. 38-43 Articles : High plasma creatine kinase : review of the literature and proposal for a diagnostic algorithm / Morandi L ; Angelini C ; Prelle A ; Pini A ; Grassi B ; Bernardi G ; Politano L ; Bruno C ; De Grandis D ; Cudia P ; Citterio A. Neurological sciences, 2006. - 27, 5, p. 303-311 Articles : Expression profiling characterization of laminin alpha-2 positive MDC / Millino C ; Bellin M ; Fanin M ; Romualdi C ; Pegoraro E ; Angelini C ; Lanfranchi G. Biochemical and biophysical research communications, 2006. - 350, 2, p. 345-351 Articles : Facioscapulohumeral muscular dystrophy and occurrence of heart arrhythmia / Trevisan CP ; Pastorello E ; Armani M ; Angelini C ; Nante G ; Tomelleri G ; Tonin P ; Mongini T ; Palmucci L ; Galluzzi G ; Tupler RG ; Barchitta A. European neurology, 2006. - 56, 1, p. 1-5 Articles : The glucocorticoid receptor N363S polymorphism and steroid response in Duchenne dystrophy / Bonifati DM ; Witchel SF ; Ermani M ; Hoffman EP ; Angelini C ; Pegoraro E. Journal of neurology, neurosurgery and psychiatry, 2006. - 77, 10, p. 1177-1179 Articles : Identification of 45 novel mutations in the nebulin gene associated with autosomal recessive nemaline myopathy / Lehtokari VL ; Pelin K ; Sandbacka M ; Ranta S ; Donner K ; Muntoni F ; Sewry C ; Angelini C ; Bushby K ; van den Bergh P ; Iannaccone S ; Laing NG ; Wallgren-Pettersson C. Human mutation, 2006. - 27, 9, p. 946-956 Articles : McArdle disease : The mutation spectrum of PYGM in a large Italian cohort / Bruno C ; Cassandrini D ; Martinuzzi A ; Toscano A ; Moggio M ; Morandi L ; Servidei S ; Mongini T ; Angelini C ; Musumeci O ; Comi GP ; Lamperti C ; Filosto M ; Zara F ; Minetti C. Human mutation, 2006. - 27, 7, p. 718 Conferences : Neuronal nitric oxide synthase (nNOS) activity and ultrastructural changes in caveolin-3 deficient muscle cause mechanical irritability (Abstract in 58th Annual Meeting of American Academy of Neurology) / Angelini C ; Fulizio L ; Nascimbeni AC ; Fanin M ; Cennacchi G. Neurology, 2006. - 66, 5, Suppl 2, p. A362 Conferences : Clinical and pathological findings in families with X-linked spinal and bulbar muscular atrophy (Kennedy's disease) (Abstract in 58th Annual Meeting of American Academy of Neurology) / Angelini C ; D'Ascenzo C ; Polo A ; Baggio L ; Palmieri A ; Vergani L ; Soraru G. Neurology, 2006. - 66, 5, Suppl 2, p. A136 Articles : Generalized lysosome-associated membrane protein-2 defect explains multisystem clinical involvement and allows leukocyte diagnostic screening in Danon disease / Fanin M ; Nascimbeni AC ; Fulizio L ; Spinazzi M ; Melacini P ; Angelini C. American journal of pathology, 2006. - 168, 4, p. 1309-1320 Articles : Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration / Bakay M ; Wang Z ; Melcon G ; Schiltz L ; Xuan J ; Zhao P ; Sartorelli V ; Seo J ; Pegoraro E ; Angelini C ; Shneiderman B ; Escolar D ; Chen YW ; Winokur ST ; Pachman LM ; Fan C ; Mandler R ; Nevo Y ; Gordon E ; Zhu Y ; Dong Y ; Wang Y ; Hoffman EP. Brain, 2006. - 129, 4, p. 996-1013 Conferences : Development and validation of SOLE, a new instrument for measuring quality of life in children with neuromuscular disorders : preliminary results (abstract : congrès international de Myologie, 2005) / Orcesi S ; Rossi M ; Gorni K ; Berardinelli A ; Beghi E ; Angelini C ; Bertini E ; Pini A ; Palmucci L ; Mercuri E ; Lanzi G. 2005. - p. 304 Articles : Clinical and molecular characterization of patients with limb-girdle muscular dystrophy type 2I / Boito C ; Melacini P ; Vianello A ; Prandini P ; Gavassini BF ; Bagattin A ; Siciliano G ; Angelini C ; Pegoraro E. Archives of neurology, 2005. - 62, 12, p. 1894-1899 Articles : Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes / Piluso G ; Politano L ; Aurino S ; Fanin M ; Ricci E ; Ventriglia VM ; Belsito A ; Totaro A ; Saccone V ; Topaloglu H ; Nascimbeni AC ; Fulizio L ; Broccolini A ; Canki-Klain N ; Comi LI ; Nigro G ; Angelini C ; Nigro V. Journal of medical genetics, 2005. - 42, p. 686-693 Articles : Dominant LMNA mutations can cause combined muscular dystrophy and peripheral neuropathy / Benedetti S ; Bertini E ; Iannaccone S ; Angelini C ; Trisciani M ; Toniolo D ; Sferrazza B ; Carrera P ; Comi G ; Ferrari M ; Quattrini A ; Previtali SC. Journal of neurology, neurosurgery and psychiatry, 2005. - 76, 7, p. 1019-1021 Articles : Muscle MRI findings in patients with limb girdle muscular dystrophy with calpain 3 deficiency (LGMD2A) and early contractures / Mercuri E ; Bushby K ; Ricci E ; Birchall D ; Pane M ; Kinali M ; Allsop J ; Nigro V ; Saenz A ; Nascimbeni A ; Fulizio L ; Angelini C ; Muntoni F. Neuromuscular disorders, 2005. - 15, 2, p. 164-171 Articles : Ultrastructural changes in dysferlinopathy support defective membrane repair mechanism / Cenacchi G ; Fanin M ; De Giorgi LB ; Angelini C. Journal of clinical pathology, 2005. - 58, 2, p. 190-195 Articles : Molecular and muscle pathology in a series of caveolinopathy patients / Fulizio L ; Chiara Nascimbeni A ; Fanin M ; Piluso G ; Politano L ; Nigro V ; Angelini C. Human mutation, 2005. - 25, p. 82-89 Articles : Correlating phenotype and genotype in the periodic paralyses / Miller TM ; Dias Da Silva MR ; Miller HA ; Kwiecinski H ; Mendell JR ; Tawil R ; McManis P ; Griggs RC ; Angelini C ; Servidei S ; Petajan J ; Dalakas MC ; Ranum LPW ; Fu YH ; Ptacek LJ. Neurology, 2004. - 63, 9, p. 1647-1655 Articles : LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophy / Prandini P ; Berardinelli A ; Fanin M ; Morello F ; Zardini E ; Pichiecchio A ; Uggetti C ; Lanzi G ; Angelini C ; Pegoraro E. Neurology, 2004. - 63, 6, p. 1118-1121 Articles : Molecular diagnosis in LGMD2A : mutation analysis or protein testing ? / Fanin M ; Fulizio L ; Nascimbeni AC ; Spinazzi M ; Piluso G ; Ventriglia VM ; Ruzza G ; Siciliano G ; Trevisan CP ; Politano L ; Nigro V ; Angelini C. Human mutation, 2004. - 24, 1, p. 52-62 Articles : Motor function-muscle strength relationship in spinal muscular atrophy / Merlini L ; Bertini E ; Minetti C ; Mongini T ; Morandi L ; Angelini C ; Vita G. Muscle and nerve, 2004. - 29, 4, p. 548-552 Articles : Morphological changes in late onset acid maltase deficient patients with splicing gene mutation / Angelini C ; Cenacchi G ; Nascimbeni AC ; Fulizio L. Acta myologica, 2003. - XXII, p. 90-96 Articles : Role of gabapentin in spinal muscular atrophy : results of a multicenter, randomized Italian study / Merlini L ; Solari A ; Vita G ; Bertini E ; Minetti C ; Mongini T ; Mazzoni E ; Angelini C ; Morandi L. Journal of child neurology, 2003. - 18, p. 537-541 Articles : Loss of calpain-3 autocatalytic activity in LGMD2A patients with normal protein expression / Fanin M ; Chiara Nascimbeni A ; Fulizio L ; Trevisan CP ; Meznaric-Petrusa M ; Angelini C. American journal of pathology, 2003. - 163, 5, p. 1929-1936 Articles : Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha2 (LAMA2) deficiency / Tezak Z ; Prandini P ; Boscaro M ; Marin A ; Devaney JM ; Marino M ; Fanin M ; Trevisan CP ; Park J ; Tyson W ; Finkel RS ; Garcia C ; Angelini C ; Hoffman EP ; Pegoraro E. Human mutation, 2003. - 21, 2, p. 103-111 Articles : Advances and perspectives in muscular dystrophies / Angelini C. Basic applied myology, 2002. - 12,1, p. 17-25 Articles : Defective assembly of sarcoglycan complex in patients with Beta-sarcoglycan gene mutations. Study of aneural and innervated cultured myotubes / Fanin M ; Angelini C. Neuropathology and applied neurobiology, 2002. - 28, p. 190-199 Articles : Muscle pathology in dysferlin deficiency / Fanin M ; Angelini C. Neuropathology and applied neurobiology, 2002. - 28, p. 461-470 Articles : Molecular update and therapeutic trials in muscle disorders of glycogen and lipid metabolism / Angelini C. Acta myologica, 2002. - 21, p. 51 Articles : Epidemiology of myotonic dystrophy in Italy : re-apprisal after genetic diagnosis / Siciliano G ; Manca ML ; Gennarelli M ; Angelini C ; Rocchi A ; Iudice A ; Miorin M ; Mostacciuolo ML. Clinical genetics, 2001. - 59, p. 344-349 Articles : Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy / Aoki M ; Liu J ; Richard I ; Bashir R ; Britton S ; Keers SM ; Oeltjen J ; Brown HEV ; Marchand S ; Bourg N ; Beley C ; McKenna-Yasek D ; Arahata K ; Bohlega S ; Cupler EJ ; Illa I ; Majneh I ; Barohn RJ ; Urtizberea JA ; Fardeau M ; Amato AA ; Angelini C ; Bushby K ; Beckmann JS ; Brown RH Jr. Neurology, 2001. - 57, p. 271-278 Articles : Heart transplantation in patients with inherited myopathies associated with end-stage cardiomyopathy : Molecular and biochemical defects on cardiac and skeletal muscle / Melacini P ; Gambino A ; Caforio AL ; Barchitta A ; Valente ML ; Angelini A ; Fanin M ; Thiene G ; Angelini C ; Casarotto D ; Danieli GA ; Dalla Volta S. Transplantation proceedings, 2001. - 33, 1-2, p. 1596-1599 Articles : Caspase 3 expression correlates with skeletal muscle apoptosis in Duchenne and Facioscapulo human muscular dystrophy. A potential target for pharmacological treatment / Sandri M ; El Meslemani AH ; Sandri C ; Schjerling P ; Vissing K ; Andersen JL ; Rossini K ; Carraro U ; Angelini C. Journal of neuropathology and experimental neurology, 2001. - 60, 3, p. 302-312 Articles : Calpain-3 and dysferlin protein screening in patients with limb-girdle dystrophy and myopathy / Fanin M ; Pegoraro E ; Matsuda-Asada C ; Brown RH Jr ; Angelini C. Neurology, 2001. - 56, p. 660-665 Articles : New therapies in muscular dystrophies / Angelini C ; Bonifati DM. Neurological sciences, 2000. - 21, 5, p. S919-S924 Articles : Distal Myopathies / Angelini C ; Fanin M ; Vlak M ; Padovan R. Acta myologica, 2000. - XIX, p. 221-225 Articles : A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophy / Pegoraro E ; Fanin M ; Trevisan CP ; Angelini C ; Hoffman EP. Neurology, 2000. - 55, 8, p. 1128-1134 Articles : A multicenter, double-blind, randomized trial of Deflazacort versus Prednisone in Duchenne muscular dystrophy / Bonifati MD ; Ruzza G ; Bonometto PP ; Berardinelli A ; Gorni K ; Orcesi S ; Lanzi G ; Angelini C. Muscle and nerve, 2000. - 23, 9, p. 1344-1347 Articles : Cognitive impairment and (CTG)n expansion in myotonic dystrophy patients / Perini GI ; Menegazzo E ; Ermani M ; Zara M ; Gemma A ; Ferruzza E ; Gennarelli M ; Angelini C. Biological psychiatry, 1999. - 46, p. 425-431 Articles : Could utrophin rescue the myocardium of patients with dystrophin gene mutations ? / Fanin M ; Melacini P ; Angelini C ; Danieli GA. Journal of molecular and cellular cardiology, 1999. - 31, 8, p. 1501-1508 Articles : Regeneration in sarcoglycanopathies : expression studies of sarcoglycans and other muscle proteins / Fanin M ; Angelini C. Journal of the neurological sciences, 1999. - 165, 2, p. 170-177 Articles : Clinical and neuroimaging study of central nervous system in congenital myotonic dystrophy / Martinello F ; Piazza A ; Pastorello E ; Angelini C ; Trevisan CP. Journal of neurology, 1999. - 246, 3, p. 186-192 Articles : The clinical spectrum of sarcoglycanopathies / Angelini C ; Fanin M ; Freda MP ; Duggan DJ ; Siciliano G ; Hoffman EP. Neurology, 1999. - 52, p. 176-179 Articles : Calpain III mutation analysis of a heterogeneous limb-girdle muscular dystrophy population / Chou FL ; Angelini C ; Daentl D ; Garcia C ; Greco C ; Hausmanowa-Petrusewicz I ; Fidzianska A ; Wessel H ; Hoffman EP. Neurology, 1999. - 52, 5, p. 1015-1020 Articles : Heart involvement in muscular dystrophies due to sarcoglycan gene mutations / Melacini P ; Fanin M ; Duggan DJ ; Freda MP ; Berardinelli A ; Danieli GA ; Barchitta A ; Hoffman EP ; Dalla Volta S ; Angelini C. Muscle and nerve, 1999. - 22, 4, p. 473-479 Articles : Fours years od steroid treatment in Duchenne muscular dystrophy / Bonifati DM ; Bonometto PP ; Ruzza GP ; Angelini C. Neuromuscular disorders, 1998. - 8, 3, p. 267 Articles : Cardiac transplantation in a Duchenne muscular dystrophy carrier / Melacini P ; Fanin M ; Angelini A ; Pegoraro E ; Livi U ; Danieli GA ; Hoffman EP ; Thiene G ; Dalla Volta S ; Angelini C. Neuromuscular disorders, 1998. - 8, 8, p. 585-590 Articles : Clinical features and laboratory findings of patients with proximal myotonic myopathy (PROMM) in Italy : analysis of 50 patients / Meola G ; Sansone V ; Rotondo G ; Nobile-Orazio E ; Mongini T ; Angelini C ; Toscano A. Muscle and nerve, 1998. - Suppl 7, p. s157 Articles : Sarcoglycanopathies are rare disorders : experience with steroid treatments / Angelini C ; Fanin M ; Pegora E ; Menegazzo E ; Ruzza GP. Neuromuscular disorders, 1998. - 8, 3, p.272 Articles : Congenital muscular dystrophy with partial merosin deficiency and late onset epilepsy / Martinello F ; Angelini C ; Trevisan CP. Neurology, 1998. - 40, p. 37-45 Articles : Laminin alpha-2 muscular dystrophy. Genotype/phenotype studies of 22 patients / Pegoraro E ; Marks H ; Garcia CA ; Crawford T ; Mancias P ; Connolly AM ; Fanin M ; Martinello F ; Trevisan CP ; Angelini C ; Stella A ; Munk RL ; Servidei S ; Bonnemann CC ; Bertorini T ; Acsadi G ; Thompson CE ; Gagnon D ; Hoganson G ; Carver V ; Zimmerman RA ; Hoffman EP ; Scavina M. Neurology, 1998. - 51, p. 101-110 Articles : Steroids in the management of duchenne (DMD) and lim-girdle muscular dystrophy (LGMD2D) / Angelini C ; Bonifati DM ; Ruzza G ; Ermani M. Muscle and nerve, 1998. - Suppl 7, p. s71 Articles : Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy / Liu J ; Aoki M ; Illa I ; Wu C ; Fardeau M ; Angelini C ; Serrano C ; Urtizberea JA ; Hentati F ; Ben Hamida M ; Bohlega S ; Culper EJ ; Amato AA ; Bossie K ; Oeltjen J ; McKenna-Yasek D ; Hosler BA ; Schurr E ; Arahata K ; De Jong PJ ; Brown RH Jr ; Bejaoui K. Nature genetics, 1998. - 20, p. 31-36 Articles : Steroids in muscular dystrophy : where do we stand ? / Dubrovsky AL ; Angelini C ; Bonifati DM ; Pegoraro E ; Mesa L. Neuromuscular disorders, 1998. - 8, 6, p. 380-384 Articles : Homozygous alpha sarcoglycan mutation in two siblings : one asymptomatic and one steroid responsive mild limb girdle muscular dystrophy patient / Angelini C ; Fanin M ; Menegazzo E ; Freda MP ; Duggan DJ ; Hoffman EP. Muscle and nerve, 1998. - 21, 6, p. 769-775 Articles : Prognostic factors in mild dystrophinopathies / Angelini C ; Fanin M ; Freda MP ; Martinello F ; Miorin M ; Melacini P ; Siciliano G ; Pegoraro E ; Rosa M ; Danieli GA. Journal of the neurological sciences, 1996. - 142, p. 70-78 Articles : Correlation between muscle atrophy, male hypogonadism and DNA expansion in myotonic dystrophy / Menegazzo E ; Mastrogiacomo I ; Bonanni G ; Pagani E ; Santarossa C ; Novell G ; Angelini C. Acta cardiomiologica, 1995. - 1, p. 25-33 Articles : Deflazacort in Duchenne dystrophy : study of long-term effect / Angelini C ; Pegoraro E ; Turella E ; Intino MT ; Pini A ; Costa C. Muscle and nerve, 1994. - 17, p. 386-391 Articles : Enormous dystrophin in a patient with Becker muscular dystrophy / Angelini C ; Beggs AH ; Hoffman EP ; Fanin M ; Kunkel LM. Neurology, 1990. - 40, 5, p. 808-812 Articles : Improved diagnosis of Becker muscular dystrophy by dystrophin testing / Hoffman EP ; Kunkel LM ; Angelini C ; Clarke A ; Johnson M ; Harris JB. Neurology, 1989. - 39, 8, p. 1011-1017 Articles : Psychiatric disturbances associated with myasthenia gravis / Magni G ; Micaglio GF ; Lalli R ; Bejato L ; Candeago MR ; Merskey H ; Angelini C. Acta psychiatrica Scandinavica, 1988. - 77, 4, p. 443-445 Articles : Quantitative histopathology in congenital myopathies / Micaglio G ; Ceccato MB ; Trevisan C ; Angelini C. Rivista di neurologia, 1987. - 57, 4, p. 261-268 Articles : Guanidine hydrochloride in infantile and juvenile spinal muscular atrophy. A double blind controlled study / Angelini C ; Micaglio GF ; Trevisan C. Acta neurologica, 1980. - 2, 6, p. 460-465

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