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Marina Fanin

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Annalaura Torella; Corrado Angelini; Francesca Del Vecchio Blanco; Marina Fanin; Arcomaria Garofalo; Lucia Morandi; Margherita Mutarelli; Enrico Peterle; Giulio Piluso; Giulia Ricci; Rossella Rispoli; Marco Savarese; Gabriele Siciliano; Vincenzo Nigro
Next-Generation Sequencing Identifies Transportin 3 as the Causative Gene for LGMD1F.
Anna Chiara Nascimbeni; Corrado Angelini; Marina Fanin; Eva Masiero; Marco Sandri
Impaired autophagy contributes to muscle atrophy in glycogen storage disease type II patients.
Anna Chiara Nascimbeni; Corrado Angelini; Marina Fanin; E Masiero; Marco Sandri
The role of autophagy in the pathogenesis of glycogen storage disease type II (GSDII).

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All Publications

2013: Annalaura Torella; Corrado Angelini; Francesca Del Vecchio Blanco; Marina Fanin; Arcomaria Garofalo; Lucia Morandi; Margherita Mutarelli; Enrico Peterle; Giulio Piluso; Giulia Ricci; Rossella Rispoli; Marco Savarese; Gabriele Siciliano; Vincenzo Nigro
Next-Generation Sequencing Identifies Transportin 3 as the Causative Gene for LGMD1F.
PloS one 2013;8(5):e63536.
2012: Anna Chiara Nascimbeni; Corrado Angelini; Marina Fanin; Eva Masiero; Marco Sandri
Impaired autophagy contributes to muscle atrophy in glycogen storage disease type II patients.
Autophagy 2012;8(11):1697-700.
2012: Anna Chiara Nascimbeni; Corrado Angelini; Marina Fanin; E Masiero; Marco Sandri
The role of autophagy in the pathogenesis of glycogen storage disease type II (GSDII).
Cell death and differentiation 2012;19(10):1698-708.
2012: Luisa Piva; Gianni Soraru; Corrado Angelini; Andrea Barp; Luca Bello; Mario Ermani; Marina Fanin; Bruno F Gavassini; Eric P Hoffman; Elena Pegoraro
TGFBR2 but not SPP1 genotype modulates osteopontin expression in Duchenne muscular dystrophy muscle.
The Journal of pathology 2012;228(2):251-9.
2012: Giulia Ricci; Isabella Scionti; Rossella Tupler; Leda Volpi; Virna Zampa; Greta Alì; Corrado Angelini; Marina Fanin; Luisa Politano; Gabriele Siciliano
Rippling muscle disease and facioscapulohumeral dystrophy-like phenotype in a patient carrying a heterozygous CAV3 T78M mutation and a D4Z4 partial deletion: Further evidence for "double trouble" overlapping syndromes.
Neuromuscular disorders : NMD 2012;22(6):534-40.
2011: Mafalda Cacciottolo; Imma Rosaria Caserta; Marina Fanin; Carlo Minetti; Gelsomina Numitone; Giulio Piluso; Luisa Politano; Enzo Ricci; Corrado Angelini; Stefania Aurino; Vincenzo Nigro
Muscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutations.
European journal of human genetics : EJHG 2011;19(9):974-80.
2011: Angelica Anichini; Marina Fanin; Christine Vianey-Saban; Denise Cassandrini; Chiara Fiorillo; Claudio Bruno; Corrado Angelini
Genotype-phenotype correlations in a large series of patients with muscle type CPT II deficiency.
Neurological research 2011;33(1):24-32.
2010: Valentina Papa; Lucia Tarantino; Paola Preda; Lucilla Badiali De Giorgi; Marina Fanin; Elena Pegoraro; Corrado Angelini; Giovanna Cenacchi
The role of ultrastructural examination in storage diseases.
Ultrastructural pathology 2010;34(5):243-51.
2010: Anna Chiara Nascimbeni; Marina Fanin; Elisabetta Tasca; Corrado Angelini
Transcriptional and translational effects of intronic CAPN3 gene mutations.
Human mutation 2010;31(9):E1658-69.
2010: Corrado Angelini; L Nardetto; C Borsato; R Padoan; Marina Fanin; Anna Chiara Nascimbeni; E Tasca
The clinical course of calpainopathy (LGMD2A) and dysferlinopathy (LGMD2B).
Neurological research 2010;32(1):41-6.
2009: Sergio Salvatori; Sandra Furlan; Marina Fanin; Anne Picard; Ebe Pastorello; Vincenzo Romeo; Carlo Pietro Trevisan; Corrado Angelini
Comparative transcriptional and biochemical studies in muscle of myotonic dystrophies (DM1 and DM2).
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2009;30(3):185-92.
2009: Corrado Angelini; Claudio Semplicini; Paola Tonin; Massimiliano Filosto; Elena Pegoraro; Gianni Soraru; Marina Fanin
Progress in Enzyme Replacement Therapy in Glycogen Storage Disease Type II.
Therapeutic advances in neurological disorders 2009;2(3):143-53.
2009: Marina Fanin; Anna Chiara Nascimbeni; Elisabetta Tasca; Corrado Angelini
How to tackle the diagnosis of limb-girdle muscular dystrophy 2A.
European journal of human genetics : EJHG 2009;17(5):598-603.
2009: Marina Fanin; Anna Chiara Nascimbeni; S Aurino; E Tasca; Elena Pegoraro; Vincenzo Nigro; Corrado Angelini
Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes.
Neurology 2009;72(16):1432-5.
2009: Marina Fanin; Elisabetta Tasca; Anna Chiara Nascimbeni; Corrado Angelini
Sarcolemmal neuronal nitric oxide synthase defect in limb-girdle muscular dystrophy: an adverse modulating factor in the disease course?
Journal of neuropathology and experimental neurology 2009;68(4):383-90.
2009: S Martignago; Marina Fanin; E Albertini; Elena Pegoraro; Corrado Angelini
Muscle histopathology in myasthenia gravis with antibodies against MuSK and AChR.
Neuropathology and applied neurobiology 2009;35(1):103-10.
2009: Caterina Millino; Marina Fanin; Andrea Vettori; Paolo Laveder; Maria Luisa Mostacciuolo; Corrado Angelini; Gerolamo Lanfranchi
Different atrophy-hypertrophy transcription pathways in muscles affected by severe and mild spinal muscular atrophy.
BMC medicine 2009;7():14.
2008: Elena Pegoraro; C Borsato; Federico Dal Bello; Roberto Stramare; Marina Fanin; Giorgio Palu; Corrado Angelini
Sphingomonas paucimobilis associated with localised calf myositis.
Journal of neurology, neurosurgery, and psychiatry 2008;79(10):1194-5.
2008: Stefano Gastaldello; Simona D'Angelo; Susanna Franzoso; Marina Fanin; Corrado Angelini; Romeo Betto; Dorianna Sandonà
Inhibition of proteasome activity promotes the correct localization of disease-causing alpha-sarcoglycan mutants in HEK-293 cells constitutively expressing beta-, gamma-, and delta-sarcoglycan.
The American journal of pathology 2008;173(1):170-81.
2008: Anna Chiara Nascimbeni; Marina Fanin; Elisabetta Tasca; Corrado Angelini
Molecular pathology and enzyme processing in various phenotypes of acid maltase deficiency.
Neurology 2008;70(8):617-26.
2007: Chiara A Boito; Marina Fanin; Bruno F Gavassini; Giovanna Cenacchi; Corrado Angelini; Elena Pegoraro
Biochemical and ultrastructural evidence of endoplasmic reticulum stress in LGMD2I.
Virchows Archiv : an international journal of pathology 2007;451(6):1047-55.
2007: Marina Fanin; L Nardetto; Anna Chiara Nascimbeni; E Tasca; Marco Spinazzi; R Padoan; Corrado Angelini
Correlations between clinical severity, genotype and muscle pathology in limb girdle muscular dystrophy type 2A.
Journal of medical genetics 2007;44(10):609-14.
2007: Nina Barisić; Jasminka Jakić-Razumović; Miroslav Harjacek; Marina Fanin; Hanns Lochmüller; Ivan Lehman; Corrado Angelini
Childhood dermatomyositis associated with intracranial tumor and liver cysts.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2007;11(2):76-80.
2007: Marina Fanin; Anna Chiara Nascimbeni; Corrado Angelini
Screening of calpain-3 autolytic activity in LGMD muscle: a functional map of CAPN3 gene mutations.
Journal of medical genetics 2007;44(1):38-43.
2006: Caterina Millino; Milena Bellin; Marina Fanin; Chiara Romualdi; Elena Pegoraro; Corrado Angelini; Gerolamo Lanfranchi
Expression profiling characterization of laminin alpha-2 positive MDC.
Biochemical and biophysical research communications 2006;350(2):345-51.
2006: Marina Fanin; Anna Chiara Nascimbeni; Corrado Angelini
Muscle protein analysis in the detection of heterozygotes for recessive limb girdle muscular dystrophy type 2B and 2E.
Neuromuscular disorders : NMD 2006;16(11):792-9.
2006: Chiara Pizzanelli; Michelangelo Mancuso; Renato Galli; Anna Choub; Marina Fanin; Anna Chiara Nascimbeni; Gabriele Siciliano; Luigi Murri
Epilepsy and limb girdle muscular dystrophy type 2A: double trouble, serendipitous finding or new phenotype?
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2006;27(2):134-6.
2006: Marina Fanin; Anna Chiara Nascimbeni; Luigi Fulizio; Marco Spinazzi; Paola Melacini; Corrado Angelini
Generalized lysosome-associated membrane protein-2 defect explains multisystem clinical involvement and allows leukocyte diagnostic screening in Danon disease.
The American journal of pathology 2006;168(4):1309-20.
2006: Roberta Lanzillo; Stefania Aurino; Marina Fanin; M Aguennoz; F Vitale; Chiara Fiorillo; Emanuele Miraglia del Giudice; Vincenzo Nigro; Lucio Santoro
Early onset calpainopathy with normal non-functional calpain 3 level.
Developmental medicine and child neurology 2006;48(4):304-6.
2005: Sergio Salvatori; Marina Fanin; Carlo Pietro Trevisan; Sandra Furlan; S Reddy; J I Nagy; Corrado Angelini
Decreased expression of DMPK: correlation with CTG repeat expansion and fibre type composition in myotonic dystrophy type 1.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2005;26(4):235-42.
2005: Giulio Piluso; Luisa Politano; Stefania Aurino; Marina Fanin; Enzo Ricci; V M Ventriglia; A Belsito; A Totaro; V Saccone; Haluk Topaloglu; Anna Chiara Nascimbeni; Luigi Fulizio; A Broccolini; Nina Canki-Klain; Lucia I Comi; Ge Nigro; Corrado Angelini; Vincenzo Nigro
Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes.
Journal of medical genetics 2005;42(9):686-93.
2005: Marina Fanin; Anna Chiara Nascimbeni; Luigi Fulizio; Corrado Angelini
The frequency of limb girdle muscular dystrophy 2A in northeastern Italy.
Neuromuscular disorders : NMD 2005;15(3):218-24.
2005: Giovanna Cenacchi; Marina Fanin; LB De Giorgi; Corrado Angelini
Ultrastructural changes in dysferlinopathy support defective membrane repair mechanism.
Journal of clinical pathology 2005;58(2):190-5.
2005: Luigi Fulizio; Anna Chiara Nascimbeni; Marina Fanin; Giulio Piluso; Luisa Politano; Vincenzo Nigro; Corrado Angelini
Molecular and muscle pathology in a series of caveolinopathy patients.
Human mutation 2005;25(1):82-9.
2004: Paola Prandini; Angela Berardinelli; Marina Fanin; F Morello; Elisabetta Zardini; Anna Pichiecchio; Carla Uggetti; Giovanni Lanzi; Corrado Angelini; Elena Pegoraro
LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophy.
Neurology 2004;63(6):1118-21.
2004: Marina Fanin; Luigi Fulizio; Anna Chiara Nascimbeni; Marco Spinazzi; Giulio Piluso; V M Ventriglia; G Ruzza; Gabriele Siciliano; Carlo Pietro Trevisan; Luisa Politano; Vincenzo Nigro; Corrado Angelini
Molecular diagnosis in LGMD2A: mutation analysis or protein testing?
Human mutation 2004;24(1):52-62.
2003: Marina Fanin; Anna Chiara Nascimbeni; Luigi Fulizio; Carlo Pietro Trevisan; Marija Meznaric-Petrusa; Corrado Angelini
Loss of calpain-3 autocatalytic activity in LGMD2A patients with normal protein expression.
The American journal of pathology 2003;163(5):1929-36.
2003: Marina Fanin; Paola Melacini; Chiara A Boito; Elena Pegoraro; Corrado Angelini
LGMD2E patients risk developing dilated cardiomyopathy.
Neuromuscular disorders : NMD 2003;13(4):303-9.
2003: Chiara A Boito; Marina Fanin; Gabriele Siciliano; Corrado Angelini; Elena Pegoraro
Novel sarcoglycan gene mutations in a large cohort of Italian patients.
Journal of medical genetics 2003;40(5):e67.
2003: Andrea Martinuzzi; Elena Sartori; Marina Fanin; Anna Chiara Nascimbeni; Lucia Valente; Corrado Angelini; Gabriele Siciliano; Tiziana Mongini; Paola Tonin; Giuliano Tomelleri; Antonio Toscano; Luciano Merlini; Laurence A Bindoff; Stefano Bertelli
Phenotype modulators in myophosphorylase deficiency.
Annals of neurology 2003;53(4):497-502.
2003: Zivana Tezak; Paola Prandini; Marco Boscaro; Alessandra Marin; Joseph M Devaney; Michael Marino; Marina Fanin; Carlo Pietro Trevisan; Julie Park; Weslie Tyson; R Finkel; Carlos Garcia; Corrado Angelini; Eric Hoffman; Elena Pegoraro
Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency.
Human mutation 2003;21(2):103-11.
2002: Stefano Campanaro; Chiara Romualdi; Marina Fanin; Barbara Celegato; Beniamina Pacchioni; Silvia Trevisan; Paolo Laveder; Cristiano De Pitta; Elena Pegoraro; Yukiko K Hayashi; Giorgio Valle; Corrado Angelini; Gerolamo Lanfranchi
Gene expression profiling in dysferlinopathies using a dedicated muscle microarray.
Human molecular genetics 2002;11(26):3283-98.
2002: Marina Fanin; Corrado Angelini
Muscle pathology in dysferlin deficiency.
Neuropathology and applied neurobiology 2002;28(6):461-70.
2002: Luisa Toffolatti; Barbara Cardazzo; Carlo Nobile; Gian Antonio Danieli; Francesca Gualandi; Francesco Muntoni; Stephen Abbs; Patrizia Zanetti; Corrado Angelini; Alessandra Ferlini; Marina Fanin; Tomaso Patarnello
Investigating the mechanism of chromosomal deletion: characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin gene.
Genomics 2002;80(5):523-30.
2002: Marina Fanin; Corrado Angelini
Defective assembly of sarcoglycan complex in patients with beta-sarcoglycan gene mutations. Study of aneural and innervated cultured myotubes.
Neuropathology and applied neurobiology 2002;28(3):190-9.
2002: Elena Pegoraro; Fulvio Cepollaro; Paola Prandini; Alessandra Marin; Marina Fanin; Carlo Pietro Trevisan; Abdul Hassib El-Messlemani; Guido Tarone; Eva Engvall; Eric Hoffman; Corrado Angelini
Integrin alpha 7 beta 1 in muscular dystrophy/myopathy of unknown etiology.
The American journal of pathology 2002;160(6):2135-43.
2001: Marina Fanin; Elena Pegoraro; C Matsuda-Asada; R H Brown; Corrado Angelini
Calpain-3 and dysferlin protein screening in patients with limb-girdle dystrophy and myopathy.
Neurology 2001;56(5):660-5.
2001: Paola Melacini; Antonio Gambino; Alida L P Caforio; Agata Barchitta; Marialuisa Valente; Annalisa Angelini; Marina Fanin; Gaetano Thiene; Corrado Angelini; Dino Casarotto; Gian Antonio Danieli; Sergio Dalla Volta
Heart transplantation in patients with inherited myopathies associated with end-stage cardiomyopathy: molecular and biochemical defects on cardiac and skeletal muscle.
Transplantation proceedings 2001;33(1-2):1596-9.
2000: Elena Pegoraro; Marina Fanin; Carlo Pietro Trevisan; Corrado Angelini; Eric Hoffman
A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophy.
Neurology 2000;55(8):1128-34.
2000: Domenico Marco Bonifati; Carlo Ori; Carlo Riccardo Rossi; S Caira; Marina Fanin; Corrado Angelini
Neuromuscular damage after hyperthermic isolated limb perfusion in patients with melanoma or sarcoma treated with chemotherapeutic agents.
Cancer chemotherapy and pharmacology 2000;46(6):517-22.
2000: Marina Fanin; Eric Hoffman; Corrado Angelini; Elena Pegoraro
Private beta- and gamma-sarcoglycan gene mutations: evidence of a founder effect in Northern Italy.
Human mutation 2000;16(1):13-7.
2000: Leonardo Salviati; Anna Maria Laverda; Lucia Zancan; Marina Fanin; Corrado Angelini; Marija Meznaric-Petrusa
Acute quadriplegic myopathy in a 17-month-old boy.
Journal of child neurology 2000;15(1):63-6.
1999: Marina Fanin; Paola Melacini; Corrado Angelini; Gian Antonio Danieli
Could utrophin rescue the myocardium of patients with dystrophin gene mutations?
Journal of molecular and cellular cardiology 1999;31(8):1501-8.
1999: Elena Pegoraro; Marina Fanin; Corrado Angelini; Eric Hoffman
Prenatal diagnosis in a family affected with beta-sarcoglycan muscular dystrophy.
Neuromuscular disorders : NMD 1999;9(5):323-5.
1999: Marina Fanin; Corrado Angelini
Regeneration in sarcoglycanopathies: expression studies of sarcoglycans and other muscle proteins.
Journal of the neurological sciences 1999;165(2):170-7.
1999: Andrea Martinuzzi; G Schievano; Anna Chiara Nascimbeni; Marina Fanin
McArdle's disease. The unsolved mystery of the reappearing enzyme.
The American journal of pathology 1999;154(6):1893-7.
1999: Paola Melacini; Marina Fanin; DJ Duggan; MP Freda; Angela Berardinelli; Gian Antonio Danieli; Agata Barchitta; Eric Hoffman; Sergio Dalla Volta; Corrado Angelini
Heart involvement in muscular dystrophies due to sarcoglycan gene mutations.
Muscle & nerve 1999;22(4):473-9.
1999: Corrado Angelini; Marina Fanin; MP Freda; DJ Duggan; G Siciliano; Eric Hoffman
The clinical spectrum of sarcoglycanopathies.
Neurology 1999;52(1):176-9.
1998: Paola Melacini; Marina Fanin; Annalisa Angelini; Elena Pegoraro; Ugolino Livi; Gian Antonio Danieli; Eric Hoffman; Gaetano Thiene; Sergio Dalla Volta; Corrado Angelini
Cardiac transplantation in a Duchenne muscular dystrophy carrier.
Neuromuscular disorders : NMD 1998;8(8):585-90.
1998: Elena Pegoraro; H Marks; C A Garcia; Thomas O Crawford; Pedro Mancias; Anne M Connolly; Marina Fanin; F Martinello; Carlo Pietro Trevisan; Corrado Angelini; A Stella; Mena Scavina; R L Munk; Serenella Servidei; C C Bönnemann; Tulio Bertorini; Gyula Acsadi; C E Thompson; D Gagnon; G Hoganson; V Carver; R A Zimmerman; Eric Hoffman
Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients.
Neurology 1998;51(1):101-10.
1998: Corrado Angelini; Marina Fanin; E Menegazzo; MP Freda; DJ Duggan; Eric Hoffman
Homozygous alpha-sarcoglycan mutation in two siblings: one asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patient.
Muscle & nerve 1998;21(6):769-75.
1997: Marina Fanin; DJ Duggan; Maria Luisa Mostacciuolo; F Martinello; MP Freda; Gianni Soraru; Carlo Pietro Trevisan; Eric Hoffman; Corrado Angelini
Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutations.
Journal of medical genetics 1997;34(12):973-7.
1997: Gregorio Brevetti; Marina Fanin; Vincenzo De Amicis; Rosalba Carrozzo; Francesco Di Lello; VD Martone; Corrado Angelini
Changes in skeletal muscle histology and metabolism in patients undergoing exercise deconditioning: effect of propionyl-L-carnitine.
Muscle & nerve 1997;20(9):1115-20.
1997: DJ Duggan; J R Gorospe; Marina Fanin; Eric Hoffman; Corrado Angelini
Mutations in the sarcoglycan genes in patients with myopathy.
The New England journal of medicine 1997;336(9):618-24.
1996: Paola Melacini; Marina Fanin; Gian Antonio Danieli; C Villanova; F Martinello; M Miorin; MP Freda; M Miorelli; Maria Luisa Mostacciuolo; Giuseppe Fasoli; Corrado Angelini; Sergio Dalla Volta
Myocardial involvement is very frequent among patients affected with subclinical Becker's muscular dystrophy.
Circulation 1996;94(12):3168-75.
1996: Elizabeth McNally; David Duggan; J R Gorospe; Carsten G Bönnemann; Marina Fanin; Elena Pegoraro; Hart G W Lidov; Satoru Noguchi; Eijiro Ozawa; R S Finkel; R P Cruse; Corrado Angelini; Louis Kunkel; Eric Hoffman
Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy.
Human molecular genetics 1996;5(11):1841-7.
1996: Paola Melacini; A Vianello; C Villanova; Marina Fanin; M Miorin; Corrado Angelini; Sergio Dalla Volta
Cardiac and respiratory involvement in advanced stage Duchenne muscular dystrophy.
Neuromuscular disorders : NMD 1996;6(5):367-76.
1996: Carlo Pietro Trevisan; F Martinello; E Ferruzza; Marina Fanin; M Chevallay; Fernando M S Tomé
Brain alterations in the classical form of congenital muscular dystrophy. Clinical and neuroimaging follow-up of 12 cases and correlation with the expression of merosin in muscle.
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 1996;12(10):604-10.
1996: Corrado Angelini; Marina Fanin; MP Freda; F Martinello; M Miorin; Paola Melacini; Gabriele Siciliano; Elena Pegoraro; M Rosa; Gian Antonio Danieli
Prognostic factors in mild dystrophinopathies.
Journal of the neurological sciences 1996;142(1-2):70-8.
1996: DJ Duggan; Marina Fanin; Elena Pegoraro; Corrado Angelini; Eric Hoffman
alpha-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutations.
Journal of the neurological sciences 1996;140(1-2):30-9.
1996: Marina Fanin; MP Freda; libero vitiello; Gian Antonio Danieli; Elena Pegoraro; Corrado Angelini
Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size?
Muscle & nerve 1996;19(9):1154-60.
1996: A Martinuzzi; S Tsujino; Lodovica Vergani; G Schievano; M Cadaldini; L Bartoloni; Marina Fanin; Gabriele Siciliano; Sara Shanske; S DiMauro; Corrado Angelini
Molecular characterization of myophosphorylase deficiency in a group of patients from northern Italy.
Journal of the neurological sciences 1996;137(1):14-9.
1995: Marina Fanin; Gian Antonio Danieli; M Cadaldini; M Miorin; libero vitiello; Corrado Angelini
Dystrophin-positive fibers in Duchenne dystrophy: origin and correlation to clinical course.
Muscle & nerve 1995;18(10):1115-20.
1994: Gabriele Siciliano; Marina Fanin; Corrado Angelini; Luca Pollina; M Miorin; F A Saad; MP Freda; A Muratorio
Prevalent cardiac involvement in dystrophin Becker type mutation.
Neuromuscular disorders : NMD 1994;4(4):381-6.
1994: Corrado Angelini; Marina Fanin; Elena Pegoraro; MP Freda; M Cadaldini; F Martinello
Clinical-molecular correlation in 104 mild X-linked muscular dystrophy patients: characterization of sub-clinical phenotypes.
Neuromuscular disorders : NMD 1994;4(4):349-58.
1994: Marina Fanin; Elena Pegoraro; Corrado Angelini
Absence of dystrophin and spectrin in regenerating muscle fibers from Becker dystrophy patients.
Journal of the neurological sciences 1994;123(1-2):88-94.
1994: Maria Luisa Mostacciuolo; M Miorin; libero vitiello; Alessandra Rampazzo; Marina Fanin; Corrado Angelini; Gian Antonio Danieli
Occurrence of two different intragenic deletions in two male relatives affected with Duchenne muscular dystrophy.
American journal of medical genetics 1994;50(1):84-6.
1993: Paola Melacini; Marina Fanin; Gian Antonio Danieli; Giuseppe Fasoli; C Villanova; Corrado Angelini; libero vitiello; M Miorelli; Gianfranco Buja; Maria Luisa Mostacciuolo
Cardiac involvement in Becker muscular dystrophy.
Journal of the American College of Cardiology 1993;22(7):1927-34.
1993: A Martinuzzi; Lodovica Vergani; R Carrozzo; Marina Fanin; L Bartoloni; Corrado Angelini; Valerie Askanas; W King Engel
Expression of muscle-type phosphorylase in innervated and aneural cultured muscle of patients with myophosphorylase deficiency.
The Journal of clinical investigation 1993;92(4):1774-80.
1993: Marina Fanin; Eric Hoffman; F A Saad; A Martinuzzi; Gian Antonio Danieli; Corrado Angelini
Dystrophin-positive myotubes in innervated muscle cultures from Duchenne and Becker muscular dystrophy patients.
Neuromuscular disorders : NMD 1993;3(2):119-27.
1993: Corrado Angelini; Paola Melacini; M L Valente; Heinz Reichmann; R Carrozzo; Marina Fanin; Lodovica Vergani; Giovanni M Boffa; A Martinuzzi; Giuseppe Fasoli
Hypertrophic cardiomyopathy with mitochondrial myopathy. A new phenotype of complex II defect.
Japanese heart journal 1993;34(1):63-77.
1993: Corrado Angelini; E Menegazzo; Marina Fanin
Multifactorial study of inflammatory myopathies. Report of 29 cases.
Italian journal of neurological sciences 1993;14(1):69-76.
1993: Maria Luisa Mostacciuolo; M Miorin; Elena Pegoraro; Marina Fanin; Franco Schiavon; libero vitiello; F A Saad; Corrado Angelini; Gian Antonio Danieli
Reappraisal of the incidence rate of Duchenne and Becker muscular dystrophies on the basis of molecular diagnosis.
Neuroepidemiology 1993;12(6):326-30.
1992: Marina Fanin; Gian Antonio Danieli; libero vitiello; L Senter; Corrado Angelini
Prevalence of dystrophin-positive fibers in 85 Duchenne muscular dystrophy patients.
Neuromuscular disorders : NMD 1992;2(1):41-5.
1990: Lodovica Vergani; Marina Fanin; A Martinuzzi; A Galassi; A Appi; R Carrozzo; M Rosa; Corrado Angelini
Liver fatty acid-binding protein in two cases of human lipid storage.
Molecular and cellular biochemistry 1990;98(1-2):225-30.
1990: Corrado Angelini; A H Beggs; Eric Hoffman; Marina Fanin; Louis Kunkel
Enormous dystrophin in a patient with Becker muscular dystrophy.
Neurology 1990;40(5):808-12.