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61.
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Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15. [electronic resource] by
- Martínez Murillo, F
- Kobayashi, H
- Pegoraro, E
- Galluzzi, G
- Creel, G
- Mariani, C
- Farina, E
- Ricci, E
- Alfonso, G
- Pauli, R M
- Hoffman, E P
Producer: 19990809
In:
Neurology vol. 53
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62.
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CAG repeat length in androgen receptor gene is not associated with amyotrophic lateral sclerosis. [electronic resource] by
- Bruson, A
- Sambataro, F
- Querin, G
- D'Ascenzo, C
- Palmieri, A
- Agostini, J
- Gaiani, A
- Angelini, C
- Galbiati, M
- Poletti, A
- Pennuto, M
- Pegoraro, E
- Clementi, M
- Soraru, G
Producer: 20130411
In:
European journal of neurology vol. 19
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63.
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Brain involvement in myotonic dystrophies: neuroimaging and neuropsychological comparative study in DM1 and DM2. [electronic resource] by
- Romeo, Vincenzo
- Pegoraro, E
- Ferrati, C
- Squarzanti, F
- Sorarù, G
- Palmieri, A
- Zucchetta, P
- Antunovic, L
- Bonifazi, E
- Novelli, G
- Trevisan, C P
- Ermani, M
- Manara, R
- Angelini, C
Producer: 20110324
In:
Journal of neurology vol. 257
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64.
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Right hemisphere dysfunction and emotional processing in ALS: an fMRI study. [electronic resource] by
- Palmieri, A
- Naccarato, M
- Abrahams, S
- Bonato, M
- D'Ascenzo, C
- Balestreri, S
- Cima, V
- Querin, G
- Dal Borgo, R
- Barachino, L
- Volpato, C
- Semenza, C
- Pegoraro, E
- Angelini, C
- Sorarù, G
Producer: 20111110
In:
Journal of neurology vol. 257
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65.
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Cerebellar ataxia and coenzyme Q10 deficiency. [electronic resource] by
- Lamperti, C
- Naini, A
- Hirano, M
- De Vivo, D C
- Bertini, E
- Servidei, S
- Valeriani, M
- Lynch, D
- Banwell, B
- Berg, M
- Dubrovsky, T
- Chiriboga, C
- Angelini, C
- Pegoraro, E
- DiMauro, S
Producer: 20030423
In:
Neurology vol. 60
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66.
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No effect of AR polyG polymorphism on spinal and bulbar muscular atrophy phenotype. [electronic resource] by
- Bertolin, C
- Querin, G
- Da Re, E
- Sagnelli, A
- Bello, L
- Cao, M
- Muscas, M
- Pennuto, M
- Ermani, M
- Pegoraro, E
- Mariotti, C
- Gellera, C
- Hanna, M G
- Pareyson, D
- Fratta, P
- Sorarù, G
Producer: 20171221
In:
European journal of neurology vol. 23
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67.
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Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy. [electronic resource] by
- McNally, E M
- Duggan, D
- Gorospe, J R
- Bönnemann, C G
- Fanin, M
- Pegoraro, E
- Lidov, H G
- Noguchi, S
- Ozawa, E
- Finkel, R S
- Cruse, R P
- Angelini, C
- Kunkel, L M
- Hoffman, E P
Producer: 19970311
In:
Human molecular genetics vol. 5
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68.
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SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy. [electronic resource] by
- Pegoraro, E
- Hoffman, E P
- Piva, L
- Gavassini, B F
- Cagnin, S
- Ermani, M
- Bello, L
- Soraru, G
- Pacchioni, B
- Bonifati, M D
- Lanfranchi, G
- Angelini, C
- Kesari, A
- Lee, I
- Gordish-Dressman, H
- Devaney, J M
- McDonald, C M
Producer: 20110214
In:
Neurology vol. 76
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69.
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Genetic and biochemical normalization in female carriers of Duchenne muscular dystrophy: evidence for failure of dystrophin production in dystrophin-competent myonuclei. [electronic resource] by
- Pegoraro, E
- Schimke, R N
- Garcia, C
- Stern, H
- Cadaldini, M
- Angelini, C
- Barbosa, E
- Carroll, J
- Marks, W A
- Neville, H E
- Marks, H
- Appleton, S
- Toriello, H
- Wessel, H B
- Donnelly, J
- Bernes, S M
- Taber, J W
- Weiss, L
- Hoffman, E P
Producer: 19950523
In:
Neurology vol. 45
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70.
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Respiratory and cardiac function in congenital muscular dystrophies with alpha dystroglycan deficiency. [electronic resource] by
- Pane, M
- Messina, S
- Vasco, G
- Foley, A R
- Morandi, L
- Pegoraro, E
- Mongini, T
- D'Amico, A
- Bianco, F
- Lombardo, M E
- Scalise, R
- Bruno, C
- Berardinelli, A
- Pini, A
- Moroni, I
- Mora, M
- Toscano, A
- Moggio, M
- Comi, G
- Santorelli, F M
- Bertini, E
- Muntoni, F
- Mercuri, E
Producer: 20130107
In:
Neuromuscular disorders : NMD vol. 22
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71.
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Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years. [electronic resource] by
- Angelini, C
- Semplicini, C
- Ravaglia, S
- Bembi, B
- Servidei, S
- Pegoraro, E
- Moggio, M
- Filosto, M
- Sette, E
- Crescimanno, G
- Tonin, P
- Parini, R
- Morandi, L
- Marrosu, G
- Greco, G
- Musumeci, O
- Di Iorio, G
- Siciliano, G
- Donati, M A
- Carubbi, F
- Ermani, M
- Mongini, T
- Toscano, A
Producer: 20121017
In:
Journal of neurology vol. 259
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72.
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LOPED study: looking for an early diagnosis in a late-onset Pompe disease high-risk population. [electronic resource] by
- Musumeci, O
- la Marca, G
- Spada, M
- Mondello, S
- Danesino, C
- Comi, G P
- Pegoraro, E
- Antonini, G
- Marrosu, G
- Liguori, R
- Morandi, L
- Moggio, M
- Massa, R
- Ravaglia, S
- Di Muzio, A
- Filosto, M
- Tonin, P
- Di Iorio, G
- Servidei, S
- Siciliano, G
- Angelini, C
- Mongini, T
- Toscano, A
Producer: 20160418
In:
Journal of neurology, neurosurgery, and psychiatry vol. 87
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73.
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Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients. [electronic resource] by
- Pegoraro, E
- Marks, H
- Garcia, C A
- Crawford, T
- Mancias, P
- Connolly, A M
- Fanin, M
- Martinello, F
- Trevisan, C P
- Angelini, C
- Stella, A
- Scavina, M
- Munk, R L
- Servidei, S
- Bönnemann, C C
- Bertorini, T
- Acsadi, G
- Thompson, C E
- Gagnon, D
- Hoganson, G
- Carver, V
- Zimmerman, R A
- Hoffman, E P
Producer: 19980730
In:
Neurology vol. 51
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74.
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Phenotypic clustering of lamin A/C mutations in neuromuscular patients. [electronic resource] by
- Benedetti, S
- Menditto, I
- Degano, M
- Rodolico, C
- Merlini, L
- D'Amico, A
- Palmucci, L
- Berardinelli, A
- Pegoraro, E
- Trevisan, C P
- Morandi, L
- Moroni, I
- Galluzzi, G
- Bertini, E
- Toscano, A
- Olivè, M
- Bonne, G
- Mari, F
- Caldara, R
- Fazio, R
- Mammì, I
- Carrera, P
- Toniolo, D
- Comi, G
- Quattrini, A
- Ferrari, M
- Previtali, S C
Producer: 20071015
In:
Neurology vol. 69
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75.
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POMT1 and POMT2 mutations in CMD patients: a multicentric Italian study. [electronic resource] by
- Messina, S
- Mora, M
- Pegoraro, E
- Pini, A
- Mongini, T
- D'Amico, A
- Pane, M
- Aiello, C
- Bruno, C
- Biancheri, R
- Berardinelli, A
- Boito, C
- Farina, L
- Morandi, L
- Moroni, I
- Pezzani, R
- Pichiecchio, A
- Ricci, E
- Ruggieri, A
- Saredi, S
- Scuderi, C
- Tessa, A
- Toscano, A
- Tortorella, G
- Trevisan, C P
- Uggetti, C
- Santorelli, F M
- Bertini, E
- Mercuri, E
Producer: 20081105
In:
Neuromuscular disorders : NMD vol. 18
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76.
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Congenital muscular dystrophies with cognitive impairment. A population study. [electronic resource] by
- Messina, S
- Bruno, C
- Moroni, I
- Pegoraro, E
- D'Amico, A
- Biancheri, R
- Berardinelli, A
- Boffi, P
- Cassandrini, D
- Farina, L
- Minetti, C
- Moggio, M
- Mongini, T
- Mottarelli, E
- Pane, M
- Pantaleoni, C
- Pichiecchio, A
- Pini, A
- Ricci, E
- Saredi, S
- Sframeli, M
- Tortorella, G
- Toscano, A
- Trevisan, C P
- Uggetti, C
- Vasco, G
- Comi, G P
- Santorelli, F M
- Bertini, E
- Mercuri, E
Producer: 20100927
In:
Neurology vol. 75
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77.
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Revisiting mitochondrial ocular myopathies: a study from the Italian Network. [electronic resource] by
- Orsucci, D
- Angelini, C
- Bertini, E
- Carelli, V
- Comi, G P
- Federico, A
- Minetti, C
- Moggio, M
- Mongini, T
- Santorelli, F M
- Servidei, S
- Tonin, P
- Ardissone, A
- Bello, L
- Bruno, C
- Ienco, E Caldarazzo
- Diodato, D
- Filosto, M
- Lamperti, C
- Moroni, I
- Musumeci, O
- Pegoraro, E
- Primiano, G
- Ronchi, D
- Rubegni, A
- Salvatore, S
- Sciacco, M
- Valentino, M L
- Vercelli, L
- Toscano, A
- Zeviani, M
- Siciliano, G
- Mancuso, M
Producer: 20180418
In:
Journal of neurology vol. 264
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78.
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Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study. [electronic resource] by
- Mercuri, E
- Messina, S
- Bruno, C
- Mora, M
- Pegoraro, E
- Comi, G P
- D'Amico, A
- Aiello, C
- Biancheri, R
- Berardinelli, A
- Boffi, P
- Cassandrini, D
- Laverda, A
- Moggio, M
- Morandi, L
- Moroni, I
- Pane, M
- Pezzani, R
- Pichiecchio, A
- Pini, A
- Minetti, C
- Mongini, T
- Mottarelli, E
- Ricci, E
- Ruggieri, A
- Saredi, S
- Scuderi, C
- Tessa, A
- Toscano, A
- Tortorella, G
- Trevisan, C P
- Uggetti, C
- Vasco, G
- Santorelli, F M
- Bertini, E
Producer: 20090625
In:
Neurology vol. 72
Availability: No items available.
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79.
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Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort study. [electronic resource] by
- Mazzone, E
- Vasco, G
- Sormani, M P
- Torrente, Y
- Berardinelli, A
- Messina, S
- D'Amico, A
- Doglio, L
- Politano, L
- Cavallaro, F
- Frosini, S
- Bello, L
- Bonfiglio, S
- Zucchini, E
- De Sanctis, R
- Scutifero, M
- Bianco, F
- Rossi, F
- Motta, M C
- Sacco, A
- Donati, M A
- Mongini, T
- Pini, A
- Battini, R
- Pegoraro, E
- Pane, M
- Gasperini, S
- Previtali, S
- Napolitano, S
- Martinelli, D
- Bruno, C
- Vita, G
- Comi, G
- Bertini, E
- Mercuri, E
Producer: 20110916
In:
Neurology vol. 77
Availability: No items available.
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80.
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Reliability of the North Star Ambulatory Assessment in a multicentric setting. [electronic resource] by
- Mazzone, E S
- Messina, S
- Vasco, G
- Main, M
- Eagle, M
- D'Amico, A
- Doglio, L
- Politano, L
- Cavallaro, F
- Frosini, S
- Bello, L
- Magri, F
- Corlatti, A
- Zucchini, E
- Brancalion, B
- Rossi, F
- Ferretti, M
- Motta, M G
- Cecio, M R
- Berardinelli, A
- Alfieri, P
- Mongini, T
- Pini, A
- Astrea, G
- Battini, R
- Comi, G
- Pegoraro, E
- Morandi, L
- Pane, M
- Angelini, C
- Bruno, C
- Villanova, M
- Vita, G
- Donati, M A
- Bertini, E
- Mercuri, E
Producer: 20091015
In:
Neuromuscular disorders : NMD vol. 19
Availability: No items available.
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