Results
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LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophy. [electronic resource] by
- Prandini, P
- Berardinelli, A
- Fanin, M
- Morello, F
- Zardini, E
- Pichiecchio, A
- Uggetti, C
- Lanzi, G
- Angelini, C
- Pegoraro, E
Producer: 20050518
In:
Neurology vol. 63
Availability: No items available.
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46.
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Genetic variation in KIFAP3 is associated with an upper motor neuron-predominant phenotype in amyotrophic lateral sclerosis. [electronic resource] by
- Orsetti, V
- Pegoraro, E
- Cima, V
- D'Ascenzo, C
- Palmieri, A
- Querin, G
- Volpe, M
- Ermani, M
- Angelini, C
- Sorarù, G
Producer: 20111207
In:
Neuro-degenerative diseases vol. 8
Availability: No items available.
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47.
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ALS risk but not phenotype is affected by ataxin-2 intermediate length polyglutamine expansion. [electronic resource] by
- Sorarù, G
- Clementi, M
- Forzan, M
- Orsetti, V
- D'Ascenzo, C
- Querin, G
- Palmieri, A
- Ermani, M
- Angelini, C
- Pegoraro, E
Producer: 20110818
In:
Neurology vol. 76
Availability: No items available.
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48.
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49.
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Assessment of patients with idiopathic inflammatory myopathies and isolated creatin-kinase elevation. [electronic resource] by
- Iaccarino, L
- Pegoraro, E
- Bello, L
- Bettio, S
- Borella, E
- Nalotto, L
- Semplicini, C
- Sorarù, G
- Ghirardello, A
- Doria, A
Producer: 20150522
In:
Auto- immunity highlights vol. 5
Availability: No items available.
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Unimpaired Neuropsychological Performance and Enhanced Memory Recall in Patients with Sbma: A Large Sample Comparative Study. [electronic resource] by
- Marcato, S
- Kleinbub, J R
- Querin, G
- Pick, E
- Martinelli, I
- Bertolin, C
- Cipolletta, S
- Pegoraro, E
- Sorarù, G
- Palmieri, A
Producer: 20191028
In:
Scientific reports vol. 8
Availability: No items available.
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53.
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54.
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No evidence of cardiomyopathy in spinal and bulbar muscular atrophy. [electronic resource] by
- Querin, G
- Melacini, P
- D'Ascenzo, C
- Morandi, L
- Mazzini, L
- Silani, V
- Romito, S
- Mandrioli, J
- Raimondi, M
- Pegoraro, E
- Soraru', G
Producer: 20140602
In:
Acta neurologica Scandinavica vol. 128
Availability: No items available.
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55.
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Prognostic factors in mild dystrophinopathies. [electronic resource] by
- Angelini, C
- Fanin, M
- Freda, M P
- Martinello, F
- Miorin, M
- Melacini, P
- Siciliano, G
- Pegoraro, E
- Rosa, M
- Danieli, G A
Producer: 19970207
In:
Journal of the neurological sciences vol. 142
Availability: No items available.
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56.
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Cardiac transplantation in a Duchenne muscular dystrophy carrier. [electronic resource] by
- Melacini, P
- Fanin, M
- Angelini, A
- Pegoraro, E
- Livi, U
- Danieli, G A
- Hoffman, E P
- Thiene, G
- Dalla Volta, S
- Angelini, C
Producer: 19990624
In:
Neuromuscular disorders : NMD vol. 8
Availability: No items available.
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57.
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A novel SACS mutation results in non-ataxic spastic paraplegia and peripheral neuropathy. [electronic resource] by
- Gregianin, E
- Vazza, G
- Scaramel, E
- Boaretto, F
- Vettori, A
- Leonardi, E
- Tosatto, S C E
- Manara, R
- Pegoraro, E
- Mostacciuolo, M L
Producer: 20151022
In:
European journal of neurology vol. 20
Availability: No items available.
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58.
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Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy. [electronic resource] by
- Pegoraro, E
- Mancias, P
- Swerdlow, S H
- Raikow, R B
- Garcia, C
- Marks, H
- Crawford, T
- Carver, V
- Di Cianno, B
- Hoffman, E P
Producer: 19970123
In:
Annals of neurology vol. 40
Availability: No items available.
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59.
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60.
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Detection of new paternal dystrophin gene mutations in isolated cases of dystrophinopathy in females. [electronic resource] by
- Pegoraro, E
- Schimke, R N
- Arahata, K
- Hayashi, Y
- Stern, H
- Marks, H
- Glasberg, M R
- Carroll, J E
- Taber, J W
- Wessel, H B
Producer: 19940630
In:
American journal of human genetics vol. 54
Availability: No items available.
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