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Results of search for 'au:"Fanin, M"', page 1 of 4
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Authors
Angelini, C
Carrozzo, R
Dalla Volta, S
Danieli, G A
Duggan, D J
Fanin, M
Freda, M P
Hoffman, E P
Martinello, F
Martinuzzi, A
Melacini, P
Miorin, M
Mostacciuolo, M L
Nascimbeni, A C
Nigro, V
Pegoraro, E
Siciliano, G
Trevisan, C P
Vergani, L
Vitiello, L
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Topics
Adolescent
Adult
Biopsy
Child
Child, Preschool
Cytoskeletal Proteins
Dystrophin
Female
Humans
Immunohistochemistry
Male
Middle Aged
Muscle, Skeletal
Muscular Dystrophies
Mutation
Phenotype
analysis
chemistry
genetics
metabolism
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English
Your search returned 67 results.
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1.
Defective assembly of sarcoglycan complex in patients with beta-sarcoglycan gene mutations. Study of aneural and innervated cultured myotubes.
[electronic resource]
by
Fanin, M
Angelini, C
Producer:
20020802
In:
Neuropathology and applied neurobiology
vol. 28
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2.
Muscle pathology in dysferlin deficiency.
[electronic resource]
by
Fanin, M
Angelini, C
Producer:
20030123
In:
Neuropathology and applied neurobiology
vol. 28
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3.
Regeneration in sarcoglycanopathies: expression studies of sarcoglycans and other muscle proteins.
[electronic resource]
by
Fanin, M
Angelini, C
Producer:
19991004
In:
Journal of the neurological sciences
vol. 165
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4.
Absence of dystrophin and spectrin in regenerating muscle fibers from Becker dystrophy patients.
[electronic resource]
by
Fanin, M
Pegoraro, E
Angelini, C
Producer:
19940919
In:
Journal of the neurological sciences
vol. 123
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5.
Multifactorial study of inflammatory myopathies. Report of 29 cases.
[electronic resource]
by
Angelini, C
Menegazzo, E
Fanin, M
Producer:
19930514
In:
Italian journal of neurological sciences
vol. 14
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6.
Screening of calpain-3 autolytic activity in LGMD muscle: a functional map of CAPN3 gene mutations.
[electronic resource]
by
Fanin, M
Nascimbeni, A C
Angelini, C
Producer:
20070130
In:
Journal of medical genetics
vol. 44
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7.
Muscle atrophy in Limb Girdle Muscular Dystrophy 2A: a morphometric and molecular study.
[electronic resource]
by
Fanin, M
Nascimbeni, A C
Angelini, C
Producer:
20141118
In:
Neuropathology and applied neurobiology
vol. 39
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8.
McArdle's disease. The unsolved mystery of the reappearing enzyme.
[electronic resource]
by
Martinuzzi, A
Schievano, G
Nascimbeni, A
Fanin, M
Producer:
19990714
In:
The American journal of pathology
vol. 154
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9.
Could utrophin rescue the myocardium of patients with dystrophin gene mutations?
[electronic resource]
by
Fanin, M
Melacini, P
Angelini, C
Danieli, G A
Producer:
19990908
In:
Journal of molecular and cellular cardiology
vol. 31
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10.
Private beta- and gamma-sarcoglycan gene mutations: evidence of a founder effect in Northern Italy.
[electronic resource]
by
Fanin, M
Hoffman, E P
Angelini, C
Pegoraro, E
Producer:
20000822
In:
Human mutation
vol. 16
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11.
Prenatal diagnosis in a family affected with beta-sarcoglycan muscular dystrophy.
[electronic resource]
by
Pegoraro, E
Fanin, M
Angelini, C
Hoffman, E P
Producer:
19990825
In:
Neuromuscular disorders : NMD
vol. 9
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12.
Novel sarcoglycan gene mutations in a large cohort of Italian patients.
[electronic resource]
by
Boito, C
Fanin, M
Siciliano, G
Angelini, C
Pegoraro, E
Producer:
20030805
In:
Journal of medical genetics
vol. 40
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13.
LGMD2E patients risk developing dilated cardiomyopathy.
[electronic resource]
by
Fanin, M
Melacini, P
Boito, C
Pegoraro, E
Angelini, C
Producer:
20030819
In:
Neuromuscular disorders : NMD
vol. 13
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14.
Ultrastructural changes in dysferlinopathy support defective membrane repair mechanism.
[electronic resource]
by
Cenacchi, G
Fanin, M
De Giorgi, L B
Angelini, C
Producer:
20050307
In:
Journal of clinical pathology
vol. 58
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15.
Muscle histopathology in myasthenia gravis with antibodies against MuSK and AChR.
[electronic resource]
by
Martignago, S
Fanin, M
Albertini, E
Pegoraro, E
Angelini, C
Producer:
20090309
In:
Neuropathology and applied neurobiology
vol. 35
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16.
Cardioembolic stroke in Danon disease.
[electronic resource]
by
Spinazzi, M
Fanin, M
Melacini, P
Nascimbeni, A C
Angelini, C
Producer:
20080513
In:
Clinical genetics
vol. 73
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17.
The role of autophagy in the pathogenesis of glycogen storage disease type II (GSDII).
[electronic resource]
by
Nascimbeni, A C
Fanin, M
Masiero, E
Angelini, C
Sandri, M
Producer:
20130114
In:
Cell death and differentiation
vol. 19
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18.
Prevalence of dystrophin-positive fibers in 85 Duchenne muscular dystrophy patients.
[electronic resource]
by
Fanin, M
Danieli, G A
Vitiello, L
Senter, L
Angelini, C
Producer:
19921022
In:
Neuromuscular disorders : NMD
vol. 2
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19.
A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophy.
[electronic resource]
by
Pegoraro, E
Fanin, M
Trevisan, C P
Angelini, C
Hoffman, E P
Producer:
20001207
In:
Neurology
vol. 55
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20.
Calpain-3 and dysferlin protein screening in patients with limb-girdle dystrophy and myopathy.
[electronic resource]
by
Fanin, M
Pegoraro, E
Matsuda-Asada, C
Brown, R H
Angelini, C
Producer:
20010419
In:
Neurology
vol. 56
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