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Results of search for 'au:"Filosto, M"', page 1 of 2
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Authors
Angelini, C
Antonini, G
Bertolasi, L
Carelli, V
Comi, G P
DiMauro, S
Filosto, M
Mancuso, M
Marini, M
Moggio, M
Mongini, T
Morandi, L
Musumeci, O
Rizzuto, N
Scarpelli, M
Siciliano, G
Tomelleri, G
Tonin, P
Toscano, A
Vattemi, G
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Adolescent
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Age of Onset
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Brain
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Creatine Kinase
DNA, Mitochondrial
Female
Glycogen Storage Disease Type II
Humans
Immunohistochemistry
Male
Middle Aged
Muscle, Skeletal
Muscular Diseases
Mutation
genetics
metabolism
pathology
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1.
Mitochondrial diseases: a nosological update.
[electronic resource]
by
Filosto, M
Mancuso, M
Producer:
20070605
In:
Acta neurologica Scandinavica
vol. 115
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2.
Spinal muscular atrophy and mitochondrial DNA depletion. Response to Berber et al. (2003) Acta Neuropathol 105:245-251.
[electronic resource]
by
Mancuso, M
Filosto, M
Hirano, M
DiMauro, S
Producer:
20030711
In:
Acta neuropathologica
vol. 105
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3.
Eyelid ptosis from sympathetic nerve dysfunction mistaken as myopathy: a simple test to identify this condition.
[electronic resource]
by
Tomelleri, G
Vattemi, G
Filosto, M
Tonin, P
Producer:
20070524
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 78
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4.
Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mitochondrial diseases.
[electronic resource]
by
Filosto, M
Tonin, P
Vattemi, G
Savio, C
Rizzuto, N
Tomelleri, G
Producer:
20030423
In:
Neuropathology and applied neurobiology
vol. 29
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5.
T-cell anti-apoptotic mechanisms in inflammatory myopathies.
[electronic resource]
by
Vattemi, G
Tonin, P
Filosto, M
Spagnolo, M
Rizzuto, N
Tomelleri, G
Producer:
20001222
In:
Journal of neuroimmunology
vol. 111
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6.
Expression of late myogenic differentiation markers in sarcoplasmic masses of patients with myotonic dystrophy.
[electronic resource]
by
Vattemi, G
Tomelleri, G
Filosto, M
Savio, C
Rizzuto, N
Tonin, P
Producer:
20050316
In:
Neuropathology and applied neurobiology
vol. 31
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7.
Reversible upper limb muscle weakness with selective loss of thick filaments.
[electronic resource]
by
Vattemi, G
Tonin, P
Filosto, M
Savio, C
Rizzuto, N
Tomelleri, G
Producer:
20040416
In:
Neurology
vol. 61
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8.
A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia.
[electronic resource]
by
Spagnolo, M
Tomelleri, G
Vattemi, G
Filosto, M
Rizzuto, N
Tonin, P
Producer:
20010830
In:
Neuromuscular disorders : NMD
vol. 11
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9.
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case report.
[electronic resource]
by
Filosto, M
Tonin, P
Vattemi, G
Bongiovanni, L G
Rizzuto, N
Tomelleri, G
Producer:
20020206
In:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
vol. 22
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10.
Dermatomyositis and retroperitoneal germ cell cancer.
[electronic resource]
by
Vattemi, G
Tonin, P
Martignoni, G
Filosto, M
Marchioretto, F
Rizzuto, N
Tomelleri, G
Producer:
20010322
In:
European neurology
vol. 45
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11.
The role of muscle biopsy in investigating isolated muscle pain.
[electronic resource]
by
Filosto, M
Tonin, P
Vattemi, G
Bertolasi, L
Simonati, A
Rizzuto, N
Tomelleri, G
Producer:
20070206
In:
Neurology
vol. 68
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12.
McArdle disease and sporadic inclusion body myositis.
[electronic resource]
by
Scarpelli, M
Vattemi, G
Filosto, M
Krause, S
Marini, M
Tomelleri, G
Tonin, P
Producer:
20091013
In:
Neuropathology and applied neurobiology
vol. 35
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13.
A non-syndromic hearing loss caused by very low levels of the mtDNA A3243G mutation.
[electronic resource]
by
Mancuso, M
Filosto, M
Forli, F
Rocchi, A
Berrettini, S
Siciliano, G
Murri, L
Producer:
20040910
In:
Acta neurologica Scandinavica
vol. 110
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14.
Axillary injection of botulinum A toxin in a patient with muscle cramps associated with severe axillary hyperhidrosis.
[electronic resource]
by
Filosto, M
Bertolasi, L
Fincati, E
Priori, A
Tomelleri, G
Chieregato, G
Rizzuto, N
Producer:
20020103
In:
Acta neurologica Belgica
vol. 101
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15.
POLG mutations causing ophthalmoplegia, sensorimotor polyneuropathy, ataxia, and deafness.
[electronic resource]
by
Mancuso, M
Filosto, M
Bellan, M
Liguori, R
Montagna, P
Baruzzi, A
DiMauro, S
Carelli, V
Producer:
20050114
In:
Neurology
vol. 62
Online resources:
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16.
A novel mitochondrial tRNAPhe mutation causes MERRF syndrome.
[electronic resource]
by
Mancuso, M
Filosto, M
Mootha, V K
Rocchi, A
Pistolesi, S
Murri, L
DiMauro, S
Siciliano, G
Producer:
20041220
In:
Neurology
vol. 62
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17.
Late-Onset Glycogen Storage Disease Type 2.
[electronic resource]
by
Filosto, M
Cotelli, M S
Vielmi, V
Todeschini, A
Rinaldi, F
Rota, S
Scarpelli, M
Padovani, A
Publication details:
Current molecular medicine
2014
In:
Current molecular medicine
vol. 14
Online resources:
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18.
Sarcoidosis and inclusion body myositis.
[electronic resource]
by
Vattemi, G
Tonin, P
Marini, M
Guadagnin, M L
Dal Pra, B
Simonati, A
Filosto, M
Tomelleri, G
Producer:
20081014
In:
Rheumatology (Oxford, England)
vol. 47
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19.
Expression of protein kinase C isoforms and interleukin-1beta in myofibrillar myopathy.
[electronic resource]
by
Vattemi, G
Tonin, P
Mora, M
Filosto, M
Morandi, L
Savio, C
Dal Pra, I
Rizzuto, N
Tomelleri, G
Producer:
20041026
In:
Neurology
vol. 62
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20.
The brain in late-onset glycogenosis II: a structural and functional MRI study.
[electronic resource]
by
Borroni, Barbara
Cotelli, M S
Premi, E
Gazzina, S
Cosseddu, M
Formenti, A
Gasparotti, R
Filosto, M
Padovani, A
Producer:
20140715
In:
Journal of inherited metabolic disease
vol. 36
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