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Lamperti, C.
379
results:
Search for persons
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Online (379)
Mediatypes
E-Books (1)
Articles (Online) (131)
Bookchapter (Online) (2)
OpenAccess-fulltext (245)
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1
Primary mitochondrial myopathy: 12-month follow-up results ..:
Montano, V.
;
Lopriore, P.
;
Gruosso, F.
...
Journal of Neurology. 269 (2022) 12 - p. 6555-6565 , 2022
Link:
https://doi.org/10.1007/..
?
2
Adult-onset mitochondrial movement disorders: a national pi..:
Montano, V.
;
Orsucci, D.
;
Carelli, V.
...
Journal of Neurology. 269 (2021) 3 - p. 1413-1421 , 2021
Link:
https://doi.org/10.1007/..
?
3
MITOCHONDRIAL DISEASES (Posters):
Bertini, E.
;
Verrigni, D.
;
Battaglia, D.
...
Neuromuscular Disorders. 28 (2018) - p. S84 , 2018
Link:
https://doi.org/10.1016/..
?
4
Revisiting mitochondrial ocular myopathies: a study from th..:
Orsucci, D.
;
Angelini, C.
;
Bertini, E.
...
Journal of Neurology. 264 (2017) 8 - p. 1777-1784 , 2017
Link:
https://doi.org/10.1007/..
?
5
AAV9-based gene therapy partially ameliorates the clinical ..:
Di Meo, I
;
Marchet, S
;
Lamperti, C
..
Gene Therapy. 24 (2017) 10 - p. 661-667 , 2017
Link:
https://doi.org/10.1038/..
?
6
Dysregulated mitophagy and mitochondrial transport in senso..:
Liao, C.
;
Diot, A.
;
Ashley, N.
...
Neuromuscular Disorders. 25 (2015) - p. S185-S186 , 2015
Link:
https://doi.org/10.1016/..
?
7
T.P.18:
Sciacco, M.
;
Ronchi, D.
;
Ripolone, M.
...
Neuromuscular Disorders. 24 (2014) 9-10 - p. 869-870 , 2014
Link:
https://doi.org/10.1016/..
?
8
Evaluation of muscle biopsy in late-onset GSDII patients be..:
Violano, R
;
Ripolone, M
;
Lucchini, V
...
BMC Musculoskeletal Disorders. 14 (2013) S2 - p. , 2013
Link:
https://doi.org/10.1186/..
?
9
A case of Leber hereditary optic neuropathy plus dystonia c..:
Saracchi, Enrico
;
DiFrancesco, J. C.
;
Brighina, L.
...
Neurological Sciences. 34 (2012) 3 - p. 407-408 , 2012
Link:
https://doi.org/10.1007/..
?
10
New molecular findings in congenital myopathies due to sele..:
Cagliani, R.
;
Fruguglietti, M.E.
;
Berardinelli, A.
...
Journal of the Neurological Sciences. 300 (2011) 1-2 - p. 107-113 , 2011
Link:
https://doi.org/10.1016/..
?
11
P3.5 Oxidative defect in a large cohort of genetically-dete..:
Berardinelli, A.
;
Fagiolari, G.
;
Vallejo, D.
...
Neuromuscular Disorders. 21 (2011) 9-10 - p. 683 , 2011
Link:
https://doi.org/10.1016/..
?
12
Multi-system neurological disease is common in patients wit..:
Yu-Wai-Man, P.
;
Griffiths, P.G.
;
Gorman, G.S.
...
Brain. 133 (2010) 3 - p. 771-786 , 2010
Link:
https://doi.org/10.1093/..
?
13
G.P.9.06 Infantile inflammatory myopathy presenting as SMAR..:
Crugnola, V.
;
Colombo, I.
;
Rossetti, G.
...
Neuromuscular Disorders. 19 (2009) 8-9 - p. 596 , 2009
Link:
https://doi.org/10.1016/..
?
14
G.P.15.09 Unexpected high percentage of asymptomatic subjec..:
Bonifazi, E.
;
Lamperti, C.
;
Fiorillo, C.
...
Neuromuscular Disorders. 19 (2009) 8-9 - p. 649-650 , 2009
Link:
https://doi.org/10.1016/..
?
15
Neuropathological study of skeletal muscle, heart, liver, a..:
Lamperti, C.
;
Salani, S.
;
Lucchiari, S.
...
Journal of Inherited Metabolic Disease. 32 (2009) S1 - p. 161-168 , 2009
Link:
https://doi.org/10.1007/..
1-15