Powerhouse failure and oxidative damage in autosomal recessive spastic ataxia of Charlevoix-Saguenay
Criscuolo, Chiara, Procaccini, C., Meschini, M. C., Cianflone, A., Carbone, R., Doccini, S., Devos, D., Nesti, C., Vuillaume, I., Pellegrino, M., Filla, A., De Michele, G., Matarese, G., Santorelli, F. M.
Published in Journal of neurology (01.12.2015)
Published in Journal of neurology (01.12.2015)
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Clinical and neuroimaging features of the m.10197G>A mtDNA mutation: New case reports and expansion of the phenotype variability
Tolomeo, D., Rubegni, A., Severino, M., Pochiero, F., Bruno, C., Cassandrini, D., Madeo, A., Doccini, S., Pedemonte, M., Rossi, A., D'Amore, F., Donati, M.A., Di Rocco, M., Santorelli, F.M., Nesti, C.
Published in Journal of the neurological sciences (15.04.2019)
Published in Journal of the neurological sciences (15.04.2019)
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Journal Article
Investigation of interactions between poly-L-lysine-coated boron nitride nanotubes and C2C12 cells: up-take, cytocompatibility, and differentiation
Ciofani, G, Ricotti, L, Danti, S, Moscato, S, Nesti, C, D'Alessandro, D, Dinucci, D, Chiellini, F, Pietrabissa, A, Petrini, M, Menciassi, A
Published in International journal of nanomedicine (01.01.2010)
Published in International journal of nanomedicine (01.01.2010)
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Journal Article
Diagnostic approach to mitochondrial disorders: the need for a reliable biomarker
Mancuso, M, Orsucci, D, Coppedè, F, Nesti, C, Choub, A, Siciliano, G
Published in Current molecular medicine (01.12.2009)
Published in Current molecular medicine (01.12.2009)
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Journal Article
Autoimmunity to CD38 and GAD in Type I and Type II diabetes: CD38 and HLA genotypes and clinical phenotypes
ANTONELLI, A, TUOMI, T, NANNIPIERI, M, FALLAHI, P, NESTI, C, OKAMOTO, H, GROOP, L, FERRANNINI, E
Published in Diabetologia (01.09.2002)
Published in Diabetologia (01.09.2002)
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Journal Article
Myelinated retinal fibers in autosomal recessive spastic ataxia of Charlevoix-Saguenay
Vingolo, E. M., Di Fabio, R., Salvatore, S., Grieco, G., Bertini, E., Leuzzi, V., Nesti, C., Filla, A., Tessa, A., Pierelli, F., Santorelli, F. M., Casali, C.
Published in European journal of neurology (01.09.2011)
Published in European journal of neurology (01.09.2011)
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Journal Article
Large deletion mutation of SPAST in a multi-generation family from Sardinia
Racis, L., Di Fabio, R., Tessa, A., Guillot, F., Storti, E., Piccolo, F., Nesti, C., Tedde, A., Pierelli, F., Agnetti, V., Santorelli, F. M., Casali, C.
Published in European journal of neurology (01.06.2014)
Published in European journal of neurology (01.06.2014)
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Journal Article
Type 2 diabetes in hepatitis C-related mixed cryoglobulinaemia patients
Antonelli, A., Ferri, C., Fallahi, P., Sebastiani, M., Nesti, C., Barani, L., Barale, R., Ferrannini, E.
Published in Rheumatology (Oxford, England) (01.02.2004)
Published in Rheumatology (Oxford, England) (01.02.2004)
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Journal Article
Thyroid involvement in patients with overt HCV-related mixed cryoglobulinaemia
Antonelli, A., Ferri, C., Fallahi, P., Giuggioli, D., Nesti, C., Longombardo, G., Fadda, P., Pampana, A., Maccheroni, M., Ferrannini, E.
Published in QJM : An International Journal of Medicine (01.08.2004)
Published in QJM : An International Journal of Medicine (01.08.2004)
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Journal Article
Anti‐CD38 autoimmunity in patients with chronic autoimmune thyroiditis or Graves' disease
Antonelli, A., Fallahi, P., Nesti, C., Pupilli, C., Marchetti, P., Takasawa, S., Okamoto, H., Ferrannini, E.
Published in Clinical and experimental immunology (01.12.2001)
Published in Clinical and experimental immunology (01.12.2001)
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Journal Article
Lack of association between mtDNA haplogroups and Alzheimer's disease in Tuscany
Mancuso, M, Nardini, M, Micheli, D, Rocchi, A, Nesti, C, Giglioli, N J, Petrozzi, L, Rossi, C, Ceravolo, R, Bacci, A, Choub, A, Ricci, G, Tognoni, G, Manca, M L, Siciliano, G, Murri, L
Published in Neurological sciences (01.06.2007)
Published in Neurological sciences (01.06.2007)
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Journal Article
G.P.3.10 Oxidative stress biomarkers are related to disease severity in mitochondrial myopathies, and may be modified by a cysteine donor
Mancuso, M, Orsucci, D, Gerfo, A. Lo, Santoro, G, Nesti, C, Rocchi, A, Petrozzi, L, Galetta, F, Siciliano, G
Published in Neuromuscular disorders : NMD (01.09.2009)
Published in Neuromuscular disorders : NMD (01.09.2009)
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Journal Article
Expression of a novel human sialidase encoded by the NEU2 gene
Monti, Eugenio, Preti, Augusto, Nesti, Carlo, Ballabio, Andrea
Published in Glycobiology (Oxford) (01.12.1999)
Published in Glycobiology (Oxford) (01.12.1999)
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Journal Article
Mitochondrial syndromic sensorineural hearing loss
Forli, F, Passetti, S, Mancuso, M, Seccia, V, Siciliano, G, Nesti, C, Berrettini, S
Published in Bioscience reports (01.06.2007)
Published in Bioscience reports (01.06.2007)
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Journal Article
G.P.3.08 Myoclonic epilepsy, cortical dysplasia and mitochondrial complex I deficiency: A case report
Nesti, C, Mancuso, M, Petrozzi, L, Santorelli, F.M, Rocchi, A, Ali, G, Tessa, A, LoGerfo, A, Iudice, A, Siciliano, G
Published in Neuromuscular disorders : NMD (01.09.2009)
Published in Neuromuscular disorders : NMD (01.09.2009)
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Journal Article
Isonymy and the genetic structure of Switzerland. II. Isolation by distance
Rodriguez-Larralde, A, Scapoli, C, Beretta, M, Nesti, C, Mamolini, E, Barrai, I
Published in Annals of human biology (01.11.1998)
Published in Annals of human biology (01.11.1998)
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Journal Article
Isonymy and Isolation by Distance in Germany
RODRIGUEZ-LARRALDE, A., BARRAI, I., NESTI, C., MAMOLINI, E., SCAPOLI, C.
Published in Human biology (01.12.1998)
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Published in Human biology (01.12.1998)
Journal Article
Reversible valproate-induced subacute encephalopathy caused by a mitochondrial DNA variant
De Michele, G., Sorrentino, P., Ruggiero, L., De Michele, G., Peluso, S., Antenora, A., Nesti, C., Santorelli, F.M., Filla, A.
Published in Journal of the neurological sciences (15.10.2017)
Published in Journal of the neurological sciences (15.10.2017)
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