In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria.

অনুযায়ী Chomyn, A, Meola, G, Bresolin, N, Lai, S T, Scarlato, G, Attardi, G
প্রকাশিত 1991

Platelet-mediated transformation of mtDNA-less human cells: analysis of phenotypic variability among clones from normal individuals--and complementation behavior of the tRNALys mut...

অনুযায়ী Chomyn, A., Lai, S. T., Shakeley, R., Bresolin, N., Scarlato, G., Attardi, G.
প্রকাশিত 1994

Body building and myoglobinuria: report of three cases

অনুযায়ী Doriguzzi, C, Palmucci, L, Mongini, T, Arnaudo, E, Bet, L, Bresolin, N
প্রকাশিত 1988

Anti-MuSK-Positive Myasthenia Gravis in a Patient with Parkinsonism and Cognitive Impairment

অনুযায়ী Lanfranconi, S., Corti, S., Baron, P., Conti, G., Borellini, L., Bresolin, N., Bersano, A.
প্রকাশিত 2011

Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency.

অনুযায়ী Doriguzzi, C, Palmucci, L, Mongini, T, Bresolin, N, Bet, L, Comi, G, Lala, R
প্রকাশিত 1989

Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF).

অনুযায়ী Zeviani, M, Amati, P, Bresolin, N, Antozzi, C, Piccolo, G, Toscano, A, DiDonato, S
প্রকাশিত 1991

Growth factors in ischemic stroke

অনুযায়ী Lanfranconi, S, Locatelli, F, Corti, S, Candelise, L, Comi, G P, Baron, P L, Strazzer, S, Bresolin, N, Bersano, A
প্রকাশিত J Cell Mol Med (2011)

Intragenic inversion of mtDNA: a new type of pathogenic mutation in a patient with mitochondrial myopathy.

অনুযায়ী Musumeci, O, Andreu, A L, Shanske, S, Bresolin, N, Comi, G P, Rothstein, R, Schon, E A, DiMauro, S
প্রকাশিত 2000

Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant disease.

অনুযায়ী Zeviani, M, Bresolin, N, Gellera, C, Bordoni, A, Pannacci, M, Amati, P, Moggio, M, Servidei, S, Scarlato, G, DiDonato, S
প্রকাশিত 1990

An evolutionary history of the selectin gene cluster in humans

অনুযায়ী Fumagalli, M, Fracassetti, M, Cagliani, R, Forni, D, Pozzoli, U, Comi, G P, Marini, F, Bresolin, N, Clerici, M, Sironi, M
প্রকাশিত 2012

IgD Multiple Myeloma Paraproteinemia as a Cause of Myositis

অনুযায়ী Colombo, I., Fruguglietti, M. E., Napoli, L., Sciacco, M., Tagliaferri, E., Della Volpe, A., Crugnola, V., Bresolin, N., Moggio, M., Prelle, A.
প্রকাশিত 2010

Morpholino-mediated SOD1 reduction ameliorates an amyotrophic lateral sclerosis disease phenotype

অনুযায়ী Nizzardo, M., Simone, C., Rizzo, F., Ulzi, G., Ramirez, A., Rizzuti, M., Bordoni, A., Bucchia, M., Gatti, S., Bresolin, N., Comi, G. P., Corti, S.
প্রকাশিত Sci Rep (2016)

Synaptotagmin 13 is neuroprotective across motor neuron diseases

অনুযায়ী Nizzardo, M., Taiana, M., Rizzo, F., Aguila Benitez, J., Nijssen, J., Allodi, I., Melzi, V., Bresolin, N., Comi, G. P., Hedlund, E., Corti, S.
প্রকাশিত Acta Neuropathol (2020)

A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood

অনুযায়ী Bassi, M, Bresolin, N, Tonelli, A, Nazos, K, Crippa, F, Baschirotto, C, Zucca, C, Bersano, A, Dolcetta, D, Boneschi, F, Barone, V, Casari, G
প্রকাশিত 2004

A Trans-Specific Polymorphism in ZC3HAV1 Is Maintained by Long-Standing Balancing Selection and May Confer Susceptibility to Multiple Sclerosis

অনুযায়ী Cagliani, R., Guerini, F. R., Fumagalli, M., Riva, S., Agliardi, C., Galimberti, D., Pozzoli, U., Goris, A., Dubois, B., Fenoglio, C., Forni, D., Sanna, S., Zara, I., Pitzalis, M., Zoledziewska, M., Cucca, F., Marini, F., Comi, G. P., Scarpini, E., Bresolin, N., Clerici, M., Sironi, M.
প্রকাশিত Mol Biol Evol (2012)

“Ears of the Lynx” MRI Sign Is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia

অনুযায়ী Pascual, B., de Bot, S.T., Daniels, M.R., França, M.C., Toro, C., Riverol, M., Hedera, P., Bassi, M.T., Bresolin, N., van de Warrenburg, B.P., Kremer, B., Nicolai, J., Charles, P., Xu, J., Singh, S., Patronas, N.J., Fung, S.H., Gregory, M.D., Masdeu, J.C.
প্রকাশিত AJNR Am J Neuroradiol (2019)