Negative pressure treatment for necrotizing fasciitis after chemotherapy

Por Melchionda, Fraia, Pession, Andrea
Publicado em 2011

Urinary retention in bilateral pontine tumour: evidence for a pontine micturition centre in humans.

Por Manente, G, Melchionda, D, Uncini, A
Publicado em 1996

Pitfalls, prevention, and treatment of hyperuricemia during tumor lysis syndrome in the era of rasburicase (recombinant urate oxidase)

Por Pession, Andrea, Melchionda, Fraia, Castellini, Claudia
Publicado em 2008

Stage I clear cell sarcoma of the kidney: is it the time for a less intensive adjuvant treatment?

Por Spreafico, Filippo, Gandola, Lorenza, Melchionda, Fraia
Publicado no Transl Pediatr (2014)

Pendred Syndrome: study of three families

Por Bigozzi, M, Melchionda, S, Casano, R, Palladino, T, Gitti, G
Publicado em 2005

Ca(2+)/H(+) exchange by acidic organelles regulates cell migration in vivo

Por Melchionda, Manuela, Pittman, Jon K., Mayor, Roberto, Patel, Sandip
Publicado no J Cell Biol (2016)

Ca(2+)/H(+) exchange by acidic organelles regulates cell migration in vivo

Por Melchionda, Manuela, Pittman, Jon K., Mayor, Roberto, Patel, Sandip
Publicado no J Exp Med (2016)

Brain water intoxication and CT hypolucencies in ovarian hyperstimulation syndrome complicating gametes intrafallopian transfer (GIFT) and tubal pregnancy.

Por Onofrj, M, Thomas, A, Melchionda, D, Fulgente, T, Costantini, A, Scesi, M
Publicado em 1996

Synergistic Cytotoxic Effect of L-Asparaginase Combined with Decitabine as a Demethylating Agent in Pediatric T-ALL, with Specific Epigenetic Signature

Por Serravalle, Salvatore, Bertuccio, Salvatore N., Astolfi, Annalisa, Melchionda, Fraia, Pession, Andrea
Publicado no Biomed Res Int (2016)

In vivo confinement promotes collective migration of neural crest cells

Por Szabó, András, Melchionda, Manuela, Nastasi, Giancarlo, Woods, Mae L., Campo, Salvatore, Perris, Roberto, Mayor, Roberto
Publicado no J Cell Biol (2016)

Rotenone Upregulates Alpha-Synuclein and Myocyte Enhancer Factor 2D Independently from Lysosomal Degradation Inhibition

Por Gessica Sala, Alessandro Arosio, Giovanni Stefanoni, Laura Melchionda, Chiara Riva, Daniele Marinig, Laura Brighina, Carlo Ferrarese
Publicado em 2013-01-01

Rotenone Upregulates Alpha-Synuclein and Myocyte Enhancer Factor 2D Independently from Lysosomal Degradation Inhibition

Por Sala, Gessica, Arosio, Alessandro, Stefanoni, Giovanni, Melchionda, Laura, Riva, Chiara, Marinig, Daniele, Brighina, Laura, Ferrarese, Carlo
Publicado em 2013

A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesions

Por Melchionda, Laura, Damseh, Nadirah S., Abu Libdeh, Bassam Y., Nasca, Alessia, Elpeleg, Orly, Zanolini, Alice, Ghezzi, Daniele
Publicado no Front Genet (2014)

Physical activity monitoring in obese people in the real life environment

Por Tarrini Giulietta, Esposti Linda, Berti Lisa, Conti Linda, Di Gioia Annalisa, Benedetti Maria, Melchionda Nazario, Giannini Sandro
Publicado em 2009-12-01

Adjuvant IL-7 or IL-15 overcomes immunodominance and improves survival of the CD8(+) memory cell pool

Por Melchionda, Fraia, Fry, Terry J., Milliron, Matthew J., McKirdy, Melissa A., Tagaya, Yutaka, Mackall, Crystal L.
Publicado em 2005

Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide search.

Por Gasparini, P, Miraglia del Giudice, E, Delaunay, J, Totaro, A, Granatiero, M, Melchionda, S, Zelante, L, Iolascon, A
Publicado em 1997

Spleen nodules: a potential hallmark of Visceral Leishmaniasis in young children

Por Melchionda, Fraia, Varani, Stefania, Carfagnini, Filomena, Belotti, Tamara, Di Muccio, Trentina, Tigani, Roberto, Bergamaschi, Rosalba, Pession, Andrea
Publicado no BMC Infect Dis (2014)

Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation

Por Donaudy, F, Zheng, L, Ficarella, R, Ballana, E, Carella, M, Melchionda, S, Estivill, X, Bartles, J R, Gasparini, P
Publicado em 2006

Mitochondrial Complex III Deficiency Caused by TTC19 Defects: Report of a Novel Mutation and Review of Literature

Por Ardissone, Anna, Granata, Tiziana, Legati, Andrea, Diodato, Daria, Melchionda, Laura, Lamantea, Eleonora, Garavaglia, Barbara, Ghezzi, Daniele, Moroni, Isabella
Publicado no JIMD Rep (2015)

Evaluation of the Ion AmpliSeq SARS-CoV-2 Research Panel by Massive Parallel Sequencing

Por Federica Alessandrini, Sara Caucci, Valerio Onofri, Filomena Melchionda, Adriano Tagliabracci, Patrizia Bagnarelli, Laura Di Sante, Chiara Turchi, Stefano Menzo
Publicado em 2020-08-01