Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Valeria Guaran"'
Autor:
Micol Busi, Elena Olivetto, Stefano Volinia, Valeria Guaran, Edi Simoni, Patrizia Trevisi, Alessandro Martini, Alessandro Castiglione, Laura Astolfi, Marco Galasso
Publikováno v:
International Journal of Molecular Medicine
Mutations in mitochondrial DNA (mtDNA) have been shown to be an important cause of sensorineural hearing loss (SNHL). In this study, we performed a clinical and genetic analysis of 169 hearing-impaired patients and some of their relatives suffering f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46e6c8c7295e00f153be48e7a1b2096d
https://doi.org/10.3892/ijmm.2013.1470
https://doi.org/10.3892/ijmm.2013.1470
Autor:
M. Grabiele, Satz Mengensatzproduktion, Sakari Knuutila, C.Y. Nagamachi, A. Montaldi, G. Capone, Y. Matsuda, Laura Astolfi, D. Baldo, A. Membrillo, A. Alghisi, Riikka Räty, M.O. Pereyra, G. Anaya, Druck Reinhardt Druck Basel, T.S. Sczepanski, T.E. Sfakianakis, L.M.M. Nardozza, M.R. Vicari, C. Rossi, S. Demyda-Peyrás, Alessandro Castiglione, V.G.D. Orrico, Neda Mosakhani, V. Nogaroto, K. Pawlina, K. Yamada, J.P. O'Byran, D. Cardozo, Giulia Zeri, Anne Tyybäkinoja, R.F. Artoni, Donato Gemmati, C. Nishida, M. Moreno-Millán, S. Ishishita, J. Ishijima, Erkki Elonen, M.C.S.P. Cernach, Roberto Bovo, S.S. Takeno, M. Bugno-Poniewierska, J. Faivovich, M.I. Melaragno, J.C. Pieczarka, Marja-Liisa Karjalainen-Lindsberg, J. Busciglio, D.K. Griffin, T. Yamazaki, A. Martini, S.S. Bhatt, Valeria Guaran, C.F.B. Haddad, G.F. Catroli, T. Liehr, M.C. de Almeida, R.S. Guilherme, Elisa Orioli, P. Suárez, P.S. Bernarde, K.J. Gardiner
Publikováno v:
Cytogenetic and Genome Research. 141:I-IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::476a29dc60ef024bc875ddc157399b51
https://doi.org/10.1159/000356038
https://doi.org/10.1159/000356038
Publikováno v:
Audiological Medicine. 10:160-166
Meniere's disease is a disabling disorder presenting with crises of aural fullness, tinnitus, hearing loss and vertigo. The hallmark of the pathology is a labyrinthine hydrops, but its pathogenesis remains unclear. This unknown aetiology explains the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c17882f1d35719ff04bacd9c42c105b6
https://doi.org/10.3109/1651386x.2012.714192
https://doi.org/10.3109/1651386x.2012.714192
Autor:
Claude Jolly, Elena Olivetto, Nicola Marchetti, Edi Simoni, Alberto Cavazzini, Alessandro Martini, Laura Astolfi, Valeria Guaran
Publikováno v:
Journal of biomedical materials research. Part B, Applied biomaterials. 102(2)
Anti-inflammatory drugs can minimize the trauma and inflammation in the inner ear caused by cochlear implantation surgery. For this reason, much effort has recently been devoted to finding the best way to administer these anti-inflammatory drugs for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a16727b209667ea9d0300eedb66e7f9
https://pubmed.ncbi.nlm.nih.gov/23997036
https://pubmed.ncbi.nlm.nih.gov/23997036
Autor:
T. Volo, Enzo Emanuelli, Patrizia Trevisi, T. Sathiyaseelan, Valeria Guaran, A. Martini, Laura Astolfi
Publikováno v:
International journal of pediatric otorhinolaryngology. 77(8)
The GJB2 gene is located on chromosome 13q12 and it encodes the connexin 26, a transmembrane protein involved in cell–cell attachment of almost all tissues. GJB2 mutations cause autosomal recessive (DFNB1) and sometimes dominant (DFNA3) non-syndrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba58f15e89f10092164aa3792323c624
https://pubmed.ncbi.nlm.nih.gov/23751281
https://pubmed.ncbi.nlm.nih.gov/23751281
Autor:
A. Montaldi, Alessandro Castiglione, A. Martini, A. Alghisi, Roberto Bovo, Valeria Guaran, Giulia Zeri, Donato Gemmati, Laura Astolfi, Elisa Orioli
The first child (proband) of nonconsanguineous Caucasian parents underwent genetic investigation because she was affected with congenital choanal atresia, heart defects and kidney hyposplasia with mild transient renal insufficiency. The direct DNA se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79719e9a15f2bbc5c4068be6a639414d
http://hdl.handle.net/11392/1839901
http://hdl.handle.net/11392/1839901
Autor:
Giorgio Lelli, Sara Ghiselli, Valeria Guaran, Elena Olivetto, Milvia Chicca, Alessandro Martini, Laura Astolfi, Edi Simoni
Publikováno v:
Oncology Reports
Cisplatin is the most common antineoplastic drug used for the therapy of solid tumours. To date, researchers have focused on the dosage to be administered for each specific tumour, mainly considering the local adverse effects. The aim of this study w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82ae71749876c6cc0180fcb011801289
https://pubmed.ncbi.nlm.nih.gov/23404427
https://pubmed.ncbi.nlm.nih.gov/23404427
Autor:
Alessandro Castiglione, Marina Taddei Masieri, Alessandra Ferlini, Patrizia Trevisi, Micol Busi, Laura Astolfi, Valeria Guaran, Alessandro Martini, Anna Ravani
Objectives Mutations in the SLC26A4 gene (7q22.3–7q31.1) are considered one of the most common causes of genetic hearing loss. There are two clinical forms related to these mutations: syndromic and non-syndromic deafness. The first one is named Pen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d779d2ace61b25b784a5f454d1bafde0
http://hdl.handle.net/11577/2510910
http://hdl.handle.net/11577/2510910
Autor:
Alessandro Martini, Maurizio Previati, Valeria Guaran, Elisa Corbacella, Irene Lanzoni, Silvano Capitani, Sara Magosso
Publikováno v:
Europe PubMed Central
Scopus-Elsevier
Scopus-Elsevier
Cis-diamminedichloroplatinum (II) cisplatin (CDDP) is an organometallic compound frequently used in anti-cancer therapy, in particular ovarian, testicular, and head and neck tumors. We found cisplatin was effective against human promyelocytic leukemi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e587e0a912ce9d8fca0b1dc487960da
http://europepmc.org/abstract/med/16865238
http://europepmc.org/abstract/med/16865238