Search the collection

9 results for Fiorini,+Claudio

Sort by:

Sort by

Limit results to:

20 per page

9 results for Fiorini,+Claudio

Export to excel

Export record to excel

File type to download

Beta version

Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 1
ArticlesPeer ReviewedFull Text
Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNALys
Author / Creator:Capristo, Mariantonietta ; Del Dotto, Valentina ; Tropeano, Concetta Valentina ; Fiorini, Claudio ; Caporali, Leonardo ; La Morgia, Chiara ; Valentino, Maria Lucia ; Montopoli, Monica ; Carelli, Valerio ; Maresca, Alessandra
Publisher:New York: BioMed Central
Journal title:Molecular medicine (Cambridge, Mass.), 2022-08, Vol.28 (1), p.1-90, Article 90
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 2
ArticlesPeer ReviewedFull Text
Pathogenic mitochondrial DNA variants are associated with response to anti-VEGF therapy in ovarian cancer PDX models
Author / Creator:Boso, Daniele ; Piga, Ilaria ; Trento, Chiara ; Minuzzo, Sonia ; Angi, Eleonora ; Iommarini, Luisa ; Lazzarini, Elisabetta ; Caporali, Leonardo ; Fiorini, Claudio ; D'Angelo, Luigi ; De Luise, Monica ; Kurelac, Ivana ; Fassan, Matteo ; Porcelli, Anna Maria ; Navaglia, Filippo ; Billato, Ilaria ; Esposito, Giovanni ; Gasparre, Giuseppe ; Romualdi, Chiara ; Indraccolo, Stefano
Publisher:England: BioMed Central Ltd
Journal title:Journal of experimental & clinical cancer research, 2024-12, Vol.43 (1), p.325-17, Article 325
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 3
ArticlesPeer ReviewedFull Text
Papillary thyroid carcinoma tall cell variant shares accumulation of mitochondria, mitochondrial DNA mutations, and loss of oxidative phosphorylation complex I integrity with oncocytic tumors
Author / Creator:Tsybrovskyy, Oleksiy ; De Luise, Monica ; Biase, Dario ; Caporali, Leonardo ; Fiorini, Claudio ; Gasparre, Giuseppe ; Carelli, Valerio ; Hackl, Dominik ; Imamovic, Larisa ; Haim, Silke ; Sobrinho‐Simões, Manuel ; Tallini, Giovanni
Publisher:Hoboken, USA: John Wiley & Sons, Inc
Journal title:The journal of pathology. Clinical research, 2022-03, Vol.8 (2), p.155-168
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 4
ArticlesPeer ReviewedFull Text
Recessive MECR pathogenic variants cause an LHON-like optic neuropathy
Author / Creator:Fiorini, Claudio ; Degiorgi, Andrea ; Cascavilla, Maria Lucia ; Tropeano, Concetta Valentina ; La Morgia, Chiara ; Battista, Marco ; Ormanbekova, Danara ; Palombo, Flavia ; Carbonelli, Michele ; Bandello, Francesco ; Carelli, Valerio ; Maresca, Alessandra ; Barboni, Piero ; Baruffini, Enrico ; Caporali, Leonardo
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2024-01, Vol.61 (1), p.93-101
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 5
ArticlesPeer ReviewedFull Text
Co-occurrence of amyotrophic lateral sclerosis and Leber’s hereditary optic neuropathy: is mitochondrial dysfunction a modifier?
Author / Creator:Amore, Giulia ; Vacchiano, Veria ; La Morgia, Chiara ; Valentino, Maria L. ; Caporali, Leonardo ; Fiorini, Claudio ; Ormanbekova, Danara ; Salvi, Fabrizio ; Bartoletti-Stella, Anna ; Capellari, Sabina ; Liguori, Rocco ; Carelli, Valerio
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of neurology, 2023-01, Vol.270 (1), p.559-564
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 6
ArticlesPeer ReviewedFull Text
Spatial transcriptomics: bridging anatomy and molecular techniques for precision medicine in rare diseases
Author / Creator:Elisa, Boschetti ; Irene, Neri ; Leonardo, Caporali ; Claudio, Fiorini ; Ormanbekova, Danara ; Santino, Blando ; Carolina, Malagelada ; Carelli, Valerio ; De Giorgio, Roberto ; Ratti, Stefano ; Manzoli, Lucia
Publisher:Florence: Firenze University Press Università degli Studi di Firenze
Journal title:Italian journal of anatomy and embryology, 2024-01, Vol.128, p.123-123
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 7
ArticlesPeer ReviewedFull Text
An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder
Author / Creator:Cameli, Cinzia ; Viggiano, Marta ; Rochat, Magali J. ; Maresca, Alessandra ; Caporali, Leonardo ; Fiorini, Claudio ; Palombo, Flavia ; Magini, Pamela ; Duardo, Renée C. ; Ceroni, Fabiola ; Scaduto, Maria C. ; Posar, Annio ; Seri, Marco ; Carelli, Valerio ; Visconti, Paola ; Bacchelli, Elena ; Maestrini, Elena
Publisher:England: John Wiley & Sons, Inc
Journal title:Journal of cellular and molecular medicine, 2021-03, Vol.25 (5), p.2459-2470
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 8
ArticlesPeer ReviewedFull Text
Progression of micro-anatomical, molecular and metabolic changes affecting the liver of patients with TYMP derived mitochondrial disease
Author / Creator:Boschetti, Elisa ; Neri, Irene ; Caporali, Leonardino ; Fiorini, Claudio ; Ormanbekova, Danara ; Righi, Valeria ; Rinaldi, Rita ; D'Angelo, Roberto ; Malagelada, Carolina ; Costa, Roberta ; Cenacchi, Giovanna ; Pironi, Loris ; Carelli, Valerio ; De Giorgio, Roberto ; Ratti, Stefano ; Manzoli, Lucia
Publisher:Firenze University Press
Journal title:Italian journal of anatomy and embryology, 2023-09, Vol.127 (S1), p.46
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 9
ArticlesPeer ReviewedFull Text
Missense PDSS1 mutations in CoenzymeQ10 synthesis cause optic atrophy and sensorineural deafness
Author / Creator:Nardecchia, Francesca ; De Giorgi, Agnese ; Palombo, Flavia ; Fiorini, Claudio ; De Negri, Anna M. ; Carelli, Valerio ; Caporali, Leonardo ; Leuzzi, Vincenzo
Publisher:United States: John Wiley & Sons, Inc
Journal title:Annals of clinical and translational neurology, 2021-01, Vol.8 (1), p.247-251
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.

Export record to excel

Export this record

Export record to excel

Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNALys

Export this record

Export record to excel

Pathogenic mitochondrial DNA variants are associated with response to anti-VEGF therapy in ovarian cancer PDX models

Export this record

Export record to excel

Papillary thyroid carcinoma tall cell variant shares accumulation of mitochondria, mitochondrial DNA mutations, and loss of oxidative phosphorylation complex I integrity with oncocytic tumors

Export this record

Export record to excel

Recessive MECR pathogenic variants cause an LHON-like optic neuropathy

Export this record

Export record to excel

Co-occurrence of amyotrophic lateral sclerosis and Leber’s hereditary optic neuropathy: is mitochondrial dysfunction a modifier?

Export this record

Export record to excel

Spatial transcriptomics: bridging anatomy and molecular techniques for precision medicine in rare diseases

Export this record

Export record to excel

An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder

Export this record

Export record to excel

Progression of micro-anatomical, molecular and metabolic changes affecting the liver of patients with TYMP derived mitochondrial disease

Export this record

Export record to excel

Missense PDSS1 mutations in CoenzymeQ10 synthesis cause optic atrophy and sensorineural deafness

Refine your search