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Switching of biological therapy to dupilumab in comorbid patients with severe asthma and CRSwNP.
Published in:
European Archives of Oto-Rhino-Laryngology, 2024, v. 281, n. 6, p. 3017, doi. 10.1007/s00405-024-08461-y
By:
- Rosso, Cecilia;
- De Corso, Eugenio;
- Conti, Valerio;
- Nitro, Letizia;
- Saibene, Alberto Maria;
- Parazzini, Elena;
- Rinaldo, Rocco;
- De Pascalis, Sabrina;
- Arnone, Flavio;
- Centanni, Stefano;
- Montuori, Claudio;
- D'Auria, Leandro Maria;
- Felisati, Giovanni;
- Pipolo, Carlotta
Publication type:
Article
High definition three-dimensional exoscope (VITOM 3D) for microsurgery training: a preliminary experience.
Published in:
European Archives of Oto-Rhino-Laryngology, 2020, v. 277, n. 9, p. 2589, doi. 10.1007/s00405-020-06014-7
By:
- De Virgilio, Armando;
- Costantino, Andrea;
- Ebm, Claudia;
- Conti, Valerio;
- Mondello, Tiziana;
- Di Bari, Matteo;
- Cugini, Giovanni;
- Mercante, Giuseppe;
- Spriano, Giuseppe
Publication type:
Article
Morphometric network-based abnormalities correlate with psychiatric comorbidities and gene expression in PCDH19-related developmental and epileptic encephalopathy.
Published in:
Translational Psychiatry, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41398-024-02753-x
By:
- Lenge, Matteo;
- Balestrini, Simona;
- Napolitano, Antonio;
- Mei, Davide;
- Conti, Valerio;
- Baldassarri, Giulia;
- Trivisano, Marina;
- Pellacani, Simona;
- Macconi, Letizia;
- Longo, Daniela;
- Rossi Espagnet, Maria Camilla;
- Cappelletti, Simona;
- PCDH19 Clinical Study Group;
- Ferrari, Annarita;
- Pisano, Tiziana;
- Sicca, Federico;
- Striano, Pasquale;
- D'Incerti, Ludovico;
- Barba, Carmen;
- Specchio, Nicola
Publication type:
Article
Prospective Evaluation of Ghrelin and Des-Acyl Ghrelin Plasma Levels in Children with Newly Diagnosed Epilepsy: Evidence for Reduced Ghrelin-to-Des-Acyl Ghrelin Ratio in Generalized Epilepsies.
Published in:
Journal of Personalized Medicine, 2022, v. 12, n. 4, p. 527, doi. 10.3390/jpm12040527
By:
- Costa, Anna-Maria;
- Lo Barco, Tommaso;
- Spezia, Elisabetta;
- Conti, Valerio;
- Roli, Laura;
- Marini, Lorenza;
- Minghetti, Sara;
- Caramaschi, Elisa;
- Pietrangelo, Laura;
- Pecoraro, Luca;
- D'Achille, Fabio;
- Accorsi, Paola;
- Trenti, Tommaso;
- Melani, Federico;
- Marini, Carla;
- Guerrini, Renzo;
- Darra, Francesca;
- Bergonzini, Patrizia;
- Biagini, Giuseppe
Publication type:
Article
Multimodal fiber-probe spectroscopy allows detecting epileptogenic focal cortical dysplasia in children.
Published in:
Journal of Biophotonics, 2017, v. 10, n. 6/7, p. 896, doi. 10.1002/jbio.201600136
By:
- Anand, Suresh;
- Cicchi, Riccardo;
- Giordano, Flavio;
- Conti, Valerio;
- Buccoliero, Anna Maria;
- Guerrini, Renzo;
- Pavone, Francesco Saverio
Publication type:
Article
Profiling PI3K-AKT-MTOR variants in focal brain malformations reveals new insights for diagnostic care.
Published in:
2022
By:
- Pirozzi, Filomena;
- Berkseth, Matthew;
- Shear, Rylee;
- Gonzalez, Lorenzo;
- Timms, Andrew E;
- Sulc, Josef;
- Pao, Emily;
- Oyama, Nora;
- Forzano, Francesca;
- Conti, Valerio;
- Guerrini, Renzo;
- Doherty, Emily S;
- Saitta, Sulagna C;
- Lockwood, Christina M;
- Pritchard, Colin C;
- Dobyns, William B;
- Novotny, Edward;
- Wright, Jason N N;
- Saneto, Russell P;
- Friedman, Seth
Publication type:
journal article
Biallelic DMXL2 mutations impair autophagy and cause Ohtahara syndrome with progressive course.
Published in:
2019
By:
- Esposito, Alessandro;
- Falace, Antonio;
- Wagner, Matias;
- Gal, Moran;
- Mei, Davide;
- Conti, Valerio;
- Pisano, Tiziana;
- Aprile, Davide;
- Cerullo, Maria Sabina;
- Fusco, Antonio De;
- Giovedì, Silvia;
- Seibt, Annette;
- Magen, Daniella;
- Polster, Tilman;
- Eran, Ayelet;
- Stenton, Sarah L;
- Fiorillo, Chiara;
- Ravid, Sarit;
- Mayatepek, Ertan;
- Hafner, Hava
Publication type:
journal article
De novo mutations of the ATP6V1A gene cause developmental encephalopathy with epilepsy.
Published in:
2018
By:
- Fassio, Anna;
- Esposito, Alessandro;
- Mitsuhiro Kato;
- Hirotomo Saitsu;
- Mei, Davide;
- Marini, Carla;
- Conti, Valerio;
- Mitsuko Nakashima;
- Nobuhiko Okamoto;
- Turker, Akgun Olmez;
- Albuz, Burcu;
- Gündüz, C. Nur Semerci;
- Yanagihara, Keiko;
- Belmonte, Elisa;
- Maragliano, Luca;
- Ramsey, Keri;
- Balak, Chris;
- Siniard, Ashley;
- Narayanan, Vinodh;
- Ohba, Chihiro
Publication type:
journal article
Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene.
Published in:
Brain: A Journal of Neurology, 2013, v. 136, n. 11, p. 3378, doi. 10.1093/brain/awt249
By:
- Conti, Valerio;
- Carabalona, Aurelie;
- Pallesi-Pocachard, Emilie;
- Parrini, Elena;
- Leventer, Richard J.;
- Buhler, Emmanuelle;
- McGillivray, George;
- Michel, François J.;
- Striano, Pasquale;
- Mei, Davide;
- Watrin, Françoise;
- Lise, Stefano;
- Pagnamenta, Alistair T.;
- Taylor, Jenny C.;
- Kini, Usha;
- Clayton-Smith, Jill;
- Novara, Francesca;
- Zuffardi, Orsetta;
- Dobyns, William B.;
- Scheffer, Ingrid E.
Publication type:
Article
Genetic Basis of Brain Malformations.
Published in:
Molecular Syndromology, 2016, v. 7, n. 4, p. 220, doi. 10.1159/000448639
By:
- Parrini, Elena;
- Conti, Valerio;
- Dobyns, William B.;
- Guerrini, Renzo
Publication type:
Article
Circulating tumor cells and palbociclib treatment in patients with ER-positive, HER2-negative advanced breast cancer: results from a translational sub-study of the TREnd trial.
Published in:
2021
By:
- Galardi, Francesca;
- De Luca, Francesca;
- Biagioni, Chiara;
- Migliaccio, Ilenia;
- Curigliano, Giuseppe;
- Minisini, Alessandro M.;
- Bonechi, Martina;
- Moretti, Erica;
- Risi, Emanuela;
- McCartney, Amelia;
- Benelli, Matteo;
- Romagnoli, Dario;
- Cappadona, Silvia;
- Gabellini, Stefano;
- Guarducci, Cristina;
- Conti, Valerio;
- Biganzoli, Laura;
- Di Leo, Angelo;
- Malorni, Luca
Publication type:
journal article
Pre-Clinical Experience With the VITOM 3D and the ARTip Cruise System for Micro-Laryngeal Surgery.
Published in:
2021
By:
- De Virgilio, Armando;
- Costantino, Andrea;
- Mondello, Tiziana;
- Conti, Valerio;
- Pirola, Francesca;
- Russo, Elena;
- Mercante, Giuseppe;
- Spriano, Giuseppe
Publication type:
journal article
Genomic DNA methylation distinguishes subtypes of human focal cortical dysplasia.
Published in:
Epilepsia (Series 4), 2019, v. 60, n. 6, p. 1091, doi. 10.1111/epi.14934
By:
- Kobow, Katja;
- Coras, Roland;
- Blümcke, Ingmar;
- Kudernatsch, Manfred;
- Hamer, Hajo;
- Kasper, Burkhard S.;
- Rössler, Karl;
- Conti, Valerio;
- Guerrini, Renzo;
- Ziemann, Mark;
- Khurana, Ishant;
- Kaspi, Antony;
- Kaipananickal, Harikrishnan;
- El‐Osta, Assam;
- Feucht, Martha;
- Mühlebner, Angelika;
- Aronica, Eleonora;
- Hainfellner, Johannes A.;
- Czech, Thomas;
- Pieper, Tom
Publication type:
Article
Association of MTOR Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism.
Published in:
JAMA Neurology, 2016, v. 73, n. 7, p. 836, doi. 10.1001/jamaneurol.2016.0363
By:
- Mirzaa, Ghayda M.;
- Campbell, Catarina D.;
- Solovieff, Nadia;
- Goold, Carleton P.;
- Jansen, Laura A.;
- Menon, Suchithra;
- Timms, Andrew E.;
- Conti, Valerio;
- Biag, Jonathan D.;
- Olds, Carissa;
- Boyle, Evan August;
- Collins, Sarah;
- Ishak, Gisele;
- Poliachik, Sandra L.;
- Girisha, Katta M.;
- Kit-San Yeung;
- Yin Chung, Brian Hon;
- Rahikkala, Elisa;
- Gunter, Sonya A.;
- McDaniel, Sharon S.
Publication type:
Article
C620R mutation of the murine ret proto-oncogene: Loss of function effect in homozygotes and possible gain of function effect in heterozygotes.
Published in:
International Journal of Cancer, 2007, v. 121, n. 2, p. 292, doi. 10.1002/ijc.22378
By:
- Yin, Luo;
- Puliti, Aldamaria;
- Bonora, Elena;
- Evangelisti, Cecilia;
- Conti, Valerio;
- Tong, Wei-Min;
- Medard, Jean-Jacques;
- Lavoué, Marie-France;
- Forey, Nathalie;
- Wang, Lily C.;
- Manié, Serge;
- Morel, Gérard;
- Raccurt, Mireille;
- Wang, Zhao-Qi;
- Romeo, Giovanni
Publication type:
Article
Corpus callosum agenesis, severe mental retardation, epilepsy, and dyskinetic quadriparesis due to a novel mutation in the homeodomain of ARX.
Published in:
American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 4, p. 892, doi. 10.1002/ajmg.a.33923
By:
- Conti, Valerio;
- Marini, Carla;
- Gana, Simone;
- Sudi, Jyotsna;
- Dobyns, William B.;
- Guerrini, Renzo
Publication type:
Article
Contractions in the second polyA tract of ARX are rare, non-pathogenic polymorphisms.
Published in:
American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 1, p. 164, doi. 10.1002/ajmg.a.33753
By:
- Conti, Valerio;
- Marini, Carla;
- Mei, Davide;
- Falchi, Melania;
- Ferrari, Anna Rita;
- Guerrini, Renzo
Publication type:
Article
Autism-epilepsy phenotype with macrocephaly suggests PTEN, but not GLIALCAM, genetic screening.
Published in:
BMC Medical Genetics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2350-15-26
By:
- Marchese, Maria;
- Conti, Valerio;
- Valvo, Giulia;
- Moro, Francesca;
- Muratori, Filippo;
- Tancredi, Raffaella;
- Santorelli, Filippo M.;
- Guerrini, Renzo;
- Sicca, Federico
Publication type:
Article
A versatile clearing agent for multi-modal brain imaging.
Published in:
Scientific Reports, 2015, p. 9808, doi. 10.1038/srep09808
By:
- Costantini, Irene;
- Di Giovanna, Antonino Paolo;
- Mascaro, Anna Letizia Allegra;
- Silvestri, Ludovico;
- Müllenbroich, Marie Caroline;
- Onofri, Leonardo;
- Ghobril, Jean-Pierre;
- Markram, Henry;
- Conti, Valerio;
- Guerrini, Renzo;
- Vanzi, Francesco;
- Sacconi, Leonardo;
- Iannello, Giulio;
- Pavone, Francesco Saverio
Publication type:
Article
Somatic double-hit in MTOR and RPS6 in hemimegalencephaly with intractable epilepsy.
Published in:
Human Molecular Genetics, 2019, v. 28, n. 22, p. 3755, doi. 10.1093/hmg/ddz194
By:
- Pelorosso, Cristiana;
- Watrin, Françoise;
- Conti, Valerio;
- Buhler, Emmanuelle;
- Gelot, Antoinette;
- Yang, Xiaoxu;
- Mei, Davide;
- McEvoy-Venneri, Jennifer;
- Manent, Jean-Bernard;
- Cetica, Valentina;
- Ball, Laurel L;
- Buccoliero, Anna Maria;
- Vinck, Antonin;
- Barba, Carmen;
- Gleeson, Joseph G;
- Guerrini, Renzo;
- Represa, Alfonso
Publication type:
Article

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