Primitive Epithelioid Hemangioendothelioma (EHE) of the Pleura. A Case Report and Literature Review

Autor: Francesca M Plutino, Baldassare Mondello, Marcello Filotico

Publikováno v: Acta Scientific Medical Sciences. :13-18

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a22c4ffbc439d59e3001bdfcd4eaaaef
https://doi.org/10.31080/asms.2022.06.1113

Specie esotiche invasive di rilevanza unionale in Italia: aggiornamenti e integrazioni

Autor: C. Montagnani, R. Gentili, G. Brundu, L. Celesti‐Grapow, G. Galasso, L. Lazzaro, S. Armeli Minicante, L. Carnevali, A. T. R. Acosta, E. Agrillo, A. Alessandrini, C. Angiolini, N. M. G. Ardenghi, I. Arduini, S. Armiraglio, F. Attorre, G. Bacchetta, S. Bagella, E. Barni, G. Barone, F. Bartolucci, A. Beretta, G. Berta, R. Bolpagni, I. Bona, G. Bonari, D. Bouvet, M. Bovio, I. Briozzo, G. Brusa, F. Buldrini, S. Buono, M. Burnelli, M. Carboni, E. Carli, F. Casella, M. Castello, R. M. Ceriani, K. Cianfaglione, M. Cicutto, F. Conti, D. Dagnino, G. Domina, E. Fanfarillo, S. Fascetti, A. Ferrario, G. Ferretti, B. Foggi, L. Gariboldi, C. Giancola, D. Gigante, R. Guarino, D. Iamonico, M. Iberite, M. Kleih, V. L. A. Laface, M. Latini, V. Lazzeri, V. Lozano, S. Magrini, A. Mainetti, F. Marinangeli, F. Martini, F. Masiero, M. Massimi, L. Mazzola, P. Medagli, M. Mugnai, C. M. Musarella, G. Nicolella, S. Orsenigo, S. Peccenini, L. Pedullà, E. V. Perrino, M. Plutino, L. Podda, L. Poggio, G. Posillipo, C. Proietti, F. Prosser, A. Ranfa, M. Rempicci, G. Rivieccio, E. S. Rodi, L. Rosati, G. Salerno, A. Santangelo, F. Scalari, A. Selvaggi, G. Spampinato, A. Stinca, C. Turcato, D. Viciani, M. Vidali, M. Villani, M. Vurro, R. P. Wagensommer, T. Wilhalm, S. Citterio

La Commissione Europea (CE) ha inserito ad oggi 36 taxa esotici vegetali nella lista delle specie esotiche invasive di rilevanza unionale ai sensi del Regolamento (UE) n. 1143/2014 del Parlamento Europeo e del Consiglio, recante disposizioni volte a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::124e0e626354ff5878f94fb52754b8c7
http://hdl.handle.net/2158/1261347

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Mutation update and uncommon phenotypes in a French cohort of 96 patients withWFS1-related disorders

Autor: Brigitte Chabrol, Sylvie Bannwarth, Samira Ait-El-Mkadem, B. Vialettes, Véronique Paquis-Flucklinger, M. Plutino, M. Nicolino, Hélène Dollfus, Cécile Rouzier, P. Charles, M. Quere, Magalie Barth, A. Chaussenot

Publikováno v: Clinical Genetics. 87:430-439

WFS1 mutations are responsible for Wolfram syndrome (WS) characterized by juvenile-onset diabetes mellitus and optic atrophy, and for low-frequency sensorineural hearing loss (LFSNHL). Our aim was to analyze the French cohort of 96 patients with WFS1

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::47ea905aaf6c1f42c00f96b8c7769662
https://doi.org/10.1111/cge.12437

Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1-related disorders

Autor: A, Chaussenot, C, Rouzier, M, Quere, M, Plutino, S, Ait-El-Mkadem, S, Bannwarth, M, Barth, H, Dollfus, P, Charles, M, Nicolino, B, Chabrol, B, Vialettes, V, Paquis-Flucklinger

Publikováno v: Clinical genetics. 87(5)

WFS1 mutations are responsible for Wolfram syndrome (WS) characterized by juvenile-onset diabetes mellitus and optic atrophy, and for low-frequency sensorineural hearing loss (LFSNHL). Our aim was to analyze the French cohort of 96 patients with WFS1

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::81f0c672c9a19fb88712874334821e5a
https://pubmed.ncbi.nlm.nih.gov/24890733