Výsledky vyhledávání

The Vobarno Study

Autor: Claudia Agabiti Rosei, Enrico Agabiti Rosei, Massimo Salvetti, Anna Paini, Maurizio Castellano, M. Giacchè, Fabio Bertacchini, Carlo Aggiusti, Maria Lorenza Muiesan

Publikováno v: Panminerva Medica. 63

INTRODUCTION The Vobarno study represents the first observational study aimed to assess in a general population sample the relationship between parameters of cardiac and vascular structure (and function) and blood pressure values, measured in the cli

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b83fd328b1740cbd3105f5fe65e2ffe5
https://doi.org/10.23736/s0031-0808.21.04433-5

Zobrazit plný text záznamu

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

Autor: Patricia L. M. Dahia, Maurizio Castellano, Nicole Reisch, Carli M. J. Tops, N. Abermil, Marta Barontini, Graeme Eisenhofer, Sandra Bernaldo de Quirós, Salud Borrego, Álvaro Gómez-Graña, Nelly Burnichon, M. Giacchè, Mercedes Robledo, Emiliano Honrado, Giuseppe Opocher, Francesca Schiavi, Xavier Girerd, Elena Rapizzi, Lucía Inglada-Pérez, Esther Korpershoek, Henri J L M Timmers, Massimo Mannelli, Encarna B. Gomez-Garcia, Elisa Taschin, María-Dolores Chiara, Sara Bobisse, Alberto Cascón, Peggy Pierre, Carlos Suárez, Alexander P.A. Stegmann, Arjen R. Mensenkamp, Felix Beuschlein, Luigi Mori, Iñaki Comino-Méndez, Marinus J. Blok, Laurence Amar, Arnaud Murat, Macarena Ruiz-Ferrer, Ronald R. de Krijger, F Schillo, Frederik J. Hes, Karel Pacak, Nicole Paes Morales, Tonino Ercolino, Jacques W.M. Lenders, Rocío Letón, Miguel Urioste, Eleonora P M Corssmit, Isabelle Guilhem, Nan Qin, Anne-Paule Gimenez-Roqueplo, Giovanna Roncador, Pierre-François Plouin, Tamara Prodanov, Yves-Jean Bignon, Victoria M. Raymond, Jérôme Bertherat, Miguel Quesada-Charneco, Anna Merlo, Aguirre A. de Cubas, Philippe Chanson

Publikováno v: Clinical Cancer Research
Clinical Cancer Research, 2012, 18 (10), pp.2828-37. ⟨10.1158/1078-0432.CCR-12-0160⟩
Clinical Cancer Research, 18(10), 2828-2837. American Association for Cancer Research Inc.
Clinical Cancer Research, American Association for Cancer Research, 2012, 18 (10), pp.2828-37. ⟨10.1158/1078-0432.CCR-12-0160⟩
Clinical Cancer Research, 18, 10, pp. 2828-37
Digital.CSIC. Repositorio Institucional del CSIC
instname
Clinical Cancer Research, 18(10), 2828-2837
Clinical Cancer Research, American Association for Cancer Research, 2012, 18 (10), pp.2828-37. 〈10.1158/1078-0432.CCR-12-0160〉
Clinical Cancer Research; Vol 18
Clinical Cancer Research, 18, 2828-37

11 pages, 2 figures, 2 tables.-- Burnichón, Nelly et al.
Purpose: Pheochromocytomas (PCC) and paragangliomas (PGL) are genetically heterogeneous neural crest-derived neoplasms. Recently we identified germline mutations in a new tumor suppressor

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::741d2c9a7a3e90b407fce3123fe7e415
http://hdl.handle.net/11379/148720

Zobrazit plný text záznamu

A novel menin gene deletional mutation in a little series of Italian patients affected by apparently sporadic multiple endocrine neoplasia type 1 syndrome

Autor: Maurizio Castellano, A. Panarotto, M. Giacchè, E. Agabiti Rosei, M. C. Tacchetti, Linda Daffini, Luigi Mori, Ilenia Pirola

Aim: To perform a genetic screening for the multiple endocrine neoplasia type 1 (MEN1) gene mutations in patients affected by an apparently sporadic form of the disease, referred to an internal medicine unit of a large general hospital. Subjects and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78489a6c0e5c183406011792863aa88e
https://hdl.handle.net/11379/564564

Zobrazit plný text záznamu

Genetic mutation screening in an Italian cohort of nonsyndromic pheochromocytoma/paraganglioma patients

Autor: Maurizio Castellano, Enrico Agabiti-Rosei, F. Veglio, Rossella Tosini, M. Giacchè, Luigi Mori, A. Panarotto, Carlo Cappelli, D. Cumetti, E. Agliozzo, P. Mulatero

To assess the prevalence of genetic mutations in nonsyndromic pheochromocytoma/paraganglioma (PHEO/PGL) patients we have performed a systematic search for mutations in the succinate dehydrogenase (SDH) B, C, and D subunits, von Hippel–Lindau (VHL),

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81f6daaeca3c80d23605e5026fa3f85d
http://hdl.handle.net/11379/28824

Zobrazit plný text záznamu

Beta(2)-adrenergic receptor gene polymorphism, age, and cardiovascular phenotypes

Autor: C. Perani, Maurizio Castellano, Marina Beschi, Maria Lorenza Muiesan, Enrico Agabiti-Rosei, M. Giacchè, Damiano Rizzoni, Federica Rossi, Massimo Salvetti, Francesca Rivadossi

Publikováno v: Hypertension (Dallas, Tex. : 1979). 41(2)

Previous studies suggest that variants of the β 2 -adrenergic receptor (ADRB2) may differently affect functional responses to adrenergic stimulation, thereby possibly modulating cardiovascular and metabolic phenotypes. We examined the hypothesis tha

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95ea1a4909cdc69bb884d862ae52768e
https://pubmed.ncbi.nlm.nih.gov/12574108

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání