Sfoglia per Rivista
Guidelines for acromegaly management.
2002-01-01 Melmed, S; Casanueva, Ff; Cavagnini, F; Chanson, P; Frohman, L; Grossman, A; Ho, K; Kleinberg, D; Lamberts, S; Laws, E; Lombardi, G; Vance, Ml; Werder, Kv; Wass, J; Giustina, Andrea; Acromegaly Treatment Consensus Workshop, Participants
High prevalence of radiological vertebral fractures in women on thyroid-stimulating hormone-suppressive therapy for thyroid carcinoma
2018-01-01 Mazziotti, Gherardo; Formenti, Anna Maria; Frara, Stefano; Olivetti, Roberto; Banfi, Giuseppe; Memo, Maurizio; Maroldi, Roberto; Giubbini, Raffaele; Giustina, Andrea
High risk of congenital hypothyroidism in multiple pregnancies.
2007-01-01 Olivieri, A; Medda, E; De Angelis, S; Valensise, H; De Felice, M; Fazzini, C; Cascino, I; Cordeddu, V; Sorcini, M; Stazi, Ma; Weber, Giovanna
High-dose and high-frequency lanreotide autogel in acromegaly: A randomized, multicenter study
2017-01-01 Giustina, Andrea; Mazziotti, Gherardo; Cannavã², Salvatore; Castello, Roberto; Arnaldi, Giorgio; Bugari, Giovanna; Cozzi, Renato; Ferone, Diego; Formenti, Anna Maria; Gatti, Enza; Grottoli, Silvia; Maffei, Pietro; Maffezzoni, Filippo; Montini, Marcella; Terzolo, Massimo; Ghigo, Ezio
Hyperplastic pituitaary gland, high serum glycoprotein hormone alfa-subunit and variable circulating thyrotropin (TSH) levels as hallmark of central hypothyroidism due to mutations of the TSH-beta gene
2001-01-01 Bonomi, M; Proverbio, Mc; Weber, Giovanna; Chiumello, G; BECK PECCOZ, P; Persani, L.
Identification, characterization and biological activity of specific receptors for natural, (Ghrelin) and synthetic growth hormone secretagogues in human breast carcinomas and cell lines
2001-01-01 Cassoni, P.; Papotti, M.; Ghè, C.; Catapano, F.; Sapino, A.; Graziani, Andrea; Reissmann, T.; Deghenghi, R; Ghigo, E.; Muccioli, G.
Impact of age and antibody type on progression from single to multiple autoantibodies in type 1 diabetes relatives
2017-01-01 Bosi, Emanuele; Boulware, David C.; Becker, Dorothy J.; Buckner, Jane H.; Geyer, Susan; Gottlieb, Peter A.; Henderson, Courtney; Kinderman, Amanda; Sosenko, Jay M.; Steck, Andrea K.; Bingley, Polly J.
Impact of somatostatin analogs on the heart in acromegaly: a metaanalysis.
2007-01-01 Maison, P; Tropeano, Ai; MACQUIN MAVIER, I; Giustina, Andrea; Chanson, P.
Impaired growth hormone (GH) response to pyridostigmine in type 1 diabetic patients with exaggerated GH-releasing hormone-stimulated GH secretion.
1990-01-01 Giustina, Andrea; Bossoni, S; Cimino, A; Pizzocolo, G; Romanelli, G; Wehrenberg, Wb
Insights from a successful case of intrahepatic islet transplantation into a type 1 diabetic patient
2000-01-01 Davalli, A; Maffi, P; Socci, C; Sanvito, F; Freschi, M; – DAVALLI A. MAFFI P. SOCCI C. SANVITO F. FRESCHI M., BERTUZZI F; Falqui, L; DI CARLO, V; Pozza, G; Secchi, Antonio
Interleukin-12 and its free p40 subunit regulate immune recognition of endometrial cells: potential role in endometriosis
1998-01-01 Mazzeo, D; Viganó, P; Di Blasio, A M; Sinigaglia, F; Vignali, M; Panina-Bordignon, P
International Multicenter Validation Study of the SAGIT® Instrument in Acromegaly
2021-01-01 Giustina, Andrea; Bronstein, Marcello D; Chanson, Philippe; Petersenn, Stephan; Casanueva, Felipe F; Sert, Caroline; Houchard, Aude; Melmed, Shlomo
JAG1 Loss-Of-Function Variations as a Novel Predisposing Event in the Pathogenesis of Congenital Thyroid Defects.
2016-01-01 de Filippis, T; Marelli, F; Nebbia, G; Porazzi, P; Corbetta, S; Fugazzola, L; Gastaldi, R; Vigone, Mc; Biffanti, R; Frizziero, D; Mandarà, L; Prontera, P; Salerno, M; Maghnie, M; Tiso, N; Radetti, G; Weber, Giovanna; Persani, L.
Low vitamin D levels are associated with Long COVID syndrome in COVID-19 survivors
2023-01-01 di Filippo, Luigi; Frara, Stefano; Nannipieri, Fabrizio; Cotellessa, Alice; Locatelli, Massimo; Rovere Querini, Patrizia; Giustina, Andrea
Management of childhood-onset craniopharyngioma in Italy: A multicenter seven year follow-up study of 145 patients
2021-01-01 Zucchini, Stefano; Di Iorgi, Natascia; Pozzobon, Gabriella; Pedicelli, Stefania; Parpagnoli, Maria; Driul, Daniela; Matarazzo, Patrizia; Baronio, Federico; Crocco, Marco; Giudica, Giovanna; Partenope, Cristina; Nardini, Beatrice; Ubertini, Graziamaria; Menardi, Rachele; Guzzetti, Chiara; Iughetti, Lorenzo; Aversa, Tommaso; Di Mase, Raffaella; Cassio, Alessandra; Cianfarani, Stefano; Maghnie, Mohamad; Tuli, Gerdi; Loche, Sandro; Bruzzi, Patrizia; Wasniewska, Malgorzata; Salerno, Mariacarolina; Rutigliano, Irene; Iezzi, Maria Laura; Cherubini, Valentino; Grandone, Anna; Faienza, Mariafelicia; Tumini, Stefano; Baldoli, Cristina; Consales, Alessandro; Genitori, Lorenzo; Marras, Carlo Efisio; Milanaccio, Claudia; Mortini, Pietro; Vindigni, Marco; Zenga, Francesco; Zucchelli, Mino
Maturation of the regulation of growth hormone secretion in young males with hypogonadotropic hypogonadism pharmacologically exposed to progressive increments in serum testosterone.
1997-01-01 Giustina, Andrea; Scalvini, T; Tassi, C; Desenzani, P; Poiesi, C; Wehrenberg, Wb; Rogol, Ad; Veldhuis, Jd
Molecular analysis of the Pendred's syndrome gene and magnetic resonance imaging studies of the inner ear are essential for the diagnosis of true Pendred's syndrome
2000-01-01 Fugazzola, L; Mannavola, D; Cerutti, N; Maghnie, M; Pagella, F; Bianchi, P; Weber, Giovanna; Persani, L; BECK PECCOZ, P.
Mutation of PFN1 Gene in an Early Onset, Polyostotic Paget-like Disease
2020-01-01 Merlotti, D; Materozzi, M; Bianciardi, S; Guarnieri, V; Rendina, D; Volterrani, L; Bellan, C; Mingiano, C; Picchioni, T; Frosali, A; Orfanelli, U; Cenci, S; Gennari, L
Mutational analysis of GNAS1 in patients with Pseudohypoparathyroidism: identification of two novel mutations
2000-01-01 Mantovani, G; Romoli, R; Weber, Giovanna; Brunelli, V; DE MENIS, E; Beccio, S; BECK PECCOZ, P; Spada, A.
Neonatal Screening for Congenital Hypothyroidism: What can we learn from Discordant twins?
2019-01-01 Medda, Emanuela; Vigone, Maria Cristina; Cassio, Alessandra; Calaciura, Francesca; Costa, Pietro; Weber, Giovanna; de Filippis, Tiziana; Gelmini, Giulia; Di Frenna, Marianna; Caiulo, Silvana; Ortolano, Rita; Rotondi, Daniela; Bartolucci, Monica; Gelsomino, Rossella; De Angelis, Simona; Gabbianelli, Marco; Persani, Luca; Olivieri, Antonella
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Guidelines for acromegaly management. | 1-gen-2002 | Melmed, S; Casanueva, Ff; Cavagnini, F; Chanson, P; Frohman, L; Grossman, A; Ho, K; Kleinberg, D; Lamberts, S; Laws, E; Lombardi, G; Vance, Ml; Werder, Kv; Wass, J; Giustina, Andrea; Acromegaly Treatment Consensus Workshop, Participants | |
| High prevalence of radiological vertebral fractures in women on thyroid-stimulating hormone-suppressive therapy for thyroid carcinoma | 1-gen-2018 | Mazziotti, Gherardo; Formenti, Anna Maria; Frara, Stefano; Olivetti, Roberto; Banfi, Giuseppe; Memo, Maurizio; Maroldi, Roberto; Giubbini, Raffaele; Giustina, Andrea | |
| High risk of congenital hypothyroidism in multiple pregnancies. | 1-gen-2007 | Olivieri, A; Medda, E; De Angelis, S; Valensise, H; De Felice, M; Fazzini, C; Cascino, I; Cordeddu, V; Sorcini, M; Stazi, Ma; Weber, Giovanna | |
| High-dose and high-frequency lanreotide autogel in acromegaly: A randomized, multicenter study | 1-gen-2017 | Giustina, Andrea; Mazziotti, Gherardo; Cannavã², Salvatore; Castello, Roberto; Arnaldi, Giorgio; Bugari, Giovanna; Cozzi, Renato; Ferone, Diego; Formenti, Anna Maria; Gatti, Enza; Grottoli, Silvia; Maffei, Pietro; Maffezzoni, Filippo; Montini, Marcella; Terzolo, Massimo; Ghigo, Ezio | |
| Hyperplastic pituitaary gland, high serum glycoprotein hormone alfa-subunit and variable circulating thyrotropin (TSH) levels as hallmark of central hypothyroidism due to mutations of the TSH-beta gene | 1-gen-2001 | Bonomi, M; Proverbio, Mc; Weber, Giovanna; Chiumello, G; BECK PECCOZ, P; Persani, L. | |
| Identification, characterization and biological activity of specific receptors for natural, (Ghrelin) and synthetic growth hormone secretagogues in human breast carcinomas and cell lines | 1-gen-2001 | Cassoni, P.; Papotti, M.; Ghè, C.; Catapano, F.; Sapino, A.; Graziani, Andrea; Reissmann, T.; Deghenghi, R; Ghigo, E.; Muccioli, G. | |
| Impact of age and antibody type on progression from single to multiple autoantibodies in type 1 diabetes relatives | 1-gen-2017 | Bosi, Emanuele; Boulware, David C.; Becker, Dorothy J.; Buckner, Jane H.; Geyer, Susan; Gottlieb, Peter A.; Henderson, Courtney; Kinderman, Amanda; Sosenko, Jay M.; Steck, Andrea K.; Bingley, Polly J. | |
| Impact of somatostatin analogs on the heart in acromegaly: a metaanalysis. | 1-gen-2007 | Maison, P; Tropeano, Ai; MACQUIN MAVIER, I; Giustina, Andrea; Chanson, P. | |
| Impaired growth hormone (GH) response to pyridostigmine in type 1 diabetic patients with exaggerated GH-releasing hormone-stimulated GH secretion. | 1-gen-1990 | Giustina, Andrea; Bossoni, S; Cimino, A; Pizzocolo, G; Romanelli, G; Wehrenberg, Wb | |
| Insights from a successful case of intrahepatic islet transplantation into a type 1 diabetic patient | 1-gen-2000 | Davalli, A; Maffi, P; Socci, C; Sanvito, F; Freschi, M; – DAVALLI A. MAFFI P. SOCCI C. SANVITO F. FRESCHI M., BERTUZZI F; Falqui, L; DI CARLO, V; Pozza, G; Secchi, Antonio | |
| Interleukin-12 and its free p40 subunit regulate immune recognition of endometrial cells: potential role in endometriosis | 1-gen-1998 | Mazzeo, D; Viganó, P; Di Blasio, A M; Sinigaglia, F; Vignali, M; Panina-Bordignon, P | |
| International Multicenter Validation Study of the SAGIT® Instrument in Acromegaly | 1-gen-2021 | Giustina, Andrea; Bronstein, Marcello D; Chanson, Philippe; Petersenn, Stephan; Casanueva, Felipe F; Sert, Caroline; Houchard, Aude; Melmed, Shlomo | |
| JAG1 Loss-Of-Function Variations as a Novel Predisposing Event in the Pathogenesis of Congenital Thyroid Defects. | 1-gen-2016 | de Filippis, T; Marelli, F; Nebbia, G; Porazzi, P; Corbetta, S; Fugazzola, L; Gastaldi, R; Vigone, Mc; Biffanti, R; Frizziero, D; Mandarà, L; Prontera, P; Salerno, M; Maghnie, M; Tiso, N; Radetti, G; Weber, Giovanna; Persani, L. | |
| Low vitamin D levels are associated with Long COVID syndrome in COVID-19 survivors | 1-gen-2023 | di Filippo, Luigi; Frara, Stefano; Nannipieri, Fabrizio; Cotellessa, Alice; Locatelli, Massimo; Rovere Querini, Patrizia; Giustina, Andrea | |
| Management of childhood-onset craniopharyngioma in Italy: A multicenter seven year follow-up study of 145 patients | 1-gen-2021 | Zucchini, Stefano; Di Iorgi, Natascia; Pozzobon, Gabriella; Pedicelli, Stefania; Parpagnoli, Maria; Driul, Daniela; Matarazzo, Patrizia; Baronio, Federico; Crocco, Marco; Giudica, Giovanna; Partenope, Cristina; Nardini, Beatrice; Ubertini, Graziamaria; Menardi, Rachele; Guzzetti, Chiara; Iughetti, Lorenzo; Aversa, Tommaso; Di Mase, Raffaella; Cassio, Alessandra; Cianfarani, Stefano; Maghnie, Mohamad; Tuli, Gerdi; Loche, Sandro; Bruzzi, Patrizia; Wasniewska, Malgorzata; Salerno, Mariacarolina; Rutigliano, Irene; Iezzi, Maria Laura; Cherubini, Valentino; Grandone, Anna; Faienza, Mariafelicia; Tumini, Stefano; Baldoli, Cristina; Consales, Alessandro; Genitori, Lorenzo; Marras, Carlo Efisio; Milanaccio, Claudia; Mortini, Pietro; Vindigni, Marco; Zenga, Francesco; Zucchelli, Mino | |
| Maturation of the regulation of growth hormone secretion in young males with hypogonadotropic hypogonadism pharmacologically exposed to progressive increments in serum testosterone. | 1-gen-1997 | Giustina, Andrea; Scalvini, T; Tassi, C; Desenzani, P; Poiesi, C; Wehrenberg, Wb; Rogol, Ad; Veldhuis, Jd | |
| Molecular analysis of the Pendred's syndrome gene and magnetic resonance imaging studies of the inner ear are essential for the diagnosis of true Pendred's syndrome | 1-gen-2000 | Fugazzola, L; Mannavola, D; Cerutti, N; Maghnie, M; Pagella, F; Bianchi, P; Weber, Giovanna; Persani, L; BECK PECCOZ, P. | |
| Mutation of PFN1 Gene in an Early Onset, Polyostotic Paget-like Disease | 1-gen-2020 | Merlotti, D; Materozzi, M; Bianciardi, S; Guarnieri, V; Rendina, D; Volterrani, L; Bellan, C; Mingiano, C; Picchioni, T; Frosali, A; Orfanelli, U; Cenci, S; Gennari, L | |
| Mutational analysis of GNAS1 in patients with Pseudohypoparathyroidism: identification of two novel mutations | 1-gen-2000 | Mantovani, G; Romoli, R; Weber, Giovanna; Brunelli, V; DE MENIS, E; Beccio, S; BECK PECCOZ, P; Spada, A. | |
| Neonatal Screening for Congenital Hypothyroidism: What can we learn from Discordant twins? | 1-gen-2019 | Medda, Emanuela; Vigone, Maria Cristina; Cassio, Alessandra; Calaciura, Francesca; Costa, Pietro; Weber, Giovanna; de Filippis, Tiziana; Gelmini, Giulia; Di Frenna, Marianna; Caiulo, Silvana; Ortolano, Rita; Rotondi, Daniela; Bartolucci, Monica; Gelsomino, Rossella; De Angelis, Simona; Gabbianelli, Marco; Persani, Luca; Olivieri, Antonella |
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