Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Lino, Furlani"'
Autor:
Niccolò Faccioli, Giovanni Carbognin, Lino Furlani, Giovanni Foti, Giuseppe Malleo, Andrea Guerriero
Publikováno v:
La radiologia medica. 123:833-840
To evaluate the diagnostic accuracy of wash-out parameters calculated using multiple intermediate and delayed phases. This prospective study had institutional review board approval and informed consent was obtained from all patients. Between January
Publikováno v:
Revue du Rhumatisme. 76:1359-1362
Resume Contexte L’hypercalcemie hypocalciurique familiale (HHF) associee a la maladie a depots de cristaux de pyrophosphate de calcium dihydrate (PPCD ou CCA) est rare mais elle doit etre prise en compte dans le diagnostic differentiel d’une hype
Autor:
Lino Furlani, Stefano Mariotti, Luca Deiana, Francesca Pigliaru, Marco Losa, Francesca Perticone, Pietro Mortini
Publikováno v:
Thyroid : official journal of the American Thyroid Association. 25(4)
Patients with a thyrotropin-secreting pituitary adenoma (TSHoma) are exposed to unregulated and inappropriately high levels of thyrotropin (TSH). Given the rarity of this condition, it is not known whether this chronic TSH stimulation of the thyroid
Autor:
Stefania, Gori, Jennifer, Foglietta, Marta, Rossi, Alketa, Hamzaj, Lucia, Stocchi, Carla, Galuppo, Vincenzo, Picece, Efisio, Puxeddu, Lino, Furlani
Publikováno v:
Tumori Journal. 99:e285-e287
We present the case of a 51-year-old woman with a follicular variant of papillary thyroid carcinoma. After surgery she experienced a relapse. Chemotherapy treatment led only to disease stabilization. In August 2009, we decided to start therapy with s
Autor:
Valentina Martineti, Lino Furlani, Andrea Amorosi, Silvia Fabiani, Alberto Falchetti, Francesco Tonelli, Annamaria Morelli, Maria Luisa Brandi, Roberto Castello
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 82:2278-2282
Homozygosity for the multiple endocrine neoplasia type 1 (MEN1) gene mutation was described in two of three affected siblings of a kindred in which both parents and the third daughter were heterozygotes. Surprisingly, in the two homozygotes, the dise
Autor:
Luca Giovanella, Lino Furlani, Roberto Castello, Anna Ferrari, Alessia Palumbo, Maria Stella Graziani, Mauro Imperiali
Publikováno v:
Clinical Chemistry and Laboratory Medicine. 50
The present study was undertaken to establish serum thyroglobulin (Tg) normal reference values in a large group of healthy subjects.Four hundred and thirty-eight non-smoking healthy subjects were selected to assess the Tg reference values (209 males,
Autor:
Paola Loli, Enrico Papini, Benoit Dupas, Anna Pia, Vincenzo Toscano, Michele Zini, Franco Mantero, Iacopo Chiodini, Massimo Terzolo, Giuseppe Reimondo, Bruno Allolio, P. Garofalo, Lino Furlani, Giorgio Borretta, Antonio Stigliano, Giorgio Arnaldi, Antoine Tabarin
ObjectiveTo assess currently available evidence on adrenal incidentaloma and provide recommendations for clinical practice.DesignA panel of experts (appointed by the Italian Association of Clinical Endocrinologists (AME)) appraised the methodological
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37b01e84696ced2a36a8892dccfa06ea
http://hdl.handle.net/2318/89196
http://hdl.handle.net/2318/89196
Publikováno v:
Joint bone spine. 76(6)
Background Calcium pyrophosphate dihydrate crystal deposition disease (CPPD-CDD) has been associated to hypercalcemia. Familial hypocalciuric hypercalcemia (FHH) is a rare but important consideration in the differential diagnosis of hypercalcemia. Th
Autor:
Lino Furlani, Annamaria Morelli, Maria Luisa Brandi, Francesco Tonelli, A. Frilling, Paola Tomassetti, Alberto Falchetti, Mario Serio, Roberto Castello
Publikováno v:
Journal of endocrinological investigation. 18(5)
Multiple endocrine neoplasia type 1 (MEN 1) is an autosomal dominantly inherited disorder characterized by parathyroid hyperplasia, anterior pituitary adenomas and neoplasms of the endocrine cells of the gastroenteric tract. It has been established t