Sfoglia per Autore  

Opzioni
Mostrati risultati da 1 a 20 di 27
Titolo Data di pubblicazione Autore(i) File
Surgical enucleation of testicular leydigioma in a young child: case report and literature review 2011 Guanà, Riccardo; Mussa, Alessandro; Lala, Roberto; Tessaris, Daniele; Tessiatore, Patrizia Maiullari Erasmo; Canavese, Ferdinando
Combined treatment with bicalutamide and anastrozole in a young boy with peripheral precocious puberty due to McCune-Albright Syndrome 2012 Tessaris, Daniele; Matarazzo, Patrizia; Mussa, Alessandro; Tuli, Gerdi; Verna, Francesca; Fiore, Ludovica; Lala, Roberto
Measurement of height velocity is an useful marker for monitoring pituitary function in patients who had traumatic brain injury 2013 Bellone, S; Einaudi, S; Caputo, M; Prodam, F; Busti, A; Belcastro, S; Parlamento, S; Zavattaro, M; Verna, F; Bondone, C; Tessaris, D; Gasco, V; Bona, G; Aimaretti, G
Osteonecrosis of the jaw (ONJ) as a possible adverse side effects of bisphosphonate therapy in fibrous dysplasia and McCune-Albright syndrome 2014 P. Defabianis; A. Cimma; D. Tessaris; R. Lala
Iatrogenic acute pancreatitis due to hypercalcemia in a child with pseudohypoparathyroidism. 2014 Feyles F;Mussa A;Peiretti V;Tessaris D;Santanera A;Corrias A;de Sanctis L;Calvo L
Odontoiatric perspectives and osteonecrosis of the jaw as a possible adverse effect of bisphosphonates therapy in fibrous dysplasia and McCune-Albright syndrome. 2016 Tessaris D; Matarazzo P; Lala R; Defabianis P.
Combining Real-Time COLD-and MAMA-PCR TaqMan Techniques to Detect and Quantify R201 GNAS Mutations in the McCune-Albright Syndromeâ 2017 de Sanctis, Luisa; Galliano, Ilaria; Montanari, Paola; Matarazzo, Patrizia; Tessaris, Daniele; Bergallo, Massimiliano
Tolvaptan treatment in children with chronic hyponatremia due to inappropriate antidiuretic hormone secretion: A report of three cases 2017 Tuli, Gerdi*; Tessaris, Daniele; Einaudi, Silvia; De Sanctis, Luisa; Matarazzo, Patrizia
Compound heterozygosity for two GHR missense mutations in a patient affected by Laron Syndrome: A case report 2017 Moia, Stefania; Tessaris, Daniele; Einaudi, Silvia; De Sanctis, Luisa; Bona, Gianni; Bellone, Simonetta; Prodam, Flavia
Growth hormone—Insulin-like growth factor 1 axis hyperactivity on bone fibrous dysplasia in McCune-Albright Syndrome 2018 Tessaris, Daniele*; Boyce, Alison M; Zacharin, Margaret; Matarazzo, Patrizia; Lala, Roberto; De Sanctis, Luisa; Collins, Michael T
Genetic and Epigenetic Defects at the GNAS Locus Lead to Distinct Patterns of Skeletal Growth but Similar Early-Onset Obesity 2018 Hanna, Patrick; Grybek, Virginie; Perez de Nanclares, Guiomar; Tran, Léa C; de Sanctis, Luisa; Elli, Francesca; Errea, Javier; Francou, Bruno; Kamenicky, Peter; Linglart, Léa; Pereda, Arrate; Rothenbuhler, Anya; Tessaris, Daniele; Thiele, Susanne; Usardi, Alessia; Shoemaker, Ashley H; Kottler, Marie-Laure; Jüppner, Harald; Mantovani, Giovanna; Linglart, Agnès
Copeptin role in polyuria-polydipsia syndrome differential diagnosis and reference range in paediatric age 2018 Tuli, Gerdi; Tessaris, Daniele; Einaudi, Silvia; Matarazzo, Patrizia; De Sanctis, Luisa
X-linked hypophosphatemic rickets: An Italian experts' opinion survey 2019 Emma F.; Cappa M.; Antoniazzi F.; Bianchi M.L.; Chiodini I.; Eller Vainicher C.; Di Iorgi N.; Maghnie M.; Cassio A.; Balsamo A.; Baronio F.; De Sanctis L.; Tessaris D.; Baroncelli G.I.; Mora S.; Brandi M.L.; Weber G.; D'Ausilio A.; Lanati E.P.
Plasma cortisol and ACTH levels in 416 VLBW preterm infants during the first month of life: distribution in the AGA/SGA population 2019 Mori A.; Tuli G.; Magaldi R.; Ghirri P.; Tessaris D.; Rinaldi M.; Bagnoli F.; de Sanctis L.
Association of GNAS imprinting defects and deletions of chromosome 2 in two patients: Clues explaining phenotypic heterogeneity in pseudohypoparathyroidism type 1B/iPPSD3 2019 Elli F.M.; Desanctis L.; Maffini M.A.; Bordogna P.; Tessaris D.; Pirelli A.; Arosio M.; Linglart A.; Mantovani G.
Teriparatide (rhPTH 1–34) treatment in the pediatric age: long-term efficacy and safety data in a cohort with genetic hypoparathyroidism 2019 Tuli G.; Buganza R.; Tessaris D.; Einaudi S.; Matarazzo P.; de Sanctis L.
SHOX deficiency in children with growth impairment: evaluation of known and new auxological and radiological indicators 2020 Vannelli, Silvia; Baffico, Maria; Buganza, Raffaele; Verna, Francesca; Vinci, Giulia; Tessaris, Daniele; Di Rosa, Gianpaolo; Borraccino, Alberto; de Sanctis, Luisa
Prospective evaluation of autoimmune and non-autoimmune subclinical hypothyroidism in down syndrome children 2020 Pepe G.; Corica D.; de Sanctis L.; Salerno M.; Faienza M.F.; Tessaris D.; Tuli G.; Scala I.; Penta L.; Alibrandi A.; Pajno G.B.; Aversa T.; Wasniewska M.
Distribution of plasma copeptin levels and influence of obesity in children and adolescents 2021 Tuli, Gerdi; Munarin, Jessica; Tessaris, Daniele; Einaudi, Silvia; Matarazzo, Patrizia; de Sanctis, Luisa
Pseudohypoparathyroidism: application of the Italian common healthcare-pathway for a homogeneous clinical approach and a shared follow up 2021 Tessaris D.; Bonino E.; Weber G.; Wasniewska M.; Corica D.; Pitea M.; Scire G.; Caruso-Nicoletti M.; Fintini D.; de Sanctis L.
Mostrati risultati da 1 a 20 di 27
Legenda icone

  •  file ad accesso aperto
  •  file disponibili sulla rete interna
  •  file disponibili agli utenti autorizzati
  •  file disponibili solo agli amministratori
  •  file sotto embargo
  •  nessun file disponibile