Sfoglia per Autore
Perinatal asphyxia and hypothermic treatment from the endocrine perspective
2023-01-01 Improda, Nicola; Capalbo, Donatella; Poloniato, Antonella; Garbetta, Gisella; Dituri, Francesco; Penta, Laura; Aversa, Tommaso; Sessa, Linda; Vierucci, Francesco; Cozzolino, Mariarosaria; Vigone, Maria Cristina; Tronconi, Giulia Maria; Del Pistoia, Marta; Lucaccioni, Laura; Tuli, Gerdi; Munarin, Jessica; Tessaris, Daniele; de Sanctis, Luisa; Salerno, Mariacarolina
Successful treatment with MEK-inhibitor in a patient with NRAS-related cutaneous skeletal hypophosphatemia syndrome
2022-01-01 Carli, Diana; Cardaropoli, Simona; Tessaris, Daniele; Coppo, Paola; La Selva, Roberta; Cesario, Claudia; Lepri, Francesca Romana; Pullano, Verdiana; Palumbo, Martina; Ramenghi, Ugo; Brusco, Alfredo; Medico, Enzo; De Sanctis, Luisa; Ferrero, Giovanni Battista; Mussa, Alessandro
Genetic Testing for a Patient with Suspected 3 Beta-Hydroxysteroid Dehydrogenase Deficiency: A Case of Unreported Genetic Variants
2022-01-01 Menegatti, Elisa; Tessaris, Daniele; Barinotti, Alice; Matarazzo, Patrizia; Einaudi, Silvia
Papillary thyroid microcarcinoma in a boy with Graves' disease: a case report.
2022-01-01 Tuli, Gerdi; Munarin, Jessica; Tessaris, Daniele; Quaglino, Francesco; de Sanctis, Luisa
Distribution of plasma copeptin levels and influence of obesity in children and adolescents
2021-01-01 Tuli, Gerdi; Munarin, Jessica; Tessaris, Daniele; Einaudi, Silvia; Matarazzo, Patrizia; de Sanctis, Luisa
Incidence of primary congenital hypothyroidism and relationship between diagnostic categories and associated malformations
2021-01-01 Tuli, Gerdi; Munarin, Jessica; Tessaris, Daniele; Matarazzo, Patrizia; Einaudi, Silvia; de Sanctis, Luisa
Multidisciplinary Approach for Hypothalamic Obesity in Children and Adolescents: A Preliminary Study
2021-01-01 Tessaris, Daniele; Matarazzo, Patrizia; Tuli, Gerdi; Tuscano, Antonella; Rabbone, Ivana; Spinardi, Alessandra; Lezo, Antonella; Fenocchio, Giorgia; Buganza, Raffaele; de Sanctis, Luisa
Pseudohypoparathyroidism: application of the Italian common healthcare-pathway for a homogeneous clinical approach and a shared follow up
2021-01-01 Tessaris D.; Bonino E.; Weber G.; Wasniewska M.; Corica D.; Pitea M.; Scire G.; Caruso-Nicoletti M.; Fintini D.; de Sanctis L.
"primary Hyperparathyroidism (PHPT) in Children: Two Case Reports and Review of the Literature"
2021-01-01 Tuli G.; Munarin J.; Tessaris D.; Buganza R.; Matarazzo P.; De Sanctis L.
Prospective evaluation of autoimmune and non-autoimmune subclinical hypothyroidism in down syndrome children
2020-01-01 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.
SHOX deficiency in children with growth impairment: evaluation of known and new auxological and radiological indicators
2020-01-01 Vannelli, Silvia; Baffico, Maria; Buganza, Raffaele; Verna, Francesca; Vinci, Giulia; Tessaris, Daniele; Di Rosa, Gianpaolo; Borraccino, Alberto; de Sanctis, Luisa
Association of GNAS imprinting defects and deletions of chromosome 2 in two patients: Clues explaining phenotypic heterogeneity in pseudohypoparathyroidism type 1B/iPPSD3
2019-01-01 Elli F.M.; Desanctis L.; Maffini M.A.; Bordogna P.; Tessaris D.; Pirelli A.; Arosio M.; Linglart A.; Mantovani G.
Plasma cortisol and ACTH levels in 416 VLBW preterm infants during the first month of life: distribution in the AGA/SGA population
2019-01-01 Mori A.; Tuli G.; Magaldi R.; Ghirri P.; Tessaris D.; Rinaldi M.; Bagnoli F.; de Sanctis L.
X-linked hypophosphatemic rickets: An Italian experts' opinion survey
2019-01-01 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.
Teriparatide (rhPTH 1–34) treatment in the pediatric age: long-term efficacy and safety data in a cohort with genetic hypoparathyroidism
2019-01-01 Tuli G.; Buganza R.; Tessaris D.; Einaudi S.; Matarazzo P.; de Sanctis L.
Growth hormone—Insulin-like growth factor 1 axis hyperactivity on bone fibrous dysplasia in McCune-Albright Syndrome
2018-01-01 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
2018-01-01 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
2018-01-01 Tuli, Gerdi; Tessaris, Daniele; Einaudi, Silvia; Matarazzo, Patrizia; De Sanctis, Luisa
Combining Real-Time COLD-and MAMA-PCR TaqMan Techniques to Detect and Quantify R201 GNAS Mutations in the McCune-Albright Syndromeâ
2017-01-01 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
2017-01-01 Tuli, Gerdi*; Tessaris, Daniele; Einaudi, Silvia; De Sanctis, Luisa; Matarazzo, Patrizia
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Perinatal asphyxia and hypothermic treatment from the endocrine perspective | 2023 | Improda, Nicola; Capalbo, Donatella; Poloniato, Antonella; Garbetta, Gisella; Dituri, Francesco; Penta, Laura; Aversa, Tommaso; Sessa, Linda; Vierucci, Francesco; Cozzolino, Mariarosaria; Vigone, Maria Cristina; Tronconi, Giulia Maria; Del Pistoia, Marta; Lucaccioni, Laura; Tuli, Gerdi; Munarin, Jessica; Tessaris, Daniele; de Sanctis, Luisa; Salerno, Mariacarolina | |
| Successful treatment with MEK-inhibitor in a patient with NRAS-related cutaneous skeletal hypophosphatemia syndrome | 2022 | Carli, Diana; Cardaropoli, Simona; Tessaris, Daniele; Coppo, Paola; La Selva, Roberta; Cesario, Claudia; Lepri, Francesca Romana; Pullano, Verdiana; Palumbo, Martina; Ramenghi, Ugo; Brusco, Alfredo; Medico, Enzo; De Sanctis, Luisa; Ferrero, Giovanni Battista; Mussa, Alessandro | |
| Genetic Testing for a Patient with Suspected 3 Beta-Hydroxysteroid Dehydrogenase Deficiency: A Case of Unreported Genetic Variants | 2022 | Menegatti, Elisa; Tessaris, Daniele; Barinotti, Alice; Matarazzo, Patrizia; Einaudi, Silvia | |
| Papillary thyroid microcarcinoma in a boy with Graves' disease: a case report. | 2022 | Tuli, Gerdi; Munarin, Jessica; Tessaris, Daniele; Quaglino, Francesco; de Sanctis, Luisa | |
| 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 | |
| Incidence of primary congenital hypothyroidism and relationship between diagnostic categories and associated malformations | 2021 | Tuli, Gerdi; Munarin, Jessica; Tessaris, Daniele; Matarazzo, Patrizia; Einaudi, Silvia; de Sanctis, Luisa | |
| Multidisciplinary Approach for Hypothalamic Obesity in Children and Adolescents: A Preliminary Study | 2021 | Tessaris, Daniele; Matarazzo, Patrizia; Tuli, Gerdi; Tuscano, Antonella; Rabbone, Ivana; Spinardi, Alessandra; Lezo, Antonella; Fenocchio, Giorgia; Buganza, Raffaele; 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. | |
| "primary Hyperparathyroidism (PHPT) in Children: Two Case Reports and Review of the Literature" | 2021 | Tuli G.; Munarin J.; Tessaris D.; Buganza R.; Matarazzo P.; De Sanctis L. | |
| 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. | |
| 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 | |
| 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. | |
| 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. | |
| 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. | |
| 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. | |
| 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 | |
| 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 |
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