Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Arianna Passoni"'
Autor:
Maria Cristina Vigone, Lorenzo Andrea Bassi, Stefano Mora, Arianna Passoni, Giovanna Weber, Elena Peroni, Clara Pozzi
Publikováno v:
Hormone research in paediatrics. 81(1)
Aims: To compare the effects of liquid and tablet formulations of levothyroxine (L-T4) in 78 newborns with congenital hypothyroidism (CH). Methods: 39 patients received liquid L-T4 (group A) and 39 patients received tablets (group B). Thyroid-stimula
Autor:
Sarah Rabbiosi, Marianna Di Frenna, Giovanna Weber, Carlo Gelmetti, Francesca Cortinovis, Arianna Passoni, Maria Cristina Vigone, Giuseppe Chiumello, Luca Persani
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 25(1-2)
Consumptive hypothyroidism is a rare condition related to massive infantile hemangiomas producing an excess of the thyroid-hormone-inactivating enzyme type 3 iodothyronine deiodinase. We report the first case of consumptive hypothyroidism secondary t
Autor:
Luca Persani, Paolo Beck-Peccoz, Francesca Cortinovis, Giovanna Weber, Arianna Passoni, Davide Calebiro, Maria Cristina Vigone, Giuseppe Chiumello, Carlo Corbetta
Summary Context The guidelines of the National Academy of Clinical Biochemistry advocated the use of low bloodspot TSH (b-TSH) threshold for newborn screening of congenital hypothyroidism (CH). The impact generated by the application of this indicati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe1ed0c5784f45fa4efff6197dc46a92
Autor:
P. L. Paesano, Giovanna Weber, Maria Cristina Vigone, Arianna Passoni, Giuseppe Chiumello, Carlo Corbetta, M. Odoni, Maria Carla Proverbio, F. Dosio, Luca Persani
Publikováno v:
Journal of endocrinological investigation (Testo stamp.) 28 (2005): 516–522.
info:cnr-pdr/source/autori:Weber G, Vigone MC, Passoni A, Odoni M, Paesano PL, Dosio F, Proverbio MC, Corbetta C, Persani L, Chiumello G./titolo:Congenital hypothyroidism with gland in situ: diagnostic re-evaluation./doi:/rivista:Journal of endocrinological investigation (Testo stamp.)/anno:2005/pagina_da:516/pagina_a:522/intervallo_pagine:516–522/volume:28
Scopus-Elsevier
info:cnr-pdr/source/autori:Weber G, Vigone MC, Passoni A, Odoni M, Paesano PL, Dosio F, Proverbio MC, Corbetta C, Persani L, Chiumello G./titolo:Congenital hypothyroidism with gland in situ: diagnostic re-evaluation./doi:/rivista:Journal of endocrinological investigation (Testo stamp.)/anno:2005/pagina_da:516/pagina_a:522/intervallo_pagine:516–522/volume:28
Scopus-Elsevier
In the past, most congenital hypothyroidism (CH) children with thyroid gland in situ were considered to be affected by hormonogenesis defect. Nowadays, the improved sensitivity of neonatal screening, novel insights into the pathogenic mechanisms and
Autor:
Carlo Corbetta, Arianna Passoni, Fabio Mosca, Giovanna Weber, Rosanna Rovelli, Ludovica Maina, Giuseppe Chiumello, Andrea Corrias, Maria Cristina Vigone, Chiara Giovanettoni
Publikováno v:
Italian Journal of Pediatrics
Italian Journal of Pediatrics, Vol 36, Iss 1, p 24 (2010)
Italian Journal of Pediatrics, Vol 36, Iss 1, p 24 (2010)
Background evaluation of thyroid function in neonates born from mothers affected by autoimmune thyroiditis in order to define if a precise follow-up is necessary for these children. The influence of maternal thyroid peroxidase antibody (TPOAb) and L-
Autor:
Gabriella Pozzobon, Bruna Cammarata, Maria Antonietta Piscopo, Arianna Passoni, Elena Grechi, Giulio Frontino
Publikováno v:
Cases Journal
We report a case of bilateral cavo-ilio-femoral thrombosis in an adolescent with factor V heterozygous mutation and transient antiphospholipid antibodies secondary Varicella infection. The clinical significance of finding transient antiphospholipid a
Autor:
Laura Fugazzola, I. Zamproni, Giuseppe Chiumello, Stefania Di Candia, Giovanna Weber, Arianna Passoni, Maria Cristina Vigone, Luca Persani
Publikováno v:
Human Mutation. 26:395-395
One of the steps in thyroid hormone biosynthesis is the generation of hydrogen peroxide by dual oxidases (DUOX). Only one study reported mutations in DUOX2 gene in congenital hypothyroidism (CH) associated with total iodide organification defect (TIO