Search Results - "Macchia, P. E."

Thyroid Nodules Treated with Percutaneous Radiofrequency Thermal Ablation: A Comparative Study by Faggiano, A, Ramundo, V, Assanti, A. P, Fonderico, F, Macchia, P. E, Misso, C, Marciello, F, Marotta, V, Del Prete, M, Papini, E, Lombardi, G, Colao, A, Spiezia, S

“…Purpose: Percutaneous radiofrequency thermal ablation (RTA) was reported as an effective tool for the management of thyroid nodules (TNs). The aim of this…”
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SERS assisted sandwich immunoassay platforms for ultrasensitive and selective detection of human Thyroglobulin by Spaziani, S., Quero, G., Managò, S., Zito, G., Terracciano, D., Macchia, P.E., Galeotti, F., Pisco, M., De Luca, A.C., Cusano, A.

“…We developed an immunoassay platform for the detection of human Thyroglobulin (Tg) to be integrated with fine-needle aspiration biopsy for early detection of…”
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PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis by Macchia, Paolo Emidio, Lapi, Paola, Krude, Heiko, Pirro, Maria Teresa, Missero, Caterina, Chiovato, Luca, Souabni, Abdallah, Baserga, Mariangiola, Tassi, Vittorio, Pinchera, Aldo, Fenzi, Gianfranco, Grüters, Annette, Busslinger, Meinrad, Lauro, Roberto Di

“…Permanent congenital hypothyroidism (CH) is a common disease that occurs in 1 of 3,000-4,000 newborns. Except in rare cases due to hypothalamic or pituitary…”
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Increased Sensitivity to Thyroid Hormone in Mice with Complete Deficiency of Thyroid Hormone Receptor α by Macchia, Paolo E., Takeuchi, Yoko, Kawai, Tomoko, Cua, Kevin, Gauthier, Karine, Chassande, Olivier, Seo, Hisao, Hayashi, Yoshitaka, Samarut, Jacques, Murata, Yoshiharu, Weiss, Roy E., Refetoff, Samuel

“…Only three of the four thyroid hormone receptor (TR) isoforms, α1, β1, and β2, bind thyroid hormone (TH) and are considered to be true TRs. TRα2 binds to TH…”
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High-dose intravenous corticosteroid therapy for Graves' ophthalmopathy by MACCHIA, P. E, BAGATTINI, M, LUPOLI, G, VITALE, M, VITALE, G, FENZI, G

“…In order to compare oral and high-dose iv corticosteroid therapy for Graves' disease, 25 patients with Graves' ophthalmopathy were treated with two weekly iv…”
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Effects of treatment modalities for Graves’ hyperthyroidism on Graves’ orbitopathy: a 2015 Italian Society of Endocrinology Consensus Statement by Bartalena, L., Macchia, P. E., Marcocci, C., Salvi, M., Vermiglio, F.

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The molecular causes of thyroid dysgenesis: A systematic review by Nettore, I. C., Cacace, V., De Fusco, C., Colao, A., Macchia, P. E.

“…Background: Congenital hypothyroidism (CH) is a frequent disease occurring with an incidence of about 1/2500 newborns/year. In 80–85% of the cases CH is caused…”
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Pregnancy outcome in women treated with methimazole or propylthiouracil during pregnancy by Gianetti, E., Russo, L., Orlandi, F., Chiovato, L., Giusti, M., Benvenga, S., Moleti, M., Vermiglio, F., Macchia, P. E., Vitale, M., Regalbuto, C., Centanni, M., Martino, E., Vitti, P., Tonacchera, M.

“…Purpose Control of thyroid function in hyperthyroid women during pregnancy is based on antithyroid drugs (ATD) [propylthiouracil (PTU) and methimazole (MMI)]…”
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Thyroid function and effect of aging in combined hetero/homozygous mice deficient in thyroid hormone receptors alpha and beta genes by Weiss, RE, Chassande, O, Koo, EK, Macchia, PE, Cua, K, Samarut, J, Refetoff, S, Refetoff, S

“…The maintenance of thyroid hormone (TH) homeostasis is dependent on the synthesis and secretion of TH regulated by TSH. This is achieved, in turn, by the…”
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High-resolution melting analysis (HRM) for mutational screening of Dnajc17 gene in patients affected by thyroid dysgenesis by Nettore, I. C., Desiderio, S., De Nisco, E., Cacace, V., Albano, L., Improda, N., Ungaro, P., Salerno, M., Colao, A., Macchia, P. E.

“…Background Congenital hypothyroidism is a frequent disease occurring with an incidence of about 1/1500 newborns/year. In about 75% of the cases, CH is caused…”
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Orbital scintigraphy with [111In-diethylenetriamine pentaacetic acid-D-Phe1]-octreotide predicts the clinical response to corticosteroid therapy in patients with Graves' ophthalmopathy by COLAO, A, LASTORIA, S, FERONE, D, PIVONELLO, R, MACCHIA, P. E, VASSALLO, P, BONAVOLONTA, G, MUTO, P, LOMBARDI, G, FENZI, G

“…Corticosteroid treatment is successfully used in Graves' ophthalmopathy, and its effect varies according to the phase of the disease. The infiltration of the…”
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Thyroid function tests and characterization of thyroxine-binding globulin in the carbohydrate-deficient glycoprotein syndrome type I by Macchia, P E, Harrison, H H, Scherberg, N H, Sunthornthepfvarakul, T, Jaeken, J, Refetoff, S

“…Carbohydrate-deficient glycoprotein (CDG) syndrome is a newly recognized hereditary disorder that presents with psychomotor retardation, cerebellar ataxia,…”
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Five new families with resistance to thyroid hormone not caused by mutations in the thyroid hormone receptor β gene by POHLENZ, J, WEISS, R. E, MACCHIA, P. E, PANNAIN, S, IP TIM LAU, HO, H, REFETOFF, S

“…Resistance to thyroid hormone (RTH) is a syndrome of variable tissue hyposensitivity to TH. In 191 families, the RTH phenotype has been linked to mutations…”
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Screening for mutations in the ISL1 gene in patients with thyroid dysgenesis by Ferrara, A. M., Rossi, G., Zampella, E., Di Candia, S., Pagliara, V., Nettore, I. C., Capalbo, D., De Sanctis, L., Baserga, M., Salerno, M. C., Fenzi, G., Macchia, P. E.

“…Context: Congenital hypothyroidism (CH) is a common endocrine disorder with an incidence of 1:3000–4000 newborns. In 80–85% of cases, CH is caused by defects…”
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A mouse model for hereditary thyroid dysgenesis and cleft palate by Rodriguez-Mallon, Alina, De Felice, Mario, Macchia, Paolo Emidio, Schöler, Hans, Macchia, Vincenzo, Mariano, Angela, Mattei, Marie-Genevieve, Biffali, Elio, Ovitt, Catherine, Arra, Claudio, Di Lauro, Roberto, Anastassiadis, Konstantinos

“…Alteration of thyroid gland morphogenesis (thyroid dysgenesis) is a frequent human malformation. Among the one in three to four thousand newborns in which…”
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Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesis by Ferrara, A. M., De Sanctis, L., Rossi, G., Capuano, S., Del Prete, G., Zampella, E., Gianino, P., Corrias, A., Fenzi, G., Zannini, M., Macchia, P. E.

“…Aim : In 80–85% of cases, congenital hypothyroidism is associated with thyroid dysgenesis (TD), but only in a small percentage of cases mutations in thyroid…”
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Integrin expression in thyroid cells from normal glands and nodular goiters by Vitale, M, Bassi, V, Fenzi, G, Macchia, P E, Salzano, S, Rossi, G

“…To assess the expression of the very late antigens family of the integrin superfamily in normal and diseased thyroid glands, tissue specimens were digested to…”
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A mouse model for hereditary thyroid dysgenesis and cleft palate by DE FELICE, M, OVITT, C, MACCHIA, V, DI LAURO, R, BIFFALI, E, RODRIGUEZ-MALLON, A, ARRA, C, ANASTASSIADIS, K, MACCHIA, P. E, MATTEI, M.-G, MARIANO, A, SCHÖLER, H

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Epidermal growth factor receptor in human brain tumors by DI CARLO, A, MARIANO, A, MACCHIA, P. E, MORONI, M. C, BEGUINOT, L, MACCHIA, V

“…The expression of epidermal growth factor receptor (EGF-R) was examined in 27 primary human brain tumors (7 glioblastomas, 10 astrocytomas, 5…”
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Epidermal growth factor receptor and lipid membrane components in human lung cancers by DI CARLO, A, MARIANO, A, MACCHIA, P. E, CECERE, C, FERRANTE, G, MACCHIA, V

“…The binding of 125I-epidermal growth factor (EGF) to the plasma membranes of 54 samples of human lung tumors was determined. These included 34 squamous cell…”
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