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Items: 1 to 50 of 68

1.

Genetic interaction analysis of VEGF-A rs3025039 and VEGFR-2 rs2071559 identifies a genetic profile at higher risk to develop nodular goiter.

Molinaro A, Orlandi P, Niccolai F, Agretti P, De Marco G, Ferrarini E, Di Cosmo C, Vitti P, Piaggi P, Di Desidero T, Bocci G, Tonacchera M.

J Endocrinol Invest. 2019 Aug 2. doi: 10.1007/s40618-019-01092-9. [Epub ahead of print]

PMID:
31376092
2.

Measurement of urinary free cortisol by LC-MS-MS: adoption of a literature reference range and comparison with our current immunometric method.

Bianchi L, Campi B, Sessa MR, De Marco G, Ferrarini E, Zucchi R, Marcocci C, Vitti P, Manetti L, Saba A, Agretti P.

J Endocrinol Invest. 2019 Apr 22. doi: 10.1007/s40618-019-01050-5. [Epub ahead of print]

PMID:
31012054
3.

Papillary thyroid cancer in a patient with congenital goitrous hypothyroidism due to a novel deletion in NIS gene.

Agretti P, Bagattini B, De Marco G, Di Cosmo C, Dionigi G, Vitti P, Tonacchera M.

Endocrine. 2016 Oct;54(1):256-258. Epub 2015 Nov 13. No abstract available.

PMID:
26563437
4.

TSH elevations as the first laboratory evidence for pseudohypoparathyroidism type Ib (PHP-Ib).

Molinaro A, Tiosano D, Takatani R, Chrysis D, Russell W, Koscielniak N, Kottler ML, Agretti P, De Marco G, Ahtiainen P, Christov M, Mäkitie O, Tonacchera M, Jüppner H.

J Bone Miner Res. 2015 May;30(5):906-12. doi: 10.1002/jbmr.2408.

5.

The different requirement of L-T4 therapy in congenital athyreosis compared with adult-acquired hypothyroidism suggests a persisting thyroid hormone resistance at the hypothalamic-pituitary level.

Bagattini B, Cosmo CD, Montanelli L, Piaggi P, Ciampi M, Agretti P, Marco GD, Vitti P, Tonacchera M.

Eur J Endocrinol. 2014 Nov;171(5):615-21. doi: 10.1530/EJE-14-0621.

PMID:
25305309
6.

BRAF mutation analysis in thyroid nodules with indeterminate cytology: our experience on surgical management of patients with thyroid nodules from an area of borderline iodine deficiency.

Agretti P, Niccolai F, Rago T, De Marco G, Molinaro A, Scutari M, Di Cosmo C, Di Coscio G, Vitale M, Maccheroni M, Vitti P, Tonacchera M.

J Endocrinol Invest. 2014 Oct;37(10):1009-14. doi: 10.1007/s40618-014-0166-6. Epub 2014 Sep 7.

PMID:
25194426
7.

Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidism.

Vincenzi M, Camilot M, Ferrarini E, Teofoli F, Venturi G, Gaudino R, Cavarzere P, De Marco G, Agretti P, Dimida A, Tonacchera M, Boner A, Antoniazzi F.

BMC Endocr Disord. 2014 Aug 22;14:69. doi: 10.1186/1472-6823-14-69.

8.

Frequency and effect on serum TSH of phosphodiesterase 8B (PDE8B) gene polymorphisms in patients with sporadic nonautoimmune subclinical hypothyroidism.

Agretti P, De Marco G, Di Cosmo C, Bagattini B, Ferrarini E, Montanelli L, Vitti P, Tonacchera M.

J Endocrinol Invest. 2014 Feb;37(2):189-94. doi: 10.1007/s40618-013-0036-7. Epub 2014 Jan 9.

PMID:
24497218
9.

Presence in the pre-surgical fine-needle aspiration of potential thyroid biomarkers previously identified in the post-surgical one.

Ciregia F, Giusti L, Molinaro A, Niccolai F, Agretti P, Rago T, Di Coscio G, Vitti P, Basolo F, Iacconi P, Tonacchera M, Lucacchini A.

PLoS One. 2013 Sep 2;8(9):e72911. doi: 10.1371/journal.pone.0072911. eCollection 2013.

10.

The W520X mutation in the TSHR gene brings on subclinical hypothyroidism through an haploinsufficiency mechanism.

Moia S, Godi M, Walker GE, Roccio M, Agretti P, Tonacchera M, Berardi R, Bellone S, Prodam F, Giordano M, Bona G.

J Endocrinol Invest. 2013 Oct;36(9):716-21. doi: 10.3275/8930. Epub 2013 Apr 8.

PMID:
23563316
11.

Iodine fortification of vegetables improves human iodine nutrition: in vivo evidence for a new model of iodine prophylaxis.

Tonacchera M, Dimida A, De Servi M, Frigeri M, Ferrarini E, De Marco G, Grasso L, Agretti P, Piaggi P, Aghini-Lombardi F, Perata P, Pinchera A, Vitti P.

J Clin Endocrinol Metab. 2013 Apr;98(4):E694-7. doi: 10.1210/jc.2012-3509. Epub 2013 Mar 12.

PMID:
23482609
12.

Congenital hypothyroidism caused by a novel homozygous mutation in the thyroglobulin gene.

Agretti P, De Marco G, Di Cosmo C, Ferrarini E, Montanelli L, Bagattini B, Vitti P, Tonacchera M.

Eur J Pediatr. 2013 Jul;172(7):959-64. doi: 10.1007/s00431-013-1976-9. Epub 2013 Mar 3.

PMID:
23455760
13.

Prevalence of activating thyrotropin receptor and Gsα gene mutations in paediatric thyroid toxic adenomas: a multicentric Italian study.

Agretti P, Segni M, De Marco G, Ferrarini E, Di Cosmo C, Corrias A, Weber G, Larizza D, Calcaterra V, Pelizzo MR, Cesaretti G, Vitti P, Tonacchera M.

Clin Endocrinol (Oxf). 2013 Nov;79(5):747-9. doi: 10.1111/cen.12158. Epub 2013 May 20. No abstract available.

PMID:
23346880
14.

Non-autoimmune subclinical hypothyroidism due to a mutation in TSH receptor: report on two brothers.

Cerbone M, Agretti P, De Marco G, Improda N, Pignata C, Santamaria F, Tonacchera M, Salerno M.

Ital J Pediatr. 2013 Jan 19;39:5. doi: 10.1186/1824-7288-39-5.

15.

Clinical characteristics and genetic analysis in women with premature ovarian insufficiency.

Ferrarini E, Russo L, Fruzzetti F, Agretti P, De Marco G, Dimida A, Gianetti E, Simoncini T, Simi P, Baldinotti F, Benelli E, Pucci E, Pinchera A, Vitti P, Tonacchera M.

Maturitas. 2013 Jan;74(1):61-7. doi: 10.1016/j.maturitas.2012.09.017. Epub 2012 Oct 26.

PMID:
23107817
16.

MicroRNA expression profile helps to distinguish benign nodules from papillary thyroid carcinomas starting from cells of fine-needle aspiration.

Agretti P, Ferrarini E, Rago T, Candelieri A, De Marco G, Dimida A, Niccolai F, Molinaro A, Di Coscio G, Pinchera A, Vitti P, Tonacchera M.

Eur J Endocrinol. 2012 Sep;167(3):393-400. doi: 10.1530/EJE-12-0400. Epub 2012 Jun 22.

PMID:
22728346
17.

Metabolic engineering of the iodine content in Arabidopsis.

Landini M, Gonzali S, Kiferle C, Tonacchera M, Agretti P, Dimida A, Vitti P, Alpi A, Pinchera A, Perata P.

Sci Rep. 2012;2:338. doi: 10.1038/srep00338. Epub 2012 Mar 27.

18.

Sporadic congenital nonautoimmune hyperthyroidism caused by P639S mutation in thyrotropin receptor gene.

Agretti P, De Marco G, Biagioni M, Iannilli A, Marigliano M, Pinchera A, Vitti P, Cherubini V, Tonacchera M.

Eur J Pediatr. 2012 Jul;171(7):1133-7. doi: 10.1007/s00431-012-1702-z. Epub 2012 Feb 28.

PMID:
22371259
19.

Genetic markers to discriminate benign and malignant thyroid nodules with undetermined cytology in an area of borderline iodine deficiency.

Tonacchera M, Agretti P, Rago T, De Marco G, Niccolai F, Molinaro A, Scutari M, Candelieri A, Conforti D, Musmanno R, Di Coscio G, Basolo F, Iacconi P, Miccoli P, Pinchera A, Vitti P.

J Endocrinol Invest. 2012 Sep;35(8):754-9. Epub 2011 Oct 4.

PMID:
21979329
20.

Identification and functional analysis of novel dual oxidase 2 (DUOX2) mutations in children with congenital or subclinical hypothyroidism.

De Marco G, Agretti P, Montanelli L, Di Cosmo C, Bagattini B, De Servi M, Ferrarini E, Dimida A, Freitas Ferreira AC, Molinaro A, Ceccarelli C, Brozzi F, Pinchera A, Vitti P, Tonacchera M.

J Clin Endocrinol Metab. 2011 Aug;96(8):E1335-9. doi: 10.1210/jc.2010-2467. Epub 2011 May 11.

PMID:
21565790
21.

3-Iodothyronamine metabolism and functional effects in FRTL5 thyroid cells.

Agretti P, De Marco G, Russo L, Saba A, Raffaelli A, Marchini M, Chiellini G, Grasso L, Pinchera A, Vitti P, Scanlan TS, Zucchi R, Tonacchera M.

J Mol Endocrinol. 2011 Jul 12;47(1):23-32. doi: 10.1530/JME-10-0168. Print 2011 Aug.

PMID:
21511808
22.

Electric and magnetic fields do not modify the biochemical properties of FRTL-5 cells.

Dimida A, Ferrarini E, Agretti P, De Marco G, Grasso L, Martinelli M, Longo I, Giulietti D, Ricci A, Galimberti M, Siervo B, Licitra G, Francia F, Pinchera A, Vitti P, Tonacchera M.

J Endocrinol Invest. 2011 Mar;34(3):185-9. doi: 10.3275/7107. Epub 2010 Jun 11.

PMID:
20543553
23.

Study of potential inhibitors of thyroid iodide uptake by using CHO cells stably expressing the human sodium/iodide symporter (hNIS) protein.

Agretti P, Dimida A, De Marco G, Ferrarini E, Rodrìguez Gonzàlez JC, Santini F, Vitti P, Pinchera A, Tonacchera M.

J Endocrinol Invest. 2011 Mar;34(3):170-4. doi: 10.3275/7046. Epub 2010 May 17.

PMID:
20479570
24.

Patients affected by vitiligo and autoimmune diseases do not show antibodies interfering with the activity of the melanocortin 1 receptor.

Agretti P, De Marco G, Sansone D, Betterle C, Coco G, Dimida A, Ferrarini E, Pinchera A, Vitti P, Tonacchera M.

J Endocrinol Invest. 2010 Dec;33(11):784-8. doi: 10.3275/6933. Epub 2010 Mar 22.

PMID:
20332705
25.

Congenital hypothyroidism and late-onset goiter: identification and characterization of a novel mutation in the sodium/iodide symporter of the proband and family members.

Montanelli L, Agretti P, Marco Gd, Bagattini B, Ceccarelli C, Brozzi F, Lettiero T, Cerbone M, Vitti P, Salerno M, Pinchera A, Tonacchera M.

Thyroid. 2009 Dec;19(12):1419-25. doi: 10.1089/thy.2009.0080.

PMID:
19916865
26.

Thyrotropin-stimulating hormone receptor gene analysis in pediatric patients with non-autoimmune subclinical hypothyroidism.

Nicoletti A, Bal M, De Marco G, Baldazzi L, Agretti P, Menabò S, Ballarini E, Cicognani A, Tonacchera M, Cassio A.

J Clin Endocrinol Metab. 2009 Nov;94(11):4187-94. doi: 10.1210/jc.2009-0618. Epub 2009 Oct 9.

PMID:
19820021
27.

Identification and functional studies of two new dual-oxidase 2 (DUOX2) mutations in a child with congenital hypothyroidism and a eutopic normal-size thyroid gland.

Tonacchera M, De Marco G, Agretti P, Montanelli L, Di Cosmo C, Freitas Ferreira AC, Dimida A, Ferrarini E, Ramos HE, Ceccarelli C, Brozzi F, Pinchera A, Vitti P.

J Clin Endocrinol Metab. 2009 Nov;94(11):4309-14. doi: 10.1210/jc.2009-0426. Epub 2009 Sep 29.

PMID:
19789206
28.

Presence of a putative steroidal allosteric site on glycoprotein hormone receptors.

Rossi M, Dimida A, Ferrarini E, Silvano E, De Marco G, Agretti P, Aloisi G, Simoncini T, Di Bari L, Tonacchera M, Giorgi F, Maggio R.

Eur J Pharmacol. 2009 Nov 25;623(1-3):155-9. doi: 10.1016/j.ejphar.2009.09.029. Epub 2009 Sep 17.

PMID:
19766106
29.

Functional studies of new TSH receptor (TSHr) mutations identified in patients affected by hypothyroidism or isolated hyperthyrotrophinaemia.

De Marco G, Agretti P, Camilot M, Teofoli F, Tatò L, Vitti P, Pinchera A, Tonacchera M.

Clin Endocrinol (Oxf). 2009 Feb;70(2):335-8. doi: 10.1111/j.1365-2265.2008.03333.x. Epub 2008 Aug 22.

PMID:
18727713
30.

Endothelin-1 up-regulates p115RhoGEF in embryonic rat cardiomyocytes during the hypertrophic response.

Porchia F, Papucci M, Gargini C, Asta A, De Marco G, Agretti P, Tonacchera M, Mazzoni MR.

J Recept Signal Transduct Res. 2008;28(3):265-83. doi: 10.1080/10799890802084515 .

PMID:
18569527
31.

Thyroid hormone action in the adult brain: gene expression profiling of the effects of single and multiple doses of triiodo-L-thyronine in the rat striatum.

Diez D, Grijota-Martinez C, Agretti P, De Marco G, Tonacchera M, Pinchera A, de Escobar GM, Bernal J, Morte B.

Endocrinology. 2008 Aug;149(8):3989-4000. doi: 10.1210/en.2008-0350. Epub 2008 May 8.

32.

A fast method to detect cell surface expression of thyrotropin receptor (TSHr): the microchip flow cytometry analysis.

Agretti P, De Marco G, Capodanno A, Ferrarini E, Dimida A, Sansone D, Collecchi P, Pinchera A, Vitti P, Tonacchera M.

Thyroid. 2007 Sep;17(9):861-8.

PMID:
17705697
33.

Identification of TSH receptor mutations in three families with resistance to TSH.

Tonacchera M, Di Cosmo C, De Marco G, Agretti P, Banco M, Perri A, Gianetti E, Montanelli L, Vitti P, Pinchera A.

Clin Endocrinol (Oxf). 2007 Nov;67(5):712-8. Epub 2007 Aug 13.

PMID:
17697008
35.

Genetic analysis of the PAX8 gene in children with congenital hypothyroidism and dysgenetic or eutopic thyroid glands: identification of a novel sequence variant.

Tonacchera M, Banco ME, Montanelli L, Di Cosmo C, Agretti P, De Marco G, Ferrarini E, Ordookhani A, Perri A, Chiovato L, Santini F, Vitti P, Pinchera A.

Clin Endocrinol (Oxf). 2007 Jul;67(1):34-40. Epub 2007 Apr 15.

PMID:
17437516
36.

Markers of cell proliferation, apoptosis, and angiogenesis in thyroid adenomas: a comparative immunohistochemical and genetic investigation of functioning and nonfunctioning nodules.

Viacava P, Bocci G, Tonacchera M, Fanelli G, DeServi M, Agretti P, Berti E, Goletti O, Aretini P, Resta ML, Bevilacqua G, Naccarato AG.

Thyroid. 2007 Mar;17(3):191-7.

PMID:
17381350
37.

Genetic analysis of the follicle stimulating hormone receptor gene in women with polycystic ovary syndrome.

Orio F Jr, Ferrarini E, Cascella T, Dimida A, Palomba S, Gianetti E, Colao A, Agretti P, Vitti P, Lombardi G, Pinchera A, Tonacchera M.

J Endocrinol Invest. 2006 Dec;29(11):975-82.

PMID:
17259794
38.

Effects of a thyroid-stimulating human monoclonal autoantibody (M22) on functional activity of LH and FSH receptors.

Tonacchera M, Ferrarini E, Dimida A, Agretti P, De Marco G, Pinchera A, Sanders J, Evans M, Richards T, Furmaniak J, Smith BR.

Thyroid. 2006 Nov;16(11):1085-9.

PMID:
17123334
39.

The thyroid disruptor 1,1,1-trichloro-2,2-bis(p-chlorophenyl)-ethane appears to be an uncompetitive inverse agonist for the thyrotropin receptor.

Rossi M, Dimida A, Dell'anno MT, Trincavelli ML, Agretti P, Giorgi F, Corsini GU, Pinchera A, Vitti P, Tonacchera M, Maggio R.

J Pharmacol Exp Ther. 2007 Jan;320(1):465-74. Epub 2006 Oct 24.

PMID:
17062616
40.

The sodium-iodide symporter expression in placental tissue at different gestational age: an immunohistochemical study.

Di Cosmo C, Fanelli G, Tonacchera M, Ferrarini E, Dimida A, Agretti P, De Marco G, Vitti P, Pinchera A, Bevilacqua G, Naccarato AG, Viacava P.

Clin Endocrinol (Oxf). 2006 Oct;65(4):544-8.

PMID:
16984250
41.

Poorly specific binding of thyroglobulin to orbital fibroblasts from patients with Graves' ophthalmopathy.

Lisi S, Botta R, Agretti P, Sellari-Franceschini S, Marcocci C, Pinchera A, Marinò M.

J Endocrinol Invest. 2005 May;28(5):420-4.

PMID:
16075925
42.

Evidence for protein and mRNA TSHr expression in fibroblasts from patients with thyroid-associated ophthalmopathy (TAO) after adipocytic differentiation.

Agretti P, De Marco G, De Servi M, Marcocci C, Vitti P, Pinchera A, Tonacchera M.

Eur J Endocrinol. 2005 May;152(5):777-84.

PMID:
15879364
43.

Relative potencies and additivity of perchlorate, thiocyanate, nitrate, and iodide on the inhibition of radioactive iodide uptake by the human sodium iodide symporter.

Tonacchera M, Pinchera A, Dimida A, Ferrarini E, Agretti P, Vitti P, Santini F, Crump K, Gibbs J.

Thyroid. 2004 Dec;14(12):1012-9.

PMID:
15650353
44.

Absence of interference of serum IgGs from patients with breast cancer and thyroid autoimmunity on the function of human iodide symporter gene stably transfected in CHO cells.

Fierabracci P, Pinchera A, Tonacchera M, Agretti P, De Marco G, Albertini S, Conforti G, Seregni E, Agresti R, Grasso L, Giani C.

J Endocrinol Invest. 2004 Oct;27(9):862-5.

PMID:
15648551
45.

Low prevalence of thyrotropin receptor mutations in a large series of subjects with sporadic and familial nonautoimmune subclinical hypothyroidism.

Tonacchera M, Perri A, De Marco G, Agretti P, Banco ME, Di Cosmo C, Grasso L, Vitti P, Chiovato L, Pinchera A.

J Clin Endocrinol Metab. 2004 Nov;89(11):5787-93.

PMID:
15531543
46.

Gonadotrophin receptor blocking antibodies measured by the use of cell lines stably expressing human gonadotrophin receptors are not detectable in women with 46,XX premature ovarian failure.

Tonacchera M, Ferrarini E, Dimida A, Agretti P, De Marco G, De Servi M, Gianetti E, Chiovato L, Pucci E, Pra CD, Betterle C, Aghini-Lombardi F, Vitti P, Pinchera A.

Clin Endocrinol (Oxf). 2004 Sep;61(3):376-81.

PMID:
15355455
47.

Genetic analysis of TTF-2 gene in children with congenital hypothyroidism and cleft palate, congenital hypothyroidism, or isolated cleft palate.

Tonacchera M, Banco M, Lapi P, Di Cosmo C, Perri A, Montanelli L, Moschini L, Gatti G, Gandini D, Massei A, Agretti P, De Marco G, Vitti P, Chiovato L, Pinchera A.

Thyroid. 2004 Aug;14(8):584-8.

PMID:
15320969
48.

The sodium-iodide symporter protein is always present at a low expression and confined to the cell membrane in nonfunctioning nonadenomatous nodules of toxic nodular goitre.

Tonacchera M, Viacava P, Fanelli G, Agretti P, De Marco G, De Servi M, Di Cosmo C, Chiovato L, Pinchera A, Vitti P.

Clin Endocrinol (Oxf). 2004 Jul;61(1):40-5.

PMID:
15212643
49.

TSH receptor antibodies do not alter the function of gonadotropin receptors stably expressed in eukaryotic cells.

Tonacchera M, Ferrarini E, Dimida A, Agretti P, De Marco G, De Servi M, Chiovato L, Cetani F, Vitti P, Pinchera A.

Eur J Endocrinol. 2004 Mar;150(3):381-7.

PMID:
15012625
50.

Genetic screening for melanocortin-4 receptor mutations in a cohort of Italian obese patients: description and functional characterization of a novel mutation.

Santini F, Maffei M, Ceccarini G, Pelosini C, Scartabelli G, Rosellini V, Chiellini C, Marsili A, Lisi S, Tonacchera M, Agretti P, Chiovato L, Mammoli C, Vitti P, Pinchera A.

J Clin Endocrinol Metab. 2004 Feb;89(2):904-8.

PMID:
14764812

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