Fenzi G - Search Results

1

Cloning, chromosomal localization and identification of polymorphisms in the human thyroid transcription factor 2 gene (TITF2).

Macchia PE, Mattei MG, Lapi P, Fenzi G, Di Lauro R. Macchia PE, et al. Among authors: fenzi g. Biochimie. 1999 May;81(5):433-40. doi: 10.1016/s0300-9084(99)80092-3. Biochimie. 1999. PMID: 10403172

2

Mutations in the gene encoding thyroid transcription factor-1 (TTF-1) are not a frequent cause of congenital hypothyroidism (CH) with thyroid dysgenesis.

Lapi P, Macchia PE, Chiovato L, Biffali E, Moschini L, Larizza D, Baserga M, Pinchera A, Fenzi G, Di Lauro R. Lapi P, et al. Among authors: fenzi g. Thyroid. 1997 Jun;7(3):383-7. doi: 10.1089/thy.1997.7.383. Thyroid. 1997. PMID: 9226207

3

PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis.

Macchia PE, Lapi P, Krude H, Pirro MT, Missero C, Chiovato L, Souabni A, Baserga M, Tassi V, Pinchera A, Fenzi G, Grüters A, Busslinger M, Di Lauro R. Macchia PE, et al. Among authors: fenzi g. Nat Genet. 1998 May;19(1):83-6. doi: 10.1038/ng0598-83. Nat Genet. 1998. PMID: 9590296

4

Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesis.

Ferrara AM, De Sanctis L, Rossi G, Capuano S, Del Prete G, Zampella E, Gianino P, Corrias A, Fenzi G, Zannini M, Macchia PE. Ferrara AM, et al. Among authors: fenzi g. J Endocrinol Invest. 2009 Mar;32(3):238-41. doi: 10.1007/BF03346459. J Endocrinol Invest. 2009. PMID: 19542741

5

Screening for mutations in the ISL1 gene in patients with thyroid dysgenesis.

Ferrara AM, Rossi G, Zampella E, Di Candia S, Pagliara V, Nettore IC, Capalbo D, De Sanctis L, Baserga M, Salerno MC, Fenzi G, Macchia PE. Ferrara AM, et al. Among authors: fenzi g. J Endocrinol Invest. 2011 Jul-Aug;34(7):e149-52. doi: 10.3275/7331. Epub 2010 Nov 8. J Endocrinol Invest. 2011. PMID: 21060249

6

Missense mutation in the transcription factor NKX2-5: a novel molecular event in the pathogenesis of thyroid dysgenesis.

Dentice M, Cordeddu V, Rosica A, Ferrara AM, Santarpia L, Salvatore D, Chiovato L, Perri A, Moschini L, Fazzini C, Olivieri A, Costa P, Stoppioni V, Baserga M, De Felice M, Sorcini M, Fenzi G, Di Lauro R, Tartaglia M, Macchia PE. Dentice M, et al. Among authors: fenzi g. J Clin Endocrinol Metab. 2006 Apr;91(4):1428-33. doi: 10.1210/jc.2005-1350. Epub 2006 Jan 17. J Clin Endocrinol Metab. 2006. PMID: 16418214

7

Pendrin is a novel in vivo downstream target gene of the TTF-1/Nkx-2.1 homeodomain transcription factor in differentiated thyroid cells.

Dentice M, Luongo C, Elefante A, Ambrosio R, Salzano S, Zannini M, Nitsch R, Di Lauro R, Rossi G, Fenzi G, Salvatore D. Dentice M, et al. Among authors: fenzi g. Mol Cell Biol. 2005 Nov;25(22):10171-82. doi: 10.1128/MCB.25.22.10171-10182.2005. Mol Cell Biol. 2005. PMID: 16260629 Free PMC article.

8

Orbital scintigraphy with [111In-diethylenetriamine pentaacetic acid-D-phe1]-octreotide predicts the clinical response to corticosteroid therapy in patients with Graves' ophthalmopathy.

Colao A, Lastoria S, Ferone D, Pivonello R, Macchia PE, Vassallo P, Bonavolonta G, Muto P, Lombardi G, Fenzi G. Colao A, et al. Among authors: fenzi g. J Clin Endocrinol Metab. 1998 Nov;83(11):3790-4. doi: 10.1210/jcem.83.11.5274. J Clin Endocrinol Metab. 1998. PMID: 9814448 Clinical Trial.

9

High-dose intravenous corticosteroid therapy for Graves' ophthalmopathy.

Macchia PE, Bagattini M, Lupoli G, Vitale M, Vitale G, Fenzi G. Macchia PE, et al. Among authors: fenzi g. J Endocrinol Invest. 2001 Mar;24(3):152-8. doi: 10.1007/BF03343835. J Endocrinol Invest. 2001. PMID: 11314743 Clinical Trial.

10

Integrin expression in thyroid cells from normal glands and nodular goiters.

Vitale M, Bassi V, Fenzi G, Macchia PE, Salzano S, Rossi G. Vitale M, et al. Among authors: fenzi g. J Clin Endocrinol Metab. 1993 Jun;76(6):1575-9. doi: 10.1210/jcem.76.6.8501165. J Clin Endocrinol Metab. 1993. PMID: 8501165

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