Moschini L - Search Results

1

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. Tonacchera M, et al. Among authors: moschini l. Thyroid. 2004 Aug;14(8):584-8. doi: 10.1089/1050725041692864. Thyroid. 2004. PMID: 15320969

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: moschini l. Thyroid. 1997 Jun;7(3):383-7. doi: 10.1089/thy.1997.7.383. Thyroid. 1997. PMID: 9226207

3

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: moschini l. 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

4

Risk factors for congenital hypothyroidism: results of a population case-control study (1997-2003).

Medda E, Olivieri A, Stazi MA, Grandolfo ME, Fazzini C, Baserga M, Burroni M, Cacciari E, Calaciura F, Cassio A, Chiovato L, Costa P, Leonardi D, Martucci M, Moschini L, Pagliardini S, Parlato G, Pignero A, Pinchera A, Sala D, Sava L, Stoppioni V, Tancredi F, Valentini F, Vigneri R, Sorcini M. Medda E, et al. Among authors: moschini l. Eur J Endocrinol. 2005 Dec;153(6):765-73. doi: 10.1530/eje.1.02048. Eur J Endocrinol. 2005. PMID: 16322381

5

[Re-evaluation of the diagnosis in congenital hypothyroidism].

Costa P, Sambuco L, Olivieri A, Fazzini C, Sorcini M, Vendemmiati V, Valentini F, Moschini L. Costa P, et al. Among authors: moschini l. Ann Ist Super Sanita. 1998;34(3):343-7. Ann Ist Super Sanita. 1998. PMID: 10052172 Italian.

6

[The instrumental and clinical laboratory follow-up of congenital hypothyroidism].

Moschini L, Costa P, D'Addio A. Moschini L, et al. Ann Ist Super Sanita. 1994;30(3):335-8. Ann Ist Super Sanita. 1994. PMID: 7880001 Italian.

7

[Congenital hypothyroidism: organization and coordination of neonatal screening in Italy].

Carta S, Grandolfo ME, Moschini L, Olivieri A, Stazi A, Fazzini C, Battisti P, Timperi F, Sorcini M. Carta S, et al. Among authors: moschini l. Ann Ist Super Sanita. 1991;27(2):311-8. Ann Ist Super Sanita. 1991. PMID: 1755585 Review. Italian.

8

Longitudinal assessment of children with congenital hypothyroidism detected by neonatal screening.

Moschini L, Costa P, Marinelli E, Maggioni G, Sorcini Carta M, Fazzini C, Diodato A, Sabini G, Grandolfo ME, Carta S, et al. Moschini L, et al. Helv Paediatr Acta. 1986 Dec;41(5):415-24. Helv Paediatr Acta. 1986. PMID: 3818328

9

[2 cases of Beckwith-Wiedemann syndrome. Morphogenetic characteristics, cardiac involvement and current diagnostic possibilities].

D'Addio AP, Moschini L, Sistopaoli F, Marinelli E, Vitarelli A. D'Addio AP, et al. Among authors: moschini l. Minerva Pediatr. 1994 Nov;46(11):509-15. Minerva Pediatr. 1994. PMID: 7870009 Italian.

10

Familial thyroxine-binding globulin deficiency detected in a pilot screening program for congenital hypothyroidism.

Carta Sorcini M, Moschini L, Fiore L, Tomarchio S, Di Irio MG, Gilardi E, Romagnoli C, Currò V, Carta S. Carta Sorcini M, et al. Among authors: moschini l. J Endocrinol Invest. 1982 Jan-Feb;5(1):21-5. doi: 10.1007/BF03350477. J Endocrinol Invest. 1982. PMID: 6808051

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