Baserga M - Search Results

1

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: baserga m. 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

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

3

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: baserga m. Eur J Endocrinol. 2005 Dec;153(6):765-73. doi: 10.1530/eje.1.02048. Eur J Endocrinol. 2005. PMID: 16322381

4

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: baserga m. Nat Genet. 1998 May;19(1):83-6. doi: 10.1038/ng0598-83. Nat Genet. 1998. PMID: 9590296

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: baserga m. 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

Congenital hypothyroidism in Calabria: epidemiological and clinical aspects.

Baserga M, Pullano MN. Baserga M, et al. Ann Ist Super Sanita. 2009;45(4):443-6. doi: 10.1590/s0021-25712009000400015. Ann Ist Super Sanita. 2009. PMID: 20061667

7

[Diabetes, hypothyroidism and celiac disease in Down's syndrome. A case report].

Rosso C, Cecere G, Concolino D, Baserga M. Rosso C, et al. Among authors: baserga m. Minerva Pediatr. 1997 Oct;49(10):483-5. Minerva Pediatr. 1997. PMID: 9557494 Italian.

8

Chromosomal instability in multiple endocrine neoplasia type 1. Cytogenetic evaluation with DEB test.

Tomassetti P, Cometa G, Del Vecchio E, Baserga M, Faccioli P, Bosoni D, Paolucci G, Barbara L. Tomassetti P, et al. Among authors: baserga m. Cancer Genet Cytogenet. 1995 Feb;79(2):123-6. doi: 10.1016/0165-4608(95)98126-j. Cancer Genet Cytogenet. 1995. PMID: 7889502

9

[Evaluation of the varus-valgus knee in a group of calabrian children].

Talarico V, Baserga M, Fuiano L, Mattace F, Mastria G, Arcuri V. Talarico V, et al. Among authors: baserga m. Pediatr Med Chir. 2011 Mar-Apr;33(2):80-4. Pediatr Med Chir. 2011. PMID: 22111290 Italian.

10

[Nailfold capillaroscopy in the study of microcirculation in childhood].

Baserga M, Bonacci E, Cammarota MG, D'Amico N. Baserga M, et al. Minerva Pediatr. 1996 Jul-Aug;48(7-8):297-301. Minerva Pediatr. 1996. PMID: 8965760 Italian.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

95 results

Search Page

Filters