De Brasi D - Search Results

1

Thyroid transcription factor 1 phosphorylation is not required for protein kinase A-dependent transcription of the thyroglobulin promoter.

Feliciello A, Allevato G, Musti AM, De Brasi D, Gallo A, Avvedimento VE, Gottesman ME. Feliciello A, et al. Among authors: de brasi d. Cell Growth Differ. 2000 Dec;11(12):649-54. Cell Growth Differ. 2000. PMID: 11149600

2

Reversible inhibition of a thyroid-specific trans-acting factor by Ras.

Avvedimento VE, Musti AM, Ueffing M, Obici S, Gallo A, Sanchez M, DeBrasi D, Gottesman ME. Avvedimento VE, et al. Genes Dev. 1991 Jan;5(1):22-8. doi: 10.1101/gad.5.1.22. Genes Dev. 1991. PMID: 1989905 Free article.

3

Inverted duplication of 15q with terminal deletion in a multiple malformed newborn with intrauterine growth failure and lethal phenotype.

Genesio R, De Brasi D, Conti A, Borghese A, Di Micco P, Di Costanzo P, Paladini D, Ungaro P, Nitsch L. Genesio R, et al. Among authors: de brasi d. Am J Med Genet A. 2004 Aug 1;128A(4):422-8. doi: 10.1002/ajmg.a.30112. Am J Med Genet A. 2004. PMID: 15264291

4

Inv dup del (1)(pter-->q44::q44-->q42:) with the classical phenotype of trisomy 1q42-qter.

De Brasi D, Rossi E, Giglio S, D'Agostino A, Titomanlio L, Farina V, Andria G, Sebastio G. De Brasi D, et al. Among authors: d agostino a. Am J Med Genet. 2001 Nov 22;104(2):127-30. doi: 10.1002/ajmg.1589. Am J Med Genet. 2001. PMID: 11746042

5

Short stature and azoospermia in a patient with Y chromosome long arm deletion.

De Rosa M, De Brasi D, Zarrilli S, Paesano L, Pivonello R, D'Agostino A, Longobardi S, Merola B, Lupoli G, Ogata T, Lombardi G. De Rosa M, et al. Among authors: de brasi d, d agostino a. J Endocrinol Invest. 1997 Nov;20(10):623-8. doi: 10.1007/BF03346921. J Endocrinol Invest. 1997. PMID: 9438922

6

Cloverleaf skull anomaly and de novo trisomy 4p.

de Brasi D, Perone L, di Micco P, Andria G, Sebastio G, Iaccarino E, Pinto L, Aliberti F. de Brasi D, et al. J Med Genet. 1999 May;36(5):422-4. J Med Genet. 1999. PMID: 10353793 Free PMC article. No abstract available.

7

Case of Myhre syndrome with autism and peculiar skin histological findings.

Titomanlio L, Marzano MG, Rossi E, D'Armiento M, De Brasi D, Vega GR, Andreucci MV, Orsini AV, Santoro L, Sebastio G. Titomanlio L, et al. Among authors: de brasi d, d armiento m. Am J Med Genet. 2001 Oct 1;103(2):163-5. doi: 10.1002/ajmg.1517. Am J Med Genet. 2001. PMID: 11568925

8

Unbalanced translocation (3;5)(q26.1;p14): a clinical report.

Rossi M, Di Micco P, Perone L, De Brasi D, Guzzetta V, Andreucci MV, Vega GR, Marzano MG, Iaccarino E, Andria G. Rossi M, et al. Among authors: de brasi d. Am J Med Genet. 2002 Jul 15;110(4):353-8. doi: 10.1002/ajmg.10440. Am J Med Genet. 2002. PMID: 12116209 Review.

9

New syndrome with generalized lipodystrophy and a distinctive facial appearance: confirmation of Keppen-Lubinski syndrome?

De Brasi D, Brunetti-Pierri N, Di Micco P, Andria G, Sebastio G. De Brasi D, et al. Am J Med Genet A. 2003 Mar 1;117A(2):194-5. doi: 10.1002/ajmg.a.10936. Am J Med Genet A. 2003. PMID: 12567423 No abstract available.

10

Mild Wolf-Hirschhorn phenotype and partial GH deficiency in a patient with a 4p terminal deletion.

Titomanlio L, Romano A, Conti A, Genesio R, Salerno M, De Brasi D, Nitsch L, Del Giudice E. Titomanlio L, et al. Among authors: de brasi d. Am J Med Genet A. 2004 Jun 1;127A(2):197-200. doi: 10.1002/ajmg.a.20667. Am J Med Genet A. 2004. PMID: 15108211

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

70 results

Search Page

Filters