Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

422 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
The E180splice mutation in the GHR gene causing Laron syndrome: witness of a Sephardic Jewish exodus from the Iberian Peninsula to the New World?
Gonçalves FT, Fridman C, Pinto EM, Guevara-Aguirre J, Shevah O, Rosembloom AL, Hwa V, Cassorla F, Rosenfeld RG, Lins TS, Damiani D, Arnhold IJ, Laron Z, Jorge AA. Gonçalves FT, et al. Among authors: damiani d. Am J Med Genet A. 2014 May;164A(5):1204-8. doi: 10.1002/ajmg.a.36444. Epub 2014 Mar 24. Am J Med Genet A. 2014. PMID: 24664892
Ullrich-Turner syndrome: relevance of searching for Y chromosome fragments.
Damiani D, Guedes DR, Fellous M, Barbaux S, McElreavey K, Kalil J, Goldberg AC, Moreira-Filho CA, Barbosa A, Della Manna T, Dichtchekenian V, Setian N. Damiani D, et al. J Pediatr Endocrinol Metab. 1999 Nov-Dec;12(6):827-31. doi: 10.1515/jpem.1999.12.6.827. J Pediatr Endocrinol Metab. 1999. PMID: 10614539
Polycystic Ovary Syndrome among Obese Adolescents.
Ybarra M, Franco RR, Cominato L, Sampaio RB, Sucena da Rocha SM, Damiani D. Ybarra M, et al. Among authors: damiani d. Gynecol Endocrinol. 2018 Jan;34(1):45-48. doi: 10.1080/09513590.2017.1359250. Epub 2017 Jul 29. Gynecol Endocrinol. 2018. PMID: 28758509 Free article.
[Multicentric study of Brazilian patients with 21-hydroxylase deficiency: a genotype-phenotype correlation].
Bachega TA, Billerbeck AE, Parente EB, Lemos-Marini SH, Baptista MT, Mello MP, Guerra G Jr, Kuperman H, Setian N, Damiani D, Torres N, Castro Md, Mendonça BB. Bachega TA, et al. Among authors: damiani d. Arq Bras Endocrinol Metabol. 2004 Oct;48(5):697-704. doi: 10.1590/s0004-27302004000500016. Epub 2005 Mar 7. Arq Bras Endocrinol Metabol. 2004. PMID: 15761541 Review. Portuguese.
Glibenclamide unresponsiveness in a Brazilian child with permanent neonatal diabetes mellitus and DEND syndrome due to a C166Y mutation in KCNJ11 (Kir6.2) gene.
Della Manna T, Battistim C, Radonsky V, Savoldelli RD, Damiani D, Kok F, Pearson ER, Ellard S, Hattersley AT, Reis AF. Della Manna T, et al. Among authors: damiani d. Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1350-5. doi: 10.1590/s0004-27302008000800024. Arq Bras Endocrinol Metabol. 2008. PMID: 19169493
422 results