Scommegna S - Search Results

1

Longitudinal hormonal evaluation in a patient with disorder of sexual development, 46,XY karyotype and one NR5A1 mutation.

Pedace L, Laino L, Preziosi N, Valentini MS, Scommegna S, Rapone AM, Guarino N, Boscherini B, De Bernardo C, Marrocco G, Majore S, Grammatico P. Pedace L, et al. Among authors: scommegna s. Am J Med Genet A. 2014 Nov;164A(11):2938-46. doi: 10.1002/ajmg.a.36729. Epub 2014 Aug 26. Am J Med Genet A. 2014. PMID: 25160005

2

Disorders of sex development: a genetic study of patients in a multidisciplinary clinic.

Laino L, Majore S, Preziosi N, Grammatico B, De Bernardo C, Scommegna S, Rapone AM, Marrocco G, Bottillo I, Grammatico P. Laino L, et al. Among authors: scommegna s. Endocr Connect. 2014 Dec;3(4):180-92. doi: 10.1530/EC-14-0085. Epub 2014 Sep 23. Endocr Connect. 2014. PMID: 25248670 Free PMC article.

3

Vaginoplasty for disorders of sex development.

Guarino N, Scommegna S, Majore S, Rapone AM, Ungaro L, Morrone A, Grammatico P, Marrocco GA. Guarino N, et al. Among authors: scommegna s. Front Endocrinol (Lausanne). 2013 Mar 11;4:29. doi: 10.3389/fendo.2013.00029. eCollection 2013. Front Endocrinol (Lausanne). 2013. PMID: 23483838 Free PMC article.

4

Lucci-Cordisco E, Scommegna S, Orteschi D, Galeazzi D, Neri G, Boscherini B. Lucci-Cordisco E, et al. Among authors: scommegna s. Am J Med Genet A. 2012 Nov;158A(11):2750-5. doi: 10.1002/ajmg.a.35579. Epub 2012 Sep 17. Am J Med Genet A. 2012. PMID: 22987613

5

A novel heterozygous SOX2 mutation causing anophthalmia/microphthalmia with genital anomalies.

Pedace L, Castori M, Binni F, Pingi A, Grammatico B, Scommegna S, Majore S, Grammatico P. Pedace L, et al. Among authors: scommegna s. Eur J Med Genet. 2009 Jul-Aug;52(4):273-6. doi: 10.1016/j.ejmg.2009.02.007. Epub 2009 Feb 28. Eur J Med Genet. 2009. PMID: 19254784

6

Molecular characterization of 6 unrelated Italian patients with 5alpha-reductase type 2 deficiency.

Baldinotti F, Majore S, Fogli A, Marrocco G, Ghirri P, Vuerich M, Tumini S, Boscherini B, Vetri M, Scommegna S, Rinaldi R, Simi P, Grammatico P. Baldinotti F, et al. Among authors: scommegna s. J Androl. 2008 Jan-Feb;29(1):20-8. doi: 10.2164/jandrol.107.002592. Epub 2007 Jul 3. J Androl. 2008. PMID: 17609295 Free article.

7

Neonatal identification of pituitary aplasia: a life-saving diagnosis. Review of five cases.

Scommegna S, Galeazzi D, Picone S, Farinelli E, Agostino R, Bozzao A, Boscherini B, Cianfarani S. Scommegna S, et al. Horm Res. 2004;62(1):10-6. doi: 10.1159/000077661. Epub 2004 Apr 1. Horm Res. 2004. PMID: 15073433

8

Endocrine and neuropsychological assessment in a child with a novel mutation of thyroid hormone receptor: response to 12-month triiodothyroacetic acid (TRIAC) therapy.

Torre P, Bertoli M, Di Giovanni S, Scommegna S, Conte C, Novelli G, Cianfarani S. Torre P, et al. Among authors: scommegna s. J Endocrinol Invest. 2005 Jul-Aug;28(7):657-62. doi: 10.1007/BF03347267. J Endocrinol Invest. 2005. PMID: 16218051

9

Alloimmune neonatal neutropenia treated with rHuG-CSF.

Ruggiero A, Pesaresi A, Scommegna S, Giordano P, Mastrangelo S, Riccardi R. Ruggiero A, et al. Among authors: scommegna s. Pediatr Med Chir. 1999 Jan-Feb;21(1):27-8. Pediatr Med Chir. 1999. PMID: 10451893

10

Growth in disorders of adrenal hyperfunction.

Savage MO, Scommegna S, Carroll PV, Ho JT, Monson JP, Besser GM, Grossman AB. Savage MO, et al. Among authors: scommegna s. Horm Res. 2002;58 Suppl 1:39-43. doi: 10.1159/000064767. Horm Res. 2002. PMID: 12373013 Review.

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

17 results

Search Page

Filters