Valenzise M - Search Results

1

A Rare Case of Precocious Puberty in a Child with a Novel GATA-4 Gene Mutation: Implications for Disorders of Sex Development (DSD) and Review of the Literature.

Aversa T, Luppino G, Corica D, Pepe G, Valenzise M, Coco R, Li Pomi A, Wasniewska M. Aversa T, et al. Among authors: valenzise m. Genes (Basel). 2023 Aug 16;14(8):1631. doi: 10.3390/genes14081631. Genes (Basel). 2023. PMID: 37628683 Free PMC article. Review.

2

TTF-2/FOXE1 gene polymorphisms in Sicilian patients with permanent primary congenital hypothyroidism.

Santarpia L, Valenzise M, Di Pasquale G, Arrigo T, San Martino G, Cicciò MP, Trimarchi F, De Luca F, Benvenga S. Santarpia L, et al. Among authors: valenzise m. J Endocrinol Invest. 2007 Jan;30(1):13-9. doi: 10.1007/BF03347390. J Endocrinol Invest. 2007. PMID: 17318017

3

Altered B cell homeostasis and Toll-like receptor 9-driven response in patients affected by autoimmune polyglandular syndrome Type 1: Altered B cell phenotype and dysregulation of the B cell function in APECED patients.

Perri V, Gianchecchi E, Scarpa R, Valenzise M, Rosado MM, Giorda E, Crinò A, Cappa M, Barollo S, Garelli S, Betterle C, Fierabracci A. Perri V, et al. Among authors: valenzise m. Immunobiology. 2017 Feb;222(2):372-383. doi: 10.1016/j.imbio.2016.09.001. Epub 2016 Sep 9. Immunobiology. 2017. PMID: 27622939

4

Hallerman-Streiff syndrome: patient with decreased GH and insulin-like growth factor-1.

Damiano Salpietro C, Briuglia S, Valeria Merlino M, Piraino B, Valenzise M, Dallapiccola B. Damiano Salpietro C, et al. Among authors: valenzise m. Am J Med Genet A. 2004 Mar 1;125A(2):216-8. doi: 10.1002/ajmg.a.20399. Am J Med Genet A. 2004. PMID: 14981729 No abstract available.

5

Interactions among pro-inflammatory cytokines, IGF system and thyroid function in pre-pubertal obese subjects.

Street ME, Smerieri A, Montanini L, Predieri B, Iughetti L, Valenzise M, De Luca F, Vigone M, Weber G, Maghnie M, Bernasconi S. Street ME, et al. Among authors: valenzise m. J Biol Regul Homeost Agents. 2013 Jan-Mar;27(1):259-66. J Biol Regul Homeost Agents. 2013. PMID: 23489706

6

Hair as a diagnostic tool in dysmorphology.

Silengo M, Valenzise M, Sorasio L, Ferrero GB. Silengo M, et al. Among authors: valenzise m. Clin Genet. 2002 Oct;62(4):270-2. doi: 10.1034/j.1399-0004.2002.620403.x. Clin Genet. 2002. PMID: 12372052

7

Evaluation of the autoimmune regulator (AIRE) gene mutations in a cohort of Italian patients with autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy (APECED) and in their relatives.

Cervato S, Mariniello B, Lazzarotto F, Morlin L, Zanchetta R, Radetti G, De Luca F, Valenzise M, Giordano R, Rizzo D, Giordano C, Betterle C. Cervato S, et al. Among authors: valenzise m. Clin Endocrinol (Oxf). 2009 Mar;70(3):421-8. doi: 10.1111/j.1365-2265.2008.03318.x. Epub 2008 Jun 27. Clin Endocrinol (Oxf). 2009. PMID: 18616706

8

Malformations following methimazole exposure in utero: an open issue.

Ferraris S, Valenzise M, Lerone M, Divizia MT, Rosaia L, Blaid D, Nemelka O, Ferrero GB, Silengo M. Ferraris S, et al. Among authors: valenzise m. Birth Defects Res A Clin Mol Teratol. 2003 Dec;67(12):989-92. doi: 10.1002/bdra.10098. Birth Defects Res A Clin Mol Teratol. 2003. PMID: 14745920

9

Hair changes in congenital disorders of glycosylation (CDG type 1).

Silengo M, Valenzise M, Pagliardini S, Spada M. Silengo M, et al. Among authors: valenzise m. Eur J Pediatr. 2003 Feb;162(2):114-5. doi: 10.1007/s00431-002-1054-1. Eur J Pediatr. 2003. PMID: 12607543 No abstract available.

10

Oral, facial, digital, vertebral anomalies with psychomotor delay: a mild form of OFD type Gabrielli?

Ferrero GB, Valenzise M, Franco B, Defilippi C, Gregato G, Corsello G, Pepe E, Silengo M. Ferrero GB, et al. Among authors: valenzise m. Am J Med Genet. 2002 Dec 1;113(3):291-4. doi: 10.1002/ajmg.10815. Am J Med Genet. 2002. PMID: 12439899

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