Esposito S - Search Results

1

Juvenile Moyamoya and Craniosynostosis in a Child with Deletion 1p32p31: Expanding the Clinical Spectrum of 1p32p31 Deletion Syndrome and a Review of the Literature.

Prontera P, Rogaia D, Mencarelli A, Ottaviani V, Sallicandro E, Guercini G, Esposito S, Bersano A, Merla G, Stangoni G. Prontera P, et al. Among authors: esposito s. Int J Mol Sci. 2017 Sep 17;18(9):1998. doi: 10.3390/ijms18091998. Int J Mol Sci. 2017. PMID: 28926972 Free PMC article. Review.

2

Update on the Management of Pediatric Acute Osteomyelitis and Septic Arthritis.

Castellazzi L, Mantero M, Esposito S. Castellazzi L, et al. Among authors: esposito s. Int J Mol Sci. 2016 Jun 1;17(6):855. doi: 10.3390/ijms17060855. Int J Mol Sci. 2016. PMID: 27258258 Free PMC article. Review.

3

Infectious Diseases: Pathophysiology, Diagnostics and Prevention.

Esposito S. Esposito S. Int J Mol Sci. 2016 Sep 2;17(9):1464. doi: 10.3390/ijms17091464. Int J Mol Sci. 2016. PMID: 27598145 Free PMC article.

4

Lung Involvement in Children with Hereditary Autoinflammatory Disorders.

Tarantino G, Esposito S, Andreozzi L, Bracci B, D'Errico F, Rigante D. Tarantino G, et al. Among authors: esposito s. Int J Mol Sci. 2016 Dec 15;17(12):2111. doi: 10.3390/ijms17122111. Int J Mol Sci. 2016. PMID: 27983684 Free PMC article. Review.

5

Biomarkers in Pediatric Community-Acquired Pneumonia.

Principi N, Esposito S. Principi N, et al. Among authors: esposito s. Int J Mol Sci. 2017 Feb 19;18(2):447. doi: 10.3390/ijms18020447. Int J Mol Sci. 2017. PMID: 28218726 Free PMC article. Review.

6

Autosomal Dominant PTH Gene Signal Sequence Mutation in a Family With Familial Isolated Hypoparathyroidism.

Cinque L, Sparaneo A, Penta L, Mencarelli A, Rogaia D, Esposito S, Fabrizio FP, Baorda F, Verrotti A, Falorni A, Stangoni G, Hendy GN, Guarnieri V, Prontera P. Cinque L, et al. Among authors: esposito s. J Clin Endocrinol Metab. 2017 Nov 1;102(11):3961-3969. doi: 10.1210/jc.2017-00250. J Clin Endocrinol Metab. 2017. PMID: 28938448

7

Epileptogenic Brain Malformations and Mutations in Tubulin Genes: A Case Report and Review of the Literature.

Mencarelli A, Prontera P, Stangoni G, Mencaroni E, Principi N, Esposito S. Mencarelli A, et al. Among authors: esposito s. Int J Mol Sci. 2017 Oct 29;18(11):2273. doi: 10.3390/ijms18112273. Int J Mol Sci. 2017. PMID: 29109381 Free PMC article. Review.

8

Report of a Novel SHOX Missense Variant in a Boy With Short Stature and His Mother With Leri-Weill Dyschondrosteosis.

Lucchetti L, Prontera P, Mencarelli A, Sallicandro E, Mencarelli A, Cofini M, Leonardi A, Stangoni G, Penta L, Esposito S. Lucchetti L, et al. Among authors: esposito s. Front Endocrinol (Lausanne). 2018 Apr 10;9:163. doi: 10.3389/fendo.2018.00163. eCollection 2018. Front Endocrinol (Lausanne). 2018. PMID: 29692759 Free PMC article.

9

A Child with a c.6923_6928dup (p.Arg2308_Met2309dup) SPTAN1 Mutation Associated with a Severe Early Infantile Epileptic Encephalopathy.

Rapaccini V, Esposito S, Strinati F, Allegretti M, Manfroi E, Miconi F, Pitzianti M, Prontera P, Principi N, Pasini A. Rapaccini V, et al. Among authors: esposito s. Int J Mol Sci. 2018 Jul 6;19(7):1976. doi: 10.3390/ijms19071976. Int J Mol Sci. 2018. PMID: 29986434 Free PMC article.

10

Expanding the Clinical Spectrum of Sotos Syndrome in a Patient with the New "c.[5867T>A]+[=]"; "p.[Leu1956Gln]+[=]" NSD1 Missense Mutation and Complex Skin Hamartoma.

Mencarelli A, Prontera P, Mencarelli A, Rogaia D, Stangoni G, Cecconi M, Esposito S. Mencarelli A, et al. Among authors: esposito s. Int J Mol Sci. 2018 Oct 16;19(10):3189. doi: 10.3390/ijms19103189. Int J Mol Sci. 2018. PMID: 30332768 Free PMC article.

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