d'Adamo AP - Search Results

1

Genetic bases of C7 deficiency: systematic review and report of a novel deletion determining functional hemizygosity.

Balduit A, Bianco AM, Mangogna A, Zicari AM, Leonardi L, Cinicola BL, Capponi M, Tommasini A, Agostinis C, d'Adamo AP, Bulla R. Balduit A, et al. Among authors: d adamo ap. Front Immunol. 2023 May 25;14:1192690. doi: 10.3389/fimmu.2023.1192690. eCollection 2023. Front Immunol. 2023. PMID: 37304269 Free PMC article.

2

A rare loss-of-function genetic mutation suggest a role of dermcidin deficiency in hidradenitis suppurativa pathogenesis.

Tricarico PM, Gratton R, Dos Santos-Silva CA, de Moura RR, Ura B, Sommella E, Campiglia P, Del Vecchio C, Moltrasio C, Berti I, D'Adamo AP, Elsherbini AMA, Staudenmaier L, Chersi K, Boniotto M, Krismer B, Schittek B, Crovella S. Tricarico PM, et al. Among authors: d adamo ap. Front Immunol. 2022 Dec 5;13:1060547. doi: 10.3389/fimmu.2022.1060547. eCollection 2022. Front Immunol. 2022. PMID: 36544771 Free PMC article.

3

A loss-of-function NCSTN mutation associated with familial Dowling Degos disease and hidradenitis suppurativa.

de Oliveira ASLE, de Siqueira RC, Nait-Meddour C, Tricarico PM, Moura R, Agrelli A, d'Adamo AP, Jamain S, Crovella S, de Fátima Medeiros Brito M, Boniotto M, Brandão LAC. de Oliveira ASLE, et al. Among authors: d adamo ap. Exp Dermatol. 2023 Nov;32(11):1935-1945. doi: 10.1111/exd.14919. Epub 2023 Sep 4. Exp Dermatol. 2023. PMID: 37665193

4

Unraveling the Epigenetic Tapestry: Decoding the Impact of Epigenetic Modifications in Hidradenitis Suppurativa Pathogenesis.

Nardacchione EM, Tricarico PM, Moura R, d'Adamo AP, Thasneem A, Suleman M, Marzano AV, Crovella S, Moltrasio C. Nardacchione EM, et al. Among authors: d adamo ap. Genes (Basel). 2023 Dec 26;15(1):38. doi: 10.3390/genes15010038. Genes (Basel). 2023. PMID: 38254928 Free PMC article. Review.

5

Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele.

Magri C, Marchina E, Sansone E, D'Adamo AP, Cappellani S, Bonfanti C, Terlenghi L, Biasiotto G, Zanella I, Sala E, Caruso A, Lombardo M, Gasparini P, De Palma G, Gennarelli M. Magri C, et al. Among authors: d adamo ap. HLA. 2023 Dec;102(6):707-719. doi: 10.1111/tan.15157. Epub 2023 Jul 19. HLA. 2023. PMID: 37469131

6

Circular RNAs Could Encode Unique Proteins and Affect Cancer Pathways.

Crudele F, Bianchi N, Terrazzan A, Ancona P, Frassoldati A, Gasparini P, D'Adamo AP, Papaioannou D, Garzon R, Wójcicka A, Gaj P, Jażdżewski K, Palatini J, Volinia S. Crudele F, et al. Among authors: d adamo ap. Biology (Basel). 2023 Mar 24;12(4):493. doi: 10.3390/biology12040493. Biology (Basel). 2023. PMID: 37106694 Free PMC article.

7

Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders.

Di Stazio M, Zanus C, Faletra F, Pesaresi A, Ziccardi I, Morgan A, Girotto G, Costa P, Carrozzi M, d'Adamo AP, Musante L. Di Stazio M, et al. Among authors: d adamo ap. Genes (Basel). 2023 Jan 18;14(2):250. doi: 10.3390/genes14020250. Genes (Basel). 2023. PMID: 36833176 Free PMC article.

8

What Is the Exact Contribution of PITX1 and TBX4 Genes in Clubfoot Development? An Italian Study.

Bianco AM, Ragusa G, Di Carlo V, Faletra F, Di Stazio M, Racano C, Trisolino G, Cappellani S, De Pellegrin M, d'Addetta I, Carluccio G, Monforte S, Andreacchio A, Dibello D, d'Adamo AP. Bianco AM, et al. Among authors: d adamo ap. Genes (Basel). 2022 Oct 27;13(11):1958. doi: 10.3390/genes13111958. Genes (Basel). 2022. PMID: 36360195 Free PMC article.

9

Incidence of Congenital Clubfoot: Preliminary Data from Italian CeDAP Registry.

Dibello D, Torelli L, Di Carlo V, d'Adamo AP, Faletra F, Mangogna A, Colin G. Dibello D, et al. Among authors: d adamo ap. Int J Environ Res Public Health. 2022 Apr 29;19(9):5406. doi: 10.3390/ijerph19095406. Int J Environ Res Public Health. 2022. PMID: 35564801 Free PMC article.

10

Things come in threes: A new complex allele and a novel deletion within the CFTR gene complicate an accurate diagnosis of cystic fibrosis.

Persico I, Feresin A, Faleschini M, Fontana G, Sirchia F, Faletra F, La Bianca M, Suergiu S, Morgutti M, Maschio M, D'Adamo AP, Raraigh KS, Savoia A, Bottega R. Persico I, et al. Among authors: d adamo ap. Mol Genet Genomic Med. 2022 Jun;10(6):e1926. doi: 10.1002/mgg3.1926. Epub 2022 Mar 29. Mol Genet Genomic Med. 2022. PMID: 35348309 Free PMC article.

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

52 results

Search Page