Cesario C - Search Results

1

Clinical and Molecular Spectrum of Sporadic Vascular Malformations: A Single-Center Study.

Diociaiuti A, Rotunno R, Pisaneschi E, Cesario C, Carnevale C, Condorelli AG, Rollo M, Di Cecca S, Quintarelli C, Novelli A, Zambruno G, El Hachem M. Diociaiuti A, et al. Among authors: cesario c. Biomedicines. 2022 Jun 20;10(6):1460. doi: 10.3390/biomedicines10061460. Biomedicines. 2022. PMID: 35740480 Free PMC article.

2

Trichothiodystrophy and Chiari malformation type I in a child: more than a coincidence?

Diociaiuti A, Pisaneschi E, Spacca B, Cesario C, Giancristoforo S, Bassi A, Zambruno G, El Hachem M. Diociaiuti A, et al. Among authors: cesario c. Eur J Dermatol. 2019 Oct 1;29(5):547-549. doi: 10.1684/ejd.2019.3662. Eur J Dermatol. 2019. PMID: 31789278 No abstract available.

3

KBG syndrome: Common and uncommon clinical features based on 31 new patients.

Gnazzo M, Lepri FR, Dentici ML, Capolino R, Pisaneschi E, Agolini E, Rinelli M, Alesi V, Versacci P, Genovese S, Cesario C, Sinibaldi L, Baban A, Bartuli A, Marino B, Cappa M, Dallapiccola B, Novelli A, Digilio MC. Gnazzo M, et al. Among authors: cesario c. Am J Med Genet A. 2020 May;182(5):1073-1083. doi: 10.1002/ajmg.a.61524. Epub 2020 Mar 3. Am J Med Genet A. 2020. PMID: 32124548

4

A novel patient with White-Sutton syndrome refines the mutational and clinical repertoire of the POGZ-related phenotype and suggests further observations.

Pascolini G, Agolini E, Fleischer N, Gulotta E, Cesario C, D'Elia G, Novelli A, Majore S, Grammatico P. Pascolini G, et al. Among authors: cesario c. Am J Med Genet A. 2020 Jul;182(7):1791-1795. doi: 10.1002/ajmg.a.61605. Epub 2020 May 2. Am J Med Genet A. 2020. PMID: 32359026

5

First Case of KRT2 Epidermolytic Nevus and Novel Clinical and Genetic Findings in 26 Italian Patients with Keratinopathic Ichthyoses.

Diociaiuti A, Castiglia D, Corbeddu M, Rotunno R, Rossi S, Pisaneschi E, Cesario C, Condorelli AG, Zambruno G, El Hachem M. Diociaiuti A, et al. Among authors: cesario c. Int J Mol Sci. 2020 Oct 18;21(20):7707. doi: 10.3390/ijms21207707. Int J Mol Sci. 2020. PMID: 33081034 Free PMC article.

6

Immunofluorescence mapping, electron microscopy and genetics in the diagnosis and sub-classification of inherited epidermolysis bullosa: a single-centre retrospective comparative study of 87 cases with long-term follow-up.

Rossi S, Castiglia D, Pisaneschi E, Diociaiuti A, Stracuzzi A, Cesario C, Mariani R, Floriddia G, Zambruno G, Boldrini R, Abeni D, Novelli A, Alaggio R, El Hachem M. Rossi S, et al. Among authors: cesario c. J Eur Acad Dermatol Venereol. 2021 Apr;35(4):1007-1016. doi: 10.1111/jdv.17060. Epub 2021 Feb 5. J Eur Acad Dermatol Venereol. 2021. PMID: 33274474

7

Self-improving dominant dystrophic epidermolysis bullosa: phenotypic variability associated with COL7A1 mutation p.Gly2037Glu.

Diociaiuti A, Guerriero C, Cesario C, Rossi S, Rotunno R, Zambruno G, El Hachem M. Diociaiuti A, et al. Among authors: cesario c. Eur J Dermatol. 2020 Dec 1;30(6):753-754. doi: 10.1684/ejd.2020.3922. Eur J Dermatol. 2020. PMID: 33459266 Free PMC article. No abstract available.

8

Two Italian Patients with ELOVL4-Related Neuro-Ichthyosis: Expanding the Genotypic and Phenotypic Spectrum and Ultrastructural Characterization.

Diociaiuti A, Martinelli D, Nicita F, Cesario C, Pisaneschi E, Macchiaiolo M, Rossi S, Condorelli AG, Zambruno G, El Hachem M. Diociaiuti A, et al. Among authors: cesario c. Genes (Basel). 2021 Feb 26;12(3):343. doi: 10.3390/genes12030343. Genes (Basel). 2021. PMID: 33652762 Free PMC article.

9

Whole Exome Sequencing Is the Minimal Technological Approach in Probands Born to Consanguineous Couples.

Peluso F, Caraffi SG, Zuntini R, Trimarchi G, Ivanovski I, Valeri L, Barbieri V, Marinelli M, Pancaldi A, Melli N, Cesario C, Agolini E, Cellini E, Radio FC, Crisafi A, Napoli M, Guerrini R, Tartaglia M, Novelli A, Gargano G, Zuffardi O, Garavelli L. Peluso F, et al. Among authors: cesario c. Genes (Basel). 2021 Jun 24;12(7):962. doi: 10.3390/genes12070962. Genes (Basel). 2021. PMID: 34202629 Free PMC article.

10

RSPO1-mutated fibroblasts from non-tumoural areas of palmoplantar keratoderma display a cancer-associated phenotype.

Dellambra E, Cordisco S, Proto V, Nicodemi EM, Didona B, Cesario C, Pisaneschi E, Valente C, Teson M, Castiglia D, Guerra L. Dellambra E, et al. Among authors: cesario c. Eur J Dermatol. 2021 Jun 1;31(3):342-350. doi: 10.1684/ejd.2021.4066. Eur J Dermatol. 2021. PMID: 34309520

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