Andrea Diociaiuti
Overview
Explore the profile of Andrea Diociaiuti including associated specialties, affiliations and a list of published articles.
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Articles
102
Citations
504
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Recent Articles
1.
Diociaiuti A, Grimaldi M, Pisaneschi E, Dentici M, Cesario C, Paolantonio G, et al.
J Dermatol
. 2025 Mar;
PMID: 40070285
No abstract available.
2.
El Hachem M, Diociaiuti A, Galeotti A, Grussu F, Gusson E, Ferretti A, et al.
Orphanet J Rare Dis
. 2025 Jan;
20(1):28.
PMID: 39819452
Background: Sturge-Weber Syndrome (SWS) is a rare, sporadic neurocutaneous disorder affecting the skin, brain, and eyes, due to somatic activating mutations in GNAQ or, less commonly, GNA11 gene. It is...
3.
Vallese S, Tancredi C, Giovannoni I, Diociaiuti A, Stracuzzi A, Rossi S, et al.
Genes Chromosomes Cancer
. 2024 Dec;
63(2):e23224.
PMID: 39660974
Fibroblastic/myofibroblastic tumors encompass a wide spectrum of lesions. Among them, plexiform myofibroblastoma (PM) represents a rare and distinctive entity recently described as mostly occurring in children and with a favorable...
4.
Zangari P, Giancotta C, Pacillo L, Colantoni N, Leone F, Amodio D, et al.
Pediatr Allergy Immunol
. 2024 Aug;
35(8):e14215.
PMID: 39105363
No abstract available.
5.
El Hachem M, Diociaiuti A, Zambruno G, Samela T, Ferretti F, Carnevale C, et al.
Ital J Pediatr
. 2024 Apr;
50(1):76.
PMID: 38637879
Background: Inherited epidermolysis bullosa (EB) is a clinically and genetically heterogeneous group of skin fragility disorders characterized by blister formation following minor trauma. Four major types are distinguished based on...
6.
Diociaiuti A, Corbeddu M, Rossi S, Pisaneschi E, Cesario C, Condorelli A, et al.
Dermatology
. 2024 Apr;
240(3):397-413.
PMID: 38588653
Background: Autosomal recessive congenital ichthyoses (ARCIs) are a clinically heterogeneous group of keratinization disorders characterized by generalized skin scaling due to mutations in at least 12 genes. The aim of...
7.
Condorelli A, Nobili R, Muglia A, Scarpelli G, Marzuolo E, De Stefanis C, et al.
J Invest Dermatol
. 2024 Jan;
144(7):1522-1533.e10.
PMID: 38237731
Recessive dystrophic epidermolysis bullosa (RDEB) is a rare skin fragility disorder caused by mutations in COL7A1. RDEB is hallmarked by trauma-induced unremitting blistering, chronic wounds with inflammation, and progressive fibrosis,...
8.
Baffa M, Filippeschi C, Tronconi G, Diociaiuti A, El Hachem M, Oranges T
Int J Dermatol
. 2023 Nov;
63(1):e19-e20.
PMID: 37950367
No abstract available.
9.
Dompmartin A, Baselga E, Boon L, Diociaiuti A, Dvorakova V, El Hachem M, et al.
J Vasc Anom (Phila)
. 2023 Jun;
4(2):e064.
PMID: 37332880
Methods: VASCERN-VASCA (https://vascern.eu/) is a European network of multidisciplinary centers for Vascular Anomalies. The Nominal Group Technique was used to establish the pathways. Two facilitators were identified: one to propose...
10.
Cammarata-Scalisi F, Diociaiuti A, Tadich A, Sandoval X, Oranges T, Filippeschi C, et al.
Ital J Dermatol Venerol
. 2023 Jun;
158(4):316-320.
PMID: 37282850
Rubinstein-Taybi Syndrome is a rare congenital multisystem syndrome inherited in an autosomal dominant pattern caused by mutations in CREBBP and EP300 genes in approximately 60% and 10% respectively. These genes...