Andrea Pietrobattista
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Explore the profile of Andrea Pietrobattista including associated specialties, affiliations and a list of published articles.
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53
Citations
554
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Recent Articles
11.
Panfili F, Pietrobattista A, Vecchio D, Gonfiantini M, Bartuli A, Macchiaiolo M
Front Genet
. 2024 Jan;
14:1255807.
PMID: 38188503
No abstract available.
12.
Paldino G, Faienza M, Cappa M, Pietrobattista A, Capalbo D, Valenzise M, et al.
Front Immunol
. 2023 Jul;
14:1172369.
PMID: 37457714
Introduction: Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) syndrome is a rare monogenic disease determined by biallelic mutations in gene, which encodes a transcription factor essential for central immune tolerance. Classic diagnosis is...
13.
Greco B, Caviglia S, Martinelli D, Grimaldi Capitello T, Liccardo D, De Nictolis F, et al.
J Inherit Metab Dis
. 2023 Jul;
46(5):906-915.
PMID: 37395264
Organic acidurias (OAs), urea-cycle disorders (UCDs), and maple syrup urine disease (MSUD) belong to the category of intoxication-type inborn errors of metabolism (IT-IEM). Liver transplantation (LTx) is increasingly utilized in...
14.
Siano M, Ametrano O, Barbato F, Sammarco E, Ranucci G, Pietrobattista A, et al.
JPGN Rep
. 2023 May;
3(4):e270.
PMID: 37168485
Materials And Methods: Here, we report a case series of 3 patients and a systematic review of the literature. Results: Hypothyroidism (mean serum TSH 52.03 mIU/L) was detected at a...
15.
Di Giorgio A, Matarazzo L, Sonzogni A, Nicastro E, Pietrobattista A, Cananzi M, et al.
Liver Int
. 2023 May;
43(7):1523-1536.
PMID: 37157951
Background And Aims: In paediatrics, porto-sinusoidal vascular disease (PSVD) is relatively unknown and probably underdiagnosed. We aimed to describe clinical phenotypes, histology and outcome of children diagnosed with PSVD. Methods:...
16.
Algeri M, Velardi E, Spada M, Galaverna F, Carta R, Vinti L, et al.
Am J Transplant
. 2023 Apr;
23(9):1446-1450.
PMID: 37061187
Hematopoietic stem cell transplantation (HSCT)-based approaches are increasingly investigated strategies to induce tolerance in recipients of solid allografts. However, in the majority of cases, these approaches rely on the infusion...
17.
Pietrobattista A, Della Volpe L, Francalanci P, Talamanca L, Monti L, Lepri F, et al.
Genes (Basel)
. 2023 Mar;
14(3).
PMID: 36981010
Zhu-Tokita-Takenouchi-Kim (ZTTK) syndrome, an intellectual disability syndrome first described in 2016, is caused by heterozygous loss-of-function variants in . Haploinsufficiency in may affect multiple genes, including those involved in the...
18.
Veraldi S, Pietrobattista A, Soglia G, Monti L, Alterio T, Mosca A, et al.
Front Pediatr
. 2023 Feb;
10:1033570.
PMID: 36741094
Sarcopenia is a clinical condition characterized by a reduction in muscle mass, which typically affects adult patients; however, it has recently been recognized in pediatric literature. Few studies in children...
19.
Colantuono R, Pavanello C, Pietrobattista A, Turri M, Francalanci P, Spada M, et al.
Front Pediatr
. 2022 Aug;
10:969081.
PMID: 35989999
Background: Lipoprotein X (LpX) - mediated extremely severe hyperlipidemia is a possible feature detectable in children with syndromic paucity of intralobular bile ducts (Alagille syndrome) but rarely in other types...
20.
Macchiaiolo M, Panfili F, Vecchio D, Cortellessa F, Gonfiantini M, Buonuomo P, et al.
Am J Med Genet A
. 2022 Jul;
188(10):2920-2931.
PMID: 35869874
POIKiloderma, tendon contractures, myopathy, pulmonary fibrosis is a congenital multisystem disorder due to FAM111B dominant variants. We present a literature review focusing on the frequency and the impact of hepatic...