Saverio Scianguetta
Overview
Explore the profile of Saverio Scianguetta including associated specialties, affiliations and a list of published articles.
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Articles
20
Citations
311
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0
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Recent Articles
1.
Casale M, Scianguetta S, Palma T, Pinfildi L, Vallefuoco G, Capellupo M, et al.
Eur J Pediatr
. 2025 Jan;
184(2):157.
PMID: 39875760
Conclusions: A screening program for SCD performed by the primary care paediatricians is feasible and relatively easy to organize. SCD affects mainly children with African family background and the scarce...
2.
Casale M, Di Girolamo M, Di Maio N, Tomeo R, Iengo M, Scianguetta S, et al.
Ann Hematol
. 2023 Sep;
103(2):623-629.
PMID: 37758964
Transfer of vaccine antibodies (Ab) from donors to recipients after transfusion of packed red blood cells (RBC) is supposed, thus affecting the recipients' response to vaccinations. In this prospective study,...
3.
Mandrile G, Barella S, Giambona A, Gigante A, Grosso M, Perrotta S, et al.
J Clin Med
. 2022 Sep;
11(18).
PMID: 36143073
Methods: The management committee of SITE selected and gathered a multidisciplinary team in order to formulate recommendations based on the available scientific evidence integrated with the opinions of experts, with...
4.
Casale M, Di Maio N, Verde V, Scianguetta S, Di Girolamo M, Tomeo R, et al.
Vaccines (Basel)
. 2021 Jun;
9(6).
PMID: 34072263
Measles, mumps and rubella (MMR) still determine significant morbidity and mortality, although a highly effective vaccine is available. Postponing the MMR vaccination until 6 months after the last red blood...
5.
Casale M, Roberti D, Mandato C, Iorio R, Caropreso M, Scianguetta S, et al.
Sci Rep
. 2020 Jun;
10(1):9683.
PMID: 32546701
Most reports of post-transplant erythrocytosis have involved kidney recipients and, so far, there have been no large studies of onset of erythrocytosis after orthotopic liver transplantation (OLT) in children. We...
6.
Perrotta S, Roberti D, Bencivenga D, Corsetto P, OBrien K, Caiazza M, et al.
N Engl J Med
. 2020 Feb;
382(9):835-844.
PMID: 32101665
Mutations in , which encodes von Hippel-Lindau tumor suppressor (VHL), are associated with divergent diseases. We describe a patient with marked erythrocytosis and prominent mitochondrial alterations associated with a severe...
7.
Casale M, Cozzolino F, Scianguetta S, Pucci P, Monaco V, Sanchez G, et al.
Clin Biochem
. 2019 Sep;
74:80-85.
PMID: 31493379
Hb variants are structurally abnormal haemoglobins which can originate a wide range of phenotypes from clinically silent conditions to very severe disorders. In many cases, diagnosis is very difficult due...
8.
Patti G, Scianguetta S, Roberti D, Di Mascio A, Balsamo A, Brugnara M, et al.
Eur J Endocrinol
. 2019 Jun;
181(3):233-244.
PMID: 31238300
Background: Autosomal dominant neurohypophyseal diabetes insipidus (adNDI) is caused by arginine vasopressin (AVP) deficiency resulting from mutations in the AVP-NPII gene encoding the AVP preprohormone. Aim: To describe the clinical...
9.
Casale M, Filosa A, Ragozzino A, Amendola G, Roberti D, Tartaglione I, et al.
Am J Hematol
. 2018 Nov;
94(3):312-318.
PMID: 30489651
The management of iron overload in thalassemia has changed dramatically since the implementation of magnetic resonance imaging, which allows detection of preclinical iron overload and prevention of clinical complications. This...
10.
Casale M, Picariello S, Corvino F, Cerasari G, Scianguetta S, Rossi F, et al.
Hemoglobin
. 2018 Sep;
42(3):213-216.
PMID: 30251901
A 20-year-old male affected by transfusion-dependent β-thalassemia (β-thal), was prescribed intensive chelation therapy with deferoxamine (DFO) and deferiprone (DFP) because of severe hepatic and cardiac iron overload and β-blocker and...