Daniela Concolino
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Explore the profile of Daniela Concolino including associated specialties, affiliations and a list of published articles.
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75
Citations
819
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Recent Articles
1.
Sestito S, Brodosi L, Ferraro S, Carella R, De Giovanni D, Mita D, et al.
Nutr Health
. 2024 Apr;
:2601060241248522.
PMID: 38651794
Maternal phenylketonuria (mPKU) is a pathologic condition occurring in the fetus of a mother with PKU that is caused by prolonged elevated intrauterine blood phenylalanine (Phe) levels, which can lead...
2.
Salvatore S, Carlino M, Sestito S, Concolino D, Agosti M, Pensabene L
Nutrients
. 2024 Feb;
16(3).
PMID: 38337634
Different nutraceuticals are often considered by parents of infants and children with abdominal pain and disorders of the gut-brain interaction. Herb extracts and natural compounds have long been used in...
3.
Crispino A, Musolino A, Buonsenso D, Caloiero M, Concolino D
J Ultrasound
. 2024 Jan;
27(2):303-314.
PMID: 38240960
Aims: Respiratory complications in Cystic Fibrosis (CF) are still the leading cause of death nowadays in these patients. High-Resolution Computed Tomography is the gold standard method for staging lung disease...
4.
Strozzi C, Di Battista C, Graziosi A, DAdamo E, Librandi M, Patacchiola R, et al.
Acta Paediatr
. 2023 Dec;
113(4):700-708.
PMID: 38156367
Aim: To investigate the effects of caffeine loading/maintenance administration on near-infrared spectroscopy cerebral, kidney and splanchnic patterns in preterm infants. Methods: We conducted a multicentre case-control prospective study in 40...
5.
Riillo C, Bonapace G, Moricca M, Sestito S, Salatino A, Concolino D
Mol Genet Metab
. 2023 Sep;
140(3):107700.
PMID: 37774431
Fabry Disease (FD) (OMIM 301500) is a metabolic X-linked inherited lysosomal storage disorder that results from the deficient activity of Alpha-Galactosidase A (Alpha-Gal), a lysosomal hydrolase that cleaves neutral glycosphingolipids...
6.
Pelaia G, Concolino D, Sabatino J
J Clin Med
. 2023 Aug;
12(15).
PMID: 37568486
Despite the long-standing neglect, there is now a mounting interest in the left atrium (LA) physiology.
7.
Di Rocco M, Vici C, Burlina A, Venturelli F, Fiumara A, Fecarotta S, et al.
Orphanet J Rare Dis
. 2023 Jul;
18(1):197.
PMID: 37480063
Background: GD and ASMD are lysosomal storage disorders that enter into differential diagnosis due to the possible overlap in their clinical manifestations. The availability of safe and effective enzymatic therapies...
8.
Bauleo A, Montesanto A, Pace V, Guarasci F, Apa R, Brando R, et al.
Genes (Basel)
. 2023 Jun;
14(6).
PMID: 37372471
Partial duplication of the short arm of chromosome 7 is a rare chromosome rearrangement. The phenotype spectrum associated with this rearrangement is extremely variable even if in the last decade...
9.
Scarpa M, Barbato A, Bisconti A, Burlina A, Concolino D, Deodato F, et al.
Intern Emerg Med
. 2023 Mar;
18(3):831-842.
PMID: 36882619
Acid sphingomyelinase deficiency (ASMD) is an ultra-rare disease, and several gaps of knowledge on various issues remain, particularly at a regional/national level. Expert opinions collected through well-defined consensus methodologies are...
10.
Risoleo M, Siciliano M, Vetri L, Bitetti I, Di Sessa A, Carotenuto M, et al.
Children (Basel)
. 2022 Nov;
9(11).
PMID: 36360407
Background: Phenylketonuria (PKU) is a rare congenital disorder caused by decreased metabolism of phenylalanine determining cerebral impairments. If untreated, PKU might lead to intellectual disability, seizures and behavioral disorders. The...