Daniela Longo
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Explore the profile of Daniela Longo including associated specialties, affiliations and a list of published articles.
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106
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1067
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Recent Articles
1.
Siri B, Greco B, Martinelli D, Cairoli S, Guarnera A, Longo D, et al.
J Inherit Metab Dis
. 2025 Jan;
48(1):e12843.
PMID: 39776112
Liver transplantation (LTx) is increasingly used in Urea Cycle Defects (UCDs) to prevent recurrent hyperammonemia and related neurological irreversible injury. Among UCDs, argininosuccinate lyase deficiency (ASLD) has a more complex...
2.
Dellepiane F, Moltoni G, Ronci S, Guarnera A, Rossi-Espagnet M, Digilio M, et al.
Biomedicines
. 2025 Jan;
12(12.
PMID: 39767685
The glycosylphosphatidylinositol (GPI) is a glycol-lipid that anchors several proteins to the cell surface. The GPI-anchor pathway is crucial for the correct function of proteins involved in cell function, and...
3.
Guarnera A, Moltoni G, Dellepiane F, Lucignani G, Rossi-Espagnet M, Campi F, et al.
Biomedicines
. 2024 Nov;
12(11).
PMID: 39595056
Bacterial meningoencephalitis in newborns is a severe and life-threatening pathology, which results from meningeal infection and the subsequent involvement of the brain parenchyma. The severity of the acute onset of...
4.
Parente F, Pedale T, Rossi-Espagnet C, Longo D, Napolitano A, Gazzellini S, et al.
Brain Topogr
. 2024 Nov;
38(1):16.
PMID: 39585450
Exclusive breastfeeding (eBF) in infancy appears to offer a developmental advantage for children's brains compared to formula-fed counterparts. Existing research has predominantly focused on global brain measures (i.e., total white/grey...
5.
Sartorelli J, Travaglini L, Colona V, Casali C, Cumbo F, DAmico A, et al.
Cerebellum
. 2024 Sep;
23(6):2408-2413.
PMID: 39312122
Bi-allelic pathogenic variants in GRID2 have been initially associated to an autosomal recessive form of spinocerebellar ataxia, namely SCAR18. Subsequently, few monoallelic cases have been described. Here we present a...
6.
Moltoni G, Lucignani G, Sgro S, Guarnera A, Rossi Espagnet M, Dellepiane F, et al.
Front Pediatr
. 2024 Sep;
12:1415603.
PMID: 39247673
Introduction: MRI examinations in the pediatric population require acquiring motionless images in the safest possible manner. At our institute, we have developed a protocol called "Good Practice" aimed at avoiding...
7.
Isolated Intracranial Hypertensions as Onset of Myelin Oligodendrocyte Glycoprotein Antibody Disease
Papetti L, Moltoni G, Longo D, Monte G, Dellepiane F, Pro S, et al.
J Clin Med
. 2024 Aug;
13(15).
PMID: 39124735
Myelin oligodendrocyte glycoprotein antibody disease (MOGAD) is characterized by multiple phenotypic conditions such as acute disseminated encephalomyelitis, optic neuritis, and myelitis. MOGAD's spectrum is expanding, with potential symptoms of increased...
8.
Valente P, Mancini F, Romanzo A, Milano G, Russo I, Mazza M, et al.
J Pediatr Hematol Oncol
. 2024 Jul;
46(6):e476-e479.
PMID: 38980895
No abstract available.
9.
gene mutations and perinatal intracranial hemorrhage in neonates: case reports and literature review
Bersani I, Ronci S, Savarese I, Piersigilli F, Micalizzi A, Maddaloni C, et al.
Front Pediatr
. 2024 Jul;
12:1417873.
PMID: 38978838
Intracranial hemorrhage may represent a complication of the perinatal period that affects neonatal morbidity and mortality. Very poor data exist about a possible association between mutations of the type IV...
10.
Sartorelli J, Longo D, Travaglini L, Orlando V, DAmico A, Bertini E, et al.
Mov Disord Clin Pract
. 2024 Jun;
11(9):1160-1162.
PMID: 38940375
No abstract available.