Carlo Gandolfo
Overview
Explore the profile of Carlo Gandolfo including associated specialties, affiliations and a list of published articles.
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Articles
97
Citations
927
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Recent Articles
1.
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...
2.
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...
3.
Guarnera A, Valente P, Pasquini L, Moltoni G, Randisi F, Carducci C, et al.
J Ophthalmol
. 2024 Feb;
2024:5993083.
PMID: 38322500
Congenital malformations of the eye represent a wide and heterogeneous spectrum of abnormalities that may be part of a complex syndrome or be isolated. Ocular malformation severity depends on the...
4.
Antonelli M, Lucignani M, Parrillo C, Grassi F, Talamanca L, Rossi Espagnet M, et al.
Digit Health
. 2023 Nov;
9:20552076231214066.
PMID: 38025111
Objective: The goal of this work is to show how to implement a mixed reality application (app) for neurosurgery planning based on neuroimaging data, highlighting the strengths and weaknesses of...
5.
Landolfo F, Giliberti P, De Rose D, Pugnaloni F, Santisi A, Columbo C, et al.
Ital J Pediatr
. 2023 Oct;
49(1):141.
PMID: 37840126
Background: The hemodynamic status of newborns with intracranial arteriovenous shunts (AVSs) may be extremely complex. Mini-invasive hemodynamic monitoring through innovative techniques such as Near-Infrared Spectroscopy (NIRS) and Pressure Recording Analytical...
6.
Del Zotto E, Grassi M, Zedde M, Zini A, Bersano A, Gandolfo C, et al.
J Neurol
. 2023 Jul;
270(11):5622-5628.
PMID: 37436563
No abstract available.
7.
Lucignani G, Vattermoli L, Rossi-Espagnet M, Guarnera A, Napolitano A, Figa-Talamanca L, et al.
Children (Basel)
. 2023 Jun;
10(6).
PMID: 37371303
Molybdenum cofactor deficiency (MoCD) is a rare and severe autosomal recessive in-born error of metabolism caused by the mutation in MOCS1, MOCS2, MOCS3 or GEPH genes, with an incidence ranging...
8.
Del Zotto E, Grassi M, Zedde M, Zini A, Bersano A, Gandolfo C, et al.
Ann Neurol
. 2023 Jun;
94(3):585-595.
PMID: 37272282
Objective: Epidemiological data to characterize the individual risk profile of patients with spontaneous cervical artery dissection (sCeAD) are rather inconsistent. Methods And Results: In the setting of the Italian Project...
9.
Campi F, De Rose D, Pugnaloni F, Ronci S, Cali M, Pro S, et al.
Front Pediatr
. 2023 Apr;
11:1111527.
PMID: 37063679
Background: Despite the latest advances in prenatal diagnosis and postnatal embolization procedures, intracranial arteriovenous shunts (AVSs) are still associated with high mortality and morbidity rates. Our aim was to evaluate...
10.
Guarnera A, Lucignani G, Parrillo C, Rossi-Espagnet M, Carducci C, Moltoni G, et al.
Children (Basel)
. 2023 Mar;
10(3).
PMID: 36980004
Background: Hypoxic-ischemic encephalopathy (HIE) is a severe pathology, and no unique predictive biomarker has been identified. Our aims are to identify associations of perinatal and outcome parameters with morphological anomalies...