Giampaolo Garani
Overview
Explore the profile of Giampaolo Garani including associated specialties, affiliations and a list of published articles.
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Articles
15
Citations
208
Followers
0
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Recent Articles
1.
Tarocco A, Morciano G, Perrone M, Cafolla C, Ferre C, Vacca T, et al.
Sci Rep
. 2022 May;
12(1):7795.
PMID: 35551488
Brain injury at birth is an important cause of neurological and behavioral disorders. Hypoxic-ischemic encephalopathy (HIE) is a critical cerebral event occurring acutely or chronically at birth with high mortality...
2.
Menin D, Ballardini E, Panebianco R, Garani G, Borgna-Pignatti C, Oster H, et al.
PLoS One
. 2022 May;
17(5):e0268083.
PMID: 35522682
Yawning is a long neglected behavioral pattern, but it has recently gained an increasing interdisciplinary attention for its theoretical implications as well as for its potential use as a clinical...
3.
Vento G, Ventura M, Pastorino R, van Kaam A, Carnielli V, Cools F, et al.
Lancet Respir Med
. 2020 Jul;
9(2):159-166.
PMID: 32687801
Background: The importance of lung recruitment before surfactant administration has been shown in animal studies. Well designed trials in preterm infants are absent. We aimed to examine whether the application...
4.
Tarocco A, Caroccia N, Morciano G, Wieckowski M, Ancora G, Garani G, et al.
Cell Death Dis
. 2019 Apr;
10(4):317.
PMID: 30962427
Melatonin, more commonly known as the sleep hormone, is mainly secreted by the pineal gland in dark conditions and regulates the circadian rhythm of the organism. Its intrinsic properties, including...
5.
Parmeggiani G, Bigoni S, Buldrini B, Garani G, Clauser L, Galie M, et al.
Mol Syndromol
. 2018 Feb;
9(1):30-37.
PMID: 29456481
Reported here is the case of a 1.8-year-old boy with a 9.6- Mb deletion in 6q13q14.1 and an 11.2-Mb deletion in 6q21q22.31, ascertained through array CGH, as the result of...
6.
Bruel A, Bigoni S, Kennedy J, Whiteford M, Buxton C, Parmeggiani G, et al.
J Med Genet
. 2017 Oct;
54(12):830-835.
PMID: 29074562
Background: Bohring-Opitz syndrome (BOS) is a rare genetic disorder characterised by a recognisable craniofacial appearance and a typical 'BOS' posture. BOS is caused by sporadic mutations of. However, several typical...
7.
Ballardini E, Tarocco A, Rosignoli C, Baldan A, Borgna-Pignatti C, Garani G
Pediatr Neurol
. 2017 Apr;
71:14-17.
PMID: 28449983
Background: Full-term neonates may have asymptomatic cranial injuries at birth and head ultrasound screening could be useful for early diagnosis. The aim of this study was to assess the prevalence...
8.
Vento G, Pastorino R, Boni L, Cota F, Carnielli V, Cools F, et al.
Trials
. 2016 Aug;
17:414.
PMID: 27538798
Background: Although beneficial in clinical practice, the INtubate-SURfactant-Extubate (IN-SUR-E) method is not successful in all preterm neonates with respiratory distress syndrome, with a reported failure rate ranging from 19 to...
9.
Tarocco A, Ballardini E, Contiero M, Garani G, Fanaro S
Case Rep Pediatr
. 2015 Nov;
2015:592053.
PMID: 26558128
[This corrects the article DOI: 10.1155/2015/591783.].
10.
Tarocco A, Ballardini E, Contiero M, Garani G, Fanaro S
Case Rep Pediatr
. 2015 May;
2015:591783.
PMID: 26000190
Multiple mutations of surfactant genes causing surfactant dysfunction have been described. Surfactant protein C (SP-C) deficiency is associated with variable clinical manifestations ranging from neonatal respiratory distress syndrome to lethal...