S DArrigo
Overview
Explore the profile of S DArrigo including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
32
Citations
160
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0
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Recent Articles
1.
Meossi C, Carrer A, Ciaccio C, Estienne M, Silipigni R, Sciacca F, et al.
J Intellect Disabil Res
. 2023 May;
67(7):679-689.
PMID: 37129092
Background: Investigating copy number variations (CNVs) such as microdeletions or microduplications can significantly contribute to discover the aetiology of neurodevelopmental disorders. 15q11.2 genomic region, including NIPA1 and NIPA2 genes, contains...
2.
Jenkinson E, Livingston J, ODriscoll M, Desguerre I, Nabbout R, Boddaert N, et al.
Clin Genet
. 2017 Apr;
93(2):228-234.
PMID: 28386946
Occludin (OCLN) is an important component of the tight junction complex, providing apical intercellular connections between adjacent cells in endothelial and epithelial tissue. In 2010 O'Driscoll et al reported mutations...
3.
Sandroni C, DArrigo S
Minerva Anestesiol
. 2014 Jan;
80(10):1105-14.
PMID: 24398444
Experimental evidence shows that derangements of arterial partial pressures of either oxygen (PaO2) and carbon dioxide (PaCO2) immediately after resuscitation from cardiac arrest may increase the severity of organ dysfunction...
4.
Prodi E, Grisoli M, Panzeri M, Minati L, Fattori F, Erbetta A, et al.
Eur J Neurol
. 2012 Jul;
20(1):138-46.
PMID: 22816526
Background And Purpose: The autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is an early-onset neurodegenerative disorder caused by mutations in the SACS gene. The disease, first described in Canadian families...
5.
Novel POMGNT1 point mutations and intragenic rearrangements associated with muscle-eye-brain disease
Saredi S, Ardissone A, Ruggieri A, Mottarelli E, Farina L, Rinaldi R, et al.
J Neurol Sci
. 2012 May;
318(1-2):45-50.
PMID: 22554691
Congenital muscular dystrophies due to defects in genes encoding proteins involved in α-dystroglycan (α-DG) glycosylation are a heterogeneous group of muscle disorders variably associated with central nervous system and eye...
6.
Chiapparini L, Savoiardo M, DArrigo S, Reale C, Zorzi G, Zibordi F, et al.
Neuropediatrics
. 2011 Aug;
42(4):159-62.
PMID: 21877312
Pantothenate kinase-associated neurodegeneration (PKAN) is a rare disorder associated with brain iron accumulation. The brain MRI abnormality consists of T2 hypointensity in the globus pallidus with a small hyperintensity in...
7.
Gitto E, Pellegrino S, DArrigo S, Barberi I, Reiter R
Eur Respir J
. 2009 Dec;
34(6):1461-9.
PMID: 19948912
The lungs of newborns are especially prone to oxidative damage induced by both reactive oxygen and reactive nitrogen species. Yet, these infants are often 1) exposed to high oxygen concentrations,...
8.
Briggs T, Wolf N, DArrigo S, Ebinger F, Harting I, Dobyns W, et al.
Am J Med Genet A
. 2008 Nov;
146A(24):3173-80.
PMID: 19012351
The combination of intracranial calcification and polymicrogyria is usually seen in the context of intrauterine infection, most frequently due to cytomegalovirus. Rare familial occurrences have been reported. We describe five...
9.
Lanzi G, DArrigo S, Termine C, Rossi M, Ferrari-Ginevra O, Mongelli A, et al.
Psychopathology
. 2006 Oct;
40(1):1-7.
PMID: 17057418
Background: Headache is a disease that has a high social impact in the paediatric as well as in the adult population, often resulting in a significant reduction in the young...
10.
Riva D, Aggio F, Vago C, Nichelli F, Andreucci E, Paruta N, et al.
Cephalalgia
. 2006 May;
26(5):596-603.
PMID: 16674769
Since cognitive and behavioural characteristics of paediatric migraine sufferers have yet to be adequately defined, in this study we assessed the effect of migraine on the interictal functioning of children...