A Chabas
Overview
Explore the profile of A Chabas including associated specialties, affiliations and a list of published articles.
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Articles
74
Citations
432
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Recent Articles
1.
Aroskay A, Martin E, Bekki S, Montana G, Randazzo L, Cartigny P, et al.
Sci Total Environ
. 2020 Nov;
750:142283.
PMID: 33182218
The deterioration of monument or building stone materials is mostly due to the growth of black crusts that cause blackening and disaggregation of the exposed surface. This study reports on...
2.
Chabas A, Fouqueau A, Attoui M, Alfaro S, Petitmangin A, Bouilloux A, et al.
Environ Sci Pollut Res Int
. 2015 Aug;
22(23):19170-83.
PMID: 26250811
An approach consisting in combining in situ and laboratory experiments is often favoured for investigating the mechanisms involved in the weathering of the materials of the cultural heritage. However, the...
3.
Lombardo T, Chabas A, Verney-Carron A, Cachier H, Triquet S, Darchy S
Environ Sci Pollut Res Int
. 2014 Apr;
21(15):9251-8.
PMID: 24723354
Glass materials are broadly used in the built environment (windows, facades, roofs, museum showcases, and solar panels) due to their optical (transparency) and thermal properties. Their interaction with the multiphase...
4.
Canals I, Elalaoui S, Pineda M, Delgadillo V, Szlago M, Jaouad I, et al.
Clin Genet
. 2010 Sep;
80(4):367-74.
PMID: 20825431
The Sanfilippo syndrome type C [mucopolysaccharidosis IIIC (MPS IIIC)] is caused by mutations in the HGSNAT gene, encoding an enzyme involved in heparan sulphate degradation. We report the first molecular...
5.
Lombardo T, Ionescu A, Chabas A, Lefevre R, Ausset P, Candau Y
Sci Total Environ
. 2009 Nov;
408(4):976-84.
PMID: 19900698
Several exposure campaigns of silica-soda-lime window glass have been performed in 30 European sites and 1 in Canada in order to understand, quantify and model the phenomenon of soiling. In...
6.
Gort L, Santamaria R, Grinberg D, Vilageliu L, Chabas A
Clin Genet
. 2007 Jul;
72(2):109-11.
PMID: 17661814
The term 'pseudodeficiency' is used in lysosomal storage diseases to denote the situation in which individuals show greatly reduced enzyme activity but remain clinically healthy. Pseudodeficiencies have been reported for...
7.
Santamaria R, Blanco M, Chabas A, Grinberg D, Vilageliu L
Clin Genet
. 2007 Feb;
71(3):273-9.
PMID: 17309651
GM1 gangliosidosis is a lysosomal storage disorder caused by the absence or reduction of lysosomal beta-galactosidase activity because of mutations in the GLB1 gene. Three major clinical forms have been...
8.
Chabas A, Duque J, Gort L
J Inherit Metab Dis
. 2006 Dec;
30(1):108.
PMID: 17171432
alpha-N-Acetylgalactosaminidase deficiency is a lysosomal disorder with clinically very different infantile and adult forms. To date, 12 patients from eight families are known. Neuroaxonal dystrophy or moderate psychomotor retardation, without...
9.
Pascual-Pascual S, Rubio P, Albajara L, Gutierrez M, Chabas A, Alvarado F
J Inherit Metab Dis
. 2006 Oct;
29(6):763.
PMID: 17041744
A patient with atypical infantile Pompe disease suffered acute respiratory insufficiency at the age of 8 years which resulted in complete immobilization and dependence on assisted ventilation. Shortly after initiation...
10.
Ionescu A, Lefevre R, Chabas A, Lombardo T, Ausset P, Candau Y, et al.
Sci Total Environ
. 2006 Jun;
369(1-3):246-55.
PMID: 16777189
Samples of silica-soda-lime float glass, a material selected as a pertinent soiling sensor, were exposed for up to 28 months at four urban sites (Athens, Krakow, London and Prague) and...