Results 241 to 250 of about 268,117 (300)

MP Simulations Without Computing MP Statistics

Proceedings, 2010
In recent years, multiple-point simulation has become an invaluable tool to integrate geological concepts in subsurface models. However, due to the high CPU and RAM demand, its use is restricted to relatively small problems with limited structural complexity. Moreover, it only allows for the simulation of univariate fields.
G. Mariethoz, P. Renard, J. Straubhaar, J. Caers   +3 more
openaire   +1 more source

Molecular characterization of MPS IIIA, MPS IIIB and MPS IIIC in Tunisian patients

Clinica Chimica Acta, 2018
__1. Letter to the editor__ In November 2011 a paper was published in the Clinica Chimica Acta by Ouesleti et al. entitled ‘Molecular characterization of MPS IIIA, MPS IIIB and MPS IIIC in Tunisian patients’. The researchers describe variants found in seven patients with a severe phenotype of Sanfilippo disease.
Deden, AC, van Slegtenhorst, Marjon, Ruijter, George, Schoonderwoerd, Kees, Huidekoper, Hidde, Oussoren, Esmeralda, Brooks, Alice, Demirdas, Serwet   +7 more
openaire   +2 more sources

Molecular characterization of MPS IIIA, MPS IIIB and MPS IIIC in Tunisian patients

Clinica Chimica Acta, 2011
Sanfilippo syndrome (mucopolysaccharidosis type III, MPS III) is a progressive disorder in which patients are characterized by severe central nervous system degeneration together with mild somatic disease. MPS III results from a deficiency in one of the four enzymes involved in the heparan sulfate degradation, with sulfamidase (SGSH), α-N ...
S, Ouesleti, V, Brunel, H, Ben Turkia, H, Dranguet, A, Miled, N, Miladi, M F, Ben Dridi, A, Lavoinne, P, Saugier-Veber, S, Bekri   +9 more
openaire   +2 more sources

Glycosaminoglycan levels for newborn screening in MPS I, MPS II and MPS III

Tijdschrift voor Kindergeneeskunde, 2013
INTRODUCTION Mucopolysaccharidoses (MPSs) are a group of lysosomal storage disorders characterized by glycosaminoglycan accumulation and severe and progressive skeletal, cardiac and/or neurological disease. To date, disease modifying therapy is available for three of the MPSs and is being developed for the other types.
Jessica de Ruijter, Minke H. de Ru, Tom Wagemans, Lodewijk IJlst, Frits A. Wijburg, N. van Vlies   +5 more
openaire   +1 more source

Index-MP and MP-index matrices

Journal of Mathematical Analysis and Applications
zbMATH Open Web Interface contents unavailable due to conflicting licenses.
Mosić, Dijana, Stanimirović, Predrag S., Kyrchei, Ivan I.   +2 more
openaire   +2 more sources

Chimie - MP/MP*-PT/PT*

2022
Bruno Fosset, Jean-Bernard Baudin, Frédéric Lahitète   +2 more
openaire   +1 more source

Physique - MP/MP*-MPI/MPI* 

2022
Bernard Salamito, Marie-Noëlle Sanz, Marc Tuloup   +2 more
openaire   +1 more source

Investigation on the adsorption and desorption behaviors of antibiotics by degradable MPs with or without UV ageing process

Journal of Hazardous Materials, 2021
Xiulei Fan, Yefeng Zou, Nan Geng
exaly  

Suspended fine particulate matter (PM2.5), microplastics (MPs), and polycyclic aromatic hydrocarbons (PAHs) in air: Their possible relationships and health implications

Environmental Research, 2021
Razegheh Akhbarizadeh, Sina Dobaradaran, Mehdi Amouei Torkmahalleh   +2 more
exaly  

Interactions between polypropylene microplastics (PP-MPs) and humic acid influenced by aging of MPs

Water Research, 2022
Hongwei Luo, Xiangliang Pan
exaly