Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Beatriz Jurkiewicz Frangipani"'
Autor:
Vaneisse Cristina Lima Monteiro, Renata B. Oliveira, Rita de Cássia de Aquino, Agatha Nogueira Previdelli, Ana Maria Martins, Beatriz Jurkiewicz Frangipani, José Araújo de Oliveira Silva, Vânia D'Almeida, Patrícia Rossetti Dearo
Publikováno v:
Nutrire. 43
Background Mucopolysaccharidosis (MPS) are inborn errors of metabolism (IEM) recognized by deficient enzymes enrolled in glycosaminoglycans catabolism. The resulting accumulation of glycosaminoglycans leads to clinical progressive and generalized man
Autor:
Pinto, A.1 aalex.pinto@nhs.net, Alfadhel, M.2 dralfadhelm@gmail.com, Akroyd, R.3 RhondaA@adhb.govt.nz, Atik Altınok, Y.4 yaseminatik@yahoo.com.tr, Bernabei, S. M.5 silviamaria.bernabei@opbg.net, Bernstein, L.6 Laurie.Bernstein@childrenscolorado.org, Bruni, G.7 giulia.bruni@meyer.it, Caine, G.8 Gillian.Caine@midyorks.nhs.uk, Cameron, E.9 Emma.Cameron@UHBristol.nhs.uk, Carruthers, R.10 rachel.carruthers@vitaflo.co.uk, Cochrane, B.11 Barbara.Cochrane@ggc.scot.nhs.uk, Daly, A.1 a.daly3@nhs.net, de Boer, F.12 f.de.boer@umcg.nl, Delaunay, S.13 Sophie.DELAUNAY@chu-rennes.fr, Dianin, A.14 alice.dianin@aovr.veneto.it, Dixon, M.15 Marjorie.Dixon@gosh.nhs.uk, Drogari, E.16 edrogari@med.uoa.gr, Dubois, S.17 sandrine.dubois@aphp.fr, Evans, S.1 evanss21@me.com, Gribben, J.18 Joanna.Eardley@gstt.nhs.uk
Publikováno v:
Orphanet Journal of Rare Diseases. 1/25/2018, Vol. 13, p1-N.PAG. 6p.