{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,4,5]],"date-time":"2022-04-05T13:15:15Z","timestamp":1649164515317},"reference-count":12,"publisher":"Elsevier BV","issue":"12","license":[{"start":{"date-parts":[[2008,12,1]],"date-time":"2008-12-01T00:00:00Z","timestamp":1228089600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Archives de P\u00e9diatrie"],"published-print":{"date-parts":[[2008,12]]},"DOI":"10.1016\/j.arcped.2008.09.014","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T08:26:22Z","timestamp":1226305582000},"page":"1760-1764","source":"Crossref","is-referenced-by-count":0,"title":["Enzymoth\u00e9rapie substitutive chez un nourrisson atteint de maladie de Pompe\u00a0: \u00e9volution cardiologique"],"prefix":"10.1016","volume":"15","author":[{"given":"R.","family":"Bonnefoy","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"F.","family":"Labarthe","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"F.","family":"Paoli","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J.","family":"Chantreuil","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.-A.","family":"Barthez","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R.","family":"Froissart","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J.","family":"Poinsot","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Chantepie","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.arcped.2008.09.014_bib1","series-title":"The metabolic and molecular bases of inherited disease","first-page":"3389","article-title":"Glycogen storage disease type II: acid \u03b1-glucosidase (acid maltase) deficiency","author":"Hirschhorn","year":"2001"},{"key":"10.1016\/j.arcped.2008.09.014_bib2","doi-asserted-by":"crossref","first-page":"267","DOI":"10.1097\/01.gim.0000218152.87434.f3","article-title":"Pompe disease diagnosis and management guidelines. ACMG practice guidelines","volume":"8","author":"Kishnani","year":"2006","journal-title":"Genet Med"},{"key":"10.1016\/j.arcped.2008.09.014_bib3","doi-asserted-by":"crossref","first-page":"S35","DOI":"10.1016\/j.jpeds.2004.01.053","article-title":"Pompe disease in infants and children","volume":"144","author":"Kishnani","year":"2004","journal-title":"J Pediatr"},{"key":"10.1016\/j.arcped.2008.09.014_bib4","unstructured":"Nicolino M. Th\u00e9rapeutique chez l\u2019enfant atteint de maladie de Pompe, r\u00e9pondeur et non r\u00e9pondeur \u00e0 l\u2019enzymoth\u00e9rapie substitutive. 1ersymposium du Comit\u00e9 d\u2019\u00e9valuation du traitement des maladies lysosomales, Paris 22 novembre 2005, http:\/\/assoc.cetl.free.fr, (Consult\u00e9 juillet 2007)."},{"key":"10.1016\/j.arcped.2008.09.014_bib5","doi-asserted-by":"crossref","first-page":"e448","DOI":"10.1542\/peds.113.5.e448","article-title":"Long-term intravenous treatment of Pompe disease with recombinant human alpha-glucosidase from milk","volume":"113","author":"Van den Hout","year":"2004","journal-title":"Pediatrics"},{"key":"10.1016\/j.arcped.2008.09.014_bib6","doi-asserted-by":"crossref","first-page":"442","DOI":"10.1007\/s10545-006-0239-6","article-title":"Limitations of enzyme replacement therapy: current and future","volume":"29","author":"Wraith","year":"2006","journal-title":"J Inherit Metab Dis"},{"key":"10.1016\/j.arcped.2008.09.014_bib7","first-page":"132","article-title":"Recombinant human acid alpha-glucosidase enzyme therapy for infantile glycogen storage disease type II: result of phase I\/II clinical trial","volume":"3","author":"Amalfitano","year":"2001","journal-title":"Genet Med"},{"key":"10.1016\/j.arcped.2008.09.014_bib8","doi-asserted-by":"crossref","first-page":"297","DOI":"10.1097\/01.gim.0000195896.04069.5f","article-title":"Electrocardiographic response to enzyme replacement therapy for Pompe disease","volume":"8","author":"Ansong","year":"2006","journal-title":"Genet Med"},{"key":"10.1016\/j.arcped.2008.09.014_bib9","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1007\/BF02265613","article-title":"The conduction system in Pompe's disease","volume":"2","author":"Bharati","year":"1982","journal-title":"Pediatr Cardiol"},{"key":"10.1016\/j.arcped.2008.09.014_bib10","doi-asserted-by":"crossref","first-page":"697","DOI":"10.1016\/S0929-693X(01)00968-X","article-title":"Myocardiopathie hypertrophique familiale associ\u00e9e \u00e0 un syndrome de Wolff-Parkinson-White r\u00e9v\u00e9lant une glycog\u00e9nose de type II","volume":"9","author":"Tabarki","year":"2002","journal-title":"Arch Pediatr"},{"key":"10.1016\/j.arcped.2008.09.014_bib11","doi-asserted-by":"crossref","first-page":"313","DOI":"10.1097\/01.gim.0000217786.79173.a8","article-title":"Ambulatory electrocardiogram analysis in infants treated with recombinant human acid \u03b1-glucosidase enzyme replacement therapy for Pompe disease","volume":"8","author":"Cook","year":"2006","journal-title":"Genet Med"},{"key":"10.1016\/j.arcped.2008.09.014_bib12","doi-asserted-by":"crossref","first-page":"99","DOI":"10.1212\/01.wnl.0000251268.41188.04","article-title":"Recombinant human acid \u03b1-glucosidase major clinical benefits in infantile-onset Pompe disease","volume":"68","author":"Kishnani","year":"2007","journal-title":"Neurology"}],"container-title":["Archives de P\u00e9diatrie"],"original-title":[],"language":"fr","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0929693X08004272?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0929693X08004272?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,12,24]],"date-time":"2018-12-24T14:52:40Z","timestamp":1545663160000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0929693X08004272"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2008,12]]},"references-count":12,"journal-issue":{"issue":"12","published-print":{"date-parts":[[2008,12]]}},"alternative-id":["S0929693X08004272"],"URL":"https:\/\/doi.org\/10.1016\/j.arcped.2008.09.014","relation":{},"ISSN":["0929-693X"],"issn-type":[{"value":"0929-693X","type":"print"}],"subject":[],"published":{"date-parts":[[2008,12]]}}}