{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,10]],"date-time":"2026-09-10T09:25:09Z","timestamp":1789032309622,"version":"build-2803163510"},"reference-count":14,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[2010,1,1]],"date-time":"2010-01-01T00:00:00Z","timestamp":1262304000000},"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":[[2010,1]]},"DOI":"10.1016\/j.arcped.2009.10.006","type":"journal-article","created":{"date-parts":[[2009,11,14]],"date-time":"2009-11-14T10:11:19Z","timestamp":1258193479000},"page":"38-41","source":"Crossref","is-referenced-by-count":6,"title":["Le syndrome de Pearson\u00a0: \u00e0 propos de 2\u00a0observations \u00e0 r\u00e9v\u00e9lation n\u00e9onatale"],"prefix":"10.1016","volume":"17","author":[{"given":"H.","family":"Collin-Ducasse","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A.-M.","family":"Maillotte","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"F.","family":"Monpoux","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"P.","family":"Boutt\u00e9","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"C.","family":"Ferrero-Vacher","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"V.","family":"Paquis","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.arcped.2009.10.006_bib1","doi-asserted-by":"crossref","first-page":"976","DOI":"10.1016\/S0022-3476(79)80286-3","article-title":"A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction","volume":"95","author":"Pearson","year":"1979","journal-title":"J Pediatr"},{"key":"10.1016\/j.arcped.2009.10.006_bib2","doi-asserted-by":"crossref","first-page":"469","DOI":"10.1111\/j.1365-2141.1995.tb05178.x","article-title":"Pearson's marrow\/pancreas syndrome: haematological features associated with deletion and duplication of mitochondrial DNA","volume":"90","author":"Smith","year":"1995","journal-title":"Br J Haematol"},{"key":"10.1016\/j.arcped.2009.10.006_bib3","doi-asserted-by":"crossref","first-page":"915","DOI":"10.1016\/0929-693X(96)87585-3","article-title":"Cytopathies mitochondriales: r\u00f4le des g\u00e8nes nucl\u00e9aires","volume":"3","author":"Paquis","year":"1999","journal-title":"Arch Pediatr"},{"key":"10.1016\/j.arcped.2009.10.006_bib4","doi-asserted-by":"crossref","first-page":"311","DOI":"10.1007\/s00431-008-0756-4","article-title":"Early neurological impairment and severe anemia in a newborn with Pearson syndrome","volume":"168","author":"Morel","year":"2009","journal-title":"Eur J Pediatr"},{"key":"10.1016\/j.arcped.2009.10.006_bib5","doi-asserted-by":"crossref","first-page":"3","DOI":"10.1023\/A:1005305422544","article-title":"Severe lactic acidosis and neonatal death in Pearson syndrome","volume":"20","author":"Muraki","year":"1997","journal-title":"J Inherit Metab Dis"},{"key":"10.1016\/j.arcped.2009.10.006_bib6","first-page":"1952","article-title":"Pearson's syndrome: a rare cause of non-immune hydrops fetalis","volume":"116","author":"Li","year":"2003","journal-title":"Chin Med J"},{"key":"10.1016\/j.arcped.2009.10.006_bib7","first-page":"572","article-title":"Two new cases with Pearson syndrome and review of Hacettepe experience","volume":"50","author":"Topalo\u011flu","year":"2008","journal-title":"Turk J Pediatr"},{"key":"10.1016\/j.arcped.2009.10.006_bib8","doi-asserted-by":"crossref","first-page":"601","DOI":"10.1172\/JCI114881","article-title":"Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy","volume":"86","author":"R\u00f6tig","year":"1990","journal-title":"J Clin Invest"},{"key":"10.1016\/j.arcped.2009.10.006_bib9","doi-asserted-by":"crossref","first-page":"44","DOI":"10.1007\/BF02072515","article-title":"Pearson bone marrow-pancreas syndrome with insulin-dependent diabetes, progressive renal tubulopathy, organic aciduria and elevated fetal haemoglobin caused by deletion and duplication of mitochondrial DNA","volume":"152","author":"Superti-Furga","year":"1993","journal-title":"Eur J Pediatr"},{"key":"10.1016\/j.arcped.2009.10.006_bib10","doi-asserted-by":"crossref","first-page":"697","DOI":"10.1023\/A:1005378527077","article-title":"The association between haematological manifestation and mtDNA deletions in Pearson syndrome","volume":"20","author":"Muraki","year":"1997","journal-title":"Inherit Metab Dis"},{"key":"10.1016\/j.arcped.2009.10.006_bib11","first-page":"361","article-title":"Fatal acidosis in a neonate with Pearson syndrome","volume":"41","author":"G\u00fcrakan","year":"1999","journal-title":"Turk J Pediatr"},{"key":"10.1016\/j.arcped.2009.10.006_bib12","doi-asserted-by":"crossref","first-page":"208","DOI":"10.1016\/j.ejpn.2006.12.008","article-title":"The neurological evolution of Pearson syndrome: case report and literature review","volume":"11","author":"Lee","year":"2007","journal-title":"Eur J Paediatr Neurol"},{"key":"10.1016\/j.arcped.2009.10.006_bib13","first-page":"39","article-title":"Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA","volume":"48","author":"McShane","year":"1991","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.arcped.2009.10.006_bib14","doi-asserted-by":"crossref","first-page":"47","DOI":"10.1023\/B:BOLI.0000016601.49372.18","article-title":"Pearson syndrome and the role of deletion dimers and duplications in the mtDNA","volume":"27","author":"Jacobs","year":"2004","journal-title":"J Inherit Metab Dis"}],"container-title":["Archives de P\u00e9diatrie"],"original-title":[],"language":"fr","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0929693X09004205?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0929693X09004205?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2021,10,14]],"date-time":"2021-10-14T02:32:54Z","timestamp":1634178774000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0929693X09004205"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2010,1]]},"references-count":14,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2010,1]]}},"alternative-id":["S0929693X09004205"],"URL":"https:\/\/doi.org\/10.1016\/j.arcped.2009.10.006","relation":{},"ISSN":["0929-693X"],"issn-type":[{"value":"0929-693X","type":"print"}],"subject":[],"published":{"date-parts":[[2010,1]]}}}