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Glucose-6-phosphatase deficiency.
Orphanet J Rare Dis. 2011 May 20;6:27. doi: 10.1186/1750-1172-6-27.
Orphanet J Rare Dis. 2011.
PMID: 21599942
Free PMC article.
Review.
[Natural history of hepatic glycogen storage diseases].
Labrune P, Eberschweiler PT, Boudjemline AM, Hubert-Buron A, Petit F, Gajdos V.
Labrune P, et al. Among authors: boudjemline am.
Presse Med. 2008 Jul-Aug;37(7-8):1172-7. doi: 10.1016/j.lpm.2007.09.023. Epub 2008 Feb 29.
Presse Med. 2008.
PMID: 18313893
Review.
French.
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Klüver Bucy syndrome following hypoglycaemic coma in a patient with glycogen storage disease type Ib.
Boudjemline AM, Isapof A, Witas JB, Petit FM, Gajdos V, Labrune P.
Boudjemline AM, et al.
J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S477-80. doi: 10.1007/s10545-010-9243-y. Epub 2010 Nov 20.
J Inherit Metab Dis. 2010.
PMID: 21103936
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Successful plasmapheresis for acute and severe unconjugated hyperbilirubinemia in a child with crigler najjar type I syndrome.
Sellier AL, Labrune P, Kwon T, Boudjemline AM, Deschènes G, Gajdos V.
Sellier AL, et al. Among authors: boudjemline am.
JIMD Rep. 2012;2:33-6. doi: 10.1007/8904_2011_40. Epub 2011 Sep 6.
JIMD Rep. 2012.
PMID: 23430851
Free PMC article.
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