Helene Ogier

Helene Ogier

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Helene Ogier

Helene Ogier

Publications by authors named "Helene Ogier"

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Doubling diet fat on sugar ratio in children with mitochondrial OXPHOS disorders: Effects of a randomized trial on resting energy expenditure, diet induced thermogenesis and body composition.

Clin Nutr 2016 12 8;35(6):1414-1422. Epub 2016 Apr 8.

Reference Center for Inherited Metabolic Diseases in Child and Adulthood, Lille University Children's Hospital Jeanne de Flandre, and RADEME EA 7364, Lille University, F-59000 Lille, France. Electronic address:

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http://dx.doi.org/10.1016/j.clnu.2016.03.015DOI Listing
December 2016

A diagnostic flow chart for POLG-related diseases based on signs sensitivity and specificity.

J Neurol Neurosurg Psychiatry 2015 Jun 11;86(6):646-54. Epub 2014 Aug 11.

INSERM U1016, Institut Cochin; CNRS UMR 8104, Paris, France Service de Biochimie Métabolique et Centre de Génétique moléculaire et chromosomique, AP-HP, GHU Pitié-Salpêtrière, Paris, France Université Paris-Descartes-Paris5, Paris, France.

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http://dx.doi.org/10.1136/jnnp-2013-306799DOI Listing
June 2015

New spastic paraplegia phenotype associated to mutation of NFU1.

Orphanet J Rare Dis 2015 Feb 8;10:13. Epub 2015 Feb 8.

Paris Diderot University - Sorbonne Paris Cité; Inserm U1141, DHU PROTECT, Robert Debré Hospital, Paris, France.

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http://dx.doi.org/10.1186/s13023-015-0237-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333890PMC
February 2015

29 French adult patients with PMM2-congenital disorder of glycosylation: outcome of the classical pediatric phenotype and depiction of a late-onset phenotype.

Orphanet J Rare Dis 2014 Dec 11;9:207. Epub 2014 Dec 11.

AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Département de Génétique, Unité Fonctionnelle de Neurogénétique moléculaire et cellulaire et Centre de Référence des Déficiences Intellectuelles de Causes Rares, 47-83 boulevard de l'hôpital, Paris, 75013, France.

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http://dx.doi.org/10.1186/s13023-014-0207-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266234PMC
December 2014

Maternal phenylketonuria: low phenylalaninemia might increase the risk of intra uterine growth retardation.

J Inherit Metab Dis 2012 Nov 5;35(6):993-9. Epub 2012 Jun 5.

Department of Pediatrics, Brest University Hospital, CHRU Morvan, 2 avenue Foch, 29200, Brest, France.

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http://dx.doi.org/10.1007/s10545-012-9491-0DOI Listing
November 2012

Vacuolation of neutrophils and acanthocytosis in child with medium chain acyl-CoA dehydrogenase deficiency.

Br J Haematol 2008 Mar 19;140(6):595. Epub 2008 Jan 19.

Service d'Hématologie Biologie, Hôpital Robert Debré, AP-HP, Paris, France.

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http://doi.wiley.com/10.1111/j.1365-2141.2007.06849.x
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http://dx.doi.org/10.1111/j.1365-2141.2007.06849.xDOI Listing
March 2008

Maternal phenylketonuria: the French survey.

Eur J Pediatr 2004 Sep 6;163(9):540-6. Epub 2004 Jul 6.

Department of Paediatrics, CHU Brabois, Allée du morvan, 54500, Vandoeuvre les Nancy, France,

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http://dx.doi.org/10.1007/s00431-004-1482-1DOI Listing
September 2004