Publications by authors named "Gaelle Blanchard"

9Publications

Systematic MRI in NF1 children under six years of age for the diagnosis of optic pathway gliomas. Study and outcome of a French cohort.

Eur J Paediatr Neurol 2016 Mar 17;20(2):275-281. Epub 2015 Dec 17.

Hôpital des Enfants, CHU Purpan, Toulouse, France; Inserm, Imagerie Cérébrale et Handicaps Neurologiques UMR 825, CHU Purpan, Toulouse, France; Université de Toulouse III - Paul Sabatier, Toulouse, France. Electronic address:

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http://dx.doi.org/10.1016/j.ejpn.2015.12.002DOI Listing
March 2016

Clinical presentation of severe viral encephalitis with known causative agents in children: a retrospective study on 16 patients hospitalized in a pediatric intensive care unit (2008-2011).

J Child Neurol 2014 Nov 23;29(11):1508-18. Epub 2014 Jan 23.

Pediatric Emergency and Intensive Care Unit, Hospices Civils de Lyon, Lyon, France University Claude Bernard Lyon 1, France.

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http://journals.sagepub.com/doi/10.1177/0883073813513330
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http://dx.doi.org/10.1177/0883073813513330DOI Listing
November 2014

A proposed diagnostic approach for infantile spasms based on a spectrum of variable aetiology.

Eur J Paediatr Neurol 2014 Mar 18;18(2):176-82. Epub 2013 Nov 18.

Pediatric Neurology Department, Hôpital Femme Mère Enfant, Centre Hospitalier Universitaire de Lyon, 59 Boulevard Pinel, 69500 Bron, France.

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http://dx.doi.org/10.1016/j.ejpn.2013.11.005DOI Listing
March 2014

Pre- and postnatal imaging of early cerebral damage in Sturge-Weber syndrome.

Pediatr Radiol 2013 Nov 23;43(11):1536-9. Epub 2013 Jul 23.

Pediatric and Fetal Imaging, Hôpital Femme Mère Enfant, 59, boulevard Pinel, 69677, Lyon-Bron, France.

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http://dx.doi.org/10.1007/s00247-013-2743-9DOI Listing
November 2013

Hashimoto's encephalopathy: identification and long-term outcome in children.

Eur J Paediatr Neurol 2013 May 4;17(3):280-7. Epub 2012 Dec 4.

Assistance Publique-Hôpitaux de Paris, Hôpitaux Universitaires Paris-Sud, Pediatric Neurology Department, Le Kremlin-Bicêtre, France.

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http://dx.doi.org/10.1016/j.ejpn.2012.11.003DOI Listing
May 2013

Mosaic 18q21.2 deletions including the TCF4 gene: a clinical report.

Am J Med Genet A 2012 Dec 19;158A(12):3174-81. Epub 2012 Nov 19.

Centre de référence des anomalies du développement, Service de Cytogénétique Constitutionnelle, Hospices Civils de Lyon, Bron, France.

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http://dx.doi.org/10.1002/ajmg.a.35588DOI Listing
December 2012

Familial nephrogenic syndrome of inappropriate antidiuresis: dissociation between aquaporin-2 and vasopressin excretion.

J Clin Endocrinol Metab 2010 Sep 14;95(9):E37-43. Epub 2010 Jul 14.

Centre de Réfé rence des Maladies Rénales Rares, Hospices Civils de Lyon, 69317 Lyon, France.

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http://dx.doi.org/10.1210/jc.2009-2524DOI Listing
September 2010