Publications by authors named "Julie Perrier"

9Publications

Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations.

Orphanet J Rare Dis 2015 Oct 15;10:135. Epub 2015 Oct 15.

CHU Nantes, Service de Génétique Médicale, Unité de Génétique Moléculaire, 9 quai Moncousu, 44093, Nantes CEDEX 1, France.

View Article

Download full-text PDF

Source
http://link.springer.com/content/pdf/10.1186%2Fs13023-015-03
Web Search
http://www.ojrd.com/content/10/1/135
Publisher Site
http://dx.doi.org/10.1186/s13023-015-0352-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608180PMC
October 2015

Clinical and electrophysiological features in a French family presenting with seipinopathy.

Neuromuscul Disord 2015 Feb 22;25(2):161-4. Epub 2014 Oct 22.

Centre de Référence Maladies Neuromusculaires Nantes - Angers, CHU de Nantes, Nantes, France; Atlantic Gene Therapy, Biotherapy Institute for Rare Diseases, Nantes, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nmd.2014.10.006DOI Listing
February 2015

Type I interferon potentiates T-cell receptor mediated induction of IL-10-producing CD4⁺ T cells.

Eur J Immunol 2013 Oct 15;43(10):2730-40. Epub 2013 Jul 15.

Department of Immunology, Unit of Cytokine Signaling, Institut Pasteur, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/eji.201242977DOI Listing
October 2013

Ring 14 chromosome presenting as early-onset isolated partial epilepsy.

Dev Med Child Neurol 2009 Nov 31;51(11):917-22. Epub 2009 Mar 31.

Department of Pediatric Neurology, Hôpital Femme Mère Enfant, Lyon, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1469-8749.2009.03292.xDOI Listing
November 2009