Francoise Meire

Francoise Meire

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Francoise Meire

Francoise Meire

Publications by authors named "Francoise Meire"

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36Publications

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Uncommon Leber "plus" disease associated with mitochondrial mutation m.11778G>A in a premature child.

J Child Neurol 2014 Aug 17;29(8):NP18-23. Epub 2013 Jul 17.

Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium.

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http://dx.doi.org/10.1177/0883073813492895DOI Listing
August 2014

Congenital fixed dilated pupils due to ACTA2- multisystemic smooth muscle dysfunction syndrome.

J Neuroophthalmol 2014 Jun;34(2):137-43

Department of Pediatric Ophthalmology (FMJR, FMM), HUDERF, ULB, Brussels, Belgium; Departments of Neuropediatrics (FF) and Ophthalmology (PD, JDZ), Ghent University, Belgium; Department of Neuropediatrics (PVB), Erasme, ULB, Brussels, Belgium; Department of Neuroradiology (GR), Foch Hospital, Paris, France; Department of Ophthalmology (FD), Erasme, ULB, Brussels, Belgium; Department of Medical Genetics (PJC), Ghent University, Ghent, Belgium; and Vista Alpina (FMJR), Sierre, Switzerland.

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http://dx.doi.org/10.1097/WNO.0000000000000090DOI Listing
June 2014

SLC24A5 mutations are associated with non-syndromic oculocutaneous albinism.

J Invest Dermatol 2014 Feb 28;134(2):568-571. Epub 2013 Aug 28.

Maladies Rares: Génétique et Métabolisme (MRGM), University Bordeaux, Bordeaux, France; Service de Génétique Médicale, CHU de Bordeaux, Bordeaux, France. Electronic address:

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http://dx.doi.org/10.1038/jid.2013.360DOI Listing
February 2014

Development of independent locomotion in children with a severe visual impairment.

Res Dev Disabil 2011 Nov-Dec;32(6):2069-74. Epub 2011 Sep 15.

University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium.

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http://dx.doi.org/10.1016/j.ridd.2011.08.017DOI Listing
February 2012

Low vision affects dynamic stability of gait.

Gait Posture 2010 Oct;32(4):547-51

Research group of Functional Morphology, Department of Biology, University of Antwerp, Belgium.

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https://linkinghub.elsevier.com/retrieve/pii/S09666362100022
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http://dx.doi.org/10.1016/j.gaitpost.2010.07.018DOI Listing
October 2010

A new locus for congenital cataract, microcornea, microphthalmia, and atypical iris coloboma maps to chromosome 2.

Ophthalmology 2009 Jan 12;116(1):154-162.e1. Epub 2008 Nov 12.

Jules-Gonin Eye Hospital, University of Lausanne, Switzerland.

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http://dx.doi.org/10.1016/j.ophtha.2008.08.044DOI Listing
January 2009

Corneal opacities in the Hallermann-Streiff syndrome.

Ophthalmic Genet 2008 Jun;29(2):61-6

Hopital Universitaire des Enfants Reine Fabiola, U.L.B., Ophthalmology Department, Brussels, Belgium.

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http://dx.doi.org/10.1080/13816810802027101DOI Listing
June 2008

A de novo SOX10 mutation causing severe type 4 Waardenburg syndrome without Hirschsprung disease.

Am J Med Genet A 2008 Apr;146A(8):1038-41

Hôpital Universitaire des Enfants Reine Fabiola, ULB, Pediatric Clinical Genetics, Brussels, Belgium.

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http://dx.doi.org/10.1002/ajmg.a.32247DOI Listing
April 2008

Orbital myositis in a child with linear scleroderma en coup de sabre.

J Pediatr Ophthalmol Strabismus 2007 Sep-Oct;44(5):264-6

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November 2007

The key role of electrophysiology in the diagnosis of visually impaired children.

Acta Ophthalmol Scand 2006 Dec;84(6):799-806

Bartiméus Institute for the Visually Impaired, Zeist, The Netherlands.

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http://dx.doi.org/10.1111/j.1600-0420.2006.00717.xDOI Listing
December 2006

Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.

Invest Ophthalmol Vis Sci 2005 Nov;46(11):4328-35

Division of Medical Molecular Genetics and Gene Diagnostics, Institute of Medical Genetics, University of Zurich, Schwerzenbach, Switzerland.

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http://dx.doi.org/10.1167/iovs.05-0526DOI Listing
November 2005

A novel mutation in the ELOVL4 gene causes autosomal dominant Stargardt-like macular dystrophy.

Invest Ophthalmol Vis Sci 2004 Dec;45(12):4263-7

Department of Human Genetics, Radboud University Nijmegen Medical Centre, Geert Grooteplein 10, PO Box 9101, 6500 HB Nijmegen, The Netherlands.

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http://dx.doi.org/10.1167/iovs.04-0078DOI Listing
December 2004

Dominant optic atrophy, sensorineural hearing loss, ptosis, and ophthalmoplegia: a syndrome caused by a missense mutation in OPA1.

Am J Ophthalmol 2004 Nov;138(5):749-55

Department of Ophthalmology and Visual Sciences, University of Utah Health Sciences Center, Salt Lake City, Utah, USA.

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http://dx.doi.org/10.1016/j.ajo.2004.06.011DOI Listing
November 2004