Publications by authors named "Monique Cordonnier"

10Publications

Three cases of molecularly confirmed Knobloch syndrome.

Ophthalmic Genet 2020 02 17;41(1):83-87. Epub 2020 Mar 17.

Department of Ophthalmology, University Hospital Erasme, Brussels, Belgium.

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http://dx.doi.org/10.1080/13816810.2020.1737948DOI Listing
February 2020

Sixth cranial nerve neuromyotonia mimicking intermittent Duane syndrome type II: case report.

Acta Neurol Belg 2017 12 18;117(4):941-942. Epub 2017 May 18.

Hôpital Erasme, Ophthalmology Department, Cliniques Universitaires de Bruxelles, Université Libre de Bruxelles, Route de Lennik 808, 1070, Brussels, Belgium.

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http://dx.doi.org/10.1007/s13760-017-0791-xDOI Listing
December 2017

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

Neuro-ophthalmological emergencies: which ocular signs or symptoms for which diseases?

Acta Neurol Belg 2013 Sep 9;113(3):215-24. Epub 2013 Mar 9.

Neuro-ophthalmology unit, Ophthalmology Department, Hôpital Erasme, Cliniques Universitaires de Bruxelles, 808, Route de Lennik, 1070, Brussels, Belgium.

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http://dx.doi.org/10.1007/s13760-013-0188-4DOI Listing
September 2013

TMEM126A mutation in a Moroccan family with autosomal recessive optic atrophy.

Mol Vis 2012 5;18:1849-57. Epub 2012 Jul 5.

Center for Medical Genetics, Hospital Erasme, ULB, 808 route de Lennik, Brussels, Belgium.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3398502PMC
November 2012

Optic neuropathy, renal failure and pulmonary sarcoidosis in a 50-year-old man: where is the link?

BMJ Case Rep 2009 20;2009. Epub 2009 Sep 20.

Erasme Hospital, Internal Medicine, Route de Lennik 808, Brussels, 1070, Belgium.

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http://dx.doi.org/10.1136/bcr.05.2009.1879DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3027998PMC
November 2011

Screening for refractive errors in children.

Compr Ophthalmol Update 2006 Mar-Apr;7(2):63-75

Université Libre de Bruxelles, Ophthalmology Department, Brussels, Belgium.

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August 2006

Congenital stationary night blindness: report of an autosomal recessive family and linkage analysis.

Am J Med Genet A 2005 Jan;132A(1):76-9

Service de Génétique Médicale, Hôpital Erasme and Laboratoire de Génétique Médicale-ULB, Brussels, Belgium.

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http://dx.doi.org/10.1002/ajmg.a.30372DOI Listing
January 2005

An unusual cause of visual loss: involvement of bilateral lateral geniculate bodies.

AJNR Am J Neuroradiol 2004 Oct;25(9):1544-8

Department of Ophthalmology, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium.

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October 2004