Sophie Walraedt

Sophie Walraedt

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Sophie Walraedt

Sophie Walraedt

Publications by authors named "Sophie Walraedt"

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Hypotonia and delayed motor development as an early presentation of Lowe syndrome: case report and literature review.

Acta Clin Belg 2019 Dec 3;74(6):460-464. Epub 2018 Dec 3.

Department of Pediatrics, Division of Pediatric Nephrology and Rheumatology, Ghent University Hospital , Ghent , Belgium.

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http://dx.doi.org/10.1080/17843286.2018.1551743DOI Listing
December 2019

Diplopia as presenting sign of Turcot syndrome.

Int Ophthalmol 2017 Feb 3;37(1):275-278. Epub 2016 May 3.

Department of Ophthalmology, Ghent University Hospital & Ghent University, De Pintelaan 185, 9000, Ghent, Belgium.

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http://dx.doi.org/10.1007/s10792-016-0246-zDOI Listing
February 2017

DETAILED CLINICAL PHENOTYPING OF OXALATE MACULOPATHY IN PRIMARY HYPEROXALURIA TYPE 1 AND REVIEW OF THE LITERATURE.

Retina 2016 Nov;36(11):2227-2235

Departments of *Ophthalmology, †Pediatric Nephrology, and ‡Nephrology, Ghent University Hospital, Ghent, Belgium; §Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium; and ¶Division of Ophthalmology and Center for Cellular & Molecular Therapeutics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

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http://dx.doi.org/10.1097/IAE.0000000000001058DOI Listing
November 2016

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