Contact
Dr. Françoise Roulez, MD

Visp

Vista Alpina 

Eye Center

Bahnhofplatz 1a
3930 Visp

Phone 027 946 70 00

Fax 027 946 70 03

Send an e-mail

 

Consultation

Monday - Friday:

8am - 12pm

1pm - 7.30pm

(On Tuesdays, Wednesdays and

Fridays until 6pm)

On Saturdays:

8am - 12pm

Appointments

by phone

Siders

Vista Alpina

Eye Center

Rue du Bourg 3
3960 Sierre

Phone 027 455 34 04

Fax 027 455 34 77

Send an e-mail

 

Consultation

Monday:

8am - 12.00pm

12.30pm - 5pm

Tuesday:

7.30am - 12pm

12.45pm - 5pm

Wednesday:

8am - 12.00pm

12.45pm - 7.45pm

Thursday and Friday:

8am - 12pm

12.45pm - 5.30pm

Saturday: closed

Appointments

by phone

Disclaimer:

Augenzentrum Vista Alpina AG and the services provided by Augenzentrum Vista Alpina are not legally or otherwise affiliated with Vista Klinik AG, Laser Vista AG, Vista Klinik Net AG or Vista Diagnostics AG.

Memberships

 

Walliser Ärzteverband (WÄV) Medical Association

Verbindung der Schweizer Ärztinnen und Ärzte (FMH) [Swiss Medical Association]

Belgian Ophthalmology Association (SBO)

Schweizerische Ophthalmologische Gesellschaft (SOG) [Swiss Ophthalmology Association]

European Paediatric Ophthalmological Society (EPOS)

French Association for Ophthalmologic Genetics (SGOF)

Awards

 

2012

du Meilleur Poster Société Belge d’Ophtalmologie (1er auteur): „Syndromic Congenital Aplasia of Iris sphincter

 

1984

Prix Fleurisse Mercier des Etudes de Médecine Université Libre de Bruxelles

Conference presentations

 

About thirty assignments at congresses or scientific conferences

Training and background

Since 2020
Specialist in pediatric ophthalmology at Vista Alpina


Since 2017
Specialist in pediatric ophthalmology, strabismus and neuro-ophthalmology at University Hospital Basel

2009 – 2017

Ophthalmologist at the Augenzentrum Vista Alpina

 

2009 – 2011

Patent examination in «European Board of Ophthalmology Examination»

 

2001 – 2009

Lecturer for paediatrics at the «Francisco Ferrer» Nursing School in Brussels

 

1999 – 2009

Lecturer for paediatrics at the «Ilya Prigogyne» Nursing School in Brussels

 

2005 – 2009

Senior physician and head of the Ophthalmology Department at the «Reine Fabiola« Children’s Hospital (ULB) Children’s Hospital in Brussels

 

2000 – 2005

Assistant senior physician at the «Reine Fabiola» (ULB) Children’s Hospital in Brussels

 

1992 – 2000

Consultant at the «Reine Fabiola» (ULB) Children’s University Hospital in Brussels and at the «Erasme» (ULB) hospital in Brussels

 

1992

Admission in ophthalmology

 

1989

FMGEMS (Foreign Medical Graduate Examination in Medical Sciences) aux U.S.A.

 

1988 – 1992

Specialised in ophthalmology at the «St Pierre» hospital in Brussels (ULB)

 

1981 – 1988

Medical studies at the Free University of Brussels, Belgium (with highest honours)

Publications

 

Primary author:

2014

Roulez F.M., Faes F., Delbeke P., Van Bogaert P., Rodesch G., De Zaetijd J., Depasse F., Coucke PJ., Meire F.: The ophthalmologist’s crucial role for children with congenital fixed dilated pupils: diagnosis of ACTA2- Multisystemic Smooth Muscle Dysfunction Syndrome. Journal of Neuroophthalmology 2014 jun 34(2): 137-43.

 

2008

Roulez F.M., Schuil J., Meire F.: Corneal opacities in the Hallermann-Streiff syndrome. Ophtalmic Genetics  jun 2008 vol.29, n°2, 61-66.

 

2007

Roulez F.M., Dangoisse C., Dufour D, Meire F.: Orbital Myositis in a child with linear scleroderma en coup de sabre. Journal of Pediatric Ophthalmology and Strabismus sep/oct 2007, vol 44 n°5, 264-6

 

2007

Roulez F.M.: Retinal pigment epithelium-desferal. Toxicité médicamenteuse dans la sphere ophtalmologique: mise à jour revue et corrigée.  Bull.Soc.Belge Ophtalmol  2007; 304: 59-66

 

Co-author:

2011

Meire F., Delpierre I., Brachet C., Roulez F., Van Nechel C., Depasse F., Christophe C., Menten B., De Baere E.: Nonsyndromic bilateral and unilateral optic nerve aplasia: first familial occurrence and potential implication of CYP26A1 and CYP26C1 genes. Mol Vis, 2011; 17: 2072-9

  

2011

D’Haene B, Meire F, Claerhout I, Kroes HY, Plomp A, Arens YH, de Ravel T, Casteels I, De Jaegere S, Hooghe S, Wuyts W, van den Ende J, Roulez F, Veenstra-Knol HE, Oldenburg RA, Giltay J, Verheij JB, de Faber JT, Menten B, De Paepe A, Kestelyn P, Leroy BP, De Baere E. : Molecular analysis in a large cohort of patients with anterior segment malformations: expanding the spectrum of FOXC1 et PITX2 mutations and copy number changes. Invest Ophtalmol Vis Sci 2011 Jan 21;52(1): 324-33.

 

2010

Désir J., Sznajer Y., Depasse F., Roulez F., Schrooyen M., Meire F., Abramowicz M. : LTBP2 null mutations in an autosomal recessive ocular syndrome with megalocornea, spherophakia, and secondary glaucoma. Eur J Hum Genet. 2010 Jul; 18(7): 761-7

  

Posters:

2012

Congrès Ophtalmologica Belgica Nov 2012 Bruxelles (Société Belge d’ Ophtalmologie SBO/BOG): «Syndromic congenital aplasia of iris sphincter» Roulez F., Faes F., Delbeke P., Van Bogaert P., Rodesch G., De Zaetijd J., Depasse F., Coucke P., Meire F

 

2012

Swiss Society of Ophthalmology (SSO-SOG), Annual Meeting  Aug 2012, Fribourg:  «Mydriase bilatérale aréflectique et CCHS avec mutation PHOX2B » Roulez F.M., Wimmersberger A., Meire F

 

2012

Congrès EPOS juin 2012 (European Pediatric Ophtalmology Society) Uppsala- Sweden: «ERM and CHRREP in very young children with NF2» Roulez F., Postolache L., Ziereisen F., Claes K., MeireF.

 

2010

Congrès EPOS oct 2010 (European Pediatric Ophtalmology Society) Bad Nauheim, Allemagne: “ Retinal neovascularisation, blepharokeratoconjunctivitis and progressive entropion in a young girl with Autosomal Dominant severe Dyskeratosis Congenita due to TINF2 gene mutation” F.M. Roulez, Y. Sznajer,  T.Vulliamy,  I.Dokal,  B.Kadz,  F.M. Meire

 

2008

Congrès  EPOS  oct 2008 (European Pediatric Ophtalmology Society) Leuven, Belgique: «LTBP2 mutation in AR microspherophakia with lens luxation and megalocornea». Roulez F., Désir J., Laes J.,  Snajer Y., Abramocicz M., Meire F

 

2007

Poster et présentation au congrès Ophtalmologia Belgica Nov 2007 (Société Belge d’Ophtalmologie SBO/BOG): «Corneal Dystrophy in the Hallerman- Streiff syndrome». Roulez F., Schuil J., Meire F.

 

2006

Congrès Ophtalmologica Belgica  Nov 2006 (Société Belge d’Ophtalmologie SBO/BOG).«A child with unexplained  intermittent ptosis». Roulez F., Lasudry J., Dufour D., Meire F.

 

2006

Congrès Ophtalmologica Belgica  Nov 2006 (Société Belge d’Ophtalmologie SBO/BOG).

«Orbital inflammatory pseudotumor and Churg Strauss Syndrome».  Roulez F,, Goffin L., Loop M., Badot V., Ferster A., Meire F.

SIWF-ISFM certificate ophthalmo surgery Vista Alpina Eye Center
Hospital certificate Vista Alpina Eye Center

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