Nathalie Voide

Publications | Phd and Masters theses

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23 publications

2024 | 2023 | 2021 | 2020 | 2019 | 2018 | 2016 | 2015 | 2013 | 2012 | 2010 |
 
Gefleckte Retina nach Kandori ist mit einer De-novo-Mutation einer heterozygoten Variante im CAMK2A-Gen assoziiert [Fleck Retina of Kandori Associated with a De Novo Mutation of a Heterozygous Variant in the CAMK2A Gene]
Voide N., Macherel M., Ranza E., 2024/04. Klinische Monatsblatter fur Augenheilkunde, 241 (4) pp. 482-484. Peer-reviewed.
 
Épidémie de myopie en pédiatrie : prise en charge, prévention et traitement [Outbreak of myopia in pediatrics : management, prevention and treatment]
Voide N., Kaeser P.F., 2023/12/20. Revue medicale suisse, 19 (855) pp. 2407-2411. Peer-reviewed.
 
Vermutetes okuläres Histoplasmose-Syndrom bei einem 5-jährigen Mädchen in einer nicht endemischen Zone [Presumed Ocular Histoplasmosis Syndrome in a Five-Year-Old Girl in a Non-Endemic Area]
Voide N., 2023/04. Klinische Monatsblatter fur Augenheilkunde, 240 (4) pp. 578-580. Peer-reviewed.
 
Kongenitale Toxoplasmose mit bilateraler Makulachorioretinitis bei einem Frühgeborenen [Congenital Toxoplasmosis with Bilateral Macular Chorioretinitis in a Premature Newborn]
Voide N., Bijon J., Crisinel P.A., Truttmann A.C., Durig J., Rossi D.C., 2021/04. Klinische Monatsblatter fur Augenheilkunde, 238 (4) pp. 431-433. Peer-reviewed.
 
Anomalies de développement de la fonction visuelle : le nourrisson «apparemment aveugle »
voide n, 2020/09/06. dans Rapport SFO de Neuro-ophtalmologie 2020 chap. 26, Elsevier Masson.
 
Atypische Retro-ILM-Blutung bei homozygoter Sichelzellerkrankung [Atypical Retro Internal Limiting Membrane Haemorrhage in Homozygous Sickle Cell Disease]
Voide N., Mantel I., Ambresin A., 2020/04. Klinische Monatsblatter fur Augenheilkunde, 237 (4) pp. 477-479. Peer-reviewed.
Les yeux des enfants
Kaeser P.-F., voide n, 2020/01/01..
 
The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosis.
Dudakova L., Evans C.J., Pontikos N., Hafford-Tear N.J., Malinka F., Skalicka P., Horinek A., Munier F.L., Voide N., Studeny P. et al., 2019/05. Experimental eye research, 182 pp. 160-166. Peer-reviewed.
 
Paralysie du IIIème nerf crânien (nerf oculomoteur),
voide n, Robert M, 2018/08/28. dans Strabologie: Approches diagnostique et thérapeutique, 3e édition 145-154 chap. 18, Elsevier Masson.
 
Spontaneous consecutive esotropia.
Voide N., Robert M.P., 2018/07. Eye, 32 (7) pp. 1197-1200. Peer-reviewed.
 
Vergleichende Studie über die Bedeutung des binokularen Spot-Vision-Screener-Autorefraktometers bei der Früherkennung visueller Störungen bei Kindern [Comparative Study of the Usefulness of the Binocular Spot Vision Screener Autorefractor in the Detection of Childhood Visual Disorders]
Voide N., Hoeckele N., Kaeser P.F., 2018/04. Klinische Monatsblatter fur Augenheilkunde, 235 (4) pp. 416-419. Peer-reviewed.
 
Acetazolamide Reduces Retinal Inner Nuclear Layer Thickness in Microcystic Macular Edema Secondary to Optic Neuropathy.
Borruat F.X., Dysli M., Voide N., Abegg M., 2018. European neurology, 79 (3-4) pp. 150-153. Peer-reviewed.
 
Atypical retro internal limiting membrane hemorrhage in homozygous sickle­ cell disease: a case report.
Ambresin Aude, Voide Nathalie, Mantel Irmela, 2018. dans EPOS.
 
Prise en charge d’un strabisme précoce, N. Voide. Réalités ophtalmologiques. Septembre 2016
voide n, 2016/09/15. dans Réalités ophtalmologiques, Réalités ophtalmologiques.
 
Œil et environnement [Eye and the environment]
Voide N., Kaeser P.F., Behar-Cohen F., 2015/12/16. Revue medicale suisse, 11 (499) pp. 2361-2365. Peer-reviewed.
 
Microcystic Macular Edema in Optic Nerve Atrophy: A Case Series.
Voide N., Borruat F.X., 2015. Klinische Monatsblatter Fur Augenheilkunde, 232 (4) pp. 455-458. Peer-reviewed.
 
Nonsurgical treatment of cyclic esotropia.
Voide N., Presset C., Klainguti G., Kaeser P.F., 2015. Journal of Aapos : the Official Publication of the American Association For Pediatric Ophthalmology and Strabismus / American Association For Pediatric Ophthalmology and Strabismus, 19 (2) pp. 196-198. Peer-reviewed.
Spectrum of digoxin-induced ocular toxicity: a case report and literature review.
Renard D., Rubli E., Voide N., Borruat F.X., Rothuizen L.E., 2015. Bmc Research Notes, 8 (1) p. 368. Peer-reviewed.
 
Strabismus secondary to ocular perforation during amniocentesis
Voide N., Kaeser P.F., Klainguti G., 2015. Klinische Monatsblätter Für Augenheilkunde, 232 (4) pp. 487-488. Peer-reviewed.
 
Isolated Horner Syndrome and Orbital Hemangioma.
Voide N., Borruat F.X., 2013. Klinische Monatsblatter Fur Augenheilkunde, 230 (4) pp. 365-366. Peer-reviewed.
 
Spectrum of ocular digoxin toxicity in the elderly: A case report
Renard D., Rubli E., Voide N., Borruat F.X., Rothuizen L., 2013. pp. e22-e23 dans 11th Congress of the European Association for Clinical Pharmacology and Therapeutics (EACPT), Clinical Therapeutics.
 
Syndrome de Horner isolé et hémangiome orbitaire : un cas exceptionnel de syndrome de Rendu-Osler-Weber
Voide N., Kawasaki A., Borruat F., 2012., Société Suisse d'Ophtalmologie pp. S105 dans Ophta.
 
Alpha-1-antitrypsin deficiency in a 78-year-old woman with isolated liver cirrhosis.
Voide N., Ardigo S., Morris M., Rubbia-Brandt L., Rougemont A.L., Morard I., Vischer U.M., 2010/02. Journal of the American Geriatrics Society, 58 (2) pp. 415-416. Peer-reviewed.
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