Search Results - "Defoort, S"

Lateral elbow tendinopathy: surgery versus extracorporeal shock wave therapy by Defoort, S., De Smet, L., Brys, P., Peers, K., Degreef, I.

“…Lateral elbow pain caused by tendinopathy – tendinosis – or tennis elbow is a highly prevalent problem. Unfortunately, no treatment method can guarantee…”
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Neuro-ophthalmologic emergencies during this COVID-19 pandemic by Defoort, S, Lamirel, C, Touitou, V, Vignal, C

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Longitudinal follow-up of vision in a neuromyelitis optica cohort by Bouyon, M, Collongues, N, Zéphir, H, Ballonzoli, L, Jeanjean, L, Lebrun, C, Chanson, JB, Blanc, F, Fleury, M, Outteryck, O, Defoort, S, Labauge, P, Vermersch, P, Speeg, C, De Seze, J

“…Background: Neuromyelitis optica (NMO) is an inflammatory disease associated with optic neuritis and myelitis. Recently, several studies showed that optical…”
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Principle of the useful field of view and normative data by Marks, C, Bouacha, I, Defoort, S, Basset, D, Moroni, C

“…The useful field of view is a test which takes into account the influence of patient attention during the evaluation of the visual field. This study aims to…”
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Is there a need for ophthalmological surveillance in the case of short-term hydroxychloroquine treatment during this COVID-19 pandemic? by Defoort-Dhellemmes, S

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Categorization of the degree of urgency according to ophthalmology procedures or situations by Arndt, C, Audrun, F, Bodaghi, B, Caujolle, J-P, Cassoux, N, Defoort, S, Delyfer, M-N, Denis, P, Doan, S, Fenolland, J-R, Giraud, J-M, Kodjikian, L, Labetoulle, M, Lasudry, J, Leveziel, N, Rousseau, A, Saadoun, D, Speeg-Schatz, C, Touhami, S, Touitou, V, Vignal, C, Zech, C

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Benign intracranial hypertension: the role of medical treatment by Dhellemmes, P, Defoort, S, Vinchon, M

“…The goal of medical treatment in benign intracranial hypertension (BIH) is to treat intracranial hypertension symptoms as well as to preserve vision. Reducing…”
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Length of optic nerve double inversion recovery hypersignal is associated with retinal axonal loss by Hadhoum, N, Hodel, J, Defoort-Dhellemmes, S, Duhamel, A, Drumez, E, Zéphir, H, Pruvo, JP, Leclerc, X, Vermersch, P, Outteryck, O

“…Objectives: To assess the association between optic nerve double inversion recovery (DIR) hypersignal length and retinal axonal loss in neuroinflammatory…”
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Clinical evaluation of video imaging technology during visual field exams by Charlier, J., Zanlonghi, X., Defoort‐Dhellemmes, S.

“…Purpose Video imaging consists in recording the entire visual field process in synchrony with the video of the patient's head. Several clinical applications…”
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Evaluation of a new technique to evaluate the visual pursuit in infants by MONTEIRO, K, CHARLIER, J, DEFOORT‐DHELLEMMES, S

“…Purpose This study presents a new technique for recording visual pursuit and its evaluation. In infants, visual acuity is usually estimated using behavioral…”
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Comparison of 2 techniques for evaluating static monocular cyclotorsion with central visual field and scanning laser ophthalmoscope by Woillez, J P, Honoré, J, Defoort, S, Hache, J C

“…To compare the angles of cyclotorsion measured by central campimetry and scanning laser ophthalmoscopy. Both methods were applied to each eye of 44 healthy…”
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Optic disc drusen in children: Advantages of various imaging modalities by Naoum, S, Bouacha, I, Drumare, I, Marks, C, Defoort-Delemmes, S

“…In children, optic disc drusen pose a diagnostic problem with papilledema when they are buried. The goal of our study is to retrospectively compare the results…”
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Abnormal respiratory cilia in non-syndromic Leber congenital amaurosis with CEP290 mutations by Papon, J F, Perrault, I, Coste, A, Louis, B, Gérard, X, Hanein, S, Fares-Taie, L, Gerber, S, Defoort-Dhellemmes, S, Vojtek, A M, Kaplan, J, Rozet, J M, Escudier, E

“…Leber congenital amaurosis (LCA) is the earliest and most severe inherited retinal degeneration. Isolated forms of LCA frequently result from mutation of the…”
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Evaluation of magnitude and phase of sweep‐visual evoked potentials by CHARLIER, J, CABON, M, ZANLONGHI, X, DEFOORT‐DHELLEMMES, S

“…Purpose Sweep visual evoked potentials (SVEP) are frequently used for the assessment of visual acuity. Several studies have shown the presence in a significant…”
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Definition of a normative basis for peripapillary nerve fibers thickness in childhood with sd‐oct by FACON, G, DEFOORT‐DHELLEMMES, S, LABALETTE, P, ROULAND, JF

“…Purpose Since its inception, optical coherence tomography (OCT) has radically changed our way to practice ophthalmology. Yet, the analysis of databases of…”
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The contribution of the useful field of view (UFOV procedure) to allow brain-damaged patients to drive again by Moroni, C., Defoort, S., Marks-Delesalle, C.

“…Visual field disorders, frequently observed in brain-damaged patients, are associated with an adverse prognosis in outcome activities as car driving. In…”
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Les urgences neuro-ophtalmologiques pendant l’infection COVID-19 by Defoort, S., Lamirel, C., Touitou, V., Vignal, C.

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Hereditary optic neuropathies: from clinical signs to diagnosis by Meunier, I, Lenaers, G, Hamel, C, Defoort-Dhellemmes, S

“…Inherited optic atrophy must be considered when working up any optic nerve involvement and any systemic disease with signs of optic atrophy, even with a…”
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Sensorineural hearing loss in OPA1‐linked disorders by BONNEAU, D, MILEA, D, LERUEZ, S, DEFOORT‐DHELLEMMES, S, CROCHET, M, LAMBLIN, J, LENAERS, G, PROCACCIO, V, REYNIER, P, BONNEAU‐AMATI, P

“…About 20% of OPA1 mutation carriers have complicated forms of dominant optic atrophy associating extra‐ocular features. Reviewing the files of 327 patients…”
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Cost‐effective molecular inversion probe‐based ABCA4 sequencing reveals deep‐intronic variants in Stargardt disease by Khan, Mubeen, Cornelis, Stéphanie S., Khan, Muhammad Imran, Elmelik, Duaa, Manders, Eline, Bakker, Sem, Derks, Ronny, Neveling, Kornelia, Vorst, Maartje, Gilissen, Christian, Meunier, Isabelle, Defoort, Sabine, Puech, Bernard, Devos, Aurore, Schulz, Heidi L., Stöhr, Heidi, Grassmann, Felix, Weber, Bernhard H. F., Dhaenens, Claire‐Marie, Cremers, Frans P. M.

“…Purpose Stargardt disease (STGD1) is caused by biallelic mutations in ABCA4, but many patients are genetically unsolved due to insensitive mutation‐scanning…”
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