Optical coherence tomography in Malattia Leventinese;Tomographie à cohérence optique dans la Malattia Leventinese

Klinische Monatsblatter fur Augenheilkunde

Volumn 222, Issue 3, 2005, Pages 180-185

  Gaillard, M C ^a   Wolfensberger, T J ^a   Uffer, S ^a   Mantel, I ^a   Pournaras, J A ^a   Schorderet, D F ^a,b   Munier, Francis L ^a,b,c  

^a UNIVERSITY OF LAUSANNE   (Switzerland)

^b Institut de Recherche en Ophtalmologie   (Switzerland)

^c HÔPITAL OPHTALMIQUE JULES GONIN   (Switzerland)

Author keywords

Drusen; EFEMP1; Fibulin 3; Malattia Leventinese; Optical coherence tomography

Indexed keywords

ADULT; AUTOSOMAL DOMINANT INHERITANCE; BRUCH MEMBRANE; CHOROID CAPILLARY LAYER; CLINICAL ARTICLE; CLINICAL FEATURE; CONFERENCE PAPER; DRUSEN; GENE MUTATION; GENETIC ANALYSIS; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; IMAGING SYSTEM; MALATTIA LEVENTINESE; OPHTHALMOSCOPY; OPTICAL COHERENCE TOMOGRAPHY; PIGMENT EPITHELIUM; RETINA ANGIOGRAPHY; RETINA MACULA DEGENERATION; TECHNIQUE; THICKNESS; ADOLESCENT; ANGIOGRAPHY; ARTICLE; CASE REPORT; CHROMOSOME ABERRATION; COMPARATIVE STUDY; CONGENITAL CORNEA DYSTROPHY; DISEASE COURSE; DOMINANT GENE; FEMALE; GENETICS; MIDDLE AGED; NUCLEOTIDE SEQUENCE; OPTIC DISK; OPTIC DISK ANOMALY; PATHOLOGY; RETINA BLOOD VESSEL; RETINA MACULA LUTEA; SENSITIVITY AND SPECIFICITY; VASCULARIZATION;

EFEMP1 PROTEIN, HUMAN; SCLEROPROTEIN;

ADOLESCENT; ADULT; ANGIOGRAPHY; CHROMOSOME ABERRATIONS; CORNEAL DYSTROPHIES, HEREDITARY; DISEASE PROGRESSION; DNA MUTATIONAL ANALYSIS; EXTRACELLULAR MATRIX PROTEINS; FEMALE; GENES, DOMINANT; HUMANS; MACULA LUTEA; MIDDLE AGED; OPHTHALMOSCOPY; OPTIC DISK; OPTIC DISK DRUSEN; PIGMENT EPITHELIUM OF EYE; RETINAL VESSELS; SENSITIVITY AND SPECIFICITY; TOMOGRAPHY, OPTICAL COHERENCE;

EID: 17244375545     PISSN: 00232165     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-857972     Document Type: Conference Paper

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