tallózása szerző szerint "Szabó Viktória"

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Leber congenital amaurosis: first genotyped Hungarian patients and report of 2 novel mutations in the CRB1 and CEP290 genes.

Vámos Rita; Kulm M; Szabó Viktória; Ahman A; Lesch Balázs; Schneider Miklós; Varsányi Balázs; Nagy Zoltán Zsolt; Németh János Tibor; Farkas Ágnes (2016)

PURPOSE: To introduce the first Hungarian patients with genetically defined Leber congenital amaurosis (LCA) and to report 2 novel mutations. METHODS: Seven otherwise healthy patients (4-29 years, 5 male and 2 female) who ...
Pathogenesis and genetic basis for retinopathy of prematurity.

Csak Krisztina; Szabó Viktória; Szabó András; Vannay Ádám (2006)

Retinopathy of prematurity (ROP) is a vasoproliferative disorder affecting preterm infants with low gestational age and birth weight. In general more than 50% of preterm infants weighing less than 1250 g at birth show ...

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