Suchergebnisse - "Sergouniotis, Panagiotis I."

PubPharm (4)

1

Clinical and genetic findings in TRPM1-related congenital stationary night blindness

enthalten in: Acta ophthalmologica | 2022

von Iosifidis, C. | Liu, J. | Gale, T. | +7

2

Genome sequencing identifies a large deletion at 13q32.1 as the cause of microcoria and childhood-onset glaucoma

enthalten in: Acta ophthalmologica | 2017

von Sergouniotis, P. | Ellingford, J. | O'Sullivan, J. | +2

3

Phenotypic findings in C1QTNF5 retinopathy (late-onset retinal degeneration)

enthalten in: Acta ophthalmologica | 2013

von Soumplis, V. | Sergouniotis, P. | Robson, A. | +4

4

A phenotypic study of congenital stationary night blindness (CSNB) associated with mutations in the GRM6 gene

enthalten in: Acta ophthalmologica | 2012

von Sergouniotis, P. | Robson, A. | Li, Z. | +4

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