Serotoninergic status in patients with hereditary vascular retinopathy syndrome von Storimans, C W J M, Fekkes, D, van Dalen, A, Bleeker-Wagemakers, E D, Oosterhuis, J A

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Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenon von TERWINDT, G. M, HAAN, J, OPHOFF, R. A, GROENEN, S. M. A, STORIMANS, C. W. J. M, LANSER, J. B. K, ROOS, R. A. C, BLEEKER-WAGEMAKERS, E. M, FRANTS, R. R, FERRARI, M. D

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Familial vascular retinopathy : a preliminary report von STORIMANS, C. W. J. M, OOSTERHUIS, J. A, VAN SCHOONEVELD, M. J, BOS, P. J. M, MAASWINKEL-MOOY, P. D

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C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy von Richards, Anna, van den Maagdenberg, Arn M J M, Jen, Joanna C, Kavanagh, David, Bertram, Paula, Spitzer, Dirk, Liszewski, M Kathryn, Barilla-LaBarca, Maria-Louise, Terwindt, Gisela M, Kasai, Yumi, McLellan, Mike, Grand, Mark Gilbert, Vanmolkot, Kaate R J, de Vries, Boukje, Wan, Jijun, Kane, Michael J, Mamsa, Hafsa, Schäfer, Ruth, Stam, Anine H, Haan, Joost, de Jong, Paulus T V M, Storimans, Caroline W, van Schooneveld, Mary J, Oosterhuis, Jendo A, Gschwendter, Andreas, Dichgans, Martin, Kotschet, Katya E, Hodgkinson, Suzanne, Hardy, Todd A, Delatycki, Martin B, Hajj-Ali, Rula A, Kothari, Parul H, Nelson, Stanley F, Frants, Rune R, Baloh, Robert W, Ferrari, Michel D, Atkinson, John P

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Rieger's eye anomaly and persistent hyperplastic primary vitreous von Storimans, Caroline W. J. M., Van Schooneveld, Mary J.

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