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Restorative Neurology and Neuroscience|May 10, 2011
Transplantation of human embryonic retina to adult rat retinaR Aramant, M Seiler, B Ehinger, et al.
Experimental Biology|January 1, 1990
Postnatal development of photoreceptor-specific proteins in mice with hereditary retinal degeneration. An immunocytochemical studyR Cantera, M von Schantz, G J Chader, et al.
Molecular Aspects of Medicine|January 1, 1997
Evaluation of the possible role of coenzyme Q10 and vitamin E in juvenile neuronal ceroid-lipofuscinosis (JNCL)T Westermarck, L Aberg, P Santavuori, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 10, 2000
Neuronal ceroid lipofuscinoses in childhoodP Santavuori, L Lauronen, E Kirveskari, et al.
Annals of Neurology|December 10, 1997
Clinical and magnetic resonance imaging findings in Batten disease: analysis of the major mutation (1.02-kb deletion)I Järvelä, T Autti, S Lamminranta, et al.
Acta Pharmacologica Et Toxicologica|August 1, 1983
Antiarrhythmic effects of tocainide and lidocaine in dogsG Aberg, R Ronfeld, L Aberg, et al.
Journal of Veterinary Internal Medicine|April 13, 2005
Acute clinical, hematologic, serologic, and polymerase chain reaction findings in horses experimentally infected with a European strain of Anaplasma phagocytophilumP Franzén, A Aspan, A Egenvall, et al.
Ophthalmic Genetics|November 12, 1998
A Swedish family with a mutation in the peripherin/RDS gene (Arg-172-Trp) associated with a progressive retinal degenerationU Ekström, S Andréasson, V Ponjavic, et al.
Ophthalmic Genetics|May 20, 1998
Phenotypic expression of autosomal dominant retinitis pigmentosa in a Swedish family expressing a Phe-211-Leu variant of peripherin/RDSU Ekström, V Ponjavic, M Abrahamson, et al.
Ophthalmic Genetics|January 5, 2000
Clinical expression of Best's vitelliform macular dystrophy in Swedish families with mutations in the bestrophin geneV Ponjavic, L Eksandh, S Andréasson, et al.
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