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Archives of Neurology|January 1, 1985
Familial hypokalemic periodic paralysis. 50-year follow-up of a large familyO J Buruma, G T Bots, L N WentJournal of the Neurological Sciences|June 1, 1991
Hereditary spastic dystonia: a new mitochondrial encephalopathy? Putaminal necrosis as a diagnostic signG W Bruyn, G J Vielvoye, L N WentThe British Journal of Ophthalmology|April 1, 1982
Primary choroidal and cutaneous melanomas, bilateral choroidal melanomas, and familial occurrence of melanomasJ A Oosterhuis, L N Went, H T LynchJournal of Medical Genetics|March 1, 1975
Haemoglobin Lepore Boston and elliptocytosis in a family of Indonesian-German ancestryL N Went, W W de Jong, S E BosClinica Chimica Acta; International Journal of Clinical Chemistry|September 16, 1975
Characterization of protoporphyrin in red blood cells of patients with erythropoietic protoporphyriaA F De Goeij, J Van Steveninck, L N WentThe British Journal of Ophthalmology|June 1, 1991
Dominant cone dystrophy starting with blue cone involvementM J van Schooneveld, L N Went, J A OosterhuisJournal of Medical Genetics|May 1, 1992
Late onset dominant cone dystrophy with early blue cone involvementL N Went, M J van Schooneveld, J A OosterhuisOphthalmic Paediatrics and Genetics|February 1, 1985
Studies in dominant optic atrophyH C Roggeveen, A P de Winter, L N WentDrugs & Aging|June 30, 2000
Clinical relevance of hyperhomocysteinaemia in atherothrombotic diseaseD A StehouwerAnnals of Human Genetics|January 1, 1976
Ages of death of children with Huntington's chorea and of their affected parentsM Vegter-van der Vlis, W S Volkers, L N WentPageof 87