L.N. Went

Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia.

Daniëlle de Vries, L.N. Went, G.W. Bruyn et al. · PubMed · 1996 · 192 citations

Life Sciences, Genetics, Molecular Genetics +16

Familial cerebral amyloid angiopathy presenting as recurrent cerebral haemorrhage

A.R. Wattendorff, G. Th. A. M. Bots, L.N. Went et al. · Journal of the Neurological Sciences · 1982 · 162 citations

Life Sciences, Neurology, Neuroscience +9

Ethical issues policy statement on Huntington's disease molecular genetics predictive test. International Huntington Association. World Federation of Neurology.

L.N. Went · Journal of Medical Genetics · 1990 · 145 citations · Full text

Life Sciences, Molecular Genetics, Neurology +10

Genetic aspects of erythropoietic protoporphyria

L.N. Went, E.C. Klasen · Annals of Human Genetics · 1984 · 135 citations

Life Sciences, Genetics, Molecular Genetics +9

Tumour spectrum in the FAMMM syndrome

Henry T. Lynch, Ramon M. Fusaro, Judith Pester et al. · British Journal of Cancer · 1981 · 120 citations

Veterinary Medicine, Oncology, Molecular Pathology +4