Colour vision, ophthalmological and linkage studies in a pedigree with a tritan defect.
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Adolescent↗
Biomedical subjects
L N Went
Publications and source records attributed to L N Went.
Comparative colour vision and other ophthalmological studies in three families with dominant inherited juvenile optic atrophy.
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Adolescent↗
Photodynamic damage of the erythrocyte membrane caused by protoporphyrin in protoporphyria and in normal red blood cells.
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Amino Acids↗
The colour vision characteristics of an observer with unilateral defective colour vision: results and analysis.
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Adaptation, Ocular↗
-Carotene as a treatment for photohypersensitivity due to erythropoietic protoporphyria.
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Administration, Oral↗
Metabolic aspects of the photodynamic effect of protoporphyrin in protoporphyria and in normal red blood cells.
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Acetylcholinesterase↗
Unilateral colour vision disturbance. A family study.
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Adult↗
Neurological studies in families with Leber's optic atrophy.
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Adult↗
Hemoglobin O arab in four negro families and its interaction with hemoglobin S and hemoglobin C.
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Acetates↗
[Hereditary compression neuropathy. A classification problem in hereditary neurologic diseases].
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Adult↗
Protoporphyrin-induced photohemolysis in protoporphyria and in normal red blood cells.
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Adult↗
Some clinical and fundamental aspects of erythropoietic protoporphyria.
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Adolescent↗
X-linked ichthyosis: linkage relationship with the Xg blood groups and other studies in a large Dutch kindred.
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Adolescent↗
Studies on African Pygmies. I. A pilot investigation of Babinga Pygmies in the Central African Republic (with an analysis of genetic distances).
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ABO Blood-Group System↗
Haemoglobin Leiden: deletion of beta-6 or 7 glutamic acid.
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Adult↗
Juvenile amyotrophic lateral sclerosis-dementia complex in a Dutch family.
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Adolescent↗
Haemoglobin J Baltimor (alpha 2 beta 2 16 gly--asp) and Haemoglobin D Punjab (alpha 2 beta 2 121 glu--gln) in two Dutch families.
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Adolescent↗
[Thalassemia in the Netherlands].
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Humans↗