British Journal of Ophthalmology · 1968 · 19 citations · 13 references
MedicineOphthalmologyOcular DiseaseOcular PathologyOphthalmic PathologyCongenital Eye AnomaliesEye DiseasePupillary AbnormalitiesPupillary DisordersAutosomal Recessive InheritanceCase Investigation ReportsMethionine MetabolismOphthalmic ManifestationsSkeletal AbnormalitiesSkeletal Changes
HOMOCYSTINURIA is an inborn error of metabolism due to deficiency of the enzyme cystathionine synthetase. This results in an increased excretion of homocystine in the urine and raised homocystine and methionine levels in the blood and cerebrospinal fluid.
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Glen W. Davidson, Danell Crase · Death Studies · 1989 · 2.9K citations
R. Neil Schimke · JAMA · 1965 · 250 citations
Diagnosis and Therapy of the Glaucomas.
Bernard Becker · Archives of Ophthalmology · 1962 · 238 citations · Full text
N. A. J. Carson, C. E. Dent, C. M. B. Field et al. · The Journal of Pediatrics · 1965 · 194 citations
HOMOCYSTINURIA, THROMBOSIS, AND THE BLOOD-PLATELETS
Lawson McDonald, Colin Bray, C. M. B. Field et al. · The Lancet · 1964 · 137 citations