| scholarly article | Q13442814 |
| P2093 | author name string | A. F. Winder | |
| P2860 | cites work | American Journal of Human Genetics | Q4744249 |
| Tear calcium levels and contact lens wear | Q33650366 | ||
| Tear glucose levels in normal people and in diabetic patients | Q33652133 | ||
| Juvenile Batten's disease: an ophthalmological assessment of 26 patients | Q33652147 | ||
| Long-term management of abetalipoproteinaemia. Possible role for vitamin E | Q34989797 | ||
| Detection of heterozygotes for tyrosinase-negative oculocutaneous albinism by hairbulb tyrosinase assay | Q35202044 | ||
| The fatty acid composition of skin and plasma lipids in Refsum's disease | Q39519097 | ||
| Heredopathia atactica polyneuritiformis (refsum's disease) treated by diet and plasma-exchange | Q39535202 | ||
| Tear physiology and dry eyes | Q39709731 | ||
| Human albinism | Q40769255 | ||
| Microheterogeneity of human galactose-1-Phosphate uridylyl transferase. Isoelectrofocusing results | Q44109174 | ||
| A rapid simplified assay for galactokinase activity in whole blood | Q52931655 | ||
| Maternal enzymes of galactose metabolism and the "inexplicable" infantile cataract. | Q53856061 | ||
| A simple spot screening test for galactosemia. | Q54083310 | ||
| Galactokinase and cataracts | Q66698637 | ||
| Albinism | Q67260684 | ||
| Osmolarity of Tear Microvolumes in Keratoconjunctivitis Sicca | Q67324592 | ||
| Modification of the radioactive method for erythrocyte galactokinase assay | Q67403291 | ||
| The origin of some enzymes in tear fluid, determined by comparative investigation with two collection methods | Q67450526 | ||
| Enzymatic micromethod for measuring galactose-1-phosphate uridylyltransferase activity in human erythrocytes | Q67652917 | ||
| Tear sodium, potassium, chloride, and calcium at various flow rates: children with cystic fibrosis and unaffected siblings with and without corneal staining | Q70001012 | ||
| Presenile cataract formation and decreased activity of galactosemic enzymes | Q71131483 | ||
| Macromelanosomes in X-linked ocular albinism | Q71240112 | ||
| Gyrate atrophy of the choroid and retina: improved visual function following reduction of plasma ornithine by diet | Q71416539 | ||
| Plasma vitamin A assay by fluorometry and use of a silicic acid column technique | Q71624939 | ||
| Improved method for measuring galactose-1-phosphate uridyl transferase activity of erythrocytes | Q72864342 | ||
| P433 | issue | 8 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | eye disease | Q3041498 |
| P304 | page(s) | 610-615 | |
| P577 | publication date | 1981-08-01 | |
| P1433 | published in | Journal of the Royal Society of Medicine | Q6296198 |
| P1476 | title | Laboratory screening for metabolic eye disease: a review | |
| Laboratory Screening for Metabolic Eye Disease: A Review | |||
| P478 | volume | 74 |
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