[ON OPTICAL VALUES IN MILD AND SEVERE MYOPIA ON THE BASIS OF ECHOGRAPHIC FINDINGS].
Explore the source record for details and available documents.
Eye↗
Biomedical subjects
A FRANCESCHETTI
Publications and source records attributed to A FRANCESCHETTI.
[DETECTION OF TOXOPLASMA IN A CASE OF SERUM-NEGATIVE CHORIORETINITIS].
Explore the source record for details and available documents.
Chorioretinitis↗
[ON THE PROGNOSIS OF REFRACTION AND THE MAGNIFYING EFFECT FOLLOWING FUKALA OPERATION BY MEANS OF ULTRASONIC EXAMINATION].
Explore the source record for details and available documents.
Humans↗
[ON THE DETECTION OF CARRIERS OF HETEROZYGOUS FEATURES IN OPHTHALMOLOGY].
Explore the source record for details and available documents.
Eye Diseases↗
[A new form of fundus albipunctatus with hemeralopia].
Explore the source record for details and available documents.
Fundus Oculi↗
[ISOLATION OF TOXOPLASMA GONDII IN A CASE OF SERO-NEGATIVE CHORIORETINITIS].
Explore the source record for details and available documents.
Chorioretinitis↗
[ALBESCENT PUNCTATE RETINOPATHY].
Explore the source record for details and available documents.
Diagnosis, Differential↗
[REVERSIBLE TAPETOID REFLEX (INVERSE MIZUO PHENOMENON) IN FEMALE CONDUCTORS OF RECESSIVE PIGMENTARY RETINOPATHY RELATED TO SEX].
Explore the source record for details and available documents.
Female↗
A curious affection of the fundus oculi: helicoid peripapillar chorioretinal degeneration. Its relation to pigmentary paravenous chorioretinal degeneration.
Explore the source record for details and available documents.
Angioid Streaks↗
[Aminoaciduria in cataract and glaucoma of congenital origin. Analogies with the Lowe-Terrey-Mac-Lachlan oculo-cerebro-renal syndrome (hyperaminoaciduria, psychomotor retardation and muscular hypotonia with cataract and glaucoma)].
Explore the source record for details and available documents.
Amino Acid Metabolism, Inborn Errors↗
[Daltonism: its relation to other sex-linked hereditary abnormalities and its importance as gene marker].
Explore the source record for details and available documents.
Biomarkers↗
Red-green blindness. Its relation to other sex-linked hereditary anomalies and its importance as a gene-marker.
Explore the source record for details and available documents.
Biomarkers↗
[On corneal dystrophy in genodermatoses with special reference to palmar and plantar keratosis. (Clinical, genetic and histological studies)].
Explore the source record for details and available documents.
Cornea↗
[Clinical, ophthalmological and genetic aspects of neuroretinal abiotrophies in pediatrics].
Explore the source record for details and available documents.
Central Nervous System Diseases↗
[Multiple abnormalities (atypical incontinentia pigmenti?, polydactylia, idiocy, coloboma of the choroid)].
Explore the source record for details and available documents.
Abnormalities, Multiple↗
[On the "Behcetin reaction"].
Explore the source record for details and available documents.
Behcet Syndrome↗