Skip to content

Biomedical subjects

S Auch-Roy-Mainguy

Publications and source records attributed to S Auch-Roy-Mainguy.

9 recordsLinked to original sources

PubMed1989

[Gronblad-Strandberg syndrome: association of angioid streaks and an elastic pseudoxanthoma (apropos of a case in a 20-year-old young woman)].

Explore the source record for details and available documents.

Adult↗

PubMed1987

[2 cases of mitochondrial cytopathy manifested ophthalmologically].

Explore the source record for details and available documents.

Adolescent↗

PubMed1984

[Binasal hemianopsia and hydrocephalus in the adult].

Explore the source record for details and available documents.

Cerebral Aqueduct↗

PubMed1984

[Malignant endocrine exophthalmos. Therapeutic problems].

Explore the source record for details and available documents.

Female↗

PubMed1983

[Optico-chiasma conflict of anterior polygonal origin (campimetric changes and attempt at physiopathogenic explanation].

Explore the source record for details and available documents.

Aged↗

PubMed1982

[Mucoceles with ophthalmic manifestations and their treatment apropos of (20 cases)].

Explore the source record for details and available documents.

Adolescent↗

PubMedDate not supplied

[A case of cholesteric granuloma of the orbit].

Explore the source record for details and available documents.

Adult↗

PubMedDate not supplied

[Mixed photoreceptor dystrophy. Apropos of two cases].

Two observations of cone-rod dystrophy are reported. It's about two brothers. The transmission way is not defined. The extinction of the scotopic ERG and the final threshold of the rod in dark adaptation shows the rod participation in this disease. In this case, the characteristics of the progressive cone dystrophy (photophobia, achromatopsia, visual capacity loss, respect of the peripheric visual field, alteration of the photopic ERG) are seen. Fundus examination and angiography are discussed and reported to the vitreofluorometry.

Adolescent↗

PubMedDate not supplied

[Familial agenesis of the lacrimal glands and ducts].

Authors report three cases of hereditary malformation of excretory lacrymal system, two children and their father. One of the two children have a lacrymal fistula. A surgical treatment was successful.

Adult↗