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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
5
|
| pubmed:dateCreated |
1990-8-16
|
| pubmed:abstractText |
Early diagnosis of retinitis pigmentosa and related diseases is based on a specific history, on perimetry of the outer isopters, and on rod/cone electroretinography. The remarkable variability of phenomenology, age of onset and genetic pattern, however, often complicate early diagnosis. Continuous consulting and documentation of the course of the disease are considered a meaningful care by the physician and represent the basis for the tasks of the geneticist.
|
| pubmed:language |
ger
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
May
|
| pubmed:issn |
0023-2165
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
196
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
273-4
|
| pubmed:dateRevised |
2010-11-18
|
| pubmed:meshHeading | |
| pubmed:year |
1990
|
| pubmed:articleTitle |
[Early diagnosis and heterogeneity of retinitis pigmentosa].
|
| pubmed:affiliation |
Neurophysiologie-Laboratorium, Augenklinik des Universitätsspitals Zürich.
|
| pubmed:publicationType |
Journal Article,
English Abstract
|