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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2001-3-6
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pubmed:abstractText |
To describe the corneal abnormalities and to measure different modalities of corneal sensitivity in corneal lattice dystrophy type II (familial amyloidosis, Finnish type, also known as gelsolin-related amyloidosis and originally as Meretoja syndrome).
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0146-0404
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
42
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
634-41
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pubmed:dateRevised |
2010-3-24
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pubmed:meshHeading |
pubmed-meshheading:11222521-Adult,
pubmed-meshheading:11222521-Aged,
pubmed-meshheading:11222521-Amyloidosis,
pubmed-meshheading:11222521-Cornea,
pubmed-meshheading:11222521-Corneal Dystrophies, Hereditary,
pubmed-meshheading:11222521-Cranial Nerve Diseases,
pubmed-meshheading:11222521-Diagnostic Techniques, Ophthalmological,
pubmed-meshheading:11222521-Female,
pubmed-meshheading:11222521-Gelsolin,
pubmed-meshheading:11222521-Humans,
pubmed-meshheading:11222521-Male,
pubmed-meshheading:11222521-Microscopy, Confocal,
pubmed-meshheading:11222521-Middle Aged,
pubmed-meshheading:11222521-Nerve Fibers,
pubmed-meshheading:11222521-Ophthalmic Nerve,
pubmed-meshheading:11222521-Sensation Disorders
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pubmed:year |
2001
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pubmed:articleTitle |
Corneal morphology and sensitivity in lattice dystrophy type II (familial amyloidosis, Finnish type).
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pubmed:affiliation |
Department of Ophthalmology, University of Helsinki, Eye Bank, PO Box 220, Fin-00029 HUS, Finland. maria.rosenberg@hus.fi
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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