Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
|
pubmed:dateCreated |
1979-3-28
|
pubmed:language |
jpn
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
0029-0203
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
10
|
pubmed:volume |
82
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
887-99
|
pubmed:dateRevised |
2011-7-28
|
pubmed:meshHeading |
pubmed-meshheading:310634-Adult,
pubmed-meshheading:310634-Cornea,
pubmed-meshheading:310634-Corneal Dystrophies, Hereditary,
pubmed-meshheading:310634-Female,
pubmed-meshheading:310634-Fuchs' Endothelial Dystrophy,
pubmed-meshheading:310634-Humans,
pubmed-meshheading:310634-Japan,
pubmed-meshheading:310634-Microscopy, Electron
|
pubmed:year |
1978
|
pubmed:articleTitle |
[The electron microscopic study of Fuchs' dystrophy: the first primary case in Japan (author's transl)].
|
pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|