Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
1988-7-29
|
pubmed:abstractText |
It is reported on a 33-year-old patient whose diagnosis "hereditary elliptocytosis" has been ensured by typical findings. References to a structural defect of erythrocyte membrane proteins resulted from the SDS-gel electrophoresis. A splenectomy improved the subjective and objective symptoms distinctly.
|
pubmed:language |
ger
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0044-2542
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
1
|
pubmed:volume |
43
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
128-9
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:3388917-Adult,
pubmed-meshheading:3388917-Blood Protein Electrophoresis,
pubmed-meshheading:3388917-Elliptocytosis, Hereditary,
pubmed-meshheading:3388917-Erythrocyte Membrane,
pubmed-meshheading:3388917-Humans,
pubmed-meshheading:3388917-Male,
pubmed-meshheading:3388917-Membrane Proteins
|
pubmed:year |
1988
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pubmed:articleTitle |
[Hereditary elliptocytosis with detection of a membrane protein defect of erythrocytes].
|
pubmed:affiliation |
Poliklinik für Innere Medizin, Medizinischen Akademie Erfurt.
|
pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|