Erythrocyte abnormalities in a hypoalphalipoproteinemia syndrome resembling fish eye disease

scientific article published on 01 August 1988

Erythrocyte abnormalities in a hypoalphalipoproteinemia syndrome resembling fish eye disease is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1111/J.1600-0609.1988.TB00888.X
P953full work available at URLhttp://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1988.tb00888.x/fullpdf
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1600-0609.1988.tb00888.x
P698PubMed publication ID3410011

P2093author name stringD. V. Godin
L. D. Wadsworth
J. Frohlich
G. Hoag
M. E. Garnett
P2860cites workDecreased fluidity of red cell membrane lipids in abetalipoproteinemiaQ24595286
Clinical, biochemical, and genetic features in familial disorders of high density lipoprotein deficiencyQ40213171
Increased susceptibility of red-blood-cell lipids to autooxidation in haemolytic statesQ45177870
Plasma lipoprotein abnormalities in heterozygotes for familial lecithin:cholesterol acyltransferase deficiency.Q51627361
Evidence for deficiency of high density lipoprotein lecithin: cholesterol acyltransferase activity (alpha-LCAT) in fish eye disease.Q54166778
Alterations in free radical tissue-defense mechanisms in streptozocin-induced diabetes in rat. Effects of insulin treatmentQ68171191
Hypoalphalipoproteinemia resembling fish eye diseaseQ69047587
Enzymatic Activities and Glutathione Content of Erythrocytes in the Newborn: Comparison with Red Cells of Older Normal Subjects and those with Comparable ReticulocytosisQ69378712
Red-cell lipids in familial alphalipoprotein deficiency (Tangier disease)Q70089012
Erythrocyte membrane alterations and plasma lipids in patients with chylomicronemia and in Tangier diseaseQ70147709
Increased erythrocyte susceptibility to lipid peroxidation in myeloproliferative disordersQ71251942
Fish eye disease: a new familial condition with massive corneal opacities and dyslipoproteinaemiaQ71595838
Familial plasma cholesterol ester deficiency. A study of the erythrocytesQ72173892
Study of erythrocytes in a hereditary hemolytic syndrome (HHS): comparison with erythrocytes in lecithin:cholesterol acyltransferase (LCAT) deficiencyQ72851344
Heinz body formation in red cell membrane disorders: its acceleration in membrane lipid abnormalitiesQ93639709
P433issue2
P407language of work or nameEnglishQ1860
P921main subjecteye diseaseQ3041498
hypoalphalipoproteinemiaQ5959167
P304page(s)176-181
P577publication date1988-08-01
P1433published inEuropean Journal of HaematologyQ15765799
P1476titleErythrocyte abnormalities in a hypoalphalipoproteinemia syndrome resembling fish eye disease
P478volume41

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