about
Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndromeMultiple organ dysfunction in a 33-year-old woman due to hereditary hemochromatosis.Increased PiZ gene frequency for alpha 1 antitrypsin in patients with genetic haemochromatosisAccumulation of iron by primary rat hepatocytes in long-term culture: changes in nuclear shape mediated by non-transferrin-bound forms of iron.Chronic iron overload in rats induces oval cells in the liver.Vitamin C: antioxidant or pro-oxidant in vivo?Expression of adhesion molecules and von Willebrand factor in human coronary artery endothelial cells incubated with differently modified hemoglobin solutions.Screening for C282Y homozygosity in a Norwegian population (HUNT2): The sensitivity and specificity of transferrin saturation.Effects of co-supplementation of iron with ascorbic acid on antioxidant--pro-oxidant balance in the guinea pig.69-year-old man with gait disturbance and Parkinsonism.
P2860
Q24562778-59CC2346-18A5-4FDD-AFAF-15342B0D656FQ33608528-DCD1FBBA-ACDA-41C0-879E-B27BC3CE8AB1Q34408182-3FEB924B-C6DB-4E26-9348-D173C7B205F2Q35765011-7EB1ED8E-28EC-428F-9DD9-09AAE1C2EA72Q35782589-2AD4FEA3-9AA5-4733-BA32-A6A79B63B043Q41197203-7B03FDFA-15C8-4CF9-883B-693961CEB467Q42436315-9FED5C3E-2375-4B70-8120-B6F58DBF229CQ43743838-587F8530-A4DC-4615-8F24-B5A8188838EBQ46830075-F7380A53-BE0A-4C44-80DD-74DC0FB37B4DQ48856920-6DD905F5-02DE-47F0-B503-4A67D0085AEC
P2860
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年学术文章
@wuu
1993年学术文章
@zh-cn
1993年学术文章
@zh-hans
1993年学术文章
@zh-my
1993年学术文章
@zh-sg
1993年學術文章
@yue
1993年學術文章
@zh
1993年學術文章
@zh-hant
name
Pathogenesis of genetic haemochromatosis.
@en
type
label
Pathogenesis of genetic haemochromatosis.
@en
prefLabel
Pathogenesis of genetic haemochromatosis.
@en
P2093
P2860
P1476
Pathogenesis of genetic haemochromatosis
@en
P2093
C Niederau
G Strohmeyer
H D Riedel
P2860
P304
P356
10.1111/J.1365-2362.1993.TB02031.X
P50
P577
1993-06-01T00:00:00Z