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1                                      Crigler-Najjar syndrome (CN) is a very rare genetic disorder cha
2                                      Crigler-Najjar syndrome is a recessively inherited disorder char
3                                      Crigler-Najjar syndrome type 1 (CN-1) is a recessively inherited
4                                      Crigler-Najjar syndrome type I is characterized by unconjugated
5 in the UGT1A1 (HUG-Br1) isozyme of a Crigler-Najjar (CN) Type I patient.
6 c bilirubin glucuronidation, causing Crigler-Najjar syndrome type 1 or 2, respectively.
7                         In contrast, Crigler-Najjar syndrome types I and II are rare genetic disorder
8 he risk of bilirubin encephalopathy (Crigler-Najjar syndrome).
9                                  For Crigler-Najjar syndrome, an inherited disorder that results in f
10 cult, is now accepted management for Crigler-Najjar type I disease but remains controversial for the
11 rubinemia in humans that suffer from Crigler-Najjar type I disease results from lesions in the UGT1A1
12 r type II patients and, recently, in Crigler-Najjar type I patients treated with human hepatocyte cel
13                                   In Crigler-Najjar type II patients and, recently, in Crigler-Najjar
14 lirubinemia in the Gunn rat model of Crigler-Najjar syndrome can be achieved with one injection of HD
15 perbilirubinemic Gunn rats (model of Crigler-Najjar syndrome type 1) resulted in hUGT1A1 expression i
16 transplantation in the management of Crigler-Najjar syndrome, type 1.
17  rat is an excellent animal model of Crigler-Najjar syndrome, type 1.
18  both alleles, whereas patients with Crigler-Najjar syndrome are homozygous for a defect that yields
19  report describes a young adult with Crigler-Najjar syndrome type II in whom kernicterus developed af
20 nduced levels noted in patients with Crigler-Najjar type 1 disease, is fatal in neonatal Ugt1(-/-) mi
21 s (n = 3), and patients (n = 4) with Crigler-Najjar type I (CN-I) syndrome.

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