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1 he risk of bilirubin encephalopathy (Crigler-Najjar syndrome).
2                                  For Crigler-Najjar syndrome, an inherited disorder that results in f
3  both alleles, whereas patients with Crigler-Najjar syndrome are homozygous for a defect that yields
4 lirubinemia in the Gunn rat model of Crigler-Najjar syndrome can be achieved with one injection of HD
5                                      Crigler-Najjar syndrome (CN) is a very rare genetic disorder cha
6                                      Crigler-Najjar syndrome is a recessively inherited disorder char
7                                      Crigler-Najjar syndrome type 1 (CN-1) is a recessively inherited
8 c bilirubin glucuronidation, causing Crigler-Najjar syndrome type 1 or 2, respectively.
9 perbilirubinemic Gunn rats (model of Crigler-Najjar syndrome type 1) resulted in hUGT1A1 expression i
10                                      Crigler-Najjar syndrome type I is characterized by unconjugated
11  report describes a young adult with Crigler-Najjar syndrome type II in whom kernicterus developed af
12 transplantation in the management of Crigler-Najjar syndrome, type 1.
13  rat is an excellent animal model of Crigler-Najjar syndrome, type 1.
14                         In contrast, Crigler-Najjar syndrome types I and II are rare genetic disorder

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