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1                                              GACI has a poor prognosis, with more than half of patien
2                                              GACI is a lethal orphan disease in which infants calcify
3                                              GACI patients present a more severe, often prenatal arte
4                                              GACI usually occurs during fetal development.
5 ) analyses of extracted primary teeth from 3 GACI subjects revealed 4-fold increased cervical cementu
6 mutations were identified in five additional GACI families with normal ENPP1 sequences.
7 be useful for selected patients with PXE and GACI.
8 ences in enamel and dentin densities between GACI and control teeth.
9 ine area, duration of GA, and configuration, GACI categories were significantly associated with incre
10 ic conditions and confirm a second locus for GACI.
11 d dramatically expanded cervical cementum in GACI teeth, including cementocyte-like cells and unusual
12  findings reveal a novel dental phenotype in GACI and identify ENPP1 genetic mutations associated wit
13  the "Geographic Atrophy Circularity Index" (GACI) was developed on the basis of area and perimeter m
14 neralized arterial calcification of infancy (GACI) due to loss-of-function mutations in the ENPP1 gen
15 neralized arterial calcification of infancy (GACI) is a rare genetic condition with varied clinical p
16 neralized arterial calcification of infancy (GACI) is a rare genetic disease that affects the circula
17 neralized arterial calcification of infancy (GACI) is an autosomal recessive disorder characterized b
18 neralized arterial calcification of infancy (GACI), characterized by severe, early-onset mineralizati
19 neralized arterial calcification of infancy (GACI), to common diseases such as hardening of the arter
20 neralized arterial calcification of infancy (GACI).
21                                Most cases of GACI are caused by mutations in the ENPP1 gene.
22 s and sequela of disease in animal models of GACI, and is accompanied by a complete clinical and biom
23                 These three conditions, PXE, GACI, and ACDC, caused by mutations in ABCC6, ENPP1, and
24                                          The GACI ranges from 0.0 to 1.0 and is categorized into 3 gr
25                                          The GACI was associated with the progression rate of GA and
26 d the aortic narrowing to be associated with GACI.
27                                  Babies with GACI are diagnosed early, generally soon after birth and
28           We first studied two siblings with GACI from a non-consanguineous family without mutations