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1 tion to counteract ectopic mineralization in pseudoxanthoma elasticum.
2 efore provides a novel model system to study pseudoxanthoma elasticum.
3 rter C6) ABC transporter are associated with pseudoxanthoma elasticum, a disease of altered elastic p
4  drug efflux pumps, are the genetic basis of Pseudoxanthoma elasticum, a disease that affects elastin
5                                              Pseudoxanthoma elasticum, a heritable ectopic mineraliza
6                 Mutations in ABCC6 result in pseudoxanthoma elasticum, a multi-system heritable conne
7 eye (3%) had neovascularization secondary to pseudoxanthoma elasticum, all showing similar ORT format
8 f all Vanderbilt Eye Institute patients with pseudoxanthoma elasticum and at least 1 set of color fun
9       This report summarizes the progress in pseudoxanthoma elasticum and other ectopic mineralizatio
10 els, resulting in the calcification disorder pseudoxanthoma elasticum and some cases of generalized a
11 nderlie the incurable calcification disorder pseudoxanthoma elasticum and some cases of generalized a
12          The prototype of such conditions is pseudoxanthoma elasticum, and related conditions with ov
13 ic atrophy independent of CNV can develop in pseudoxanthoma elasticum, causing significant vision los
14 ted a series of Abcc6(-/-) rats as models of pseudoxanthoma elasticum depicting ectopic mineralizatio
15  exemplified by familial tumoral calcinosis, pseudoxanthoma elasticum, generalized arterial calcifica
16                                              Pseudoxanthoma elasticum in humans and dystrophic cardia
17                                              Pseudoxanthoma elasticum is a multisystem ectopic minera
18                                              Pseudoxanthoma elasticum is a prototype of heritable ect
19                                              Pseudoxanthoma elasticum like fundus changes are a frequ
20                                              Pseudoxanthoma elasticum-like changes were more frequent
21                                              Pseudoxanthoma elasticum-like fundus changes are a frequ
22  several months prevented the development of pseudoxanthoma elasticum-like spontaneous calcification,
23 mately 200 mutations have been identified in pseudoxanthoma elasticum patients, the underlying struct
24 BCC6 gene cause soft-tissue calcification in pseudoxanthoma elasticum (PXE) and, in some patients, ge
25                                              Pseudoxanthoma elasticum (PXE) is a classic inherited di
26                                              Pseudoxanthoma elasticum (PXE) is a heritable disorder c
27                                              Pseudoxanthoma elasticum (PXE) is a heritable disorder m
28                                              Pseudoxanthoma elasticum (PXE) is a multisystem disorder
29                                              Pseudoxanthoma elasticum (PXE) is a multisystem ectopic
30                                              Pseudoxanthoma elasticum (PXE) is a pleiotropic multisys
31                                              Pseudoxanthoma elasticum (PXE) is a systemic heritable d
32                                              Pseudoxanthoma elasticum (PXE) is an autosomal recessive
33                                              Pseudoxanthoma elasticum (PXE) is an autosomal recessive
34                                              Pseudoxanthoma elasticum (PXE) is an autosomal recessive
35                                              Pseudoxanthoma elasticum (PXE) is caused by mutations in
36                                              Pseudoxanthoma elasticum (PXE) is caused by mutations in
37                                              Pseudoxanthoma elasticum (PXE) is caused by mutations in
38                   The pathologic hallmark of pseudoxanthoma elasticum (PXE) is ectopic mineralization
39                                  The classic pseudoxanthoma elasticum (PXE) phenotype derives from mu
40 rformed linkage analysis on 21 families with pseudoxanthoma elasticum (PXE) using 10 polymorphic mark
41 cular fundus abnormalities characteristic of pseudoxanthoma elasticum (PXE) were detected by cSLO in
42                                              Pseudoxanthoma elasticum (PXE), a multisystem disorder c
43                                              Pseudoxanthoma elasticum (PXE), a pleiotropic heritable
44                                              Pseudoxanthoma elasticum (PXE), a pleiotropic multisyste
45                                              Pseudoxanthoma elasticum (PXE), a prototype of heritable
46                                              Pseudoxanthoma elasticum (PXE), a prototypic heritable d
47                                              Pseudoxanthoma elasticum (PXE), a rare genetic disease c
48                                              Pseudoxanthoma elasticum (PXE), an autosomal recessive d
49          A characteristic feature of classic pseudoxanthoma elasticum (PXE), an autosomal recessive d
50                                              Pseudoxanthoma elasticum (PXE), characterized by connect
51 cular fundus abnormalities characteristic of pseudoxanthoma elasticum (PXE), including peau d'orange,
52          The ABCC6 gene, which is mutated in pseudoxanthoma elasticum (PXE), resided within a small r
53                 Although clinical similar to pseudoxanthoma elasticum (PXE), the skin changes were fo
54    To better understand the pathogenetics of pseudoxanthoma elasticum (PXE), we performed a mutationa
55 system have been identified in families with pseudoxanthoma elasticum (PXE).
56 ions in four candidate genes associated with pseudoxanthoma elasticum, the prototype of ectopic miner
57                In a humanized mouse model of pseudoxanthoma elasticum, we investigated whether 4-PBA
58  The fundamental question on pathogenesis of pseudoxanthoma elasticum, whether lack of ABCC6 expressi

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