1 ndylitis, primary sclerosing cholangitis and Takayasu's arteritis(3-6)-we identify that the causal ge

2 ent who fulfilled the diagnostic criteria of Takayasu's arteritis and pulmonary hypertension were inc

3  long-term survival outcome in patients with Takayasu's arteritis-associated pulmonary hypertension (

4 t they may be effective for the treatment of Takayasu's arteritis, but their role in the treatment of

5 litis (LVV), including giant cell arteritis, Takayasu's arteritis, immunoglobulin G4-related aortitis

6 r's granulomatosis, giant cell arteritis and Takayasu's arteritis in the US amounted to $150 million

7               Giant cell arteritis (GCA) and Takayasu's arteritis (TAK) are major forms of large-vess

8                                              Takayasu's arteritis (TAK) is a large-vessel vasculitis

9 logically similar to the lesions observed in Takayasu's arteritis, the nongranulomatous variant of te

10 sts: pentraxin-3 in giant cell arteritis and Takayasu's arteritis; von Willebrand factor antigen in c