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Domain Informations
Usscicomms.com lookup results from whois.nameshield.net server:
- Domain created: 2018-10-19T07:06:18Z
- Domain updated: 2024-10-17T22:20:59Z
- Domain expires: 2026-10-19T07:06:18Z 1 Year, 35 Days left
- Website age: 6 Years, 329 Days
- Registrar Domain ID: 2323122213_DOMAIN_COM-VRSN
- Registrar Url: http://www.nameshield.com
- Registrar WHOIS Server: whois.nameshield.net
- Registrar Abuse Contact Email: [email protected]
- Registrar Abuse Contact Phone: +33241182828
- Name server:
- NSA.PERF1.FR
- NSB.PERF1.COM
- NSC.PERF1.COM
Network
- inetnum : 45.60.0.0 - 45.60.255.255
- name : INCAPSULA-NET
- handle : NET-45-60-0-0-1
- status : Direct Allocation
- created : 2010-09-15
- changed : 2025-04-29
Owner
- organization : Incapsula Inc
- handle : INCAP-5
- address : Array,SAN MATEO,CA,94403,US
Abuse
- handle : IMPER7-ARIN
- name : Imperva AbuseDesk
- phone : +1-866-250-7659
- email : [email protected],[email protected]
Technical support
- handle : LCW4-ARIN
- name : Wooderson, Lee Charles
- phone : +1-469-731-2552
- email : [email protected]
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Host Informations
| Host name | 45.60.242.221 |
| IP address | 45.60.242.221 |
| Location | United States |
| Latitude | 37.751 |
| Longitude | -97.822 |
| Timezone | America/Chicago |
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www.usscicomms.com
Redirecting to https://www.usscicomms.com/respiratory/ATS2020/goh.
Usscicomms.comDA: 18 PA: 25 MOZ Rank: 43
Effects of nintedanib on dyspnea, cough and quality of life in …
Methods Trial design2 n Subjects were enrolled who had an ILD other than IPF, diagnosed by the investigator according to their usual clinical practice, reticular abnormality with traction …
Usscicomms.comDA: 18 PA: 41 MOZ Rank: 60
Effects of nintedanib in subgroups based on combined pulmonary …
Effects of nintedanib in subgroups based on combined pulmonary fibrosis and emphysema (CPFE) index at baseline Vincent Cottin,1 Christopher J Ryerson,2 Kevin R Flaherty,3 Joyce S …
Usscicomms.comDA: 18 PA: 50 MOZ Rank: 88
Antifibrotic therapy for idiopathic pulmonary fibrosis: …
Abstract. Idiopathic pulmonary fibrosis (IPF) is a progressive disease with a dismal prognosis. The average life expectancy of untreated patients with IPF is only 3 to 4 years. …
Pubmed.ncbi.nlm.nih.govDA: 23 PA: 10 MOZ Rank: 36
ATS 2023 International Conference
Washington, DC | May 19 - 24. The American Thoracic Society improves global health by advancing research, patient care, and public health in pulmonary disease, critical illness, and …
Conference.thoracic.orgDA: 23 PA: 23 MOZ Rank: 28
Safety and tolerability of nintedanib in patients with progressive ...
Methods. Patients with fibrosing ILDs other than idiopathic pulmonary fibrosis (IPF), who had experienced progression of ILD within the 24 months before screening despite …
Ncbi.nlm.nih.govDA: 20 PA: 25 MOZ Rank: 50
Antifibrotic therapy for idiopathic pulmonary fibrosis: time to treat
REVIEW Open Access Antifibrotic therapy for idiopathic pulmonary fibrosis: time to treat Toby M. Maher1,2* and Mary E. Strek3 Abstract Idiopathic pulmonary fibrosis (IPF) is a progressive …
Respiratory-research.biomedcentral.comDA: 38 PA: 40 MOZ Rank: 84
Utility of the six-minute walk test in patients with idiopathic ...
REVIEW Open Access Utility of the six-minute walk test in patients with idiopathic pulmonary fibrosis Lisa H. Lancaster1,2 Abstract The six-minute walk test (6MWT) is a simple test that is …
Mrmjournal.biomedcentral.comDA: 28 PA: 40 MOZ Rank: 75
Seminars in Oncology - ResearchGate
272 A. Masood, R.K. Kancha and J. Subramanian / Seminars in Oncology 46 (2019) 271–283 Table 1 Summary of key randomized trials of EGFR TKIs undertaken in patients with NSCLCs …
Researchgate.netDA: 20 PA: 50 MOZ Rank: 42
Time to diagnosis of idiopathic pulmonary fibrosis in the IPF-PRO ...
Introduction. Idiopathic pulmonary fibrosis (IPF) is a progressive fibrosing interstitial lung disease (ILD) with poor prognosis.1 Median survival from diagnosis of IPF is 2 to 5 years,2–4 but the …
Bmjopenrespres.bmj.comDA: 22 PA: 20 MOZ Rank: 51
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