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Domain Informations

Network
  • inetnum : 172.64.0.0 - 172.71.255.255
  • name : CLOUDFLARENET
  • handle : NET-172-64-0-0-1
  • status : Direct Allocation
  • created : 2010-07-09
  • changed : 2021-07-01
  • desc : All Cloudflare abuse reporting can be done via https://www.cloudflare.com/abuse
Owner
  • organization : Cloudflare, Inc.
  • handle : CLOUD14
  • address : Array,San Francisco,CA,94107,US
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Host Informations

  • IP address: 172.67.159.43
  • Location: United States
  • Latitude: 37.751
  • Longitude: -97.822
  • Timezone: America/Chicago

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 › Ftp: 21
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 › Dns: 53
 › Http: 80
 › Pop3: 110
 › Portmapper, rpcbind: 111
 › Microsoft RPC services: 135
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 › Imap: 143
 › Ldap: 389
 › Https: 443
 › SMB directly over IP: 445
 › Msa-outlook: 587
 › IIS, NFS, or listener RFS remote_file_sharing: 1025
 › Lotus notes: 1352
 › Sql server: 1433
 › Point-to-point tunnelling protocol: 1723
 › My sql: 3306
 › Remote desktop: 3389
 › Session Initiation Protocol (SIP): 5060
 › Virtual Network Computer display: 5900
 › X Window server: 6001
 › Webcache: 8080


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Websites Listing

We found Websites Listing below when search with cdn.rarediseases.org on Search Engine

Home - NORD (National Organization for Rare Disorders)

NORD’s Living Rare Forum and Rare Impact Awards Highlight Powerful Patient Stories and Community Rock Stars. “NORD’s patient centric conference showcased inspiring individuals, …

Rarediseases.org

Canadian Organization for Rare Disorders

The Canadian Organization for Rare Disorder's (CORD) is a non-profit organization dedicated to the enhancement of lives of all persons affected by rare disorders through an educational and …

Rarediseases.org

Canadian Addison Society - NORD (National Organization …

The Canadian Addison Society (La Societe Canadienne d'Addison) (CAS) is a non-profit, voluntary agency dedicated to providing support and educational information to individuals …

Rarediseases.org

NORD (National Organization for Rare Disorders)

ONFI ® (clobazam) tablets, for oral use, ONFI ® (clobazam) oral suspension, Brief Summary of Prescribing Information (See package insert for full Prescribing Information or visit …

Cdn.rarediseases.org

Canadian Organization for Rare Disorders

The Canadian Organization for Rare Disorders Hereby Gives Notice of its Annual General Meeting. Monday, August 19, 2019 at 3:00 PM (EDT) via teleconference CORD Annual General MeetingSeptember 13, 2022 at 3:00 PM (EDT) via …

Raredisorders.ca

Canadian “Rare Diseases: Models and Mechanisms” …

The human genome is made up of approximately 22,000 functional units known as genes. Mutations in these genes can cause thousands of rare but nonetheless serious diseases …

Genomecanada.ca

Rare Disease Foundation

There are over 8,000 known rare diseases and many more unidentified diseases that await clinical research. Foundation Specifics. 464 Individual Research Projects Seeded. $2.1M Generated. 14 Potential Cures. $8.6M Follow Up …

Rarediseasefoundation.org

Canada – Rare Disease Day 2022

To raise awareness in Toronto in 2017, the city’s 3D sign was lit up in the colours of Rare Disease Day—blue, green, pink and purple—for the whole of 28 February! Rare Disease Day …

Rarediseaseday.org

Americans has a RARE DISEASE

RARE DISEASES ARE GENETICALLY BASED.2 7,000 RARE DISEASES exist, with less than 500 FDA-approved treatments 2 Patients with RARE DISEASES are frequently misdiagnosed …

Cdn.rarediseases.org

Our Work | Canadian Organization for Rare Disorders

Right now, the approach to rare diseases is fragmented across the country and this means Canadian families with rare illnesses are facing extraordinary challenges. These include misdiagnosis, unnecessary surgeries, social …

Raredisorders.ca

Canadian 'Rare Diseases: Models & Mechanisms' Network

Mutations in the human genome can cause thousands of rare but nonetheless serious diseases impacting hundreds of thousands of Canadians (www.raredisorders.ca). The identification of a …

Genomebc.ca

News from Nord

Rare diseases while maintaining FDA’s high standards for safety and efficacy. NORD and other patient advocates provided significant input to Representatives Stearns and Towns. Continued …

Cdn.rarediseases.org

Canadian Organization for Rare Disorders - A Life Worth Living

The Canadian Organization for Rare Disorder’s (CORD) is a non-profit organization dedicated to the enhancement of lives of all persons affected by rare disorders through an educational and …

Alifeworthliving.ca

NORD® Learning – Empowering through education

NORD, a 501(c)(3) organization, is a patient advocacy organization dedicated to individuals with rare diseases and the organizations that serve them. NORD, along with its more than 330 …

Learn.rarediseases.org

OPINION: Pan-Canadian strategy needed in rare disease battle

2 days ago  · In 2019, the federal government committed to improving access to rare disease therapies by investing $1 billion over two years (2022-2023) to implement a national Rare …

Torontosun.com

PUBLICATIONS - rare-diseases.ca

Rare Diseases Equity and Funding; A Canadian Perspective Shirin Rizzardo, Nick Bansback, Craig Mitton, Carlo Marra, Larry Lynd Poster presentation – 2014 CADTH Symposium, …

Rare-diseases.ca

#rareDiseases | World CDG Organization

#rareDiseases. RE(ACT) Congress and IRDiRC Conference. Read more about RE(ACT) Congress and IRDiRC Conference; Featured Image. Date. Mar 15 2023 - Mar 18 2023. …

Worldcdg.org

Search - Rare Diseases: Models & Mechanisms Network

The RDMM registry collects information on model organism researchers and the specific genes they study. The registry is the mechanism by which the RDMM will find potential matches of …

Register.rare-diseases-catalyst-network.ca

Pan-canadian strategy needed in rare diseases battle

2022-07-13  · In 2019, the federal government committed to improving access to rare disease therapies by investing $1 billion over two years (2022-2023) to implement a national Rare …

Epaper.vancouversun.com

Home | Rare Diseases Clinical Research Network

To learn about other rare diseases, please visit the Genetic and Rare Diseases Information Center (GARD), which is an NIH program that helps the public find reliable information about …

Www1.rarediseasesnetwork.org


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