Top 100 alternative sites to solve-rd.eu

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  2. LTEliasson | Let the unsolved be solved
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  4. Solve the Unsolved - Forensic Astrologer
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  5. ejprarediseases.org
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  6. EJP RD – European Joint Programme on Rare Diseases

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  8. Chiesi Global Rare Diseases | Products for rare diseases
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  10. Cambridge Rare Disease Network - Cambridge Rare Disease Network
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  11. rarediseaseadvisor.com
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  12. Rare Disease News, Perspectives & Resources - Rare Disease Advisor
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  13. everylifefoundation.org
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  14. Rare Disease Legislative Advocates | EveryLife Foundation for Rare Diseases

  15. rarediseasefoundation.org
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  16. Rare Disease Foundation
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  18. Rare Disease Database
    Hypermobile Ehlers-Danlos syndrome and physiotherapy were the main keywords of the research. [Results] 1, articles emerged from the.

  19. rarediseasesinternational.org
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  20. Rare Diseases International
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  21. cureraredisease.org
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  22. Cure Rare Disease
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  24. Rare Diseases Ireland – Supporting rare disease patients and their families in Ireland

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  28. Rare Disease Pharmaceutical Services | Sciensus Rare
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  30. IORD - Indian Organization for Rare Diseases | A not-for-profit organization for Rare Diseases in India.

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  34. CENTOGENE - The Rare Disease Company
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  36. Journal of Rare Cardiovascular Diseases
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  38. Rare Genetic Diseases | Ultragenyx
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  40. HRA Pharma Rare Diseases
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  41. crcd.eu
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  42. Centre for Rare Cardiovascular Diseases
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  43. rarejournal.org
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  44. Rare Diseases and Orphan Drugs

  45. radico.fr
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  46. Radico - Rare Disease Cohorts
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  48. Home - Rare Disease UK
    What's the UK Rare Diseases Strategy? Where can I find information & support? How can I fundraise for Rare Disease UK? The latest news from RARE DISEASE UK... Lauren’s Story Living with Hereditary Amyloidosis One in a Million Abigail’s story Will’s Story Our work We work on ...

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  50. Rare diseases Luxembourg , we care 4 rare! - ALAN
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  52. Rare Trait Swiss- AGU Rare Disease: Aspartylglucosaminuria
    Rare Trait Swiss is a Non-Profit organization which contribute to raise awareness of an Lysosomal rare disease called AGU. Our goal is to fund the medical research to manufacture the cure for AGU kids and to fund a clinical trial using gene therapy

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  54. Tried Physio? Try Us. We Solve the Unsolvable. Physio Tauranga
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  56. Diploid - Supporting Rare Disease Diagnostics

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  58. F2G - The Rare Fungal Disease Company

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  60. Allies in Rare Disease - Global Genes
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  62. #WeWearStripes | Rare Disease Day 2021
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  63. rarediseasesacademy.de
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  64. Startseite - Rare Diseases Academy 2021

  65. ern-lung.eu
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  66. ERN-LUNG | Rare Respiratory Diseases
    WELCOME TO ERN-LUNG ERN-LUNG is a patient-centric network of European healthcare providers and patient organisations, committed Europe-wide and globally to reducing morbidity and mortality from rare lung diseases in people of all ages through patient care, advocacy, education, research and knowledge-sharing. A non-profit project of building a clinical care network for all rare diseases of the respiratory
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  68. European Conference on Rare Diseases - ECRD2020
    The ECRD is recognised globally as the largest, patient-led rare disease event in which collaborative dialogue, learning and conversation takes place, forming the groundwork to shape future rare disease policies. Leading, inspiring and engaging all stakeholders to take action, the Conference is an unrivalled opportunity to network and exchange invaluable knowledge with all stakeholders in the rare disease community – patient representatives, […]
    Author: Rare Diseases Europe

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  70. Rare Disease Day ® 2021
    The main objective of Rare Disease Day is to raise awareness with policy makers and the public of rare diseases and of their impact on the lives of patients, and to reinforce their importance as a public health priority.

  71. nirdp.org.uk
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  72. Northern Ireland Rare Disease Partnership

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  74. Radiorg – Rare Diseases organisation Belgium
    Edelweiss Awards 2021 Belgische koepel voor patiënten met een zeldzame ziekte RaDiOrg is de Belgische koepelvereniging voor mensen met een zeldzame ziekte. Wij tellen meer dan 80 verenigingen voor specifieke zeldzame ziekten en tellen ook honderden individuele leden met een ziekte waarvoor geen vereniging bestaat. Onze missie? Zorgen dat de stem van de zeldzame ziekten wordt gehoord door beleidsmakers. Het grote publiek sensibiliseren voor de zeldzame ziekten. De weg wijzen met heldere informatie. Mensen met zeldzame ziekten verbinden. Ruchtbaarheid geven aan de activiteiten voor en door mensen met zeldzame ziekten. We zijn zeldzaam, maar we zijn talrijk! Nieuws Blijf op

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  75. rda-forum.org
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  76. Rare Disease Action Forum | RDAF

  77. zogenix.com
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  78. Zogenix - Therapeutic Solutions for Rare Diseases
    Zogenix is committed to developing and commercializing transformative therapies to improve the lives of patients and their families living with rare diseases.

  79. curecmt4j.org
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  80. CureCMT4J | Advancing Treatments for Rare Diseases

  81. rdodjournal.com
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  82. Rare Disease and Orphan Drugs Journal
    Rare Disease and Orphan Drugs Journal (RDODJ) is an international, peer-reviewed, open access journal. RDODJ will report on scientific advances in the genetics of rare diseases, the molecular basis of the pathologies, and translational research on diagnosis, prevention and treatment. In addition, RDODJ aims to provide a forum for scientific studies and discussion covering the important regulatory, socio-economic and human science issues related to rare diseases and orphan drugs.
    Author: Daniel Scherman

  83. ramedis.de
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  84. RAMEDIS: Rare Metabolic Diseases Database
    The RAMEDIS system is a platform independent, web-based information system for rare metabolic diseases based on filed case reports
    Author: Bielefeld University Faculty

  85. rareve.com
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  86. RAREVE - relieve people with rare diseases
    In Rareve our mission is to relieve people with rare diseases. Build a community, knowledge base and full of support and professional help place for people. If you feel that you need help, or you can help yourself, than…

  87. ordindia.in
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  88. Organization For Rare Diseases India | ORDI
    ORDI was founded to address the many challenges in the management of rare disease in India. A lack of awareness about rare disease even among doctors means that a diagnosis can often take many years.

  89. mynormal.ca
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  90. My Normal | storytelling for rare disease health
    My Normal | storytelling for rare disease health
    Author: My Normal

  91. rdif.org.in
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  92. Home - Rare Diseases India Foundation

  93. allstripes.com
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  94. AllStripes - Be part of the solution for your rare disease
    We empower patients and communities to change the way that **** development happens in rare disease.

  95. globalgenes.org
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  96. Allies in Rare Disease - Global Genes
    Global Genes mission is to connect, empower and inspire the rare disease community. Learn more about our events, resources and communities.

  97. rdna.ca
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  98. rDNA | Rare Disease Network of Alberta
    The Rare Disease Network of Alberta (rDNA) is a non-profit corporation that was formed in 2018 to help people understand about rare diseases.

  99. rareopportunities.com
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  100. Welcome to Rare Opportunities in Primary Care, your source for information on primary care in rare diseases

  101. rd-action.eu
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  102. RD-ACTION : DATA AND POLICIES for rare diseases – RD-ACTION, the new Joint Action consisting of the member states of the European Union for

  103. coatsdiseasefoundation.org
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  104. Jack McGovern Coats' Disease - Rare Eye Disease - Home Page
    Jack McGovern Coats' Disease - Funds research to find a cure for Coats’ Disease and pediatric retinal Disease - We serve as a hub for the Coats’ Disease community

  105. satishbrothersandsons.com
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  106. CBSE 10th Class Previous Year Solved, Unsolved Question Papers
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  107. irdrjournal.com
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  108. Intractable & Rare Diseases Research - Current Issue
    BioScienceTrends
    Author: Yang D; Ren X; Lu Y; Han J

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  109. khurehealth.ca
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  110. Khure Health: Identifying Rare Disease Patients
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    Author: Drawesome

  111. 3billion.io
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  112. 3billion | Genetic test for rare disease patients
    Patients with rare genetic disease undergo long odyssey to receive a diagnosis. Visit 3billion and find how to order our rare disease genetic testing.

  113. soleno.life
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  114. Developing novel therapeutics for the treatment of rare diseases.

  115. yourdna.com
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  116. YourDNA - Tests, Answers and Rare Disease Guides
    YourDNA aims to take the mystery out of the growing world of consumer DNA tests, and DNA test results. Take back control of your DNA and your health.

  117. sareptatherapeutics.ch
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  118. Sarepta Therapeutics | Biopharmaceutical Company for Rare Diseases
    We are focused on the development of precision genetic medicines to treat rare neuromuscular and central nervous system diseases. Learn more about Sarepta.

  119. rd-rp.com
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  120. Rare Disease Research Partners – Helping people

  121. rarediseasesnetwork.org
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  122. Home | Rare Diseases Clinical Research Network
    The Rare Diseases Clinical Research Network (RDCRN), an initiative of the Office of Rare Diseases Research, NCATS, is made up of 21 disease research groups (consortia) and a Data Management and Coordinating Center that work together to improve availability of rare disease information, treatment, clinical studies, and general awareness for both patients and the medical community.

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  124. Aeglea BioTherapeutics | Rare Metabolic Disease | Home
    Aeglea BioTherapeutics is a clinical stage company developing enzyme therapies for rare metabolic diseases like Arginase 1 Deficiency and Homocystinuria.

  125. cloud-r.eu
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  126. Cloud-R | Rare disease from a community to data | Italy
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  128. Crinetics - Developing Therapies For Rare Endocrine Diseases
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  130. Voiture Conseil -
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  132. Boka ditt hotell online till väldigt låga priser! |
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  134. ⇒ Badewanne mit Dusche ++ Testsieger ++ Preisvergleich
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  136. Home - Preiser Scientific

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  144. - Mairie de Fontaine Etoupefour
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