Pages with the fewest revisions

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Showing below up to 100 results in range #51 to #150.

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  1. Research Models‏‎ (1 revision)
  2. Advocacy‏‎ (1 revision)
  3. Choosing an Internet Service Provider‏‎ (1 revision)
  4. Determine Goals‏‎ (1 revision)
  5. Expertise‏‎ (1 revision)
  6. Genetic Alliance‏‎ (1 revision)
  7. How to Get Started‏‎ (1 revision)
  8. Knowing Your Community‏‎ (1 revision)
  9. Promoting Research on a Condition‏‎ (1 revision)
  10. Advocacy Organizations List‏‎ (1 revision)
  11. Biobank and Registry External Relations‏‎ (1 revision)
  12. FARA Patient Registry Q & A‏‎ (1 revision)
  13. How to Obtain Donated Office Space‏‎ (1 revision)
  14. Leadership‏‎ (1 revision)
  15. Nonprofit Organization Sample Templates‏‎ (1 revision)
  16. Protecting Member Privacy‏‎ (1 revision)
  17. The Kitchen Table Is a Good Place to Start: Klinefelter Syndrome and Associates‏‎ (1 revision)
  18. Advocacy Resources‏‎ (1 revision)
  19. Biobank and Registry Financial Management‏‎ (1 revision)
  20. Compare Goals and Resources, with the Characteristics of the Condition‏‎ (1 revision)
  21. Developing the Organization That Can Achieve Your Goals‏‎ (1 revision)
  22. FARA Q & A‏‎ (1 revision)
  23. How to Use This Guide‏‎ (1 revision)
  24. Legislation and Policy Advocacy‏‎ (1 revision)
  25. Protecting Message Boards from Spam‏‎ (1 revision)
  26. Results and Individual Follow-up‏‎ (1 revision)
  27. The Power of Advocacy Organizations‏‎ (1 revision)
  28. Articles, Letters, and Other Media for Lay Publication‏‎ (1 revision)
  29. Blogging‏‎ (1 revision)
  30. Disease Advocacy Organization(DAO)‏‎ (1 revision)
  31. Facilitating Quality Research‏‎ (1 revision)
  32. Genetic Privacy‏‎ (1 revision)
  33. How to post a file on WikiAdvocacy‏‎ (1 revision)
  34. Obtaining and Maintaining Registry Data‏‎ (1 revision)
  35. Scholarships for your participants/families/members‏‎ (1 revision)
  36. Translational Science‏‎ (1 revision)
  37. Individual Speaker Recommendations‏‎ (1 revision)
  38. Maintaining Computer Files‏‎ (1 revision)
  39. Orphan Drug Application‏‎ (1 revision)
  40. Setting up Useful Systems‏‎ (1 revision)
  41. Travel‏‎ (1 revision)
  42. Attaining 501(c)(3) Status (Not-For-Profit Determination)‏‎ (1 revision)
  43. Getting Needs on Government and Legislative Agendas‏‎ (1 revision)
  44. Informal Offices or Regional Support Groups‏‎ (1 revision)
  45. Maintaining Your Membership‏‎ (1 revision)
  46. Publisher Recommendations‏‎ (1 revision)
  47. Sharon F. Terry‏‎ (1 revision)
  48. Using Search Tools to Get Found‏‎ (1 revision)
  49. Attending Professionals' Annual Meetings‏‎ (1 revision)
  50. Connecting Organizations‏‎ (1 revision)
  51. Financial Assets‏‎ (1 revision)
  52. Getting Needs onto the Research Agenda‏‎ (1 revision)
  53. Information about Rare Genetic Diseases‏‎ (1 revision)
  54. Matching Resources‏‎ (1 revision)
  55. Overview of WikiAdvocacy‏‎ (1 revision)
  56. Recruiting‏‎ (1 revision)
  57. Vision‏‎ (1 revision)
  58. Considering Starting a Support Group for a Condition that Already Has One?‏‎ (1 revision)
  59. Getting Your Community Interested‏‎ (1 revision)
  60. Media Access‏‎ (1 revision)
  61. Recruiting Celebrities‏‎ (1 revision)
  62. Celebrity Spokesperson‏‎ (1 revision)
  63. Getting Your Needs on Government and Legislative Agendas‏‎ (1 revision)
  64. Intended Goal‏‎ (1 revision)
  65. Media Tips‏‎ (1 revision)
  66. Patient's Bill of Rights‏‎ (1 revision)
  67. Functions of Advocacy Organization‏‎ (2 revisions)
  68. Start Using WikiAdvocacy‏‎ (2 revisions)
  69. Why Go There?‏‎ (2 revisions)
  70. Internet Services: Listserv Guidelines Netiquitte Help‏‎ (2 revisions)
  71. Charity Rating Listings‏‎ (2 revisions)
  72. Benefits of Collaboration with Advocacy Organization Community‏‎ (2 revisions)
  73. Childcare‏‎ (2 revisions)
  74. Working with a Lawyer‏‎ (2 revisions)
  75. Fundraising Appeals‏‎ (2 revisions)
  76. Internet and Web Resources‏‎ (2 revisions)
  77. Biobank Sample Collection‏‎ (2 revisions)
  78. Resources for Nonprofits‏‎ (2 revisions)
  79. Tax and Finance‏‎ (2 revisions)
  80. Clinician- and Researcher-Focused Materials‏‎ (2 revisions)
  81. Genetic Alliance BioBank‏‎ (2 revisions)
  82. Novel Meeting Formats‏‎ (2 revisions)
  83. Publications‏‎ (2 revisions)
  84. Assistive Technology‏‎ (2 revisions)
  85. Connecting Individuals‏‎ (2 revisions)
  86. Family Health History Initiative Guidelines‏‎ (2 revisions)
  87. Sibling Support‏‎ (2 revisions)
  88. Autopsies and Tissue Collection‏‎ (2 revisions)
  89. Consumer Medical Information‏‎ (2 revisions)
  90. Registries‏‎ (2 revisions)
  91. Medical Records‏‎ (3 revisions)
  92. People and Roles‏‎ (3 revisions)
  93. Webinars‏‎ (3 revisions)
  94. Barriers to Rare Disease Research‏‎ (3 revisions)
  95. Educating Membership about Research‏‎ (3 revisions)
  96. Registry and Biobank Weekly Tips‏‎ (3 revisions)
  97. Internet Services: Mailing Lists‏‎ (3 revisions)
  98. Accountants‏‎ (3 revisions)
  99. Helping Your Membership Help Your Group‏‎ (3 revisions)
  100. Children's Hopes and Dreams Foundations‏‎ (3 revisions)

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