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Showing below up to 100 results in range #1 to #100.

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  1. Additional/Supplemental Resources‏‎ (1 revision)
  2. History of Advocacy Organizations and Genetic Alliance‏‎ (1 revision)
  3. National Awareness Day‏‎ (1 revision)
  4. Press Kits‏‎ (1 revision)
  5. Research Model 3: Dominant Disorder‏‎ (1 revision)
  6. Choosing Internet Service Provider‏‎ (1 revision)
  7. Events‏‎ (1 revision)
  8. How to: Create a New Wiki Page‏‎ (1 revision)
  9. National Institutes of Health (NIH)‏‎ (1 revision)
  10. Promoting Research‏‎ (1 revision)
  11. Research Models‏‎ (1 revision)
  12. Advocacy‏‎ (1 revision)
  13. Choosing an Internet Service Provider‏‎ (1 revision)
  14. Determine Goals‏‎ (1 revision)
  15. Expertise‏‎ (1 revision)
  16. Genetic Alliance‏‎ (1 revision)
  17. How to Get Started‏‎ (1 revision)
  18. Knowing Your Community‏‎ (1 revision)
  19. Promoting Research on a Condition‏‎ (1 revision)
  20. Advocacy Organizations List‏‎ (1 revision)
  21. Biobank and Registry External Relations‏‎ (1 revision)
  22. FARA Patient Registry Q & A‏‎ (1 revision)
  23. How to Obtain Donated Office Space‏‎ (1 revision)
  24. Leadership‏‎ (1 revision)
  25. Nonprofit Organization Sample Templates‏‎ (1 revision)
  26. Protecting Member Privacy‏‎ (1 revision)
  27. Advocacy Resources‏‎ (1 revision)
  28. Biobank and Registry Financial Management‏‎ (1 revision)
  29. Compare Goals and Resources, with the Characteristics of the Condition‏‎ (1 revision)
  30. Developing the Organization That Can Achieve Your Goals‏‎ (1 revision)
  31. FARA Q & A‏‎ (1 revision)
  32. How to Use This Guide‏‎ (1 revision)
  33. Legislation and Policy Advocacy‏‎ (1 revision)
  34. Protecting Message Boards from Spam‏‎ (1 revision)
  35. Results and Individual Follow-up‏‎ (1 revision)
  36. The Kitchen Table Is a Good Place to Start: Klinefelter Syndrome and Associates‏‎ (1 revision)
  37. Articles, Letters, and Other Media for Lay Publication‏‎ (1 revision)
  38. Blogging‏‎ (1 revision)
  39. Disease Advocacy Organization(DAO)‏‎ (1 revision)
  40. Facilitating Quality Research‏‎ (1 revision)
  41. Genetic Privacy‏‎ (1 revision)
  42. How to post a file on WikiAdvocacy‏‎ (1 revision)
  43. Obtaining and Maintaining Registry Data‏‎ (1 revision)
  44. Scholarships for your participants/families/members‏‎ (1 revision)
  45. The Power of Advocacy Organizations‏‎ (1 revision)
  46. Individual Speaker Recommendations‏‎ (1 revision)
  47. Maintaining Computer Files‏‎ (1 revision)
  48. Orphan Drug Application‏‎ (1 revision)
  49. Translational Science‏‎ (1 revision)
  50. Attaining 501(c)(3) Status (Not-For-Profit Determination)‏‎ (1 revision)
  51. Getting Needs on Government and Legislative Agendas‏‎ (1 revision)
  52. Informal Offices or Regional Support Groups‏‎ (1 revision)
  53. Maintaining Your Membership‏‎ (1 revision)
  54. Publisher Recommendations‏‎ (1 revision)
  55. Setting up Useful Systems‏‎ (1 revision)
  56. Travel‏‎ (1 revision)
  57. Attending Professionals' Annual Meetings‏‎ (1 revision)
  58. Connecting Organizations‏‎ (1 revision)
  59. Financial Assets‏‎ (1 revision)
  60. Getting Needs onto the Research Agenda‏‎ (1 revision)
  61. Information about Rare Genetic Diseases‏‎ (1 revision)
  62. Matching Resources‏‎ (1 revision)
  63. Overview of WikiAdvocacy‏‎ (1 revision)
  64. Recruiting‏‎ (1 revision)
  65. Sharon F. Terry‏‎ (1 revision)
  66. Using Search Tools to Get Found‏‎ (1 revision)
  67. Considering Starting a Support Group for a Condition that Already Has One?‏‎ (1 revision)
  68. Getting Your Community Interested‏‎ (1 revision)
  69. Media Access‏‎ (1 revision)
  70. Recruiting Celebrities‏‎ (1 revision)
  71. Vision‏‎ (1 revision)
  72. Celebrity Spokesperson‏‎ (1 revision)
  73. Getting Your Needs on Government and Legislative Agendas‏‎ (1 revision)
  74. Intended Goal‏‎ (1 revision)
  75. Media Tips‏‎ (1 revision)
  76. Patient's Bill of Rights‏‎ (1 revision)
  77. Available Resources‏‎ (1 revision)
  78. Consumers and Researchers: Making It Work‏‎ (1 revision)
  79. Editing Practice‏‎ (1 revision)
  80. Getting a Biobank or Registry Started‏‎ (1 revision)
  81. Registry Questionnaires‏‎ (1 revision)
  82. Speaker selection and management‏‎ (1 revision)
  83. Characterize Condition‏‎ (1 revision)
  84. Cool Tips‏‎ (1 revision)
  85. Funding‏‎ (1 revision)
  86. Getting an ICD-9 code added for your condition‏‎ (1 revision)
  87. Internet Services‏‎ (1 revision)
  88. Meet Your Neighbors & Organizations‏‎ (1 revision)
  89. Phone Services: Going Beyond the Phone Tree‏‎ (1 revision)
  90. Registry and Biobank Ethics and Governance‏‎ (1 revision)
  91. Accepting Donations‏‎ (1 revision)
  92. Basic Formatting‏‎ (1 revision)
  93. Characterize Resources‏‎ (1 revision)
  94. Councils and Other Advisory Bodies‏‎ (1 revision)
  95. Educating Your Membership about Research‏‎ (1 revision)
  96. Funding Research by Others‏‎ (1 revision)
  97. Harnessing the Resources That Are Hard to Measure‏‎ (1 revision)
  98. Member Dues‏‎ (1 revision)
  99. Planning a Research Conference‏‎ (1 revision)
  100. Accessibility of Tools‏‎ (1 revision)

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