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Showing below up to 148 results in range #51 to #198.

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  1. People and Roles‏‎ (3 revisions)
  2. Barriers to Rare Disease Research‏‎ (3 revisions)
  3. Educating Membership about Research‏‎ (3 revisions)
  4. Webinars‏‎ (3 revisions)
  5. Registry and Biobank Weekly Tips‏‎ (3 revisions)
  6. Internet Services: Mailing Lists‏‎ (3 revisions)
  7. Accountants‏‎ (3 revisions)
  8. Helping Your Membership Help Your Group‏‎ (3 revisions)
  9. Fundraising Appeals‏‎ (2 revisions)
  10. Internet and Web Resources‏‎ (2 revisions)
  11. Working with a Lawyer‏‎ (2 revisions)
  12. Biobank Sample Collection‏‎ (2 revisions)
  13. Resources for Nonprofits‏‎ (2 revisions)
  14. Clinician- and Researcher-Focused Materials‏‎ (2 revisions)
  15. Tax and Finance‏‎ (2 revisions)
  16. Genetic Alliance BioBank‏‎ (2 revisions)
  17. Novel Meeting Formats‏‎ (2 revisions)
  18. Publications‏‎ (2 revisions)
  19. Assistive Technology‏‎ (2 revisions)
  20. Connecting Individuals‏‎ (2 revisions)
  21. Family Health History Initiative Guidelines‏‎ (2 revisions)
  22. Sibling Support‏‎ (2 revisions)
  23. Autopsies and Tissue Collection‏‎ (2 revisions)
  24. Consumer Medical Information‏‎ (2 revisions)
  25. Registries‏‎ (2 revisions)
  26. Functions of Advocacy Organization‏‎ (2 revisions)
  27. Internet Services: Listserv Guidelines Netiquitte Help‏‎ (2 revisions)
  28. Start Using WikiAdvocacy‏‎ (2 revisions)
  29. Why Go There?‏‎ (2 revisions)
  30. Charity Rating Listings‏‎ (2 revisions)
  31. Benefits of Collaboration with Advocacy Organization Community‏‎ (2 revisions)
  32. Childcare‏‎ (2 revisions)
  33. Additional/Supplemental Resources‏‎ (1 revision)
  34. History of Advocacy Organizations and Genetic Alliance‏‎ (1 revision)
  35. National Awareness Day‏‎ (1 revision)
  36. Press Kits‏‎ (1 revision)
  37. Research Model 3: Dominant Disorder‏‎ (1 revision)
  38. Choosing Internet Service Provider‏‎ (1 revision)
  39. Events‏‎ (1 revision)
  40. How to: Create a New Wiki Page‏‎ (1 revision)
  41. National Institutes of Health (NIH)‏‎ (1 revision)
  42. Promoting Research‏‎ (1 revision)
  43. Research Models‏‎ (1 revision)
  44. Advocacy‏‎ (1 revision)
  45. Choosing an Internet Service Provider‏‎ (1 revision)
  46. Determine Goals‏‎ (1 revision)
  47. Expertise‏‎ (1 revision)
  48. Genetic Alliance‏‎ (1 revision)
  49. How to Get Started‏‎ (1 revision)
  50. Knowing Your Community‏‎ (1 revision)
  51. Promoting Research on a Condition‏‎ (1 revision)
  52. Advocacy Organizations List‏‎ (1 revision)
  53. Biobank and Registry External Relations‏‎ (1 revision)
  54. FARA Patient Registry Q & A‏‎ (1 revision)
  55. How to Obtain Donated Office Space‏‎ (1 revision)
  56. Leadership‏‎ (1 revision)
  57. Nonprofit Organization Sample Templates‏‎ (1 revision)
  58. Protecting Member Privacy‏‎ (1 revision)
  59. Advocacy Resources‏‎ (1 revision)
  60. Biobank and Registry Financial Management‏‎ (1 revision)
  61. Compare Goals and Resources, with the Characteristics of the Condition‏‎ (1 revision)
  62. Developing the Organization That Can Achieve Your Goals‏‎ (1 revision)
  63. FARA Q & A‏‎ (1 revision)
  64. How to Use This Guide‏‎ (1 revision)
  65. Legislation and Policy Advocacy‏‎ (1 revision)
  66. Protecting Message Boards from Spam‏‎ (1 revision)
  67. Results and Individual Follow-up‏‎ (1 revision)
  68. The Kitchen Table Is a Good Place to Start: Klinefelter Syndrome and Associates‏‎ (1 revision)
  69. Articles, Letters, and Other Media for Lay Publication‏‎ (1 revision)
  70. Blogging‏‎ (1 revision)
  71. Disease Advocacy Organization(DAO)‏‎ (1 revision)
  72. Facilitating Quality Research‏‎ (1 revision)
  73. Genetic Privacy‏‎ (1 revision)
  74. How to post a file on WikiAdvocacy‏‎ (1 revision)
  75. Obtaining and Maintaining Registry Data‏‎ (1 revision)
  76. Scholarships for your participants/families/members‏‎ (1 revision)
  77. The Power of Advocacy Organizations‏‎ (1 revision)
  78. Individual Speaker Recommendations‏‎ (1 revision)
  79. Maintaining Computer Files‏‎ (1 revision)
  80. Orphan Drug Application‏‎ (1 revision)
  81. Translational Science‏‎ (1 revision)
  82. Attaining 501(c)(3) Status (Not-For-Profit Determination)‏‎ (1 revision)
  83. Getting Needs on Government and Legislative Agendas‏‎ (1 revision)
  84. Informal Offices or Regional Support Groups‏‎ (1 revision)
  85. Maintaining Your Membership‏‎ (1 revision)
  86. Publisher Recommendations‏‎ (1 revision)
  87. Setting up Useful Systems‏‎ (1 revision)
  88. Travel‏‎ (1 revision)
  89. Attending Professionals' Annual Meetings‏‎ (1 revision)
  90. Connecting Organizations‏‎ (1 revision)
  91. Financial Assets‏‎ (1 revision)
  92. Getting Needs onto the Research Agenda‏‎ (1 revision)
  93. Information about Rare Genetic Diseases‏‎ (1 revision)
  94. Matching Resources‏‎ (1 revision)
  95. Overview of WikiAdvocacy‏‎ (1 revision)
  96. Recruiting‏‎ (1 revision)
  97. Sharon F. Terry‏‎ (1 revision)
  98. Using Search Tools to Get Found‏‎ (1 revision)
  99. Considering Starting a Support Group for a Condition that Already Has One?‏‎ (1 revision)
  100. Getting Your Community Interested‏‎ (1 revision)
  101. Media Access‏‎ (1 revision)
  102. Recruiting Celebrities‏‎ (1 revision)
  103. Vision‏‎ (1 revision)
  104. Celebrity Spokesperson‏‎ (1 revision)
  105. Getting Your Needs on Government and Legislative Agendas‏‎ (1 revision)
  106. Intended Goal‏‎ (1 revision)
  107. Media Tips‏‎ (1 revision)
  108. Patient's Bill of Rights‏‎ (1 revision)
  109. Available Resources‏‎ (1 revision)
  110. Consumers and Researchers: Making It Work‏‎ (1 revision)
  111. Editing Practice‏‎ (1 revision)
  112. Getting a Biobank or Registry Started‏‎ (1 revision)
  113. Registry Questionnaires‏‎ (1 revision)
  114. Speaker selection and management‏‎ (1 revision)
  115. Characterize Condition‏‎ (1 revision)
  116. Cool Tips‏‎ (1 revision)
  117. Funding‏‎ (1 revision)
  118. Getting an ICD-9 code added for your condition‏‎ (1 revision)
  119. Internet Services‏‎ (1 revision)
  120. Meet Your Neighbors & Organizations‏‎ (1 revision)
  121. Phone Services: Going Beyond the Phone Tree‏‎ (1 revision)
  122. Registry and Biobank Ethics and Governance‏‎ (1 revision)
  123. Accepting Donations‏‎ (1 revision)
  124. Basic Formatting‏‎ (1 revision)
  125. Characterize Resources‏‎ (1 revision)
  126. Councils and Other Advisory Bodies‏‎ (1 revision)
  127. Educating Your Membership about Research‏‎ (1 revision)
  128. Funding Research by Others‏‎ (1 revision)
  129. Harnessing the Resources That Are Hard to Measure‏‎ (1 revision)
  130. Member Dues‏‎ (1 revision)
  131. Planning a Research Conference‏‎ (1 revision)
  132. Accessibility of Tools‏‎ (1 revision)
  133. Becoming the Organization You Imagine‏‎ (1 revision)
  134. Creating New Pages‏‎ (1 revision)
  135. Education of Members, Providers, and the Public‏‎ (1 revision)
  136. Health care Providers and Specialists‏‎ (1 revision)
  137. Mentors‏‎ (1 revision)
  138. Policy Tools & Resources‏‎ (1 revision)
  139. Research Model 1: Recessive Disorder‏‎ (1 revision)
  140. Starting Points for Planning Materials‏‎ (1 revision)
  141. Working Full-Time on Nonprofit‏‎ (1 revision)
  142. Creating a Natural History Survey‏‎ (1 revision)
  143. Emergency Preparedness‏‎ (1 revision)
  144. Internet Services: Websites, Chat Rooms, and Newsgroups‏‎ (1 revision)
  145. NAC Best Practices‏‎ (1 revision)
  146. Preparing for and Handling Publicity‏‎ (1 revision)
  147. Research Model 2: Chromosomal Disorder‏‎ (1 revision)
  148. State-Specific Issues‏‎ (1 revision)

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