The Ultra Rare Disease, Disorders, & Disabilities Foundation

Wednesday, 31 December 2014

Patient stem cells used to make dementia-in-a-dish; help identify new treatment strategy

Patient stem cells used to make dementia-in-a-dish; help identify new treatment strategy
Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 09:05 No comments:
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When Your Child’s Rare Disease Has No Cure – The Short Answer - WSJ

When Your Child’s Rare Disease Has No Cure – The Short Answer - WSJ
Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 08:48 No comments:
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Sunday, 7 December 2014

VIDEO: Tony and Mary Heffernan on loss: 'They were immense children... They are still our children, just in a different way' - Independent.ie

VIDEO: Tony and Mary Heffernan on loss: 'They were immense children... They are still our children, just in a different way' - Independent.ie
Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 06:21 No comments:
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Saturday, 6 December 2014

Cellerant to Present Phase 1 Clinical Data on Evaluation of CLT-008 in Patients With Acute Myeloid Leukemia at the 2014 American Society of Hematology Annual Meeting | Orphan Drugs Industry Insider - Oncology

Cellerant to Present Phase 1 Clinical Data on Evaluation of CLT-008 in Patients With Acute Myeloid Leukemia at the 2014 American Society of Hematology Annual Meeting | Orphan Drugs Industry Insider - Oncology
Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 08:38 1 comment:
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Join Incyte and Others to Raise Awareness of Rare Blood Cancers Called Myeloproliferative Neoplasms (MPNs) and Honor MPN Heroes | Orphan Drugs Industry Insider - Oncology

Join Incyte and Others to Raise Awareness of Rare Blood Cancers Called Myeloproliferative Neoplasms (MPNs) and Honor MPN Heroes | Orphan Drugs Industry Insider - Oncology
Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 08:28 No comments:
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Thursday, 4 December 2014

How the Autumn Statement changes the benefits system | Contact a Family

How the Autumn Statement changes the benefits system | Contact a Family
Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 08:24 No comments:
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      • Patient stem cells used to make dementia-in-a-dish...
      • When Your Child’s Rare Disease Has No Cure – The S...
      • VIDEO: Tony and Mary Heffernan on loss: 'They were...
      • Cellerant to Present Phase 1 Clinical Data on Eval...
      • Join Incyte and Others to Raise Awareness of Rare ...
      • How the Autumn Statement changes the benefits syst...
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