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  5. Chromosome 21- uniparental disomy...

Chromosome 21- uniparental disomy of

December 31, 2014

News

  • Marinus Pharmaceuticals Announces Delay to RAISE Phase 3 Clinical Tria
  • Gene therapy for thalassemia ends need for transfusions in young child
  • City of Hope awarded $4.9 million from CIRM to train future leaders in
  • The Lancet Child & Adolescent Health: Multi-system inflammatory s
  • Exercise reduces anxiety during active surveillance for prostate cance
More News

Treatment

  • Flunarizine hydrochloride
  • Everolimus
  • Eribulin mesylate
  • Dexamethasone phosphate
  • Dantrolene sodium
More Treatment

Clinical Trial

  • Sham LaserCap vs. LaserCap SD vs. LaserCap HD+
  • Comparison Between Efficacy of Topical Sildenafil 2% and Topical Minox
  • The Prevelence of IVS 1-6 (T-C) [HBB:c.92 +6 T-C] Gene Mutation in Sus
  • Validation of a Simplified Severity Score (Investigator Global Assessm
  • A Phase 2 Study Evaluating Efficacy, Safety and Tolerability of Differ
More Clinical Trial

Access Program

  • Jonsson Comprehensive Cancer Center – Progressive Metastatic Cas
  • Massachusetts General Hospital – Healthy Naturally Cycling Women
  • Kite, A Gilead Company – Relapsed/Refractory Transformed Follicu
  • Kite, A Gilead Company – Relapsed/Refractory Primary Mediastinal
  • Kite, A Gilead Company – Relapsed/Refractory High-Grade B-Cell L
More Access Program

Disease

  • Neonatal alloimmune thrombocytopenia
  • Ubiquitin Disorder
  • Pseudo-Zellweger syndrome
  • Pseudoxanthoma elasticum- dominant form
  • Pseudoxanthoma elasticum- recessive form
More Disease

Research

  • Diagnostic Efficacy of Digital Dermoscopy and Clinical Findings in Thi
  • Differences in Characteristics and Outcomes Between Asian and Non-Asia
  • Arthropathy, osteolysis, keloids, relapsing conjunctival pannus and gi
  • Fetal akinesia deformation sequence due to a congenital disorder of gl
  • One case of torsades de pointes with Aase’s syndrome induced by
More Research

Network

  • Cures Within Reach
  • NGLY1.org
  • The Twin to Twin Transfusion Syndrome Foundation
  • Fetal Health Foundation
  • Plus One Foundation
More Network
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About CheckOrphan

CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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