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  3. Pulmonary artery familial dilatation

Pulmonary artery familial dilatation

December 31, 2014

News

  • Rare Disease Companies Unite to Advocate for Life-Changing Therapies
  • Acentrus Specialty Contracts with Chiasma to Bring MYCAPSSA® (octreot
  • Exicure Announces Appointment of Brian C. Bock as Chief Financial Offi
  • AGTC Announces Expansion of Manufacturing and Analytics Capabilities t
  • Fate Therapeutics Announces Encouraging Interim Phase 1 Data for iPSC-
More News

Treatment

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

Clinical Trial

  • Micromegaly and Discrepancy Between Growth Hormone and IGF1 at the Dia
  • Observational Study of Patients Suffering From Endometriosis and Adeno
  • Long Term Follow-up Observational Study After Clinical Trials of AMG53
  • Pharmacokinetic and Safety Study of MRX-2843 in Adolescents and Adults
  • Hong Kong Follow up Protocol After EUS Gallbladder Drainage for Acute
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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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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