Skip to content
CheckOrphan
  • Home
  • About Us
  • Team
  • Log In
  • News
    • All News
    • Finance
    • Treatment
    • People
  • Videos
  • Treatments
  • Clinical Trials
  • Access Programs
    • All Access Programs
  • Diseases
  • Events
  • Networks
  • Research
Main Menu

Subscribe for Free Newsletter

Email *

Type *

* Required Field
Email Marketing Services by Benchmark

Generate RSS

  1. Home
    2. /
  2. Disease
    3. /
  3. Pseudomongolism

Pseudomongolism

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

  • Stereotactic Body Radiotherapy (SBRT) for Early Treatment of Oligometa
  • Immune and Genomic Markers in ALK+ NSCLC
  • Thulium Laser and KeraFactor for the Treatment of Androgenetic Alopeci
  • Correlation of FFR and iFR With Cardiac PET Perfusion in Patients With
  • Hyaluronic Acid in Counteracting Aphthous Stomatitis
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
Free Newsletter

Tools

Subscribe to our newsletter

Email Alerts

Rss Feeds

Print this page

Follow us on:

pw

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.
Click here to know more About Us

Your email is important to us

Each email is sent to a CheckOrphan staff member and will be answered. We only use a contact form to avoid spam.

    Copyright © 2021 CheckOrphan.
    Developed by: Gonza.io logo Powered by: Cloudscale logo