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Search Results for 'Rare Disease Patient Registries Represent A Fundamental Rese'
Rare Disease Patient Registries represent a fundamental research effor
liane-varnes
www.orpha.net
jane-oiler
RARE / ORPHAN
marina-yarberry
October RDLA Lunch Meeting/Webinar
tawny-fly
Patient Registries
luanne-stotts
Management of Rare Diseases: An Integrated Approach to Break Down Barriers and Facilitate
tatiana-dople
Community Congress Introductory Webinar
karlyn-bohler
Improving the process of rare disease treatment development
lindy-dunigan
Accessing the Accelerated Approval Pathway with a Rare Neur
karlyn-bohler
Toolkit #1: What is Rare Action Network?
aaron
The Indian Council of Medical Research initiated a network of cancer registries under
trish-goza
February 29-March3, 2016
min-jolicoeur
GRDR Update Webinar Tiina Urv, PhD
sherrill-nordquist
Rare Disease Patient and Ethics Council (RD-PEC)
celsa-spraggs
Going Beyond the Current Regulatory and Incentives Framewor
calandra-battersby
Quality
marina-yarberry
Genetic Basis of Human Disease and
jane-oiler
Registries Recording, Enumerating Creative Claims
tatyana-admore
Genetic Approaches to Rare Diseases:
alida-meadow
Tackling Rare Diseases
conchita-marotz
Rare Action network
karlyn-bohler
Analysis of imputed rare variants
celsa-spraggs
Pilot survey on on-line patient registries
trish-goza
The True Mother of Invention
mitsue-stanley
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