Rethinking the nonprofit foundation: an emerging niche in the rare disease ecosystem.

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Rethinking the nonprofit foundation: an emerging niche in the rare disease ecosystem.

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2017 nî lūn-bûn

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2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

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2017年论文

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2017年论文

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Rethinking the nonprofit foundation: an emerging niche in the rare disease ecosystem.

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Rethinking the nonprofit foundation: an emerging niche in the rare disease ecosystem.

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Rethinking the nonprofit foundation: an emerging niche in the rare disease ecosystem.

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P1476

Rethinking the nonprofit foundation: an emerging niche in the rare disease ecosystem

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P2093

Annette C Bakker

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Salvatore La Rosa

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P2860

Characterization and utilization of an international neurofibromatosis web-based, patient-entered registry: An observational study.

Activity of Selumetinib in Neurofibromatosis Type 1-Related Plexiform Neurofibromas

Achieving consensus for clinical trials: the REiNS International Collaboration.

A high-throughput molecular data resource for cutaneous neurofibromas.

MEK inhibition exhibits efficacy in human and mouse neurofibromatosis tumors.

Patient-driven search for rare disease therapies: the Fondazione Telethon success story and the strategy leading to Strimvelis.

The National Disease Research Interchange and Collaborators on: What Are the Major Hurdles to the Recovery of Human Tissue to Advance Research?

The path forward: 2015 International Children's Tumor Foundation conference on neurofibromatosis type 1, type 2, and schwannomatosis.

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1179-1182

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scholarly article

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10.15252/EMMM.201708203

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Salvatore La Rosa

Annette Bakker

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2017-09-01T00:00:00Z

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28743783

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ecosystem

rare disease

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5582408

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