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Rare Diseases Volume 1, 2013 - Issue 1

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Editorial

Introducing Rare Diseases

Patricia Szajner Landes Bioscience; Boston, MA USACorrespondence[email protected] [email protected]

Timur Yusufzai Harvard Medical School; Boston, MA USACorrespondence[email protected] [email protected]

Article: e24735 | Received 16 Apr 2013, Accepted 16 Apr 2013, Published online: 18 Apr 2013

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https://doi.org/10.4161/rdis.24735

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Articles from other publishers (6)

Mariana Carvalho de Moraes, Ivone Duarte & Rui Nunes. (2023) Assistance and Delivery of COVID-19 Vaccinations to Patients with Rare Diseases. Healthcare 11:20, pages 2781.
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Asma Naseem, Zohar Steinberg & Alessia Cavazza. (2022) Genome editing for primary immunodeficiencies: A therapeutic perspective on Wiskott-Aldrich syndrome. Frontiers in Immunology 13.
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Arun Pradhan, Tanya V. Kalin & Vladimir V. Kalinichenko. (2020) Genome Editing for Rare Diseases. Current Stem Cell Reports 6:3, pages 41-51.
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Elias L. Salfati, Emily G. Spencer, Sarah E. Topol, Evan D. Muse, Manuel Rueda, Jonathan R. Lucas, Glenn N. Wagner, Steven Campman, Eric J. Topol & Ali Torkamani. (2019) Re-analysis of whole-exome sequencing data uncovers novel diagnostic variants and improves molecular diagnostic yields for sudden death and idiopathic diseases. Genome Medicine 11:1.
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Panayiota Papasavva, Marina Kleanthous & Carsten W. Lederer. (2019) Rare Opportunities: CRISPR/Cas-Based Therapy Development for Rare Genetic Diseases. Molecular Diagnosis & Therapy 23:2, pages 201-222.
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Zh. P. Kravchuk & O. A. Rumyantseva. (2013) ORPHAN DISEASES: DIAGNOSIS, PROBLEMS, PROSPECTS. Health and Ecology Issues:4, pages 7-11.
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