ScholarWorks@Hanyang University

Orphanet Journal of Rare Diseases  open-access icon

Journal Title

  • Orphanet Journal of Rare Diseases

ISSN

  • P 1750-1172

Publisher

  • BioMed Central

Listed on(Coverage)

JCR 2007-2019
SJR 2007-2019
CiteScore 2011-2019
SCIE 2010-2021
SCOPUS 2017-2020
MEDLINE 2016-2021
DOAJ 2017-2021
EMBASE 2016-2020

OA Info.

OA open-access icon

based on the information

  • 2017;2018;2019;2020;2021;
Keywords rare diseases, orphan drugs
Review Process Blind peer review
Journal info. pages
Licences CC BY, CC0
Copyrights Yes
DOAJ Coverage
  • Added on Date : 2006-03-03T09:12:04Z
Subject(s) Medicine

Active

  • Active

    based on the information

    • SCOPUS:2020-10

Country

  • ENGLAND

Aime & Scopes

  • Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.

Homepage

Article List

1 - 3 out of 3 results.

SCIESCOPUS
Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyteGo to Linkopen access

Choi, Hyoung Soo; Choi, Qute; Kim, Jung-Ah; Im, Kyong Ok; Park, Si Nae; Park, Yoomi; Shin, Hee Young; Kang, Hyoung Jin; Kook, Hoon; Kim, Seon Young, et al.

ArticleIssue Date2019CitationORPHANET JOURNAL OF RARE DISEASES, v.14, no.1PublisherBMC
SCIESCOPUS
Frequency of hereditary neuropathy with liability to pressure palsies (HNPP) due to 17p11.2 deletion in a Korean newborn populationGo to Linkopen access

Park, Jong Eun; Noh, Seung-Jae; Oh, Mijin; Cho, Dae-Yeon; Kim, So Young; Ki, Chang-Seok

ArticleIssue Date2018CitationORPHANET JOURNAL OF RARE DISEASES, v.13, no.1, pp.1 - 4PublisherBIOMED CENTRAL LTD
SCIESCOPUS
Clinical, biochemical and molecular characterization of Korean patients with mucolipidosis II/III and successful prenatal diagnosisGo to Linkopen access

Yang, Mina; Cho, Sung Yun; Park, Hyung-Doo; Choi, Rihwa; Kim, Young Eun; Kim, Jinsup; Lee, Soo-Youn; Ki, Chang-Seok; Kim, Jong-Won; Sohn, Young Bae, et al.

ArticleIssue Date2017CitationOrphanet Journal of Rare Diseases, v.12, pp.1 - 10PublisherBioMed Central
1
CONTACT US

RSS_1.0 RSS_2.0 ATOM_1.0

222, Wangsimni-ro, Seongdong-gu, Seoul, 04763, Korea+82-2-2220-1366

COPYRIGHT © 2024 HANYANG UNIVERSITY.

Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.

BROWSE

한국어