
自引率: 5.6%
被引量: 7494
通过率: 暂无数据
审稿周期: 3.8
版面费用: 暂无数据
国人发稿量: 13
投稿须知/期刊简介:
Published by BioMed Central. ISSN: 1750-1172.<br /><br />Orphanet Journal of Rare Diseases is an open access, peer-reviewed online journal that encompasses all aspects of rare diseases and orphan drugs. The journal welcomes high quality review articles encompassing all aspects of diagnosis, clinical description, clinical work-up and management as well as aetiopathogenesis, *epidemiology, and genetic counselling of rare diseases. It brings together knowledge of basic research and clinical practice. By providing this information, crucial for optimised diagnosis and management, the Orphanet Journal of Rare Diseases aims to contribute to the improved care of patients affected by rare diseases. The journal provides researchers and clinicians with the opportunity to publish state of the art developments in the area of rare diseases and orphan drugs as well as to publish new syndromes and results of clinical trials including those with negative results.
期刊描述简介:
Published by BioMed Central. ISSN: 1750-1172. Orphanet Journal of Rare Diseases is an open access, peer-reviewed online journal that encompasses all aspects of rare diseases and orphan drugs. The journal welcomes high quality review articles encompassing all aspects of diagnosis, clinical description, clinical work-up and management as well as aetiopathogenesis, *epidemiology, and genetic counselling of rare diseases. It brings together knowledge of basic research and clinical practice. By providing this information, crucial for optimised diagnosis and management, the Orphanet Journal of Rare Diseases aims to contribute to the improved care of patients affected by rare diseases. The journal provides researchers and clinicians with the opportunity to publish state of the art developments in the area of rare diseases and orphan drugs as well as to publish new syndromes and results of clinical trials including those with negative results.
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Redefining the phenotype of alpha-methylacyl-CoA racemase (AMACR) deficiency.
被引量:- 发表:1970
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Functional benefit of joint surgery in patients with non-vascular Ehlers-Danlos syndrome: results of a retrospective study.
被引量:- 发表:1970
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Economic burden and health-related quality of life in patients with epidermolysis bullosa in Spain.
被引量:1 发表:1970
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Clinical and genetic characteristics of 100 consecutive patients with Birt-Hogg-Dubé syndrome in Eastern Chinese region.
被引量:- 发表:1970
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International expert opinion on the considerations for combining vosoritide and limb surgery: a modified delphi study.
被引量:- 发表:1970