Diagnosis, treatment, and research status of rare diseases related to birth defects-Reference-Cited by-同舟云学术

Diagnosis, treatment, and research status of rare diseases related to birth defects

Published:2023-08-31 Issue:3 Volume:12 Page:148-160
ISSN:2186-361X
Container-title:Intractable & Rare Diseases Research
language:en
Short-container-title:IRDR

Author:

Zhao Hongjuan¹,Du Chen²,Yang Guang³,Wang Yu²

Affiliation:

1. Department of Gynecology and Obstetrics, Shandong Provincial Third Hospital, Shandong University, Ji'nan, China.

2. Department of Gynecology and Obstetrics, Inner Mongolia Medical University Affiliated Hospital, Hohhot, China.

3. Department of General Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Publisher

International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA)

Subject

General Medicine

Link

https://www.jstage.jst.go.jp/article/irdr/12/3/12_2023.01052/_pdf

Reference83 articles.

1. 1. Luzzatto L, Hyry HI, Schieppati A, Costa E, Simoens S, Schaefer F, Roos JCP, Merlini G, Kaariainen H, Garattini S, Hollak CE, Remuzzi G, Second Workshop on Orphan Drugs p. Outrageous prices of orphan drugs: A call for collaboration. Lancet. 2018; 392:791-794.

2. 2. Gunne E, McGarvey C, Hamilton K, Treacy E, Lambert DM, Lynch SA. A retrospective review of the contribution of rare diseases to paediatric mortality in Ireland. Orphanet J Rare Dis. 2020; 15:311.

3. 3. Rare Diseases International. UN resolution on persons living with a rare disease. https://www.rarediseasesinternational.org/un-resolution/ (accessed May 20, 2023).

4. 4. He J, Tang M, Zhang X, Chen D, Kang Q, Yang Y, Hu J, Jin C, Song P. Incidence and prevalence of 121 rare diseases in China: Current status and challenges. Intractable Rare Dis Res. 2019; 8:89-97.

5. 5. Nguengang Wakap S, Lambert DM, Olry A, Rodwell C, Gueydan C, Lanneau V, Murphy D, Le Cam Y, Rath A. Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet database. Eur J Hum Genet. 2020; 28:165-173.