Literature DB >> 29066522

Development and progress of the National Congenital Anomaly and Rare Disease Registration Service.

Sarah Stevens1, Nicola Miller1, Jem Rashbass1.   

Abstract

Entities:  

Keywords:  congenital abnorm; data collection; disease registration; public health; rare disease

Mesh：

Year:  2017        PMID： 29066522     DOI： 10.1136/archdischild-2017-312833

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


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  2 in total

Review 1.  Defining and characterising a toolkit for the development of a successful European registry for rare liver diseases: a model for building a rare disease registry.

Authors:  Marinos Pericleous; Claire Kelly; Michael Schilsky; Anil Dhawan; Aftab Ala
Journal:  Clin Med (Lond)       Date:  2022-06-15       Impact factor: 5.410

2.  Prevalence of Down's Syndrome in England, 1998-2013: Comparison of linked surveillance data and electronic health records.

Authors:  J C Doidge; J K Morris; K L Harron; S Stevens; R Gilbert
Journal:  Int J Popul Data Sci       Date:  2020-03-19
  2 in total

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