Literature DB >> 18684747

Rare childhood diseases: how should we respond?

Y Zurynski1, K Frith, H Leonard, E Elliott.   

Abstract

Paradoxically, rare diseases are common, collectively affecting 6-10% of the population and have a huge impact on patients and families, health services, clinicians and the wider community. Accurate data are required to inform clinical practice, government policy and health service planning. We recommend a national approach, similar to that adopted in the USA and Europe, to support research and promote advocacy and equitable access to services for children with rare diseases.

Entities:  

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Year:  2008        PMID: 18684747     DOI: 10.1136/adc.2007.134940

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


  33 in total

1.  Factors Associated with Parental Adaptation to Children with an Undiagnosed Medical Condition.

Authors:  Tatiane Yanes; Linda Humphreys; Aideen McInerney-Leo; Barbara Biesecker
Journal:  J Genet Couns       Date:  2016-12-30       Impact factor: 2.537

2.  Exploring the genetic counselor's role in facilitating meaning-making: rare disease diagnoses.

Authors:  Benjamin M Helm
Journal:  J Genet Couns       Date:  2015-01-08       Impact factor: 2.537

3.  ClinGen's GenomeConnect registry enables patient-centered data sharing.

Authors:  Juliann M Savatt; Danielle R Azzariti; W Andrew Faucett; Steven Harrison; Jennifer Hart; Brandi Kattman; Melissa J Landrum; David H Ledbetter; Vanessa Rangel Miller; Emily Palen; Heidi L Rehm; Jud Rhode; Stefanie Turner; Jo Anne Vidal; Karen E Wain; Erin Rooney Riggs; Christa Lese Martin
Journal:  Hum Mutat       Date:  2018-11       Impact factor: 4.878

4.  Factors influencing practice variation in the management of nephrotic syndrome: a qualitative study of pediatric nephrology care providers.

Authors:  Susan M Samuel; Rachel Flynn; Michael Zappitelli; Allison Dart; Rulan Parekh; Maury Pinsk; Cherry Mammen; Andrew Wade; Shannon D Scott
Journal:  CMAJ Open       Date:  2017-06-07

Review 5.  Disease registries and outcomes research in children: focus on lysosomal storage disorders.

Authors:  Simon Jones; Emma James; Suyash Prasad
Journal:  Paediatr Drugs       Date:  2011-02-01       Impact factor: 3.022

6.  Pharmacotherapy challenges of Fontan-associated plastic bronchitis: a rare pediatric disease.

Authors:  Kristina Brooks; Regine L Caruthers; Kurt R Schumacher; Kathleen A Stringer
Journal:  Pharmacotherapy       Date:  2013-05-17       Impact factor: 4.705

7.  Delays in diagnosis of nephrotic syndrome in children: A survey study.

Authors:  Asha Hollis; Allison Dart; Catherine Morgan; Cherry Mammen; Michael Zappitelli; Rahul Chanchlani; Susan Samuel
Journal:  Paediatr Child Health       Date:  2018-12-28       Impact factor: 2.253

Review 8.  Genetic Counseling and Genome Sequencing in Pediatric Rare Disease.

Authors:  Alison M Elliott
Journal:  Cold Spring Harb Perspect Med       Date:  2020-03-02       Impact factor: 6.915

Review 9.  Being the Pillar for Children with Rare Diseases-A Systematic Review on Parental Quality of Life.

Authors:  Johannes Boettcher; Michael Boettcher; Silke Wiegand-Grefe; Holger Zapf
Journal:  Int J Environ Res Public Health       Date:  2021-05-08       Impact factor: 3.390

10.  Key outcomes from stakeholder workshops at a symposium to inform the development of an Australian national plan for rare diseases.

Authors:  Caron Molster; Leanne Youngs; Emma Hammond; Hugh Dawkins
Journal:  Orphanet J Rare Dis       Date:  2012-08-10       Impact factor: 4.123

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