Geographic and Specialty Access Disparities in US Pediatric Leukodystrophy Diagnosis-Reference-Cited by-同舟云学术

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Geographic and Specialty Access Disparities in US Pediatric Leukodystrophy Diagnosis

Published:2020-05 Issue: Volume:220 Page:193-199
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Grineski Sara,Morales Danielle X.,Collins Timothy,Wilkes Jacob,Bonkowsky Joshua L.

Funder

National Institutes of Health

Bray Presidential Chair in Child Neurology Research

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference28 articles.

1. Emergence of pediatric rare diseases: review of present policies and opportunities for improvement;Bavisetty;Rare Dis,2013

2. The burden of genetic disease on inpatient care in a children's hospital;McCandless;Am J Hum Genet,2004

3. Rare diseases, orphan drugs and their regulation: questions and misconceptions;Tambuyzer;Nat Rev Drug Discov,2010

4. Deep sequencing of patient genomes for disease diagnosis: when will it become routine?;Kingsmore;Sci Transl Med,2011

5. The National Institutes of Health Undiagnosed Diseases Program: insights into rare diseases;Gahl;Genet Med,2012

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Impact on physical, social, and family functioning of patients with metachromatic leukodystrophy and their family members in Japan: A qualitative study;Molecular Genetics and Metabolism Reports;2024-03

2. The impacts of adrenoleukodystrophy newborn screening on the evaluation of adrenal dysfunction in male children: An integrative literature review;Journal of Pediatric Nursing;2023-09

3. An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases;Nature Communications;2022-07-26

4. Time to Transplant in X-Linked Adrenoleukodystrophy;Journal of Child Neurology;2022-03-03

5. National U.S. Patient and Transplant Data for Krabbe Disease;Frontiers in Pediatrics;2021-11-11

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