Association of Diagnosis of Leukodystrophy With Race and Ethnicity Among Pediatric and Adolescent Patients-Reference-Cited by-同舟云学术

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Association of Diagnosis of Leukodystrophy With Race and Ethnicity Among Pediatric and Adolescent Patients

Published:2018-11-21 Issue:7 Volume:1 Page:e185031
ISSN:2574-3805
Container-title:JAMA Network Open
language:en
Short-container-title:JAMA Netw Open

Author:

Bonkowsky Joshua L.¹²,Wilkes Jacob³,Bardsley Tyler²,Urbik Veronica M.⁴,Stoddard Greg⁵

Affiliation:

1. Brain and Spine Center, Primary Children’s Hospital, Salt Lake City, Utah

2. Department of Pediatrics, University of Utah School of Medicine, Salt Lake City

3. Intermountain Healthcare, Salt Lake City, Utah

4. School of Medicine, University of Utah School of Medicine, Salt Lake City

5. Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City

Publisher

American Medical Association (AMA)

Subject

General Medicine

Link

http:///jamanetworkopen/article-pdf/1/7/e185031/17294412/bonkowsky_2018_oi_180217.pdf

Reference19 articles.

1. The burden of inherited leukodystrophies in children.;Bonkowsky;Neurology,2010

2. Trends in resource utilization by children with neurological impairment in the United States inpatient health care system: a repeat cross-sectional study.;Berry;PLoS Med,2012

3. Leukodystrophy incidence in Germany.;Heim;Am J Med Genet,1997

4. The frequency of lysosomal storage diseases in the Netherlands.;Poorthuis;Hum Genet,1999

5. Adrenoleukodystrophy: incidence, new mutation rate, and results of extended family screening.;Bezman;Ann Neurol,2001

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2. Experiences of patients with metachromatic leukodystrophy, adrenoleukodystrophy, or Krabbe disease and their family members: a qualitative systematic review;JBI Evidence Synthesis;2024-03-28

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4. A systematic review on the birth prevalence of metachromatic leukodystrophy;Orphanet Journal of Rare Diseases;2024-02-21

5. Inventory of current practices regarding hematopoietic stem cell transplantation in metachromatic leukodystrophy in Europe and neighboring countries;Orphanet Journal of Rare Diseases;2024-02-07

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