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Retricted access

Research article

First published 2012-10

Association Between Peroxisomal Biogenesis Factor 7 and Autism Spectrum Disorders in a Korean Population

MyungJa Ro, JungWon Park, Min Nam [...]

Journal of Child Neurology

Retricted access

Research article

First published 1987-10

Peroxisomal Disorders

Dinesh Talwar, Kenneth F. Swaiman

Clinical Pediatrics

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Other

First published 2009-09

Peroxisomal Dysfunction in Inflammatory Childhood White Matter Disorders: An Unexpected Contributor to Neuropathology

Inderjit Singh, Avtar K. Singh, Miguel A. Contreras

Journal of Child Neurology

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Other

First published 1999-07

Diagnosis and Follow-Up of a Case of Peroxisomal Disorder With Peroxisomal Mosaicism

Mercedes Pineda, Marisa Girós, Frank Roels [...]

Journal of Child Neurology

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Review article

First published 2005-04

Topical Review: Molecular and Neurologic Findings of Peroxisome Biogenesis Disorders

Nobuyuki Shimozawa, Tomoko Nagase, Yasuhiko Takemoto [...]

Journal of Child Neurology

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Review article

First published 2004-03

Topical Review: Molecular and Neurologic Findings of Peroxisome Biogenesis Disorders

Nobuyuki Shimozawa, Tomoko Nagase, Yasuhiko Takemoto [...]

Journal of Child Neurology

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Research article

First published 1990-08

Two Siblings with Phenotypes Mimicking Peroxisomal Disorders but with Discordant Biochemical Findings

Jacek J. Pietrzyk, Dorota Turowska-Heydel, Malgorzata Klimek [...]

Clinical Pediatrics

Open access

Research article

First published 2018

Laboratory Diagnosis of Peroxisomal Disorders in the -Omics Era and the Continued Importance of Biomarkers and Biochemical Studies

Ronald J. A. Wanders, Frédéric M. Vaz, Sacha Ferdinandusse [...]

Journal of Inborn Errors of Metabolism and Screening

Open access

Review article

First published 2015

Functions of Peroxisome Proliferator-Activated Receptor Gamma (PPARγ) in Gynecologic Disorders

Ping Ren, Yuquan Zhang, Yan Huang [...]

Clinical Medicine Insights: Oncology

Open access

Research article

First published 2016-11-7

Peroxisome biogenesis disorders

Catherine Argyriou, Maria Daniela D’Agostino, Nancy Braverman

Translational Science of Rare Diseases

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