Gas chromatography/mass spectrometry analysis of very long chain fatty acids, docosahexaenoic acid, phytanic acid and plasmalogen for the screening of peroxisomal disorders

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Quantitative Determination of Plasma C8–C26 Total Fatty Acids for the Biochemical Diagnosis of Nutritional and Metabolic Disorders

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The Role of Dietary n–6 and n–3 Fatty Acids in the Developing Brain

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Pseudo-Zellweger syndrome: Deficiencies in several peroxisomal oxidative activities

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Odd-numbered very-long-chain fatty acids from the microbial, animal and plant kingdoms

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Meibomian glands, meibum, and meibogenesis

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The genetic landscape of X-linked adrenoleukodystrophy: inheritance, mutations, modifier genes, and diagnosis

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Induction of oxiapoptophagy on 158N murine oligodendrocytes treated by 7-ketocholesterol-, 7β-hydroxycholesterol-, or 24(S)-hydroxycholesterol: Protective effects of α-tocopherol and docosahexaenoic acid (DHA; C22:6 n-3)

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Evidence of oxidative stress in very long chain fatty acid – Treated oligodendrocytes and potentialization of ROS production using RNA interference-directed knockdown of ABCD1 and ACOX1 peroxisomal proteins

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Combined Analysis of Metabolomes, Proteomes, and Transcriptomes of Hepatitis C Virus–Infected Cells and Liver to Identify Pathways Associated With Disease Development

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Outcomes of Unrelated Umbilical Cord Blood Transplantation for X-Linked Adrenoleukodystrophy

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Plasma fatty acid profiles in autism: A case-control study

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Measuring brain lipids

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Direct Microwave Transesterification of Fingertip Prick Blood Samples for Fatty Acid Determinations

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Induction of Mitochondrial Changes Associated with Oxidative Stress on Very Long Chain Fatty Acids (C22:0, C24:0, or C26:0)-Treated Human Neuronal Cells (SK-NB-E)

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Identification of a new complementation group of the peroxisome biogenesis disorders andPEX14 as the mutated gene

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The Proportion of Nervonic Acid in Serum Lipids is Associated with Serum Plasmalogen Levels and Metabolic Syndrome

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n-3 Polyunsaturated Fatty Acids Do Not Alter Immune and Inflammation Measures in Endurance Athletes

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Fatty Acid Profiles in Demented Patients: Identification of Hexacosanoic Acid (C26:0) as a Blood Lipid Biomarker of Dementia

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Overexpression of Peroxisome Proliferator-activated Receptor-α (PPARα)-regulated Genes in Liver in the Absence of Peroxisome Proliferation in Mice Deficient in both l- and d-Forms of Enoyl-CoA Hydratase/Dehydrogenase Enzymes of Peroxisomal β-Oxidation System

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Molecular and clinical aspects of peroxisomal diseases

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Metabolomics to Improve the Diagnostic Efficiency of Inborn Errors of Metabolism

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Peroxisomal Disorders: A Review on Cerebellar Pathologies

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Incidence of Abcd1 level on the induction of cell death and organelle dysfunctions triggered by very long chain fatty acids and TNF-α on oligodendrocytes and astrocytes

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Serum Fatty Acids and Cardiovascular Risk Factors in Sudden Sensorineural Hearing Loss: A Case-Control Study

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A modified Girard derivatizing reagent for universal profiling and trace analysis of aldehydes and ketones by electrospray ionization tandem mass spectrometry

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Tysnd1 Deficiency in Mice Interferes with the Peroxisomal Localization of PTS2 Enzymes, Causing Lipid Metabolic Abnormalities and Male Infertility

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Incomplete pediatric reference intervals for the management of patients with inborn errors of metabolism

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Laboratory diagnosis of disorders of peroxisomal biogenesis and function: a technical standard of the American College of Medical Genetics and Genomics (ACMG)

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Molecular and clinical findings and diagnostic flowchart of peroxisomal diseases

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Contiguous ABCD1 DXS1357E deletion syndrome: Report of an autopsy case

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Advanced Diagnostic System and Introduction of Newborn Screening of Adrenoleukodystrophy and Peroxisomal Disorders in Japan

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Impact of 7‐ketocholesterol and very long chain fatty acids on oligodendrocyte lipid membrane organization: Evaluation via LAURDAN and FAMIS spectral image analysis

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Detection of unusual very-long-chain fatty acid and ether lipid derivatives in the fibroblasts and plasma of patients with peroxisomal diseases using liquid chromatography-mass spectrometry

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Aberrant peroxisome morphology in peroxisomal beta-oxidation enzyme deficiencies

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Integrative metabolomics as emerging tool to study autophagy regulation

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X-linked adrenoleukodystrophy: Diagnostic and follow-up system in Japan

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Determination of choline and ethanolamine plasmalogens in human plasma by HPLC using radioactive triiodide (1-) ion (125I3−)

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Newly identified milder phenotype of peroxisome biogenesis disorder caused by mutated PEX3 gene

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Measurement of Ether Phospholipids in Human Plasma with HPLC–ELSD and LC/ESI–MS After Hydrolysis of Plasma with Phospholipase A1

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Modulation of Kv3.1b potassium channel level and intracellular potassium concentration in 158N murine oligodendrocytes and BV-2 murine microglial cells treated with 7-ketocholesterol, 24S-hydroxycholesterol or tetracosanoic acid (C24:0)

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Identification of long and very long chain fatty acids, plasmalogen-C16:0 and phytanic acid as new lipid biomarkers in Tunisian coronary artery disease patients

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Association of serum eicosapentaenoic acid to arachidonic acid ratio with microalbuminuria in a population of community-dwelling Japanese

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Hexacosenoyl-CoA is the most abundant very long-chain acyl-CoA in ATP binding cassette transporter D1-deficient cells

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X-linked Adrenoleukodystrophy

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Mild Zellweger syndrome due to functionally confirmed novel PEX1 variants

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A Novel Double Mutation in the ABCD1 Gene in a Patient with X-linked Adrenoleukodystrophy: Analysis of the Stability and Function of the Mutant ABCD1 Protein

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A mutation in PEX19 causes a severe clinical phenotype in a patient with peroxisomal biogenesis disorder

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Mild Zellweger syndrome due to a novel PEX6 mutation: correlation between clinical phenotype and in silico prediction of variant pathogenicity

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Dual effect of docosahexaenoic acid (attenuation or amplification) on C22:0-, C24:0-, and C26:0-Induced mitochondrial dysfunctions and oxidative stress on human neuronal SK-N-BE cells

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Ataxic form of autosomal recessive PEX10-related peroxisome biogenesis disorders with a novel compound heterozygous gene mutation and characteristic clinical phenotype

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Novel ACOX1 mutations in two siblings with peroxisomal acyl-CoA oxidase deficiency

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Atypical PEX16 peroxisome biogenesis disorder with mild biochemical disruptions and long survival

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Treatment of an adrenomyeloneuropathy patient with Lorenzo's oil and supplementation with docosahexaenoic acid-A case report

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Evidence of oxidative stress in peroxisomal disorders.

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Peroxisomal disorders

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Development of a Method for Measuring Phytanic Acid as a Lifestyle-related Disease Biomarker in Rat Serum Using Ultra-fast Liquid Chromatography-Ultraviolet Spectrophotometry Combined with a Modified 2-Nitrophenylhydrazine Derivatization Method

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Expanding the concept of peroxisomal diseases and efficient diagnostic system in Japan

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Sensitive change of iso-branched fatty acid (iso-15:0) in Bacillus pumilus PAMC 23174 in response to environmental changes

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Quantitative analyses of essential fatty acids in cereals and green vegetables by isotope dilution-gas chromatography/mass spectrometry

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Clinical aspects and adrenal functions in eleven Japanese children with X-linked adrenoleukodystrophy

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Screening for essential fatty acid deficiency in at risk infants

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Effect of Lorenzo’s Oil on Hepatic Gene Expression and the Serum Fatty Acid Level in abcd1-Deficient Mice

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Exogenous Addition of 25‐Hydroxycholesterol Reduces Level of Very Long‐Chain Fatty Acids in X‐Linked Adrenoleukodystrophy

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Mobile Messaging Through Android Phones: An Empirical Study to Unveil the Reasons Behind the Most Preferred Mobile Messaging Application Used by College Going StudentsPreprint

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Polyunsaturated fatty acid levels in rat tissues after chronic treatment with dietetic oils

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Diagnosis of Peroxisomal Disorders

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Suitability of selected chromatographic columns for analysis of fatty acids in dialyzed patients

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Maternal intake of docosahexaenoic acid decreased febrile seizure sensitivity by increasing estrogen synthesis in offspring

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HPLC ANALYSIS OF n‐3 AND n‐6 FATTY ACID LEVELS IN RAT SERUM AFTER CHRONIC TREATMENT WITH DIETETIC OILS

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Management of X-linked adrenoleukodystrophy in Morocco: actual situation

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Strange Phospholipids

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LC-MS Based Platform Simplifies Access to Metabolomics for Peroxisomal Disorders

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小児内分泌

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Peroxisome dysfunction alters metabolism of photoreceptor outer segments in human retinal pigment epitheliumPreprint

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Global approach of lipid metabolism in Age-Related Macular Degeneration (AMD)

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