Page last updated: 2024-08-23

phytanic acid and Charcot-Marie-Tooth Disease, Demyelinating, Type 4f

phytanic acid has been researched along with Charcot-Marie-Tooth Disease, Demyelinating, Type 4f in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Aubourg, P; Kremser, K; Rocchiccioli, F; Roland, MO; Singh, I1
Aubourg, P; Mohr, M; Rocchiccioli, F; Tranchant, C; Warter, JM; Zaenker, C1

Other Studies

2 other study(ies) available for phytanic acid and Charcot-Marie-Tooth Disease, Demyelinating, Type 4f

ArticleYear
Pseudo infantile Refsum's disease: catalase-deficient peroxisomal particles with partial deficiency of plasmalogen synthesis and oxidation of fatty acids.
    Pediatric research, 1993, Volume: 34, Issue:3

    Topics: Acatalasia; Amino Acid Sequence; Cells, Cultured; Diagnosis, Differential; Fatty Acids; Female; Fibroblasts; Hereditary Sensory and Motor Neuropathy; Humans; Infant, Newborn; Intracellular Membranes; Liver; Microbodies; Molecular Sequence Data; Oxidation-Reduction; Phytanic Acid; Plasmalogens; Refsum Disease; Zellweger Syndrome

1993
A new peroxisomal disease with impaired phytanic and pipecolic acid oxidation.
    Neurology, 1993, Volume: 43, Issue:10

    Topics: Adolescent; Adult; Brain; Consanguinity; Electroencephalography; Female; Genetic Carrier Screening; Hereditary Sensory and Motor Neuropathy; Homozygote; Humans; Male; Microbodies; Neural Conduction; Pedigree; Peripheral Nerves; Phytanic Acid; Pipecolic Acids

1993