phytanic acid has been researched along with Intellectual Disability in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (20.00) | 18.7374 |
| 1990's | 3 (60.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Christensen, E; Ferdinandusse, S; Gootjes, J; Skovby, F; Wanders, RJ | 1 |
| Barth, PG; Schutgens, RB; Staalman, CR; Wanders, RJ | 1 |
| Hakkola, E; Hiltunen, K; Kilponen, J; Palosaari, P | 1 |
| Carroll, JE; Hahn, DA; Rizzo, WB; Roesel, RA; van der Zalm, T | 1 |
| Björkhem, I; Ek, J; Kase, BF; Pedersen, JI; Reith, A | 1 |
1 review(s) available for phytanic acid and Intellectual Disability
| Article | Year |
|---|---|
[Peroxisomal diseases--pediatric and neurologic differential diagnosis].
Topics: Adrenoleukodystrophy; Child, Preschool; Diagnosis, Differential; Fatty Acids; Genetic Counseling; Humans; Infant; Intellectual Disability; Metabolism, Inborn Errors; Microbodies; Phytanic Acid | 1991 |
4 other study(ies) available for phytanic acid and Intellectual Disability
| Article | Year |
|---|---|
Reinvestigation of trihydroxycholestanoic acidemia reveals a peroxisome biogenesis disorder.
Topics: Amino Acid Sequence; Animals; Ataxia; Catalase; Child, Preschool; Cholestanols; Consensus Sequence; Diagnostic Errors; DNA Mutational Analysis; Dysarthria; Erythrocytes; Female; Fibroblasts; Fungi; Humans; Intellectual Disability; Mammals; Membrane Proteins; Molecular Sequence Data; Muscle Hypotonia; Oxidation-Reduction; Oxidoreductases; Peroxisomes; Phytanic Acid; Sequence Alignment; Sequence Homology, Amino Acid | 2004 |
Variant rhizomelic chondrodysplasia punctata (RCDP) with normal plasma phytanic acid: clinico-biochemical delineation of a subtype and complementation studies.
Topics: Cells, Cultured; Child; Chondrodysplasia Punctata, Rhizomelic; Female; Fibroblasts; Humans; Intellectual Disability; Phytanic Acid | 1996 |
Dyggve-Melchior-Clausen syndrome with increased pipecolic acid in plasma and urine.
Topics: Bone Diseases, Developmental; Child; Dwarfism; Fatty Acids; Fibroblasts; Humans; Intellectual Disability; Male; Microbodies; Phytanic Acid; Pipecolic Acids; Plasmalogens; Syndrome | 1991 |
Peroxisomal dysfunction in a boy with neurologic symptoms and amaurosis (Leber disease): clinical and biochemical findings similar to those observed in Zellweger syndrome.
Topics: Adrenoleukodystrophy; Biopsy; Blindness; Brain Diseases; Cells, Cultured; Diagnosis, Differential; Female; Fibroblasts; Hearing Loss, Sensorineural; Hepatomegaly; Humans; Infant; Intellectual Disability; Kidney Diseases; Liver; Liver Diseases; Male; Microbodies; Oxidation-Reduction; Phytanic Acid; Plasmalogens; Syndrome | 1986 |