Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1965 1
1966 1
1967 2
1968 3
1969 3
1970 5
1971 5
1972 3
1973 2
1974 6
1975 3
1977 1
1978 7
1979 1
1982 3
1983 2
1984 1
1985 3
1986 1
1987 5
1988 8
1989 6
1990 3
1991 6
1992 5
1993 8
1994 3
1995 1
1996 2
1997 5
1998 8
1999 5
2000 8
2001 12
2002 3
2003 7
2004 4
2005 4
2006 7
2007 6
2008 1
2009 3
2010 6
2011 4
2012 1
2013 8
2014 2
2015 2
2016 7
2017 3
2018 6
2019 1
2021 2
2022 1
2023 1

Text availability

Article attribute

Article type

Publication date

Search Results

208 results

Results by year

Filters applied: . Clear all
Page 1
The physiological functions of human peroxisomes.
Wanders RJA, Baes M, Ribeiro D, Ferdinandusse S, Waterham HR. Wanders RJA, et al. Physiol Rev. 2023 Jan 1;103(1):957-1024. doi: 10.1152/physrev.00051.2021. Epub 2022 Aug 11. Physiol Rev. 2023. PMID: 35951481 Review.
Among others these include the Zellweger spectrum disorders, X-linked adrenoleukodystrophy, and Refsum disease. To fulfill their role in metabolism, peroxisomes require continued interaction with other subcellular organelles including lipid droplets, lysosomes, the …
Among others these include the Zellweger spectrum disorders, X-linked adrenoleukodystrophy, and Refsum disease. To fulfill the …
Laboratory investigations.
Boltshauser E, Weber KP. Boltshauser E, et al. Handb Clin Neurol. 2018;154:287-298. doi: 10.1016/B978-0-444-63956-1.00017-5. Handb Clin Neurol. 2018. PMID: 29903445 Review.
Particular attention is paid to early diagnosis of treatable metabolic ataxias (such as abetalipoproteinemia, coenzyme Q10 deficiency, cerebrotendinous xanthomatosis, glucose transporter type 1 deficiency, Refsum disease, and vitamin E deficiency), but autoimmune at …
Particular attention is paid to early diagnosis of treatable metabolic ataxias (such as abetalipoproteinemia, coenzyme Q10 deficiency, cereb …
Peroxisomal disorders.
Aubourg P, Wanders R. Aubourg P, et al. Handb Clin Neurol. 2013;113:1593-609. doi: 10.1016/B978-0-444-59565-2.00028-9. Handb Clin Neurol. 2013. PMID: 23622381 Review.
The PBD group comprises four different disorders that include Zellweger syndrome (ZS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and rhizomelic chondrodysplasia punctata (RCDP). ...The single peroxisomal enzyme deficiency group comprises …
The PBD group comprises four different disorders that include Zellweger syndrome (ZS), neonatal adrenoleukodystrophy (NALD), infantile Re …
Phytanic acid consumption and human health, risks, benefits and future trends: A review.
Roca-Saavedra P, Mariño-Lorenzo P, Miranda JM, Porto-Arias JJ, Lamas A, Vazquez BI, Franco CM, Cepeda A. Roca-Saavedra P, et al. Food Chem. 2017 Apr 15;221:237-247. doi: 10.1016/j.foodchem.2016.10.074. Epub 2016 Oct 18. Food Chem. 2017. PMID: 27979198 Review.
Phytanic acid is a methyl-branched fatty acid present in the human diet, derived from the enzymatic degradation of phytol and subsequently oxidized by the rumenal microbiota and certain marine organisms. ...The aim of this work was to conduct an overview of t …
Phytanic acid is a methyl-branched fatty acid present in the human diet, derived from the enzymatic degradation of phyt …
Refsum disease, peroxisomes and phytanic acid oxidation: a review.
Wanders RJ, Jansen GA, Skjeldal OH. Wanders RJ, et al. J Neuropathol Exp Neurol. 2001 Nov;60(11):1021-31. doi: 10.1093/jnen/60.11.1021. J Neuropathol Exp Neurol. 2001. PMID: 11706932 Review.
Refsum disease was first recognized as a distinct disease entity by Sigvald Refsum in the 1940s. The discovery of markedly elevated levels of the branched-chain fatty acid phytanic acid in certain patients marked Refsum d …
Refsum disease was first recognized as a distinct disease entity by Sigvald Refsum in the 1940s. The discovery o …
Phytanic acid metabolism in health and disease.
Wanders RJ, Komen J, Ferdinandusse S. Wanders RJ, et al. Biochim Biophys Acta. 2011 Sep;1811(9):498-507. doi: 10.1016/j.bbalip.2011.06.006. Epub 2011 Jun 13. Biochim Biophys Acta. 2011. PMID: 21683154 Review.
Phytanic acid (3,7,11,15-tetramethylhexadecanoic acid) is a branched-chain fatty acid which cannot be beta-oxidized due to the presence of the first methyl group at the 3-position. Instead, phytanic acid undergoes alpha-oxidation to produ …
Phytanic acid (3,7,11,15-tetramethylhexadecanoic acid) is a branched-chain fatty acid which cannot be beta-oxidi …
Phytol in a pharma-medico-stance.
Islam MT, de Alencar MV, da Conceição Machado K, da Conceição Machado K, de Carvalho Melo-Cavalcante AA, de Sousa DP, de Freitas RM. Islam MT, et al. Chem Biol Interact. 2015 Oct 5;240:60-73. doi: 10.1016/j.cbi.2015.07.010. Epub 2015 Aug 19. Chem Biol Interact. 2015. PMID: 26296761 Review.
In the pharma-medico viewpoint, PYT and its derivatives have been evident to have antimicrobial, cytotoxic, antitumorous, antimutagenic, anti-teratogenic, antibiotic-chemotherapeutic, antidiabetic, lipid lowering, antispasmodic, anticonvulsant, antinociceptive, antioxidant, anti- …
In the pharma-medico viewpoint, PYT and its derivatives have been evident to have antimicrobial, cytotoxic, antitumorous, antimutagenic, ant …
Phytanic acid storage disease (Refsum's disease): clinical characteristics, pathophysiology and the role of therapeutic apheresis in its management.
Weinstein R. Weinstein R. J Clin Apher. 1999;14(4):181-4. doi: 10.1002/(sici)1098-1101(1999)14:4<181::aid-jca5>3.0.co;2-z. J Clin Apher. 1999. PMID: 10611628 Review.
Phytanic acid storage disease (known also as Refsum's Disease) is caused by inherited defects in the metabolic pathway for phytanic acid, a dietary branched-chain fatty acid. Poorly metabolized phytanic acid …
Phytanic acid storage disease (known also as Refsum's Disease) is caused by inherited defects in t …
Peroxisomal disorders.
Moser HW, Bergin A, Cornblath D. Moser HW, et al. Biochem Cell Biol. 1991 Jul;69(7):463-74. doi: 10.1139/o91-070. Biochem Cell Biol. 1991. PMID: 1724376 Review.
The concept that there are human disease states that are associated with abnormal peroxisomal function is of recent origin. ...The Zellweger cerebro-hepato-renal syndrome represents the most serious peroxisomal disease. It is associated with malfunction of virtually …
The concept that there are human disease states that are associated with abnormal peroxisomal function is of recent origin. ...The Ze …
Neurometabolic disease.
Moser HW. Moser HW. Curr Opin Neurol. 1998 Apr;11(2):91-5. doi: 10.1097/00019052-199804000-00002. Curr Opin Neurol. 1998. PMID: 9551286 Review.
Advances in knowledge of neurometabolic disease continues. Of great interest to the neurologist are the definitions of the molecular defects in Niemann-Pick C disease, Refsum disease, and five of the disorders of peroxisome biogenesis, including rhizom …
Advances in knowledge of neurometabolic disease continues. Of great interest to the neurologist are the definitions of the molecular …
208 results