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» Authors » V A Huszagh

V A Huszagh

Explore the profile of V A Huszagh including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 11
Citations 88
Followers 0
Related Specialties
Biochemistry
Endocrinology
Science
Co-Authors
J P Infante
Published In
Mol Cell Biochem
Nature
Mol Genet Metab
FEBS Lett
J Am Diet Assoc
Affiliations
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Recent Articles
1.
Impaired arachidonic (20:4n-6) and docosahexaenoic (22:6n-3) acid synthesis by phenylalanine metabolites as etiological factors in the neuropathology of phenylketonuria
Infante J, Huszagh V
Mol Genet Metab . 2001 Mar; 72(3):185-98. PMID: 11243724
The recent literature on polyunsaturated fatty acid metabolism in phenylketonuria (PKU) is critically analyzed. The data suggest that developmental impairment of the accretion of brain arachidonic (20:4n-6) and docosahexaenoic (22:6n-3,...
2.
Zellweger syndrome knockout mouse models challenge putative peroxisomal beta-oxidation involvement in docosahexaenoic acid (22:6n-3) biosynthesis
Infante J, Huszagh V
Mol Genet Metab . 2001 Feb; 72(1):1-7. PMID: 11161822
The putative involvement of peroxisomal beta-oxidation in the biosynthetic pathway of docosahexaenoic acid (22:6n-3, DHA) synthesis is critically reviewed in light of experiments with two recently developed knockout mouse models...
3.
Fluid needs of older adults
Huszagh V
J Am Diet Assoc . 2000 Aug; 100(7):768. PMID: 10916512
No abstract available.
4.
Secondary carnitine deficiency and impaired docosahexaenoic (22:6n-3) acid synthesis: a common denominator in the pathophysiology of diseases of oxidative phosphorylation and beta-oxidation
Infante J, Huszagh V
FEBS Lett . 2000 Feb; 468(1):1-5. PMID: 10683429
A critical analysis of the literature of mitochondrial disorders reveals that genetic diseases of oxidative phosphorylation are often associated with impaired beta-oxidation, and vice versa, and preferentially affect brain, retina,...
5.
Mechanisms of resistance to pathogenesis in muscular dystrophies
Infante J, Huszagh V
Mol Cell Biochem . 1999 Jul; 195(1-2):155-67. PMID: 10395079
A mechanistic definition of the dystrophic process is proposed, and the effects of growth factors vs. down-regulation of growth are critically analyzed. A conceptual scheme is presented to illustrate the...
6.
Analysis of the putative role of 24-carbon polyunsaturated fatty acids in the biosynthesis of docosapentaenoic (22:5n-6) and docosahexaenoic (22:6n-3) acids
Infante J, Huszagh V
FEBS Lett . 1998 Jul; 431(1):1-6. PMID: 9684854
The recent literature on the putative involvement of a single cycle of peroxisomal beta-oxidation of 24:5n-6 and 24:6n-3 polyunsaturated fatty acids in the biosynthesis of the respective docosapentaenoic (22:5n-6) and...
7.
On the molecular etiology of decreased arachidonic (20:4n-6), docosapentaenoic (22:5n-6) and docosahexaenoic (22:6n-3) acids in Zellweger syndrome and other peroxisomal disorders
Infante J, Huszagh V
Mol Cell Biochem . 1997 Mar; 168(1-2):101-15. PMID: 9062899
Alterations in the metabolism of arachidonic (20:4n-6), docosapentaenoic (22:5n-6), and docosahexaenoic (22:6n-3) acids and other polyunsaturated fatty acids in Zellweger syndrome and other peroxisomal disorders are reviewed. Previous proposals that...
8.
Laymen in scientists' clothing?
Infante J, Huszagh V
Nature . 1990 Aug; 346(6284):505. PMID: 2377221
No abstract available.
9.
The hypothetical way of progress
Huszagh V, Infante J
Nature . 1989 Mar; 338(6211):109. PMID: 2918931
No abstract available.
10.
On the nature of the Duchenne muscular dystrophy locus: a portion of a complex of related gene clusters of recent pseudoautosomal origin?
Infante J, Huszagh V
Mol Cell Biochem . 1988 Jun; 81(2):103-19. PMID: 3050449
The current hypothesis that the Duchenne/Becker muscular dystrophy locus encodes a single 2,000 kb gene is analyzed. The apparent encoding efficiency, the individual and total exon/intron ratios, and the heterogeneity...