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A Poulos

Showing results (131-140 of 198) with videos related to

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The Biochemical Journal|February 1, 1983
Studies on the structure of sphingomyelinase. Amino acid composition and heterogeneity on isoelectric focusingC S Jones, P Shankaran, D J Davidson, et al.
Acta Neuropathologica|January 1, 1992
Autopsy findings in two siblings with infantile Refsum diseaseC W Chow, A Poulos, A J Fellenberg, et al.
AJR. American Journal of Roentgenology|May 1, 1981
Gastric operation for the morbidly obeseA Poulos, K Peat, J G Lorman, et al.
Journal of Economic Entomology|October 27, 2025
Bacterial communities of fresh and aged fecal pellets in western drywood termite (Blattodea: Kalotermitidae) and their potential use as biomarkers of recent or active infestationsNicholas A Poulos, Lyna Ngor, Chow-Yang Lee, et al.
American Journal of Human Genetics|June 1, 1997
Absence of mutations raises doubts about the role of the 70-kD peroxisomal membrane protein in Zellweger syndromeB C Paton, S E Heron, P V Nelson, et al.
The Biochemical Journal|June 1, 1993
Formic acid is a product of the alpha-oxidation of fatty acids by human skin fibroblasts: deficiency of formic acid production in peroxisome-deficient fibroblastsA Poulos, P Sharp, H Singh, et al.
Journal of the American Academy of Dermatology|June 14, 2008
Unusual flexural drug reaction with epidermal pustules associated with adalimumab treatmentArni K Kristjansson, Georgann A Poulos, Timothy Chang, et al.
The Journal of Pediatrics|January 1, 1986
Dysmorphic syndrome with phytanic acid oxidase deficiency, abnormal very long chain fatty acids, and pipecolic acidemia: studies in four childrenS S Budden, N G Kennaway, N R Buist, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Plasma cis-dec-4-enoic acid measured by isotope dilution mass spectrometry; an improved assay to diagnose medium-chain acyl-CoA dehydrogenase deficiencyD W Johnson, J R Harrison, W A Norton, et al.
The Medical Journal of Australia|November 15, 1980
Enzymological diagnosis of a group of lysosomal storage diseases. Review of 5-year experience of 1600 patient-sample referralsA C Pollard, W F Carey, P V Nelson, et al.
Pageof 20

Showing results (131-140 of 198) with videos related to

Sort By:
Pageof 20
The Biochemical Journal|February 1, 1983
Studies on the structure of sphingomyelinase. Amino acid composition and heterogeneity on isoelectric focusingC S Jones, P Shankaran, D J Davidson, et al.
Acta Neuropathologica|January 1, 1992
Autopsy findings in two siblings with infantile Refsum diseaseC W Chow, A Poulos, A J Fellenberg, et al.
AJR. American Journal of Roentgenology|May 1, 1981
Gastric operation for the morbidly obeseA Poulos, K Peat, J G Lorman, et al.
Journal of Economic Entomology|October 27, 2025
Bacterial communities of fresh and aged fecal pellets in western drywood termite (Blattodea: Kalotermitidae) and their potential use as biomarkers of recent or active infestationsNicholas A Poulos, Lyna Ngor, Chow-Yang Lee, et al.
American Journal of Human Genetics|June 1, 1997
Absence of mutations raises doubts about the role of the 70-kD peroxisomal membrane protein in Zellweger syndromeB C Paton, S E Heron, P V Nelson, et al.
The Biochemical Journal|June 1, 1993
Formic acid is a product of the alpha-oxidation of fatty acids by human skin fibroblasts: deficiency of formic acid production in peroxisome-deficient fibroblastsA Poulos, P Sharp, H Singh, et al.
Journal of the American Academy of Dermatology|June 14, 2008
Unusual flexural drug reaction with epidermal pustules associated with adalimumab treatmentArni K Kristjansson, Georgann A Poulos, Timothy Chang, et al.
The Journal of Pediatrics|January 1, 1986
Dysmorphic syndrome with phytanic acid oxidase deficiency, abnormal very long chain fatty acids, and pipecolic acidemia: studies in four childrenS S Budden, N G Kennaway, N R Buist, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Plasma cis-dec-4-enoic acid measured by isotope dilution mass spectrometry; an improved assay to diagnose medium-chain acyl-CoA dehydrogenase deficiencyD W Johnson, J R Harrison, W A Norton, et al.
The Medical Journal of Australia|November 15, 1980
Enzymological diagnosis of a group of lysosomal storage diseases. Review of 5-year experience of 1600 patient-sample referralsA C Pollard, W F Carey, P V Nelson, et al.
Pageof 20