Zobrazeno 1 - 10
of 55
pro vyhledávání: '"V. G. Oberholzer"'
Autor:
V. G. Oberholzer, A. Briddon
Publikováno v:
Amino Acids. 1:247-250
By relating the increase in glutamine to the corresponding increase in valine following protein loading it has been possible to detect carriers of OCT deficiency.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35ee1b29526b1373931212003aa08ee7
https://doi.org/10.1007/bf00806922
https://doi.org/10.1007/bf00806922
Autor:
J Rode, P. B. Cotton, V. G. Oberholzer, J. R. Croker, U. Armbrecht, R. W. Stockbrügger, A. J. Teall
Publikováno v:
Microbial Ecology in Health and Disease; Vol 3, No 4 (1990)
It is still uncertain whether upper gastrointestinal bacterial overgrowth in patients with permanent achlorhydria causes malassimilation in more than just the occasional case. In an attempt to clarify this, 19 patients with pernicious anaemia who had
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0ad426c8240a8b9e757334f6c71def0
https://doi.org/10.3402/mehd.v3i4.7540
https://doi.org/10.3402/mehd.v3i4.7540
Autor:
A. Briddon, V. G. Oberholzer
Publikováno v:
Amino Acids ISBN: 9789072199041
Changes in plasma amino acid levels with varying protein intake in normal children [1–3] and in children with malnutrition, [4–6] have been well documented. These changes have led to the use of ratios between amino acids, or groups of amino acids
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75e74e8b98b890fe4674bdd47c7254b6
https://doi.org/10.1007/978-94-011-2262-7_134
https://doi.org/10.1007/978-94-011-2262-7_134
Publikováno v:
Journal of the Royal Society of Medicine. 73:588-591
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef6a4744283084c8b287c2e4ce60bac9
https://doi.org/10.1177/014107688007300812
https://doi.org/10.1177/014107688007300812
Publikováno v:
Journal of Inherited Metabolic Disease. 9:250-253
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c15a5baf820585d2df91b0f0dafedd1
https://doi.org/10.1007/bf01799720
https://doi.org/10.1007/bf01799720
Autor:
V G Oberholzer, M L Harris
Publikováno v:
Clinical Chemistry. 26:473-479
We studied conditions affecting a colorimetric assay of total orotic acid (orotic acid plus orotidine) in urine. Most interfering substances can be conveniently removed on a small column of cation-exchange resin, and an improved control reaction corr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f8d9a672f4734d75ffee18701c149bf
https://doi.org/10.1093/clinchem/26.3.0473
https://doi.org/10.1093/clinchem/26.3.0473
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 46:28-34
The clinical features and the computed tomographic appearances of the brain in seven children with ornithine carbamoyl transferase deficiency are described. Episodic vomiting and drowsiness, acute encephalopathy, failure to thrive and developmental r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9028e2c6ed71aad088706dcb81690ac7
https://doi.org/10.1136/jnnp.46.1.28
https://doi.org/10.1136/jnnp.46.1.28
Publikováno v:
Clinica Chimica Acta. 61:215-218
A complete absence of plasma carnosinase activity was observed in a series of patients with proven urea cycle defects. This finding could not be explained by age of patients, low protein intake, or inhibition of the enzyme by glutamine or carbamyl ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a961198e78aa06324021ec031fda7f5
https://doi.org/10.1016/0009-8981(75)90317-4
https://doi.org/10.1016/0009-8981(75)90317-4
Publikováno v:
Clinical Chemistry. 22:1976-1981
A column cation-exchange resin procedure for plasma ammonia was modified to require only 100 mul of plasma per determination. Mean analytical recovery of standard from resin (six samples) was 98% (range, 94-100%) as compared to a mean of 63% (range,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2791f26ddbb2772168d0c9496bfc2eb5
https://doi.org/10.1093/clinchem/22.12.1976
https://doi.org/10.1093/clinchem/22.12.1976
Autor:
E. A. Burgess, V. G. Oberholzer, J Sacks, T Valaes, S. Mantagos, S Tsagaraki, S Baibas, T. Palmer
Publikováno v:
Archives of Disease in Childhood. 53:230-234
Two newborn infants, male (A) and female (B), with lethal hyperammonaemia are described in the same family. In both, symptoms started on the second day of life. Lethargy and hypotonia were the most prominent initial findings and were followed by conv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2eabde1f314e286fffee0a0f85e116a9
https://doi.org/10.1136/adc.53.3.230
https://doi.org/10.1136/adc.53.3.230