Zobrazeno 1 - 10
of 61
pro vyhledávání: '"J. D. Teale"'
Autor:
J D Teale, P Y P Kwong
Publikováno v:
Journal of the Royal Society of Medicine. 95:381-385
The most important cause of hypoglycaemia in the presence of high insulin and C-peptide concentrations is insulinoma. However, a similar picture arises from use of sulphonylureas, which is sometimes covert. All specimens received in two years by a su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::478274834bafda3d97b3144016d89cd3
https://doi.org/10.1177/014107680209500802
https://doi.org/10.1177/014107680209500802
Autor:
J. D. Teale, Vincent Marks
Publikováno v:
Clinical Endocrinology. 49:491-498
Objective To assess the relative efficacy of hGH and glucocorticoids in the treatment of non-islet cell tumour hypoglycaemia (NICTH) by examination of their influence on the composition of the various molecular species involving tumour and mature for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b03853f69c40e5b717a5078b2a2eca00
https://doi.org/10.1046/j.1365-2265.1998.00564.x
https://doi.org/10.1046/j.1365-2265.1998.00564.x
Publikováno v:
Annals of Clinical Biochemistry: International Journal of Laboratory Medicine. 34:627-631
We investigated whether pancreatic β-cell dysfunction has a role in the pathogenesis of glucose intolerance in acromegaly by comparing plasma intact proinsulin, immunoreactive insulin, C-peptide and glucose concentrations during a 75 g oral glucose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b50d79c359701d357b14c7d80c03a92
https://doi.org/10.1177/000456329703400605
https://doi.org/10.1177/000456329703400605
Autor:
R. G. Gosling, J. M. P. Holly, R. L. Jones, J. D. Teale, R. C. Turay, E. D. Lehmann, S. C. Cwyfan-Hughes, K. D. Hopkins
Publikováno v:
Clinical Endocrinology. 45:327-331
OBJECTIVE While the effects of age on the growth hormone/insulin-like growth factor (IGF) axis are well documented, the influence of ethnic background is unknown. The differences in IGF and IGF binding proteins (IGFBPs) were investigated in two ethni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::920345c91ede2ce0dd87df62aded6228
https://doi.org/10.1046/j.1365-2265.1996.00815.x
https://doi.org/10.1046/j.1365-2265.1996.00815.x
Publikováno v:
Clinical Endocrinology. 44:727-731
A patient presented with frequent episodes of spontaneous hypoglycaemia due to a solitary fibrous tumour of pleural origin, secreting incompletely processed proinsulin-like growth factor II (big IGF-II). Somatostatin receptors were demonstrated in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::340a95da40b99968de8d418e82fa05a4
https://doi.org/10.1046/j.1365-2265.1996.721542.x
https://doi.org/10.1046/j.1365-2265.1996.721542.x
Publikováno v:
Clinica Chimica Acta. 188:31-38
IGF-1 concentrations were measured in plasma from 20 obese patients and 20 age- and sex-matched control subjects all of whom were fasting. Plasma IGF-1 concentrations were lower (p less than 0.05) in the obese individuals than in the controls. Plasma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93beeceea93dc4ef1f09fba4c00f0be2
https://doi.org/10.1016/0009-8981(90)90143-g
https://doi.org/10.1016/0009-8981(90)90143-g
Autor:
J D Teale, P Y P Kwong
Publikováno v:
Annals of Clinical Biochemistry: International Journal of Laboratory Medicine. 33:465-467
Laron-type dwarfism, I a syndrome of growth hormone (GH) receptor deficiency, is an autosomal recessive disorder caused by a variable genetic defect of the GH receptor.s-' The phenotype of the patients with Laron-type dwarfism (LTD) resembles isolate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcb99a10b8bc819001dfd4b11afdc645
https://doi.org/10.1177/000456329603300514
https://doi.org/10.1177/000456329603300514
Autor:
J. D. Teale, Gwen Wark
Publikováno v:
Clinical endocrinology. 60(4)
Summary objective To compare the outcome of different treatment options used in several cases of non-islet cell tumour hypoglycaemia (NICTH). patients Eight cases of NICTH were referred for diagnosis and monitoring following either surgical or medica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2f98708157aaa31dc8bca5ff614e058
https://pubmed.ncbi.nlm.nih.gov/15049960
https://pubmed.ncbi.nlm.nih.gov/15049960
Publikováno v:
Journal of clinical pathology. 56(9)
Adult spontaneous hypoglycaemia is not a diagnosis per se but a manifestation of a disease. Although rare, it is important to identify spontaneous hypoglycaemia and its causes because treatment may be preventative or curative. Hypoglycaemia can occur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e957b2e4efc518faa6efa3a5554d447
https://pubmed.ncbi.nlm.nih.gov/12944543
https://pubmed.ncbi.nlm.nih.gov/12944543
Publikováno v:
Journal of clinical pathology. 55(7)
Aim: To assess the extent to which biochemical analytical services contribute to the diagnosis and management of clinical cases of hypoglycaemia. Methods: All cases of confirmed hypoglycaemia, referred during a six month period, were included in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::871731e6eb7acd8c69bfcfc7bbe93d58
https://pubmed.ncbi.nlm.nih.gov/12101194
https://pubmed.ncbi.nlm.nih.gov/12101194