Zobrazeno 1 - 10
of 76
pro vyhledávání: '"J P, Miell"'
Autor:
Consuelo Pérez-Colodrero
Publikováno v:
Revista Electrónica Complutense de Investigación en Educación Musical, Vol 14 (2017)
Externí odkaz:
https://doaj.org/article/ed4d31c301824a17a4fa72d63cc71d3c
Autor:
L. Srikugan, Alan McGregor, Simon Aylwin, Martin Whyte, J. P. Miell, J. A. Gilbert, Roy Sherwood, S. Pramodh
Publikováno v:
Pituitary. 18:319-325
Purpose Recent guidelines suggest that a single prolactin measurement is adequate to confirm hyperprolactinaemia. This may lead to unnecessary investigation of artefactual hyperprolactinaemia. Prolactin measurement drawn from an indwelling cannula a
Autor:
R. I. G. Holt, Bernard Portmann, Richard J. Ross, J. P. Miell, Sue Justice, Marie-Catherine Postel-Vinay, X. Y. Shen
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 83:2532-2538
In cirrhosis, as in other conditions of protein catabolism, there is a state of acquired GH resistance, as defined by high circulating GH levels with low insulin-like growth factor I levels. However, patients with end-stage liver failure respond to s
Publikováno v:
Hepatology. 24:127-133
Hyperinsulinemic euglycemic clamps were performed on six patients with compensated alcoholic cirrhosis and on six normal comparison subjects. As in previous studies, glucose uptake in the cirrhotic patients was only 21% of the comparison value. The c
Publikováno v:
Clinical endocrinology. 62(6)
Summary Objective In the treatment of acromegaly, a ‘test dose’ of octreotide is recommended prior to the use of depot somatostatin analogue (SSA) therapy. However, there remains no consensus regarding the criteria that predict a response to trea
Publikováno v:
Diabetic Medicine. 11:590-592
The effect of recombinant insulin-like growth factor I (rhIGF-I) on ketone body concentrations was studied in a patient with the Mendenhall syndrome, a rare insulin-resistant state. Treatment with intravenous rhlGF-I for an episode of ketoacidosis le
Publikováno v:
The Journal of clinical endocrinology and metabolism. 85(4)
GH deficiency states and chronic fatigue syndrome (CFS) share several characteristics, and preliminary studies have revealed aspects of GH dysfunction in CFS. This study assessed indexes of GH function in 37 medication-free CFS patients without comor
Publikováno v:
Clinical endocrinology. 52(2)
Complications of childhood cirrhosis include abnormal growth and malnutrition, associated with abnormalities in circulating IGFs and IGFBPs. Controlled studies suggest that intensive enteral feeding enhances nutritional status. The aim was to ascerta
Publikováno v:
The Journal of clinical endocrinology and metabolism. 84(9)
Chronic liver disease is associated with GH resistance, which is characterized by high circulating GH and low insulin-like growth factor I (IGF-I) concentrations. Standard GH replacement has no effect on serum IGF-I in pediatric liver disease. The ai
Publikováno v:
Pediatric transplantation. 2(1)
Over 50% of children with established cirrhosis have evidence of growth failure and malnutrition. Orthotopic liver transplantation (OLT) is a successful treatment for many children and leads to improved growth and nutrition. Most of the anabolic acti