Zobrazeno 1 - 10
of 18
pro vyhledávání: '"C J, Kelnar"'
Autor:
P M, Crofton, C J, Kelnar
Publikováno v:
International Journal of Clinical Practice. 52:557-565
Biochemical markers of bone and collagen turnover have been found to be a valuable adjunct to measurements of bone mineral density in post-menopausal women in whom they appear to be independent predictors of osteoporosis and fracture risk. In childre
Publikováno v:
Hormone research. 69(4)
There is a scarcity of data on height as well as bone densitometry in humans with NOGGIN mutations.In 2 families with symphalangism, anthropometry, bone densitometry and genetic analysis of the NOGGIN gene were performed.In family A, the height stand
Autor:
C J Kelnar
Publikováno v:
The Journal of the Royal College of Physicians of Edinburgh. 42:32-33
The objective of this paper was to determine systematically the impact of growth hormone (GH)therapy on adult height of children with (so-called) 'idiopathic short stature' (ISS) using the Cochrane Central Register of Controlled Trials, Medline, and
Autor:
Luciano Cavallo, A Albanese, F Chiarelli, G E Butler, A. M. Pasquino, F Buzi, R Stanhope, Margherita Bozzola, C J Kelnar, Valentino Cherubini, S. L. S. Drop
Publikováno v:
Scopus-Elsevier
Idiopathic short stature (ISS) is a term used to describe the status of children with short stature that cannot be attributed to a specific cause. Many children diagnosed as having ISS have partial GH insensitivity, which can result from disturbances
Publikováno v:
Diabetic medicine : a journal of the British Diabetic Association. 18(5)
Many psycho-social factors can affect the glycaemic control of children with Type 1 diabetes, but the influence of the intelligence of the child and their parents has not been reported.Seventy-eight children and adolescents with Type 1 diabetes and t
Autor:
C J, Kelnar
Publikováno v:
Archives of disease in childhood. 83(2)
Autor:
C A, Carson, C J, Kelnar
Publikováno v:
Journal of the Royal College of Physicians of London. 34(1)
Publikováno v:
Clinical endocrinology. 49(4)
Mutations of the GNAS1 gene, which is located on chromosome 20q13.11 and encodes the alpha-subunit of the stimulatory GTP-binding protein, have been identified in patients with pseudohypoparathyroidism type Ia (PHPIa) and pseudopseudohypoparathyroidi
Publikováno v:
Diabetic medicine : a journal of the British Diabetic Association. 15(10)
To compare the hypoglycaemic symptoms reported by children with Type 1 diabetes and signs observed by and symptoms reported to their parents, 101 pairs, consisting of a child with diabetes and one of their parents, were asked to report the frequency
Autor:
P M, Crofton, S F, Ahmed, J C, Wade, R, Stephen, M W, Elmlinger, M B, Ranke, C J, Kelnar, W H, Wallace
Publikováno v:
The Journal of clinical endocrinology and metabolism. 83(9)
To investigate the effects of disease and intensive chemotherapy on bone turnover and growth in children with acute lymphoblastic leukemia (ALL), a longitudinal prospective study was carried out in 22 children, aged 1.2-13.5 yr, enrolled in the Medic