Zobrazeno 1 - 10
of 47
pro vyhledávání: '"M P, Whyte"'
Publikováno v:
Humanities & Social Sciences Communications, Vol 11, Iss 1, Pp 1-6 (2024)
Should healthcare professionals use the term ‘patient’? A patient is a social construct, in a biomedical model, in which each actor has their role to play. This model has been criticised as belonging to an era of medical hegemony and (mis)represe
Externí odkaz:
https://doaj.org/article/35056fe279c742f29f060036e8ca9ffa
Autor:
M. P. Whyte
Publikováno v:
Journal of Clinical Endocrinology & Metabolism. 81:4075-4080
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e10fedf2388718d2be785c6fa69a05b
https://doi.org/10.1210/jc.81.11.4075
https://doi.org/10.1210/jc.81.11.4075
Autor:
M. P. Whyte
Publikováno v:
Journal of Clinical Endocrinology & Metabolism. 81:2142-2148
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f05e4a4328425270357ccd488f0c7edd
https://doi.org/10.1210/jc.81.6.2142
https://doi.org/10.1210/jc.81.6.2142
Autor:
M. P. Whyte, Peter Brockhurst
Publikováno v:
Australian Dental Journal. 41:128-133
The aim of this study was to investigate the viability of autoclave sterilization of set dental gypsum models. The effects of autoclaving on the strength, surface hardness and dimensions of specimens of plaster, stone and diestone were investigated.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::779e7eb6a5cf002878c752a0b3093a91
https://doi.org/10.1111/j.1834-7819.1996.tb05926.x
https://doi.org/10.1111/j.1834-7819.1996.tb05926.x
Autor:
P S Henthorn, M P Whyte
Publikováno v:
Clinical Chemistry. 38:2501-2505
Hypophosphatasia is an inborn error of metabolism that is characterized clinically by defective bone mineralization and biochemically by deficient activity of the tissue-nonspecific isoenzyme of alkaline phosphatase (TNSALP) in serum and in tissues.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac0cbe69712faef89b6e78f47f75718b
https://doi.org/10.1093/clinchem/38.12.2501
https://doi.org/10.1093/clinchem/38.12.2501
Publikováno v:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 16(9)
In 1948, Dr. John Campbell Rathbun characterized the disorder "hypophosphatasia" when he reported paradoxically low levels of alkaline phosphatase (ALP) activity in blood and in several tissues from an infant who died with rickets and epilepsy, which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::952c215eefd666a3ac7ed1ddbc9fab27
https://pubmed.ncbi.nlm.nih.gov/11547844
https://pubmed.ncbi.nlm.nih.gov/11547844
Autor:
C A, Moore, C J, Curry, P S, Henthorn, J A, Smith, J C, Smith, P, O'Lague, S P, Coburn, D D, Weaver, M P, Whyte
Publikováno v:
American journal of medical genetics. 86(5)
We describe four pregnancies in two families in which mild hypophosphatasia, apparently transmitted as an autosomal dominant trait, manifested in utero as severe long bone bowing. Postnatally, there was spontaneous improvement of the skeletal defects
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0d20e944ddbd449534914df6b411f5f8
https://pubmed.ncbi.nlm.nih.gov/10508980
https://pubmed.ncbi.nlm.nih.gov/10508980
Publikováno v:
American journal of medical genetics. 86(5)
We describe a fifth instance of hypophosphatasia presenting with prenatal findings suggestive of a very severe bone dysplasia but with a subsequently benign course. Spontaneous improvement of long-bone angulation began prenatally. The postnatal cours
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ddd4b62c09abfe6bfe55cf51edc6ad05
https://pubmed.ncbi.nlm.nih.gov/10508985
https://pubmed.ncbi.nlm.nih.gov/10508985
Autor:
P H, Dixon, P T, Christie, C, Wooding, D, Trump, M, Grieff, I, Holm, J M, Gertner, J, Schmidtke, B, Shah, N, Shaw, C, Smith, C, Tau, D, Schlessinger, M P, Whyte, R V, Thakker
Publikováno v:
The Journal of clinical endocrinology and metabolism. 83(10)
Hypophosphatemic rickets is commonly an X-linked dominant disorder (XLH or HYP) associated with a renal tubular defect in phosphate transport and bone deformities. The XLH gene, referred to as PHEX, or formerly as PEX (phosphate regulating gene with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::550279771c76db0c82ca48e9b7311740
https://pubmed.ncbi.nlm.nih.gov/9768674
https://pubmed.ncbi.nlm.nih.gov/9768674
Publikováno v:
American journal of medical genetics. 77(3)
We describe a 5-4/12-year-old girl with the unique combination of bilateral radial ray hypoplasia and multiple epiphyseal dysplasia (MED). Radial ray hypoplasia was diagnosed at birth. MED was documented at age 4-3/12 years when she presented with le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7cd908e1372af55dfa25ab6fd969491a
https://pubmed.ncbi.nlm.nih.gov/9605584
https://pubmed.ncbi.nlm.nih.gov/9605584