Zobrazeno 1 - 10
of 60
pro vyhledávání: '"K, te Velde"'
Publikováno v:
Aquaculture Environment Interactions, Vol 14, Pp 113-125 (2022)
Increased aquaculture production can improve food and nutrition security and economic growth in developing countries, but comes with environmental risks. In recent years, aquaculture has increased tremendously in Lake Kariba, which is located on the
Externí odkaz:
https://doaj.org/article/db42cea0562e4e4b809b786564272f6b
Akademický článek
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Akademický článek
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Autor:
Britt I. Drögemöller, Louise Warnich, Reno S. Bladergroen, K. te Velde, P.M. Steijlen, M. van Geel, Jorge Frank, C.J. van Heerden, A.M. van Tuyll van Serooskerken, Pamela Poblete-Gutiérrez
Publikováno v:
British Journal of Dermatology. 166:261-265
Summary Background Variegate porphyria (VP) is due to a partial deficiency of protoporphyrinogen oxidase (PPOX), the seventh enzyme in the haem biosynthetic pathway. Clinically, VP is characterized by photosensitivity and acute neurovisceral attacks
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::660ba701b3e87d60945c214f610c03b1
https://doi.org/10.1111/j.1365-2133.2011.10606.x
https://doi.org/10.1111/j.1365-2133.2011.10606.x
Autor:
K. Te Velde, Hervé Puy, Jérôme Lamoril, V. Da Silva, Laurent Gouya, F. W. M. De Rooij, Jean Charles Deybach, Pavel Martásek, R. Rosipal, Yves Nordmann
Publikováno v:
Human Mutation, 13, 44-53. Wiley-Liss Inc.
Hereditary coproporphyria (HC) is an acute hepatic porphyria with autosomal dominant inheritance caused by deficient activity of coproporphyrinogen III oxidase (CPO). Clinical manifestations of the disease are characterized by acute attacks of neurol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f0e038f379e38928413ba22074578dd
https://doi.org/10.1002/(sici)1098-1004(1999)13:1<44::aid-humu5>3.0.co
https://doi.org/10.1002/(sici)1098-1004(1999)13:1<44::aid-humu5>3.0.co
Autor:
A M, van Tuyll van Serooskerken, B I, Drögemöller, K, Te Velde, R S, Bladergroen, P M, Steijlen, P, Poblete-Gutiérrez, M, van Geel, C J, van Heerden, L, Warnich, J, Frank
Publikováno v:
The British journal of dermatology. 166(2)
Variegate porphyria (VP) is due to a partial deficiency of protoporphyrinogen oxidase (PPOX), the seventh enzyme in the haem biosynthetic pathway. Clinically, VP is characterized by photosensitivity and acute neurovisceral attacks that can manifest s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::81f370fe7f8684a71fdfc07bd698049f
https://pubmed.ncbi.nlm.nih.gov/22268855
https://pubmed.ncbi.nlm.nih.gov/22268855
Autor:
G J, Beukeveld, C M, Bijleveld, F, Kuipers, H G, Kreeftenberg, J R, Huizenga, K, te Velde, B G, Wolthers
Publikováno v:
European journal of clinical chemistry and clinical biochemistry : journal of the Forum of European Clinical Chemistry Societies. 33(7)
The Enterotest string test is an easy and non-invasive method for sampling duodenal fluid, which has been successfully used for the analysis of duodenal microflora, as well as biliary bile acid and lipid composition. The method was evaluated for dete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7f9de8fea56aa272ae452f4b8874ea14
https://pubmed.ncbi.nlm.nih.gov/7548456
https://pubmed.ncbi.nlm.nih.gov/7548456
Evaluation of a first-line spectrophotometric screening test for increased urine porphyrin excretion
Publikováno v:
Annals of clinical biochemistry. 32
We compared a spectrophotometric screening test for urine porphyrin concentration with a high performance liquid chromatography (HPLC) method. The screening test gave lower values than those obtained by HPLC, but the overall correlation was good. Occ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bb080a60d5386820b62bdf5423d2273
https://pubmed.ncbi.nlm.nih.gov/7785947
https://pubmed.ncbi.nlm.nih.gov/7785947
Publikováno v:
American journal of human genetics. 51(3)
Acute intermittent porphyria (AIP) is an autosomal dominant disease characterized by a partial deficiency of porphobilinogen (PBG) deaminase. Different subtypes of the disease have been defined, and more than 10 different mutations have been describe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::00954677b0215580d08d8dccb009c3eb
https://pubmed.ncbi.nlm.nih.gov/1496994
https://pubmed.ncbi.nlm.nih.gov/1496994
Autor:
M. K. te Velde, N. C. van der Vaart, R. M. Jungblut, H. J. Kettelarij, H. A. Wierenga, Eduard Matheus Johannes Niessen, P. J. A. Derks, R. Gersmann, D. A. Benoy, W. Hoving, R. van der Wilk
Publikováno v:
SID Symposium Digest of Technical Papers. 33:1396
The design and technologies used in the industrial development of a Hopping Electron Cathode (HEC) for CRT application are described. This contribution focuses on the developmnet of: (1) a “Low-drive” current modulator, (2) a HEC funnel with well
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::400fa87be0c402a94206ac33d688184f
https://doi.org/10.1889/1.1830208
https://doi.org/10.1889/1.1830208