Zobrazeno 1 - 10
of 21
pro vyhledávání: '"E. C. Klasen"'
Publikováno v:
Clinical Genetics. 29:211-215
A significantly higher number of PI ZZ and PI MZ individuals was found in a flaccid lung population as compared to internal and healthy controls. The relative risk for ZZ is 12.5 and for MZ 1.8. We conclude that if a PI MZ individual does develop lun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::340b6a7dcab6ccc904c0d09fa5ad0e7a
https://doi.org/10.1111/j.1399-0004.1986.tb00814.x
https://doi.org/10.1111/j.1399-0004.1986.tb00814.x
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 149(36)
To determine the number and type of medical specialists in Dutch hospitals that were authors of scientific papers published in English in the field of clinical drug research in the period 1997/'03.Descriptive.PubMed was searched for articles on clini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b3724e77873be364e9aa97e1fa83265d
https://pubmed.ncbi.nlm.nih.gov/16171111
https://pubmed.ncbi.nlm.nih.gov/16171111
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 147(28)
This paper describes the laborious and lengthy path to clarification and disclosure in a case of fraud in a neurological pharmaceutical clinical trial in the Netherlands. A Dutch neurologist was suspected of irregularities within the context of the '
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0e23a82997837e841da8ad3a1475b68e
https://pubmed.ncbi.nlm.nih.gov/14526626
https://pubmed.ncbi.nlm.nih.gov/14526626
Autor:
H L, Hoeksema, E C, Klasen
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 145(1)
The Council for Medical and Health Research (MW-NWO) assessed the scientific quality of research proposals submitted to the Dutch Investigative Medicine Fund, and analysed if there had been changes over time in the proportion of proposals which the M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::34e9ea7208d3947cd436f5b9f8d7fdac
https://pubmed.ncbi.nlm.nih.gov/11198965
https://pubmed.ncbi.nlm.nih.gov/11198965
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 143(1)
In the Netherlands, the SGO Health Research Promotion Programme was carried out from 1986 until 1997. The aim of the programme was to strengthen patient-oriented clinical research in specific fields of medicine. Some of the programme sections certain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d5329e471ad8538f8b950e2cdc7069b5
https://pubmed.ncbi.nlm.nih.gov/10086099
https://pubmed.ncbi.nlm.nih.gov/10086099
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 141(25)
The enhancement of clinical scientific research in the Netherlands is being stimulated to a substantial extent by the introduction and stimulation of a training model aimed at the combined training of physicians to both a general practitioner or spec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d7e89d2ebb5ef5c8015d66db1236b921
https://pubmed.ncbi.nlm.nih.gov/9380169
https://pubmed.ncbi.nlm.nih.gov/9380169
Autor:
E. C. Klasen, T. Nukiwa, Marten H. Hofker, Rune R. Frants, D. Curiel, M. Nelen, Ronald G. Crystal
Publikováno v:
Biochemical and Biophysical Research Communications. 155:634-642
Cosmid clones containing alpha 1-antitrypsin (alpha 1AT) gene sequences were observed to contain alpha 1AT-like sequences approximately 12 kb downstream of the authentic alpha 1AT gene. Restriction mapping suggested the alpha 1AT-like gene lacks prom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af7df99a55d0c8156e2b852d6efc2ec0
https://doi.org/10.1016/s0006-291x(88)80542-4
https://doi.org/10.1016/s0006-291x(88)80542-4
Autor:
E. C. Klasen, L. N. Went
Publikováno v:
Annals of Human Genetics. 48:105-117
Summary An exhaustive study of erythropoietic protoporphyria in the Netherlands led to the discovery of 200 patients with this disorder in 91 families. In 46 of these families a single patient occurred. A study of parents, sibs and children led to th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b638be7e1ce0b05b0ef8b80c16fe346e
https://doi.org/10.1111/j.1469-1809.1984.tb01006.x
https://doi.org/10.1111/j.1469-1809.1984.tb01006.x
Autor:
D.M. van den Boomgaard, I. Biemond, E C Klasen, C. B. H. W. Lamers, A.S. Peña, J. Kreuning, J. G Goedhard
Publikováno v:
Digestion. 39:20-25
Hereditary alpha 1-antitrypsin (alpha 1-AT) deficiency has been suggested to be associated with peptic ulcer disease. Since the serum concentration of the enzyme is the result of both hereditary and nonhereditary factors, we have studied not only the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94b0788b4e4d13520e3e9badf1e1031c
https://doi.org/10.1159/000199603
https://doi.org/10.1159/000199603
Publikováno v:
Human Heredity. 37:340-344
2,000 male individuals randomly selected from three different areas in The Netherlands were phenotyped for apolipoprotein E. The apolipoprotein E gene frequencies and phenotype distribution did not differ significantly from that of previously studied
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6de6d719f1bfb332a26636286aa8229
https://doi.org/10.1159/000153731
https://doi.org/10.1159/000153731