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pro vyhledávání: '"J.G. Post"'
Akademický článek
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Autor:
Olga Aneziris, Andrew Hale, J.G. Post, Joy I. H. Oh, Ben J. M. Ale, Linda J. Bellamy, Ioannis A. Papazoglou
Publikováno v:
Journal of Loss Prevention in the Process Industries. 16:575-591
This paper presents an integrated quantitative risk assessment method for hazardous installations, taking into account management as well as technical design and producing risk level measures. The key components of the I-Risk methodology are the tech
Publikováno v:
Journal of Loss Prevention in the Process Industries. 15:545-554
This paper presents the technical model of an Integrated Quantitative Risk Assessment method, taking into account management as well as technical design and producing risk level measures. The basic steps of the technical model consist in developing a
Publikováno v:
Journal of Hazardous Materials. 61:371-374
In Dutch environmental pollution policy, great importance is attached to the assessment of hazards due to failures and accidents in industrial installations. In particular, for the aquatic environment a systematic approach was developed to be used in
Publikováno v:
Radiotherapy and Oncology. 37:124-130
The aim of this project was to measure the irradiation tolerance of normal (non tumour bearing) mouse bladder after previous intravesical photodynamic therapy (PDT). Illumination with a range of light doses at 24 h after Photofrin was used as the ini
Autor:
Marleen Simon, Theo M. Starink, Ingrid P.C. Krapels, Arjen R. Mensenkamp, Josef Frank, Martijn H. Breuning, M.A.M. van Steensel, Sadhanna Badeloe, Susan Shanley, Fred H. Menko, D.L. Smit, R.J.A. van Moorselaar, K.Y. van Spaendonck, Jean-Pierre Bayley, J.G. Post, Cora M. Aalfs, Lies H. Hoefsloot
Publikováno v:
Clinical Genetics, 79(1), 49-59. Wiley-Blackwell
Clinical Genetics, 79(1), 49-59. Wiley-Blackwell Publishing Ltd
Clinical genetics, 79(1), 49-59. Wiley-Blackwell
Clinical Genetics, 79, 1, pp. 49-59
Clinical Genetics, 79, 49-59
Smit, D L, Mensenkamp, A R, Badeloe, S, Breuning, M H, Simon, M E H, van Spaendonck, K Y, Aalfs, C M, Post, J G, Shanley, S, Krapels, I P C, Hoefsloot, L H, van Moorselaar, R J A, Starink, T M, Bayley, J P, Frank, J, van Steensel, M A M & Menko, F H 2011, ' Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis ', Clinical Genetics, vol. 79, no. 1, pp. 49-59 . https://doi.org/10.1111/j.1399-0004.2010.01486.x
Clinical Genetics, 79(1), 49-59
Clinical Genetics, 79(1), 49-59. Wiley
Clinical Genetics, 79(1), 49-59. Wiley-Blackwell Publishing Ltd
Clinical genetics, 79(1), 49-59. Wiley-Blackwell
Clinical Genetics, 79, 1, pp. 49-59
Clinical Genetics, 79, 49-59
Smit, D L, Mensenkamp, A R, Badeloe, S, Breuning, M H, Simon, M E H, van Spaendonck, K Y, Aalfs, C M, Post, J G, Shanley, S, Krapels, I P C, Hoefsloot, L H, van Moorselaar, R J A, Starink, T M, Bayley, J P, Frank, J, van Steensel, M A M & Menko, F H 2011, ' Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis ', Clinical Genetics, vol. 79, no. 1, pp. 49-59 . https://doi.org/10.1111/j.1399-0004.2010.01486.x
Clinical Genetics, 79(1), 49-59
Clinical Genetics, 79(1), 49-59. Wiley
Heterozygous fumarate hydratase (FH) germline mutations cause hereditary leiomyomatosis and renal cell cancer (HLRCC), an autosomal dominant syndrome characterized by multiple cutaneous piloleiomyomas, uterine leiomyomas and papillary type 2 renal ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0decdfe95d2f547037c7481687e3b9be
https://research.vumc.nl/en/publications/865b593b-29ea-4803-aac4-2ef13831efe9
https://research.vumc.nl/en/publications/865b593b-29ea-4803-aac4-2ef13831efe9
Akademický článek
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Autor:
H. Baksteen, J. Kuiper, M. Damen, M. Konstandinidou, J.G. Post J. Oh, O. Aneziris, L. J. Bellamy, Ioannis A. Papazoglou, M. L. Mud, Bloemhoff A
Publikováno v:
Safety, Reliability and Risk Analysis ISBN: 9780429176418
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2afbabd39b31059128edf12997323413
https://doi.org/10.1201/9781482266481-114
https://doi.org/10.1201/9781482266481-114
Autor:
J. Kuiper, H. Baksteen, M. Mud, M. Damen, O. Aneziris, J.G. Post J. Oh, M. Konstandinidou, I.A. Papazoglou, L. J. Bellamy
Publikováno v:
Safety, Reliability and Risk Analysis ISBN: 9780429176418
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b5c6d7efc308e3ce7bb6890e023872d
https://doi.org/10.1201/9781482266481-113
https://doi.org/10.1201/9781482266481-113
Publikováno v:
Clinical Neurology and Neurosurgery. 99:99-101
Middle-aged patients who initially present with a progressive cerebellar ataxia, in the absence of a known familial pattern are often referred to under the descriptive diagnosis of ‘idiopathic’ late onset cerebellar ataxia. If these patients in t