Zobrazeno 1 - 10 of 265 pro vyhledávání: '"J. Lafourcade"'
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EOR Back Produced Water Treatment: Media Selection to Improve Filtration Efficiency
Autor: P. Pedenaud, N. Lesage, J. Lafourcade, C. Sagne, G. Munduru, M. Jouanolou, H. Foraison, P. Cordelier
Publikováno v: IOR 2019 – 20th European Symposium on Improved Oil Recovery.
Summary Polymer flooding is one of the most advanced enhanced oil recovery techniques to improve production. It is a cost-effective method due to the properties of polymers, mainly its capacity to develop suitable viscosities when diluted, leading to
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ec54b0058fd989db990fa28b30fe2b8e
https://doi.org/10.3997/2214-4609.201900137
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3
P12.23 Tumor growth model applied for meningiomas: first clinical validation
Autor: Benjamin Taton, Hugues Loiseau, J. Lafourcade, Vivien Pianet, Olivier Saut, J. Joie, Guy Kantor, A. Bigourdan, Thierry Colin
Publikováno v: Neuro-Oncology. 19:iii99-iii100
Context: Meningiomas account for 30% of primary brain tumors. A dramatic increasing of their incidence with an annual percentage change ranging from 2 to 4.5% has recently been highlighted by several sources including either symptomatic or asymptomat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::527d60c29fc0c637d215d9173ca937e9
https://doi.org/10.1093/neuonc/nox036.380
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5
Familial aggregation of malignant melanoma/dysplastic naevi and tumours of the nervous system: an original syndrome of tumour proneness
Autor: M, Bahuau, D, Vidaud, M, Kujas, A, Palangié, B, Assouline, M, Chaignaud-Lebreton, M, Prieur, M, Vidaud, J P, Harpey, J, Lafourcade, B, Caille
Publikováno v: Annales de genetique. 40(2)
A five-generation family is here reported in which several members developed malignant melanoma, dysplastic naevi, astrocytoma in all grades, benign or malignant schwannoma, neurofibroma, or meningioma in a single instance. Significant cosegregation
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::70c603275ff7a0b9a16f952af627fb62
https://pubmed.ncbi.nlm.nih.gov/9259954
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6
[The r(22) syndrome, Apropos of 4 new cases]
Autor: M O, Rethore, B, Noël, J, Couturier, M, Prieur, J, Lafourcade, J, Lejeune
Publikováno v: Annales de genetique. 19(2)
Four patients with a ring derived from chromosome n 22 - r(22)-are reported. The clinical syndrome is described, based on the description of these patients and ten others already reported in the litterature. The "doe's eye" anomaly appears to be the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ae9232addd0c85b0f384ca4256297078
https://pubmed.ncbi.nlm.nih.gov/822770
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7
Increased activity of adenine phosphoribosyl transferase in a child trisomic for 16q22.2 to 16qter due to malsegregation of a t(1621) (q22.2q222)pat
Autor: M O, Rethoré, J, Lafourcade, J, Couturier, J P, Harpey, M, Hamet, R, Engler, L G, Alcindor, J, Lejeune
Publikováno v: La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris. 58(45)
Two cousins with trisomy for the distal third of 16q due to a familial translocation, t(16;21)(q22.2;q22.2), are reported. The APRT gene locus could be assigned to 16q22.2 to 16qter. The phenotypic similarities of the first patient, who had trisomy 1
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::747ab89ef15d31328bf38943baff5e7b
https://pubmed.ncbi.nlm.nih.gov/6297060
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