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Träfflista för sökning "WFRF:(Kohne H) srt2:(1998-1999)"

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Numrering	Referens	Omslagsbild	Hitta
1.	Wils, J, et al. (författare) Evaluation of clinical efficacy of new medical treatments in advanced colorectal cancer. Results of a workshop organized by the EORTC GITCCG. European Organization for Research and Treatment of Cancer 1998 Ingår i: Tumori. ; , s. 335- Bokkapitel (övrigt vetenskapligt/konstnärligt)
2.	Wils, J, et al. (författare) Evaluation of clinical efficacy of new medical treatments in advanced colorectal cancer. Results of a workshop organized by the EORTC GITCCG. European Organization for Research and Treatment of Cancer. Gastrointestinal Tract Cancer Cooperative Group 1998 Ingår i: Tumori. - : SAGE Publications. - 0300-8916. ; 84:3, s. 335-347 Tidskriftsartikel (refereegranskat)abstract During the last few years several factors have contributed to an increasing change in the medical treatment of advanced colorectal cancer. Among them are the more general acceptance of the impact of chemotherapy on quality of life and survival in first as well as in second-line treatment, the introduction of new drugs and the definition of novel endpoints which can roughly be defined as “patient benefit”. For this reason the European Organization for Research and Treatment of Cancer (EORTC) Gastrointestinal Tract Cancer Cooperative Group (GITCCG) felt it was appropriate to organize a workshop with experts from different countries and national groups to discuss in depth several aspects concerning the treatment of patients with advanced colorectal cancer.
3.	Cario, Holger, et al. (författare) A microdeletion syndrome due to a 3-Mb deletion on 19q13.2--Diamond-Blackfan anemia associated with macrocephaly, hypotonia, and psychomotor retardation 1999 Ingår i: Clinical Genetics. - : Wiley. - 0009-9163 .- 1399-0004. ; 55:6, s. 487-92 Tidskriftsartikel (refereegranskat)abstract We report on a boy with congenital pure red blood cell aplasia [Diamond Blackfan anemia (DBA)] and severe congenital hypotonia, macrocephaly, hypertelorism, a broad and tall forehead, medial epicanthus, and facial hypotonia with mouth-breathing and drooling, an affable and out-going personality, and a general psychomotor retardation. These features show similarity to the phenotype of the X-linked FG syndrome. DBA was diagnosed at the age of 4 months, and the boy underwent treatment with transfusion and with prednisolone. He had a normal 46, XY karyotype, but fluorescence in situ hybridization (FISH) analysis to metaphase chromosomes revealed a 3-Mb deletion on 19q13.2. This chromosomal region has previously been linked to the DBA phenotype and one 19q13 microdeletion has been identified in a patient with DBA. This deletion coincides with the deletion reported here. We suggest that the complex phenotype of our patient, including both DBA and the associated features, represent a microdeletion syndrome.

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Typ av publikation: tidskriftsartikel (2); bokkapitel (1)

Typ av innehåll: refereegranskat (2); övrigt vetenskapligt/konstnärligt (1)

Författare/redaktör: Evans, J. (2); Cunningham, D (2); Glimelius, B (2); Kiebert, G (2); Kerr, D (2); Labianca, R (2); visa fler...; Scheithauer, W. (2); Curran, D (2); Bleiberg, H (2); Wils, J (2); Blijham, G (2); Rougier, P (2); Conroy, T (2); Therasse, P (2); Ducreux, M (2); Sahmoud, T (2); Blazeby, J (2); Nordlinger, B. (2); Sobrero, A. (2); Hutchinson, G (2); Diaz-Rubio, E (2); Ahmedzai, S (2); Kohne, H (2); Langendijk, R (2); Nitti, D (2); et, al. (1); Gustavsson, P (1); Dahl, Niklas (1); Van Cutsem, E (1); Cario, Holger (1); Bode, H. (1); Kohne, E. (1); Schmoll, HJ (1); Wagener, T. (1); Wilke, J (1); Marinus, A (1); visa färre...

Lärosäte: Uppsala universitet (2); Karolinska Institutet (1)

Språk: Engelska (3)

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