Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Mikael Donnér"'
Publikováno v:
Acta Medica Scandinavica. 208:407-410
A case of recurrent pulmonary embolism, secondary to thrombosis in an aneurysm of the popliteal vein is described. The source of embolism was not obvious clinically, and it was discovered only after venography. The anomaly was amenable to surgical in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::253e19cc6584fbd6c8ec4c9edbe1fdc2
https://doi.org/10.1111/j.0954-6820.1980.tb01222.x
https://doi.org/10.1111/j.0954-6820.1980.tb01222.x
Autor:
Nils Mandahl, Carl-Magnus Kullendorff, Måus Åkerman, Fredrik Mertens, Mikael Donnér, Thomas Wiebe
Publikováno v:
Medical and Pediatric Oncology. 32:79-83
BACKGROUND: Ewing sarcoma is associated with a nonrandom pattern of primary and secondary chromosomal aberrations. Whereas the finding of rearrangements of chromosome 22, usually in the form of a balanced translocation t(11;22)(q24;q12), is important
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21505e484fb4e9946d3f5af4523ead15
https://doi.org/10.1002/(sici)1096-911x(199902)32:2<79::aid-mpo1>3.0.co
https://doi.org/10.1002/(sici)1096-911x(199902)32:2<79::aid-mpo1>3.0.co
Publikováno v:
Medical and Pediatric Oncology. 30:156-159
Background and procedure During a 13-year period, 22 children were treated for rhabdomyosarcoma (RMS). In 18 of these patients chromosome analysis was attempted on material from tumor biopsies, fine needle aspiration biopsies and/or bone marrow sampl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8f6d7faacf9d67872541610592f1816
https://doi.org/10.1002/(sici)1096-911x(199803)30:3<156::aid-mpo5>3.0.co
https://doi.org/10.1002/(sici)1096-911x(199803)30:3<156::aid-mpo5>3.0.co
Autor:
Inga Hägerstrand, Felix Mitelman, Carl-Magnus Kullendorff, Fredrik Mertens, Nils Mandahl, Sverre Heim, Mikael Donnér
Publikováno v:
Cancer Genetics and Cytogenetics. 81:135-138
A retroperitoneal neurofibrosarcoma infiltrating the spine of a 2-year-old boy was investigated cytogenetically three times over a 5-month period. The first sample, from a diagnostic fine-needle aspiration biopsy, had a supernumerary i(1)(q10) as the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18105d05f3151a19f087f19bb912b8b8
https://doi.org/10.1016/0165-4608(94)00214-v
https://doi.org/10.1016/0165-4608(94)00214-v
Publikováno v:
British Journal of Haematology. 78:403-407
Summary. Besides having a large number of restriction fragment length polymorphisms (RFLP) the von Willebrand factor (vWF) gene contains several sequence polymorphisms in the coding regions. Eight nucleotide substitutions have been reported in two or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0761347dd5f332a45618281f09649d26
https://doi.org/10.1111/j.1365-2141.1991.tb04455.x
https://doi.org/10.1111/j.1365-2141.1991.tb04455.x
Publikováno v:
European Journal of Haematology. 57:178-179
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8fe77e053911d99ba7698be887749a2d
https://doi.org/10.1111/j.1600-0609.1996.tb01357.x
https://doi.org/10.1111/j.1600-0609.1996.tb01357.x
Autor:
Felix Mitelman, Bertil Johansson, Mikael Donnér, Mattias Höglund, Bodil Strömbeck, Patrik Andreasson
Publikováno v:
British journal of haematology. 98(1)
The cytogenetically unidentifiable t(12;21) (p12;q22), resulting in ETV6/CBFA2 fusion, is the most frequent chromosomal aberration in childhood acute lymphoblastic leukaemia (ALL). We report a variant, ider(21) (q10)t(12;21)(p12;q22), which was shown
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db67acb55eeba63ca6af9ed984a8e10b
https://pubmed.ncbi.nlm.nih.gov/9233588
https://pubmed.ncbi.nlm.nih.gov/9233588
Publikováno v:
Medical and Pediatric Oncology. 41:486-487
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d95095cdac079e2a974133605d6ea59c
https://doi.org/10.1002/mpo.10391
https://doi.org/10.1002/mpo.10391
Autor:
Lars Holmberg, Thorsen S, Björn Dahlbäck, Ann-Charlotte Kristoffersson, Erik Berntorp, Scheibel E, Inga Marie Nilsson, Mikael Donnér
Publikováno v:
Europe PubMed Central
Recently, several von Willebrand factor gene mutations resulting in type IIA von Willebrand's disease have been reported. We examined 8 patients from Sweden and Denmark with this phenotype and found two new candidate mutations and a hitherto unknown
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e4a61e3548332c00ba88a02c221fb62
https://pubmed.ncbi.nlm.nih.gov/8348943
https://pubmed.ncbi.nlm.nih.gov/8348943
Publikováno v:
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c83953e48f3aace2781277dcd6f48e3
https://pubmed.ncbi.nlm.nih.gov/1473591
https://pubmed.ncbi.nlm.nih.gov/1473591