Zobrazeno 1 - 10
of 58
pro vyhledávání: '"V, Parlier"'
Autor:
Audrey S. Baur, Christiane Meugé-Moraw, V. Parlier, Martine Jotterand, P.M. Schmidt, Françoise Delacrétaz
Publikováno v:
European Journal of Haematology. 64:71-79
CD34/QBEND10 immunostaining has been assessed in 150 bone marrow biopsies (BMB) including 91 myelodysplastic syndromes (MDS), 16 MDS-related AML, 25 reactive BMB, and 18 cases where RA could neither be established nor ruled out. All cases were review
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c03666fd3c9f896fe9f561b4f503c7b5
https://doi.org/10.1034/j.1600-0609.2000.90047.x
https://doi.org/10.1034/j.1600-0609.2000.90047.x
Publikováno v:
Leukemia. 11:964-970
Deletions of sequences centromeric to the p-arm breakpoint have been described in a subset of patients with inv(16) and acute myeloid leukemia (AML) and reported to be associated with a relatively good prognosis. We have investigated 16 p deletions i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7f1cdec66deb9cbc7a8f746bb1855dd
https://doi.org/10.1038/sj.leu.2400681
https://doi.org/10.1038/sj.leu.2400681
Autor:
Andreas Tobler, M. Jotterand Bellomo, P.M. Schmidt, E. Haller, Ph. Beris, V. Parlier, G. van Melle
Publikováno v:
Cancer Genetics and Cytogenetics. 81:158-165
The predictive potential of six selected factors was assessed in 72 patients with primary myelodysplastic syndrome using univariate and multivariate logistic regression analysis of survival at 18 months. Factors were age (above median of 69 years), d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1161bd4513814f8835fb1041ab4bc936
https://doi.org/10.1016/0165-4608(94)00220-6
https://doi.org/10.1016/0165-4608(94)00220-6
Autor:
Ph. Beris, Andreas Tobler, V. Parlier, G. van Melle, M. Jotterand Bellomo, P.M. Schmidt, E. Haller
Publikováno v:
Cancer Genetics and Cytogenetics. 78:219-231
One hundred and nine patients with primary myelodysplastic syndrome (MDS) were classified according to the French-American-British (FAB) criteria: 27 refractory anemia (RA, 25%), 26 RA with ringed sideroblasts (RARS, 24%), 16 RA with excess of blasts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56271409863441110209de8392f1bb43
https://doi.org/10.1016/0165-4608(94)90094-9
https://doi.org/10.1016/0165-4608(94)90094-9
Autor:
P. A. Miescher, Sakari Knuutila, Ph. Beris, M. Jotterand Bellomo, Marianne Tiainen, V. Parlier
Publikováno v:
British Journal of Haematology. 81:296-304
Paroxysmal nocturnal haemoglobinuria (PNH) was diagnosed in a 20-year-old male patient who suffered from anaemia since the age of 11. Eighteen years after diagnosis, PNH transformed into refractory anaemia with ringed sideroblasts (RARS). Trisomy 8 w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c676fbbf4727459731826dd40a7d98aa
https://doi.org/10.1111/j.1365-2141.1992.tb08223.x
https://doi.org/10.1111/j.1365-2141.1992.tb08223.x
Publikováno v:
Cancer Genetics and Cytogenetics. 59:138-160
Defects of 3q in bands q21 and q26 have been reported in more than 70 cases of acute nonlymphocytic leukemia (ANLL), myelodysplastic syndrome (MDS), and myeloproliferative disorder (MPD) in blast crisis. In this paper three additional patients are de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad6d70e80d6712359701c90a58cd2a81
https://doi.org/10.1016/0165-4608(92)90208-p
https://doi.org/10.1016/0165-4608(92)90208-p
We report on two elderly patients with newly diagnosed acute myeloid leukemia (AML) who were treated in palliative intention because of comorbidities and intermediate or poor risk cytogenetics. Both received G-CSF to reduce the risk of infection rela
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ccc64f800331f1e64297504e48e561e
Publikováno v:
Cancer Genetics and Cytogenetics. 46:157-172
Fifty-four patients with myelodysplastic syndrome (MDS) (35 men and 19 women aged 34–92 years) were studied cytogenetically. Bone marrow cell culture and chromosome preparation were performed according to four different protocols used in parallel:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b6f57ab7012ded27f43f356492960c3
https://doi.org/10.1016/0165-4608(90)90101-f
https://doi.org/10.1016/0165-4608(90)90101-f
Autor:
André Tichelli, D. Mühlematter, Thomas Kühne, Urs Hess, Mario Bargetzi, Jakob Passweg, Christine Cabrol, V. Parlier, Alois Gratwohl, Sandrine Meyer-Monard, Martine Jotterand
Publikováno v:
Leukemia. 20(2)
We evaluated the impact of genetic analysis combining cytogenetics and broad molecular screening on leukemia diagnosis according to World Health Organization (WHO) and on genetic risk assignment. A two-step nested multiplex RT-PCR assay was used that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4aae2ecb999aec780f0cb136e9273d7
https://pubmed.ncbi.nlm.nih.gov/16408102
https://pubmed.ncbi.nlm.nih.gov/16408102
Autor:
Martine Jotterand, Valérie Beyer, D. Mühlematter, Guy van Melle, V. Parlier, Chantal Castagné
Publikováno v:
Cancer genetics and cytogenetics. 147(2)
We applied a dual-color interphase in situ fluorescence hybridization (I-FISH) technique using centromeric probes specific to chromosomes 7 and 8 on 20 control samples in order to define the statistical model best suited to determine cutoff values fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f53e47a5f5b2c36ada7f34d64969688
https://pubmed.ncbi.nlm.nih.gov/14623458
https://pubmed.ncbi.nlm.nih.gov/14623458