نتایج جستجو برای: cytogenetic risk groups

تعداد نتایج: 1591243  

Journal: :International journal of biology and chemistry 2021

The study utilized molecular-genetic, cytogenetic, and statistical analyzes methods. A cytogenetic molecular genetic analysis of the inhabitants villages Amangeldy, Belbulak, in whose territory warehouses unused pesticides are located, was carried out. Residents Basshi village, on which there no products disposal pesticides, were taken as control. Cytogenetic showed a high level chromosomal abe...

Journal: :British journal of haematology 2002
Alan K Burnett Keith Wheatley Anthony H Goldstone Richard F Stevens Ian M Hann John H K Rees Georgina Harrison

Patients under 55 years in the United Kingdom Medical Research Council Acute Myeloid Leukaemia 10 trial who entered complete remission were tissue typed (n = 1063). Four hundred and nineteen had a matched sibling donor and 644 had no match. When compared on a donor versus no donor basis the relapse risk was reduced in the donor arm (36%vs 52%; P = 0.001) and the disease-free survival (DFS) impr...

2014
Aristoteles Giagounidis Ghulam J Mufti Moshe Mittelman Guillermo Sanz Uwe Platzbecker Petra Muus Dominik Selleslag Odile Beyne-Rauzy Peter te Boekhorst Consuelo del Cañizo Agnès Guerci-Bresler Lars Nilsson Michael Lübbert Bruno Quesnel Arnold Ganser David Bowen Brigitte Schlegelberger Gudrun Göhring Tommy Fu Bouchra Benettaib Eva Hellström-Lindberg Pierre Fenaux

OBJECTIVE A subset analysis of the randomised, phase 3, MDS-004 study to evaluate outcomes in patients with International Prognostic Scoring System (IPSS)-defined Low-/Intermediate (Int)-1-risk myelodysplastic syndromes (MDS) with isolated del(5q). METHODS Patients received lenalidomide 10 mg/d (days 1-21; n = 47) or 5 mg/d (days 1-28; n = 43) on 28-d cycles or placebo (n = 45). From the plac...

Journal: :Environmental Health Perspectives 2001
Z Smerhovsky K Landa P Rössner M Brabec Z Zudova N Hola Z Pokorna J Mareckova D Hurychova

We used cytogenetic analysis to carry out a cohort study in which the major objective was to test the association between frequency of chromosomal aberrations and subsequent risk of cancer. In spite of the extensive use of the cytogenetic analysis of human peripheral blood lymphocytes in biomonitoring of exposure to various mutagens and carcinogens on an ecologic level, the long-term effects of...

2016
Kyung-Ho Jeong Young-Jin Song Jin-Yeong Han Ki-Uk Kim

BACKGROUND The purpose of the study is to reveal the association of cytogenetic compltyexi and peritumoral edema volume (PTEV) and its prognostic significance in high-grade astrocytoma patients by culturing patient tumor cells. METHODS Twenty-seven high-grade astrocytoma patients were divided into three groups according to karyotype complexity: normal, non-complex karyotype (NCK), and complex...

2013
Jaap Brand Martin H van Vliet Leonie de Best Peter JM Valk Henk E Viëtor Bob Löwenberg Erik H van Beers

High levels of BAALC, ERG, EVI1 and MN1 expression have been associated with shorter overall survival in AML but standardized and clinically validated assays are lacking. We have therefore developed and optimized an assay for standardized detection of these prognostic genes for patients with intermediate cytogenetic risk AML. In a training set of 147 intermediate cytogenetic risk cases we perfo...

Journal: :Rossijskij žurnal detskoj gematologii i onkologii 2022

Background . Recovery of children with acute lymphoblastic leukemia (ALL) was one the most significant achievements clinical oncohematology XX century. Success in treatment ALL became possible due to comprehensive (clinical, morphoimmunological, cytogenetic) diagnostics and development differentiated, risk-adapted protocols. The German group BFM (Berlin–Frankfurt–Munster) a pioneer creating eff...

Journal: :Journal of medical genetics 1969
P L Monteleone J A Monteleone J Grzegocki

Chromosome abnormalities in structure as well as number have often been found to be associated with congenital anomalies in humans. Numerous genetic mechanisms have been postulated to explain the cytogenetic alterations. Wallace and Anderson (1964) reported a patient with numerous congenital anomalies whose chromosomal analysis revealed 45 chromosomes with a translocation deletion involving mem...

Journal: :Haematologica 2014
Gabriel Etienne Stéphanie Dulucq Franck-Emmanuel Nicolini Stéphane Morisset Marie-Pierre Fort Anna Schmitt Madeleine Etienne Sandrine Hayette Eric Lippert Caroline Bureau Isabelle Tigaud Didier Adiko Gérald Marit Josy Reiffers François-Xavier Mahon

Sustained imatinib treatment in chronic myeloid leukemia patients can result in complete molecular response allowing discontinuation without relapse. We set out to evaluate the frequency of complete molecular response in imatinib de novo chronic phase chronic myeloid leukemia patients, to identify base-line and under-treatment predictive factors of complete molecular response in patients achiev...

2016
Yuan Jian Xiaolei Chen Huixing Zhou Wanqiu Zhu Nian Liu Chuanying Geng Wenming Chen

The identification of specific cytogenetic abnormalities by interphase fluorescence in situ hybridization (i-FISH) has become a routine procedure for prognostic stratification of multiple myeloma (MM) patients. In this study, the prognostic significance of cytogenetic abnormalities detected by interphase fluorescence in situ hybridization (iFISH) in 229 newly diagnosed multiple myeloma patients...

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