Zobrazeno 1 - 10
of 109
pro vyhledávání: '"E. Kuhlein"'
Autor:
A. Robert, P. Rachieru-Sourisseau, N. Dastugue, E. Kuhlein, A. Chassevent, L. Baranger, F. Geneviève
Publikováno v:
International Journal of Laboratory Hematology. 32:288-298
The DNA index (DI) is a prognostic factor in childhood acute lymphoblastic leukemia (ALL). The accuracy of DI measurement is important for treatment stratification: hyperdiploidy with DI > or = 1.16 is predictive of favorable prognosis whereas hypodi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2182fd9583f4a7671f6e283823c65e5
https://doi.org/10.1111/j.1751-553x.2009.01189.x
https://doi.org/10.1111/j.1751-553x.2009.01189.x
Autor:
A.-L. Debard, Jean-François Emile, Gilles Salles, Jean-Philippe Jais, Jean-Pierre Farcet, E. Kuhlein, Olivier Casasnovas, Christian Gisselbrecht, Pierre Feugier, Marie C. Béné, M. Labalette, A. Plonquet, M.H. Delfau-Larue, Claire Rabian, Corinne Haioun
Publikováno v:
Annals of Oncology. 18:1209-1215
Background: Lymphocytopenia is a prognostic factor in Hodgkin's disease. In diffuse large B-cell lymphoma (DLBCL), data are much less established, in spite of numerous reports on immune system–lymphoma interactions. This study addresses the prognos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a6717cc76ab52c72a1c308752c75502
https://doi.org/10.1093/annonc/mdm110
https://doi.org/10.1093/annonc/mdm110
Autor:
C, Fossat, M, Roussel, I, Arnoux, V, Asnafi, C, Brouzes, F, Garnache-Ottou, M C, Jacob, E, Kuhlein, E, Macintyre-Davi, A, Plesa, N, Robillard, J, Tkaczuk, N, Ifrah, H, Dombret, M C, Béné, A, Baruchel, R, Garand
Publikováno v:
Cytometry. Part B, Clinical cytometry.
Background: Minimal residual disease (MRD) assessment provides a powerful prognostic factor for therapeutic stratification in acute lymphoblastic leukemia (ALL). Multiparameter flow cytometry (MFC) has the potential for a rapid and sensitive identifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d42107d6a04e9bf2479f9a8c820377b6
https://pubmed.ncbi.nlm.nih.gov/25270227
https://pubmed.ncbi.nlm.nih.gov/25270227
Publikováno v:
Archives de Pédiatrie. 5:280-284
Resume Le diagnostic des maladies inflammatoires de revelation neonatale est parfois retrospectif, propose apres une tongue errance, elle-meme source d'agressivite et de iatrogenie. Observation. Un patient, âge de 6 ans, souffre depuis sa naissance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f062a3a97d717157016e8838d62ff77b
https://doi.org/10.1016/s0929-693x(97)89369-4
https://doi.org/10.1016/s0929-693x(97)89369-4
Publikováno v:
Immunogenetics. 59(1)
A new mutation of the CD40LG gene that encodes the CD40 ligand molecule was characterized in a young patient harboring a hyper-IgM with immunodeficiency syndrome. Inactivation of CD40LG gene resulted from the insertion of an AluYb8 element in exon 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98dca75bc67d3ff073349f0df21e2654
https://pubmed.ncbi.nlm.nih.gov/17146684
https://pubmed.ncbi.nlm.nih.gov/17146684
Autor:
Michael Zühlsdorf, W.-D. Ludwig, A. Derolf, Anna Porwit-MacDonald, Kyra Michalova, Walter Knapp, T. Haas, Richard Garand, P Leme zcaron, I Marinov, Gian Luigi Castoldi, P Talmant, E Kuhlein, A. Orfao, Estella Matutes, M. B. Van't Veer, C. Schoch, Zuzana Zemanova, M C Béné, T Haferlach
Publikováno v:
Leukemia, 20(4), 725-728. Nature Publishing Group
Near-tetraploid acute myeloid leukemias (NT-AML) constitute an unusual presentation defined by blasts containing 80–104 chromosomes without aberrant near-diploid metaphases. Only about 60 NT-AML cases have been described so far in the literature.1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1349f0f335d1051d8b3e432eed970969
https://pure.eur.nl/en/publications/1fffbf9e-89a3-4e24-9de4-7dd0ea9e32b9
https://pure.eur.nl/en/publications/1fffbf9e-89a3-4e24-9de4-7dd0ea9e32b9
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 5(3)
Diagnosis of inflammatory non-infectious diseases with a neonatal onset is often retrospective. It may lead to aggressive and iatrogenic procedures.A 6-year-old boy was suffering, since birth, from recurrent febrile attacks including rashes, gastroin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0e2b267182a23f204d97574e66cb22fb
https://pubmed.ncbi.nlm.nih.gov/10327995
https://pubmed.ncbi.nlm.nih.gov/10327995
Publikováno v:
Genetic counseling (Geneva, Switzerland). 10(1)
22q11.2 deletion is a common genetic disorder characterised by a wide spectrum of clinical manifestations. To date no simple genotype-phenotype correlation has been established. Moreover, several reports have mentioned phenotypic discordance between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b0a0b31286e562a39e398103bf73c84f
https://pubmed.ncbi.nlm.nih.gov/10191428
https://pubmed.ncbi.nlm.nih.gov/10191428
Autor:
R, Garand, E, Duchayne, D, Blanchard, N, Robillard, E, Kuhlein, O, Fenneteau, F, Salomon-Nguyen, M J, Grange, P, Rousselot, C, Demur
Publikováno v:
British journal of haematology. 90(4)
We describe eight cases of erythroleukaemia distinct from FAB-AML M6, which demonstrate minimal erythroid differentiation not associated with a myeloblastic component. Three infants (including a Down's syndrome) and two adults presented with a de nov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6fee656930fe87d58834b40f2d3f0a11
https://pubmed.ncbi.nlm.nih.gov/7669665
https://pubmed.ncbi.nlm.nih.gov/7669665