Výsledky vyhledávání - Irina Golovleva

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  1. 1
    Congenital dyserythropoietic anemia type III (CDA III) is caused by a mutation in kinesin family member, KIF23

    Congenital dyserythropoietic anemia type III (CDA III) is caused by a mutation in kinesin family member, KIF23 Autor Maria Liljeholm, Andrew F. Irvine, Ann-Louise Vikberg, Anna Norberg, Stacy Month, Herbert Sandström, Anders Wåhlin, Masanori Mishima, Irina Golovleva

    Vydáno 2013
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    Artigo
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  2. 2
    Loss of chromosomes is the primary event in near-haploid and low-hypodiploid acute lymphoblastic leukemia

    Loss of chromosomes is the primary event in near-haploid and low-hypodiploid acute lymphoblastic leukemia Autor Shahideh Safavi, Erik Forestier, Irina Golovleva, Gisela Barbany, Karolin H. Nord, Anthony V. Moorman, Christine J. Harrison, B Johansson, Kajsa Paulsson

    Vydáno 2012
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    Carta
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  3. 3
    Direct Visualization of<i>Propionibacterium acnes</i>in Prostate Tissue by Multicolor Fluorescent In Situ Hybridization Assay

    Direct Visualization of<i>Propionibacterium acnes</i>in Prostate Tissue by Multicolor Fluorescent In Situ Hybridization Assay Autor Oleg A. Alexeyev, Ingrid Marklund, Beverley A. Shannon, Irina Golovleva, Jan Olsson, Charlotte I.J. Andersson, Iréne Eriksson, Ronald J. Cohen, Fredrik Elgh

    Vydáno 2007
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    Artigo
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  4. 4
    The clinical impact of <i><scp>IKZF</scp>1</i> deletions in paediatric B‐cell precursor acute lymphoblastic leukaemia is independent of minimal residual disease stratification in Nordic Society for Paediatric Haematology and Oncology treatment protocols used between 1992 and 2013

    The clinical impact of <i><scp>IKZF</scp>1</i> deletions in paediatric B‐cell precursor acute lymphoblastic leukaemia is independent of minimal residual disease stratification in N... Autor Linda Olsson, Ingegerd Öfverholm, Ulrika Norén‐Nyström, Vasilios Zachariadis, Jessica Nordlund, Helene Sjögren, Irina Golovleva, Ann Nordgren, Kajsa Paulsson, Mats Heyman, Gisela Barbany, Bertil Johansson

    Vydáno 2015
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    Artigo
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  5. 5
    Mutations in Collagen, Type XVII, Alpha 1 (<i>COL17A1</i>) Cause Epithelial Recurrent Erosion Dystrophy (ERED)

    Mutations in Collagen, Type XVII, Alpha 1 (<i>COL17A1</i>) Cause Epithelial Recurrent Erosion Dystrophy (ERED) Autor Frida Jönsson, Berit Byström, Alice E. Davidson, Ludvig J. Backman, Therese G. Kellgren, Stephen J. Tuft, Timo Koskela, Patrik Rydén, Ola Sandgren, Patrik Danielson, Alison J. Hardcastle, Irina Golovleva

    Vydáno 2015
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  6. 6
    Alterations in the expression, structure and function of progesterone receptor membrane component-1 (PGRMC1) in premature ovarian failure

    Alterations in the expression, structure and function of progesterone receptor membrane component-1 (PGRMC1) in premature ovarian failure Autor Mahmoud Mansouri, Jens Schuster, Jitendra Badhai, Eva-Lena Stattin, Ralf Lösel, Martin Wehling, Birgit Carlsson, Outi Hovatta, P.O. Karlström, Irina Golovleva, Daniela Toniolo, Silvia Bione, John J. Peluso, Niklas Dahl

    Vydáno 2008
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  7. 7
    Outcome of <i>ETV6/RUNX1</i>‐positive childhood acute lymphoblastic leukaemia in the NOPHO‐ALL‐1992 protocol: frequent late relapses but good overall survival

    Outcome of <i>ETV6/RUNX1</i>‐positive childhood acute lymphoblastic leukaemia in the NOPHO‐ALL‐1992 protocol: frequent late relapses but good overall survival Autor Erik Forestier, Mats Heyman, Mette K. Andersen, K. Autio, Elisabeth Blennow, Georg Borgström, Irina Golovleva, Sverre Heim, Kristina Heinonen, Randi Hovland, Jóhann Heiðar Jóhannsson, Gitte Kerndrup, Ann Nordgren, Richard Rosenquist, Birgitta Swolin, Bertil Johansson

    Vydáno 2008
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  8. 8
    High modal number and triple trisomies are highly correlated favorable factors in childhood B-cell precursor high hyperdiploid acute lymphoblastic leukemia treated according to the NOPHO ALL 1992/2000 protocols

    High modal number and triple trisomies are highly correlated favorable factors in childhood B-cell precursor high hyperdiploid acute lymphoblastic leukemia treated according to the... Autor Kajsa Paulsson, Erik Forestier, Mette Klarskov Andersen, K. Autio, Gisela Barbany, G.H. Borgström, Lucia Cavelier, Irina Golovleva, Sverre Heim, Kristiina Heinonen, Randi Hovland, Jóhann Heiðar Jóhannsson, Eigil Kjeldsen, Ann Nordgren, Lars Palmqvist, Bertil Johansson

    Vydáno 2013
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    Artigo
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  9. 9
    Comprehensive variant spectrum of the <i>CNGA3</i> gene in patients affected by achromatopsia

    Comprehensive variant spectrum of the <i>CNGA3</i> gene in patients affected by achromatopsia Autor Maria Solaki, Britta Baumann, Peggy Reuter, Sten Andréasson, Isabelle Audo, Carmen Ayuso, Ghassan Balousha, Francesco Benedicenti, David G. Birch, Pierre Bitoun, Delphine Blain, Béatrice Bocquet, Kari Branham, Jaume Catalá‐Mora, Elfride De Baere, Hélène Dollfus, Mohammed Falana, Roberto Giorda, Irina Golovleva, Irène Gottlob, John R. Heckenlively, Samuel G. Jacobson, Kaylie Webb-Jones, Herbert Jägle, Andreas Janecke, Ulrich Kellner, Petra Lišková, Birgit Lorenz, Loreto Martorell, André Messias, Isabelle Meunier, Fernanda Belga Ottoni Porto, Eleni Papageorgiou, Astrid S. Plomp, Thomy de Ravel, Charlotte Reiff, Agnes B. Renner, Thomas Rosenberg, Günther Rudolph, R. Salati, Emin Cumhur Şener, Paul A. Sieving, Franco Stanzial, Elias I. Traboulsi, Stephen H. Tsang, Balázs Varsányi, Richard G. Weleber, Ditta Zobor, Katarína Štingl, Bernd Wissinger, Susanne Kohl

    Vydáno 2022
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