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Disease‐causing mutations in the XIAP BIR2 domain impair NOD2‐dependent immune signalling
Author / Creator:Damgaard, Rune Busk ; Fiil, Berthe Katrine ; Speckmann, Carsten ; Yabal, Monica ; Stadt, Udo zur ; Bekker‐Jensen, Simon ; Jost, Philipp J. ; Ehl, Stephan ; Mailand, Niels ; Gyrd‐Hansen, Mads
Publisher:London: Nature Publishing Group UK
Journal title:EMBO molecular medicine, 2013-08, Vol.5 (8), p.1278-1295
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Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A
Author / Creator:Stadt, Udo Zur ; Beutel, Karin ; Kolberg, Susanne ; Schneppenheim, Reinhard ; Kabisch, Hartmut ; Janka, Gritta ; Hennies, Hans Christian
Publisher:Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Journal title:Human mutation, 2006-01, Vol.27 (1), p.62-68
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Recent advances in the diagnosis and treatment of hemophagocytic lymphohistiocytosis
Author / Creator:Bode, Sebastian FN ; Lehmberg, Kai ; Maul-Pavicic, Andrea ; Vraetz, Thomas ; Janka, Gritta ; Stadt, Udo ; Ehl, Stephan
Publisher:England: BioMed Central Ltd
Journal title:Arthritis research & therapy, 2012-01, Vol.14 (3), p.213-213
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Characterization of novel, recurrent genomic rearrangements as sensitive MRD targets in childhood B-cell precursor ALL
Author / Creator:Udo zur Stadt ; Malik Alawi ; Adao, Manuela ; Indenbirken, Daniela ; Escherich, Gabriele ; Horstmann, Martin A
Publisher:London: Springer Nature B.V
Journal title:Blood cancer journal (New York), 2019-11, Vol.9, p.1-11
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Quantification of minimal residual disease (MRD) in acute lymphoblastic leukemia (ALL) using amplicon-fusion-site polymerase chain reaction (AFS-PCR)
Author / Creator:Weber, Axel ; Taube, Sylvia ; zur Stadt, Udo ; Horstmann, Martin ; Krohn, Knut ; Bradtke, Jutta ; Teigler-Schlegel, Andrea ; Leiblein, Sabine ; Christiansen, Holger
Publisher:England: BioMed Central Ltd
Journal title:Experimental hematology & oncology, 2012-11, Vol.1 (1), p.33-33, Article 33
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In Vivo Imaging Enables High Resolution Preclinical Trials on Patients’ Leukemia Cells Growing in Mice
Author / Creator:Terziyska, Nadia ; Alves, Catarina Castro ; Groiss, Volker ; Schneider, Katja ; Farkasova, Katarina ; Ogris, Manfred ; Wagner, Ernst ; Ehrhardt, Harald ; Brentjens, Renier J. ; zur Stadt, Udo ; Horstmann, Martin ; Quintanilla-Martinez, Leticia ; Jeremias, Irmela
Publisher:United States: Public Library of Science
Journal title:PloS one, 2012-12, Vol.7 (12), p.e52798
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STXBP2 mutations in children with familial haemophagocytic lymphohistiocytosis type 5
Author / Creator:Cetica, Valentina ; Santoro, Alessandra ; Gilmour, Kimberly C ; Sieni, Elena ; Beutel, Karin ; Pende, Daniela ; Marcenaro, Stefania ; Koch, Florian ; Grieve, Samantha ; Wheeler, Rachel ; Zhao, Fang ; zur Stadt, Udo ; Griffiths, Gillian M ; Aricò, Maurizio
Publisher:London: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2010-09, Vol.47 (9), p.595-600
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Disease‐causing mutations in the XIAP BIR 2 domain impair NOD 2‐dependent immune signalling
Author / Creator:Damgaard, Rune Busk ; Fiil, Berthe Katrine ; Speckmann, Carsten ; Yabal, Monica ; Stadt, Udo zur ; Bekker‐Jensen, Simon ; Jost, Philipp J. ; Ehl, Stephan ; Mailand, Niels ; Gyrd‐Hansen, Mads
Publisher:Frankfurt: EMBO Press
Journal title:EMBO molecular medicine, 2013-08, Vol.5 (8), p.1278-1295
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Six novel mutations in the PRF1 gene in children with haemophagocytic lymphohistiocytosis
Author / Creator:Clementi, Rita ; zur Stadt, Udo ; Savoldi, Gianfranco ; Varotto, Stefania ; Conter, Valentino ; De Fusco, Carmela ; Notarangelo, Luigi D ; Schneider, Marion ; Klersy, Catherine ; Janka, Gritta ; Danesino, Cesare ; Aricò, Maurizio
Publisher:London: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2001-09, Vol.38 (9), p.643-646
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Characterization of IG-MYC-breakpoints and their application for quantitative minimal disease monitoring in high-risk pediatric Burkitt-lymphoma and -leukemia
Author / Creator:Möker, Paula ; zur Stadt, Udo ; Zimmermann, Martin ; Alawi, Malik ; Mueller, Stephanie ; Finger, Jasmin ; Knörr, Fabian ; Riquelme, Amambay ; Oschlies, Ilske ; Klapper, Wolfram ; Bradtke, Jutta ; Burkhardt, Birgit ; Woessmann, Wilhelm ; Damm-Welk, Christine
Publisher:London: Nature Publishing Group
Journal title:Leukemia, 2022-09, Vol.36 (9), p.2343-2346
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Effective Immunological Guidance of Genetic Analyses Including Exome Sequencing in Patients Evaluated for Hemophagocytic Lymphohistiocytosis
Author / Creator:Ammann, Sandra ; Lehmberg, Kai ; zur Stadt, Udo ; Klemann, Christian ; Bode, Sebastian F. N. ; Speckmann, Carsten ; Janka, Gritta ; Wustrau, Katharina ; Rakhmanov, Mirzokhid ; Fuchs, Ilka ; Hennies, Hans C. ; Ehl, Stephan
Publisher:New York: Springer US
Journal title:Journal of clinical immunology, 2017-11, Vol.37 (8), p.770-780
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Genotype–phenotype study of familial haemophagocytic lymphohistiocytosis type 3
Author / Creator:Sieni, Elena ; Cetica, Valentina ; Santoro, Alessandra ; Beutel, Karin ; Mastrodicasa, Elena ; Meeths, Marie ; Ciambotti, Benedetta ; Brugnolo, Francesca ; zur Stadt, Udo ; Pende, Daniela ; Moretta, Lorenzo ; Griffiths, Gillian M ; Henter, Jan-Inge ; Janka, Gritta ; Aricò, Maurizio
Publisher:London: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2011-05, Vol.48 (5), p.343-352
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Late-onset hemophagocytic lymphohistiocytosis (HLH) in an adult female with Griscelli syndrome type 2 (GS2)
Author / Creator:Henkes, Martin ; Finke, Jürgen ; Warnatz, Klaus ; Ammann, Sandra ; Stadt, Udo Zur ; Janka, Gritta ; Brugger, Wolfram
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Annals of hematology, 2015-06, Vol.94 (6), p.1057-1060
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Novel Patient with Late-Onset Familial Hemophagocytic Lymphohistiocytosis with STXBP2 Mutations Presenting with Autoimmune Hepatitis, Neurological Manifestations and Infections Associated with Hypogam...
Author / Creator:Esmaeilzadeh, Hossein ; Bemanian, Mohammad Hasan ; Nabavi, Mohammad ; Arshi, Saba ; Fallahpour, Morteza ; Fuchs, Ilka ; zur Stadt, Udo ; Warnatz, Klaus ; Ammann, Sandra ; Ehl, Stephan ; Lehmberg, Kai ; Rezaei, Nima
Publisher:Boston: Springer US
Journal title:Journal of clinical immunology, 2015-01, Vol.35 (1), p.22-25
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STXBP2 mutations in children with Familial Hemophagocytic Lymphohistiocytosis type 5
Author / Creator:Cetica, Valentina ; Santoro, Alessandra ; Gilmour, Kimberly ; Sieni, Elena ; Pende, Daniela ; Marcenaro, Stefania ; Koch, Florian ; Grieve, Samantha ; Wheeler, Rachel ; Zhao, Roseanne ; Zur Stadt, Udo ; Griffiths, Gillian M ; Arico', Maurizio
Publisher:BMJ Publishing Group
Journal title:Journal of medical genetics, 2010-08, Vol.47 (9)
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GENOTYPE-PHENOTYPE STUDY OF FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS TYPE 3
Author / Creator:Sieni, Elena ; Cetica, Valentina ; Santoro, Alessandra ; Beutel, Karin ; Mastrodicasa, Elena ; Meeths, Marie ; Ciambotti, Benedetta ; Brugnolo, Francesca ; Zur Stadt, Udo ; Pende, Daniela ; Moretta, Lorenzo ; Griffiths, Gillian M. ; Henter, Jan-Inge ; Janka, Gritta ; Arico, Maurizio
Publisher:BMJ Publishing Group
Journal title:Journal of medical genetics, 2011-01, Vol.48 (5)
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Quantification of minimal residual disease
Author / Creator:Weber, Axel ; Taube, Sylvia ; zur Stadt, Udo ; Horstmann, Ma ; Krohn, Knut ; Bradtke, Jutta ; Teigler-Schlegel, Andrea ; Leiblein, Sabine ; Christiansen, Holger
Publisher:BioMed Central Ltd
Journal title:Experimental hematology & oncology, 2012-11, Vol.1
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ArticlesPeer ReviewedFull Text
Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses ofPRF1, UNC13D, STX11, andRAB27A
Author / Creator:Stadt, Udo Zur ; Beutel, Karin ; Kolberg, Susanne ; Schneppenheim, Reinhard ; Kabisch, Hartmut ; Janka, Gritta ; Hennies, Hans Christian
Journal title:Human mutation, 2006-01, Vol.27 (1), p.62-68
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Fatal Epstein-Barr virus infection in a case of familial hemophagocytic lymphohistiocytosis with syntaxin-11 mutation Fatal Epstein-Barr virus infection in a case of familial hemophagocytic lymphohist...
Author / Creator:Meryem Albayrak ; Zühre Kaya ; Ebru Yilmaz-Keskin ; Udo Zur Stadt ; Ulker Koçak ; Türkiz Gürsel
Publisher:Hacettepe University Institute of Child Health
Journal title:Turkish journal of pediatrics, 2009-08, Vol.51 (4)
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Fatal Epstein-Barr virus infection in a case of familial hemophagocytic lymphohistiocytosis with syntaxin-11 mutation
Author / Creator:Albayrak, Meryem ; Kaya, Zühre ; Yilmaz-Keskin, Ebru ; Stadt, Udo Zur ; Koçak, Ulker ; Gürsel, Türkiz
Publisher:Turkey: Hacettepe University Faculty of Medicine
Journal title:Turkish journal of pediatrics, 2009-07, Vol.51 (4), p.371-374
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Showing 1 to 20 of 21 results

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Disease‐causing mutations in the XIAP BIR2 domain impair NOD2‐dependent immune signalling

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Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A

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Recent advances in the diagnosis and treatment of hemophagocytic lymphohistiocytosis

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Characterization of novel, recurrent genomic rearrangements as sensitive MRD targets in childhood B-cell precursor ALL

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Quantification of minimal residual disease (MRD) in acute lymphoblastic leukemia (ALL) using amplicon-fusion-site polymerase chain reaction (AFS-PCR)

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In Vivo Imaging Enables High Resolution Preclinical Trials on Patients’ Leukemia Cells Growing in Mice

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STXBP2 mutations in children with familial haemophagocytic lymphohistiocytosis type 5

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Disease‐causing mutations in the XIAP BIR 2 domain impair NOD 2‐dependent immune signalling

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Six novel mutations in the PRF1 gene in children with haemophagocytic lymphohistiocytosis

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Characterization of IG-MYC-breakpoints and their application for quantitative minimal disease monitoring in high-risk pediatric Burkitt-lymphoma and -leukemia

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Effective Immunological Guidance of Genetic Analyses Including Exome Sequencing in Patients Evaluated for Hemophagocytic Lymphohistiocytosis

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Genotype–phenotype study of familial haemophagocytic lymphohistiocytosis type 3

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Late-onset hemophagocytic lymphohistiocytosis (HLH) in an adult female with Griscelli syndrome type 2 (GS2)

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Novel Patient with Late-Onset Familial Hemophagocytic Lymphohistiocytosis with STXBP2 Mutations Presenting with Autoimmune Hepatitis, Neurological Manifestations and Infections Associated with Hypogam...

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STXBP2 mutations in children with Familial Hemophagocytic Lymphohistiocytosis type 5

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GENOTYPE-PHENOTYPE STUDY OF FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS TYPE 3

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Quantification of minimal residual disease

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Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses ofPRF1, UNC13D, STX11, andRAB27A

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Fatal Epstein-Barr virus infection in a case of familial hemophagocytic lymphohistiocytosis with syntaxin-11 mutation Fatal Epstein-Barr virus infection in a case of familial hemophagocytic lymphohist...

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Fatal Epstein-Barr virus infection in a case of familial hemophagocytic lymphohistiocytosis with syntaxin-11 mutation

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