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Manuela Krumbholz

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Methods in Molecular Biology (Clifton, N.J.)|December 16, 2020
Liquid Biopsies in Ewing SarcomaManuela Krumbholz, Markus Metzler
Journal of Molecular Medicine (Berlin, Germany)|August 14, 2010
Intracellular ROS level is increased in fibroblasts of triple A syndrome patientsBarbara Kind, Katrin Koehler, Manuela Krumbholz, et al.
Journal of Cellular and Molecular Medicine|June 15, 2019
Large amplicon droplet digital PCR for DNA-based monitoring of pediatric chronic myeloid leukaemiaManuela Krumbholz, Katharina Goerlitz, Christian Albert, et al.
Leukemia & Lymphoma|June 3, 2014
Response monitoring of infant acute myeloid leukemia treatment by quantification of the tumor specific MLL-FNBP1 fusion geneManuela Krumbholz, Ronny Jung, Jutta Bradtke, et al.
Journal of Pediatric Hematology/Oncology|October 9, 2012
Novel MLL2 mutation in Kabuki syndrome with hypogammaglobulinemia and severe chronic thrombopeniaFlorian Brackmann, Manuela Krumbholz, Thorsten Langer, et al.
European Journal of Pediatrics|January 4, 2008
Three siblings with triple A syndrome with a novel frameshift mutation in the AAAS gene and a review of 17 independent patients with the frequent p.Ser263Pro mutationTatjana Milenković, Katrin Koehler, Manuela Krumbholz, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|July 11, 2008
Triple A syndrome mimicking ALSMaria Strauss, Katrin Koehler, Manuela Krumbholz, et al.
Leukemia Research|November 7, 2012
Identification of the genomic BCR-ABL1 fusion sequence from blood specimen stored on filter paperMatthias Karl, Manuela Krumbholz, Josephine T Tauer, et al.
Plos One|February 27, 2013
Genomic EWS-FLI1 fusion sequences in Ewing sarcoma resemble breakpoint characteristics of immature lymphoid malignanciesManfred Berger, Uta Dirksen, Andreas Braeuninger, et al.
European Journal of Human Genetics : EJHG|July 17, 2008
Axonal neuropathy with unusual pattern of amyotrophy and alacrima associated with a novel AAAS mutation p.Leu430PheKatrin Koehler, Knut Brockmann, Manuela Krumbholz, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Methods in Molecular Biology (Clifton, N.J.)|December 16, 2020
Liquid Biopsies in Ewing SarcomaManuela Krumbholz, Markus Metzler
Journal of Molecular Medicine (Berlin, Germany)|August 14, 2010
Intracellular ROS level is increased in fibroblasts of triple A syndrome patientsBarbara Kind, Katrin Koehler, Manuela Krumbholz, et al.
Journal of Cellular and Molecular Medicine|June 15, 2019
Large amplicon droplet digital PCR for DNA-based monitoring of pediatric chronic myeloid leukaemiaManuela Krumbholz, Katharina Goerlitz, Christian Albert, et al.
Leukemia & Lymphoma|June 3, 2014
Response monitoring of infant acute myeloid leukemia treatment by quantification of the tumor specific MLL-FNBP1 fusion geneManuela Krumbholz, Ronny Jung, Jutta Bradtke, et al.
Journal of Pediatric Hematology/Oncology|October 9, 2012
Novel MLL2 mutation in Kabuki syndrome with hypogammaglobulinemia and severe chronic thrombopeniaFlorian Brackmann, Manuela Krumbholz, Thorsten Langer, et al.
European Journal of Pediatrics|January 4, 2008
Three siblings with triple A syndrome with a novel frameshift mutation in the AAAS gene and a review of 17 independent patients with the frequent p.Ser263Pro mutationTatjana Milenković, Katrin Koehler, Manuela Krumbholz, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|July 11, 2008
Triple A syndrome mimicking ALSMaria Strauss, Katrin Koehler, Manuela Krumbholz, et al.
Leukemia Research|November 7, 2012
Identification of the genomic BCR-ABL1 fusion sequence from blood specimen stored on filter paperMatthias Karl, Manuela Krumbholz, Josephine T Tauer, et al.
Plos One|February 27, 2013
Genomic EWS-FLI1 fusion sequences in Ewing sarcoma resemble breakpoint characteristics of immature lymphoid malignanciesManfred Berger, Uta Dirksen, Andreas Braeuninger, et al.
European Journal of Human Genetics : EJHG|July 17, 2008
Axonal neuropathy with unusual pattern of amyotrophy and alacrima associated with a novel AAAS mutation p.Leu430PheKatrin Koehler, Knut Brockmann, Manuela Krumbholz, et al.
Pageof 5