Hasil Pencarian - Heidi Rossmann

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  1. 1
    A Novel Nonsense Mutation of the AGL Gene in a Romanian Patient with Glycogen Storage Disease Type IIIa

    A Novel Nonsense Mutation of the AGL Gene in a Romanian Patient with Glycogen Storage Disease Type IIIa oleh Anca Zimmermann, Heidi Rossmann, Simona Bucerzan, Paula Grigorescu-Sido

    Diterbitkan 2016-01-01
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  2. 2
    Impact of glutathione peroxidase-1 deficiency on macrophage foam cell formation and proliferation: implications for atherogenesis.

    Impact of glutathione peroxidase-1 deficiency on macrophage foam cell formation and proliferation: implications for atherogenesis. oleh Fei Cheng, Michael Torzewski, Adriana Degreif, Heidi Rossmann, Antje Canisius, Karl J Lackner

    Diterbitkan 2013-01-01
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  3. 3
    Central Venous Access Devices (CVAD) in Pediatric Oncology Patients—A Single-Center Retrospective Study Over More Than 9 Years

    Central Venous Access Devices (CVAD) in Pediatric Oncology Patients—A Single-Center Retrospective Study Over More Than 9 Years oleh Olaf Beck, Oliver Muensterer, Sarah Hofmann, Heidi Rossmann, Alicia Poplawski, Jörg Faber, Jan Gödeke

    Diterbitkan 2019-06-01
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  4. 4
    Hereditary Spherocytosis: Can Next-Generation Sequencing of the Five Most Frequently Affected Genes Replace Time-Consuming Functional Investigations?

    Hereditary Spherocytosis: Can Next-Generation Sequencing of the Five Most Frequently Affected Genes Replace Time-Consuming Functional Investigations? oleh Friederike Häuser, Heidi Rossmann, Anke Adenaeuer, Annette Shrestha, Dana Marandiuc, Claudia Paret, Jörg Faber, Karl J. Lackner, Bernhard Lämmle, Olaf Beck

    Diterbitkan 2023-11-01
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  5. 5
    Distribution of estimated glomerular filtration rate and determinants of its age dependent loss in a German population-based study

    Distribution of estimated glomerular filtration rate and determinants of its age dependent loss in a German population-based study oleh Thomas Waas, Andreas Schulz, Johannes Lotz, Heidi Rossmann, Norbert Pfeiffer, Manfred E. Beutel, Irene Schmidtmann, Thomas Münzel, Philipp S. Wild, Karl J. Lackner

    Diterbitkan 2021-05-01
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  6. 6
    Evidence for the utility of cfDNA plasma concentrations to predict disease severity in COVID-19: a retrospective pilot study

    Evidence for the utility of cfDNA plasma concentrations to predict disease severity in COVID-19: a retrospective pilot study oleh Katharina Hoeter, Elmo Neuberger, Susanne Fischer, Manuel Herbst, Ema Juškevičiūtė, Kira Enders, Heidi Rossmann, Martin F. Sprinzl, Perikles Simon, Marc Bodenstein, Michael Schaefer

    Diterbitkan 2023-09-01
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  7. 7
    Differential Inhibition of Platelet Reactivity by Dual Therapy With Aspirin and Low-Dose Rivaroxaban in Peripheral Arterial Disease: A Pilot Study

    Differential Inhibition of Platelet Reactivity by Dual Therapy With Aspirin and Low-Dose Rivaroxaban in Peripheral Arterial Disease: A Pilot Study oleh Kerstin Jurk, Korbinian F. Rothenaicher, Kathrin Groß, Heidi Rossmann, Gerhard Weißer, Irene Schmidtmann, Thomas Münzel, Thomas Münzel, Christine Espinola-Klein, Christine Espinola-Klein

    Diterbitkan 2022-05-01
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  8. 8
    Diagnosis of Hereditary TTP Caused by Homozygosity for a Rare Complex ADAMTS13 Allele After Salmonella Infection in a 43-Year-Old Asylum Seeker

    Diagnosis of Hereditary TTP Caused by Homozygosity for a Rare Complex ADAMTS13 Allele After Salmonella Infection in a 43-Year-Old Asylum Seeker oleh Ralph Wendt, Ralph Wendt, Sven Kalbitz, Felix Otto, Tanja Falter, Joachim Beige, Joachim Beige, Joachim Beige, Heidi Rossmann, Bernhard Lämmle, Bernhard Lämmle, Bernhard Lämmle

    Diterbitkan 2021-02-01
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  9. 9
    Novel <i>GATA1</i> Variant Causing a Bleeding Phenotype Associated with Combined Platelet α-/δ-Storage Pool Deficiency and Mild Dyserythropoiesis Modified by a <i>SLC4A1</i> Variant

    Novel <i>GATA1</i> Variant Causing a Bleeding Phenotype Associated with Combined Platelet α-/δ-Storage Pool Deficiency and Mild Dyserythropoiesis Modified by a <i>SLC4A1</i> Varian... oleh Kerstin Jurk, Anke Adenaeuer, Stefanie Sollfrank, Kathrin Groß, Friederike Häuser, Andreas Czwalinna, Josef Erkel, Nele Fritsch, Dana Marandiuc, Martin Schaller, Karl J. Lackner, Heidi Rossmann, Frauke Bergmann

    Diterbitkan 2022-09-01
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  10. 10
    Protective behavior and SARS-CoV-2 infection risk in the population – Results from the Gutenberg COVID-19 study

    Protective behavior and SARS-CoV-2 infection risk in the population – Results from the Gutenberg COVID-19 study oleh Rieke Baumkötter, Simge Yilmaz, Daniela Zahn, Katharina Fenzl, Jürgen H. Prochaska, Heidi Rossmann, Irene Schmidtmann, Alexander K. Schuster, Manfred E. Beutel, Karl J. Lackner, Thomas Münzel, Philipp S. Wild

    Diterbitkan 2022-10-01
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  11. 11
    Prevalence of Overweight and Obesity, Its Complications, and Progression in a 10-Year Follow-Up in the Gutenberg Health Study (GHS)

    Prevalence of Overweight and Obesity, Its Complications, and Progression in a 10-Year Follow-Up in the Gutenberg Health Study (GHS) oleh Tanja Falter, Anita M. Hennige, Andreas Schulz, Alexander Gieswinkel, Johannes Lotz, Heidi Rossmann, Manfred Beutel, Matthias Michal, Norbert Pfeiffer, Irene Schmidtmann, Thomas Münzel, Philipp S. Wild, Karl J. Lackner

    Diterbitkan 2023-10-01
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  12. 12
    Hypermethylation of RAD9A intron 2 in childhood cancer patients, leukemia and tumor cell lines suggest a role for oncogenic transformation

    Hypermethylation of RAD9A intron 2 in childhood cancer patients, leukemia and tumor cell lines suggest a role for oncogenic transformation oleh Danuta Galetzka, Julia Böck, Lukas Wagner, Marcus Dittrich, Olesja Sinizyn, Marco Ludwig, Heidi Rossmann, Claudia Spix, Markus Radsak, Peter Scholz-Kreisel, Johanna Mirsch, Matthias Linke, Walburgis Brenner, Manuela Marron, Alicia Poplawski, Thomas Haaf, Heinz Schmidberger, Dirk Prawitt

    Diterbitkan 2022-01-01
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  13. 13
    Genetics and beyond--the transcriptome of human monocytes and disease susceptibility.

    Genetics and beyond--the transcriptome of human monocytes and disease susceptibility. oleh Tanja Zeller, Philipp Wild, Silke Szymczak, Maxime Rotival, Arne Schillert, Raphaele Castagne, Seraya Maouche, Marine Germain, Karl Lackner, Heidi Rossmann, Medea Eleftheriadis, Christoph R Sinning, Renate B Schnabel, Edith Lubos, Detlev Mennerich, Werner Rust, Claire Perret, Carole Proust, Viviane Nicaud, Joseph Loscalzo, Norbert Hübner, David Tregouet, Thomas Münzel, Andreas Ziegler, Laurence Tiret, Stefan Blankenberg, François Cambien

    Diterbitkan 2010-01-01
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  14. 14
    Integrating genome-wide genetic variations and monocyte expression data reveals trans-regulated gene modules in humans.

    Integrating genome-wide genetic variations and monocyte expression data reveals trans-regulated gene modules in humans. oleh Maxime Rotival, Tanja Zeller, Philipp S Wild, Seraya Maouche, Silke Szymczak, Arne Schillert, Raphaele Castagné, Arne Deiseroth, Carole Proust, Jessy Brocheton, Tiphaine Godefroy, Claire Perret, Marine Germain, Medea Eleftheriadis, Christoph R Sinning, Renate B Schnabel, Edith Lubos, Karl J Lackner, Heidi Rossmann, Thomas Münzel, Augusto Rendon, Cardiogenics Consortium, Jeanette Erdmann, Panos Deloukas, Christian Hengstenberg, Patrick Diemert, Gilles Montalescot, Willem H Ouwehand, Nilesh J Samani, Heribert Schunkert, David-Alexandre Tregouet, Andreas Ziegler, Alison H Goodall, François Cambien, Laurence Tiret, Stefan Blankenberg

    Diterbitkan 2011-12-01
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  15. 15
    CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis

    CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis oleh Nafisa Nuzhat, Kristof Van Schil, Sandra Liakopoulos, Miriam Bauwens, Alfredo Dueñas Rey, Stephan Käseberg, Melanie Jäger, Jason R. Willer, Jennifer Winter, Hanh M. Truong, Nuria Gruartmoner, Mattias Van Heetvelde, Joachim Wolf, Robert Merget, Sabine Grasshoff-Derr, Jo Van Dorpe, Anne Hoorens, Heidi Stöhr, Luke Mansard, Anne-Françoise Roux, Thomas Langmann, Katharina Dannhausen, David Rosenkranz, Karl M. Wissing, Michel Van Lint, Heidi Rossmann, Friederike Häuser, Peter Nürnberg, Holger Thiele, Ulrich Zechner, Jillian N. Pearring, Elfride De Baere, Hanno J. Bolz

    Diterbitkan 2023-04-01
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  16. 16
    Biallelic MAD2L1BP (p31comet) mutation is associated with mosaic aneuploidy and juvenile granulosa cell tumors

    Biallelic MAD2L1BP (p31comet) mutation is associated with mosaic aneuploidy and juvenile granulosa cell tumors oleh Ghada M. H. Abdel-Salam, Susanne Hellmuth, Elise Gradhand, Stephan Käseberg, Jennifer Winter, Ann-Sophie Pabst, Maha M. Eid, Holger Thiele, Peter Nürnberg, Birgit S. Budde, Mohammad Reza Toliat, Ines B. Brecht, Christopher Schroeder, Axel Gschwind, Stephan Ossowski, Friederike Häuser, Heidi Rossmann, Mohamed S. Abdel-Hamid, Ibrahim Hegazy, Ahmed G. Mohamed, Dominik T. Schneider, Aida Bertoli-Avella, Peter Bauer, Jillian N. Pearring, Rolph Pfundt, Alexander Hoischen, Christian Gilissen, Dennis Strand, Ulrich Zechner, Soha A. Tashkandi, Eissa A. Faqeih, Olaf Stemmann, Susanne Strand, Hanno J. Bolz

    Diterbitkan 2023-11-01
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