Результати пошуку - Schmitt, Bernhard
- Показ 1 - 15 результатів із 15
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1
The quantitation of buffering action I. A formal & general approach за авторством Schmitt, Bernhard M
Опубліковано 2005Текст -
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The quantitation of buffering action II. Applications of the formal & general approach за авторством Schmitt, Bernhard M
Опубліковано 2005Текст -
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An improved method for real-time monitoring of membrane capacitance in Xenopus laevis oocytes. за авторством Schmitt, Bernhard M, Koepsell, Hermann
Опубліковано 2002Текст -
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Closed-Loop Acoustic Stimulation During Sleep in Children With Epilepsy: A Hypothesis-Driven Novel Approach to Interact With Spike-Wave Activity and Pilot Data Assessing Feasibilit... за авторством Fattinger, Sara, Heinzle, Bigna Bölsterli, Ramantani, Georgia, Abela, Lucia, Schmitt, Bernhard, Huber, Reto
Опубліковано 2019Текст -
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Cirrhosis Associated with Pyridoxal 5′-Phosphate Treatment of Pyridoxamine 5′-Phosphate Oxidase Deficiency за авторством Sudarsanam, Annapurna, Singh, Harry, Wilcken, Bridget, Stormon, Michael, Arbuckle, Susan, Schmitt, Bernhard, Clayton, Peter, Earl, John, Webster, Richard
Опубліковано 2014Текст -
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Glutamine supplementation in a child with inherited GS deficiency improves the clinical status and partially corrects the peripheral and central amino acid imbalance за авторством Häberle, Johannes, Shahbeck, Noora, Ibrahim, Khalid, Schmitt, Bernhard, Scheer, Ianina, O’Gorman, Ruth, Chaudhry, Farrukh A, Ben-Omran, Tawfeg
Опубліковано 2012Текст -
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Na/HCO(3) Cotransporters in Rat Brain: Expression in Glia, Neurons, and Choroid Plexus за авторством Schmitt, Bernhard M., Berger, Urs V., Douglas, Robert M., Bevensee, Mark O., Hediger, Matthias A., Haddad, Gabriel G., Boron, Walter F.
Опубліковано 2000Текст -
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Rapid turnover of DnaA at replication origin regions contributes to initiation control of DNA replication за авторством Schenk, Katrin, Hervás, Ana B., Rösch, Thomas C., Eisemann, Marc, Schmitt, Bernhard A., Dahlke, Stephan, Kleine-Borgmann, Luise, Murray, Seán M., Graumann, Peter L.
Опубліковано 2017Текст -
11
DNA methylation profiles of bronchoscopic biopsies for the diagnosis of lung cancer за авторством Goldmann, Torsten, Schmitt, Bernhard, Müller, Julia, Kröger, Maren, Scheufele, Swetlana, Marwitz, Sebastian, Nitschkowski, Dörte, Schneider, Marc A., Meister, Michael, Muley, Thomas, Thomas, Michael, Kugler, Christian, Rabe, Klaus F., Siebert, Reiner, Reck, Martin, Ammerpohl, Ole
Опубліковано 2021Текст -
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A Novel Multivalent OspA Vaccine against Lyme Borreliosis Is Safe and Immunogenic in an Adult Population Previously Infected with Borrelia burgdorferi Sensu Lato за авторством Wressnigg, Nina, Barrett, P. Noel, Pöllabauer, Eva-Maria, O'Rourke, Maria, Portsmouth, Daniel, Schwendinger, Michael G., Crowe, Brian A., Livey, Ian, Dvorak, Thomas, Schmitt, Bernhard, Zeitlinger, Markus, Kollaritsch, Herwig, Esen, Meral, Kremsner, Peter G., Jelinek, Tomas, Aschoff, Roland, Weisser, Roland, Naudts, Ingomar F. K., Aichinger, Gerald
Опубліковано 2014Текст -
13
Identification of a Loss-of-Function Mutation in the Context of Glutaminase Deficiency and Neonatal Epileptic Encephalopathy за авторством Rumping, Lynne, Büttner, Benjamin, Maier, Oliver, Rehmann, Holger, Lequin, Maarten, Schlump, Jan-Ulrich, Schmitt, Bernhard, Schiebergen-Bronkhorst, Birgit, Prinsen, Hubertus C. M. T., Losa, Michele, Fingerhut, Ralph, Lemke, Johannes R., Zwartkruis, Fried J. T., Houwen, Roderick H. J., Jans, Judith J. M., Verhoeven-Duif, Nanda M., van Hasselt, Peter M., Jamra, Rami
Опубліковано 2018Текст -
14
Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency) за авторством Mills, Philippa B., Footitt, Emma J., Mills, Kevin A., Tuschl, Karin, Aylett, Sarah, Varadkar, Sophia, Hemingway, Cheryl, Marlow, Neil, Rennie, Janet, Baxter, Peter, Dulac, Olivier, Nabbout, Rima, Craigen, William J., Schmitt, Bernhard, Feillet, François, Christensen, Ernst, De Lonlay, Pascale, Pike, Mike G., Hughes, M. Imelda, Struys, Eduard A., Jakobs, Cornelis, Zuberi, Sameer M., Clayton, Peter T.
Опубліковано 2010Текст -
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The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study за авторством Papuc, Sorina M., Abela, Lucia, Steindl, Katharina, Begemann, Anaïs, Simmons, Thomas L., Schmitt, Bernhard, Zweier, Markus, Oneda, Beatrice, Socher, Eileen, Crowther, Lisa M., Wohlrab, Gabriele, Gogoll, Laura, Poms, Martin, Seiler, Michelle, Papik, Michael, Baldinger, Rosa, Baumer, Alessandra, Asadollahi, Reza, Kroell-Seger, Judith, Schmid, Regula, Iff, Tobias, Schmitt-Mechelke, Thomas, Otten, Karoline, Hackenberg, Annette, Addor, Marie-Claude, Klein, Andrea, Azzarello-Burri, Silvia, Sticht, Heinrich, Joset, Pascal, Plecko, Barbara, Rauch, Anita
Опубліковано 2018Текст