Development of Hemolytic Anemia in a Nivolumab-Treated Patient with Refractory Metastatic Squamous Cell Skin Cancer and Chronic Lymphatic Leukemia

por Schwab, K.S., Heine, A., Weimann, T., Kristiansen, G., Brossart, P.
Publicado 2016

Microwave-to-optical transduction with erbium ions coupled to planar photonic and superconducting resonators

por Rochman, Jake, Xie, Tian, Bartholomew, John G., Schwab, K. C., Faraon, Andrei
Publicado 2023

Ornithine transcarbamylase deficiency combined with type 1 diabetes mellitus - a challenge in clinical and dietary management

por Grünert, Sarah C, Villavicencio-Lorini, Pablo, Wermuth, Bendicht, Lehnert, Willy, Sass, Jörn Oliver, Schwab, K Otfried
Publicado 2013

Clinical and neurocognitive outcome in symptomatic isovaleric acidemia

por Grünert, Sarah C, Wendel, Udo, Lindner, Martin, Leichsenring, Michael, Schwab, K Otfried, Vockley, Jerry, Lehnert, Willy, Ensenauer, Regina
Publicado 2012

Medium-chain acyl-CoA dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screening

por Grünert, Sarah C., Wehrle, A., Villavicencio-Lorini, P., Lausch, E., Vetter, B., Schwab, K. O., Tucci, S., Spiekerkoetter, U.
Publicado 2015

Overweight and Obesity Based on Four Reference Systems in 18,382 Paediatric Patients with Type 1 Diabetes from Germany and Austria

por Flechtner-Mors, M., Schwab, K. O., Fröhlich-Reiterer, E. E., Kapellen, T. M., Meissner, T., Rosenbauer, J., Stachow, R., Holl, R. W.
Publicado 2015

Diurnal variation of phenylalanine and tyrosine concentrations in adult patients with phenylketonuria: subcutaneous microdialysis is no adequate tool for the determination of amino...

por Grünert, Sarah C, Brichta, Corinna M, Krebs, Andreas, Clement, Hans-Willi, Rauh, Reinhold, Fleischhaker, Christian, Hennighausen, Klaus, Sass, Jörn Oliver, Schwab, K Otfried
Publicado 2013

Prevalence of type 1 and type 2 diabetes in children and adolescents in Germany from 2002 to 2020: A study based on electronic health record data from the DPV registry

por Stahl‐Pehe, Anna, Kamrath, Clemens, Prinz, Nicole, Kapellen, Thomas, Menzel, Ulrike, Kordonouri, Olga, Schwab, K. Otfried, Bechtold‐Dalla Pozza, Susanne, Rosenbauer, Joachim, Holl, Reinhard W.
Publicado 2022

Pädiatrie

por Karall, D., Meisinger, B., Grissenauer, G., Scholl-Bürgi, S., Heinz-Erian, P., Lagler, Florian, Sass, J. O., Grünert, S., Nussbaumer, E.-M., Schwab, K. O., Mönch, E., Hofer, A., Haberlandt, E., Oppl, V., Sperl, W., Spiekerkötter, U., Baumgartner Sigl, S., Stöckler-Ipsiroglu, S.
Publicado 2010

3-methylcrotonyl-CoA carboxylase deficiency: Clinical, biochemical, enzymatic and molecular studies in 88 individuals

por Grünert, Sarah C, Stucki, Martin, Morscher, Raphael J, Suormala, Terttu, Bürer, Celine, Burda, Patricie, Christensen, Ernst, Ficicioglu, Can, Herwig, Jürgen, Kölker, Stefan, Möslinger, Dorothea, Pasquini, Elisabetta, Santer, René, Schwab, K Otfried, Wilcken, Bridget, Fowler, Brian, Yue, Wyatt W, Baumgartner, Matthias R
Publicado 2012

Different pathways of molecular pathophysiology underlie cognitive and motor tauopathy phenotypes in transgenic models for Alzheimer’s disease and frontotemporal lobar degeneration...

por Melis, V., Zabke, C., Stamer, K., Magbagbeolu, M., Schwab, K., Marschall, P., Veh, R. W., Bachmann, S., Deiana, S., Moreau, P.-H., Davidson, K., Harrington, K. A., Rickard, J. E., Horsley, D., Garman, R., Mazurkiewicz, M., Niewiadomska, G., Wischik, C. M., Harrington, C. R., Riedel, G., Theuring, F.
Publicado 2014

Mutations in SELENBP1, encoding a novel human methanethiol oxidase, cause extra-oral halitosis

por Pol, Arjan, Renkema, G. Herma, Tangerman, Albert, Winkel, Edwin G., Engelke, Udo F., de Brouwer, Arjan P. M., Lloyd, Kent C., Araiza, Renee S., van den Heuvel, Lambert, Omran, Heymut, Olbrich, Heike, Elberink, Marijn Oude, Gilissen, Christian, Rodenburg, Richard J., Sass, Jörn Oliver, Schwab, K. Otfried, Schäfer, Hendrik, Venselaar, Hanka, Sequeira, J. Silvia, Op den Camp, Huub J.M., Wevers, Ron A.
Publicado 2017