Metagenomic abundance estimation and diagnostic testing on species level

Tekijä Lindner, Martin S., Renard, Bernhard Y.
Julkaistu 2013

Metagenomic Profiling of Known and Unknown Microbes with MicrobeGPS

Tekijä Lindner, Martin S., Renard, Bernhard Y.
Julkaisussa PLoS One (2015)

Newborn screening by tandem mass spectrometry for glutaric aciduria type 1: a cost-effectiveness analysis

Tekijä Pfeil, Johannes, Listl, Stefan, Hoffmann, Georg F, Kölker, Stefan, Lindner, Martin, Burgard, Peter
Julkaistu 2013

Pipasic: similarity and expression correction for strain-level identification and quantification in metaproteomics

Tekijä Penzlin, Anke, Lindner, Martin S., Doellinger, Joerg, Dabrowski, Piotr Wojtek, Nitsche, Andreas, Renard, Bernhard Y.
Julkaistu 2014

Neonatal Screening for Congenital Metabolic and Endocrine Disorders: Results From Germany for the Years 2006–2018

Tekijä Lüders, Anja, Blankenstein, Oliver, Brockow, Inken, Ensenauer, Regina, Lindner, Martin, Schulze, Andreas, Nennstiel, Uta
Julkaisussa Dtsch Arztebl Int (2021)

High blood pressure, a red flag for the neonatal manifestation of urea cycle disorders

Tekijä Teufel, Ulrike, Burgard, Peter, Meyburg, Jochen, Lindner, Martin, Poeschl, Johannes, Ruef, Peter, Hoffmann, Georg F., Kölker, Stefan
Julkaisussa Orphanet J Rare Dis (2019)

Clinical and neurocognitive outcome in symptomatic isovaleric acidemia

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

Medium-Chain Acyl-CoA Dehydrogenase Deficiency: Evaluation of Genotype-Phenotype Correlation in Patients Detected by Newborn Screening

Tekijä Gramer, Gwendolyn, Haege, Gisela, Fang-Hoffmann, Junmin, Hoffmann, Georg F., Bartram, Claus R., Hinderhofer, Katrin, Burgard, Peter, Lindner, Martin
Julkaisussa JIMD Rep (2015)

A framework to start the debate on neonatal screening policies in the EU: an Expert Opinion Document

Tekijä Cornel, Martina C, Rigter, Tessel, Weinreich, Stephanie S, Burgard, Peter, Hoffmann, Georg F, Lindner, Martin, Gerard Loeber, J, Rupp, Kathrin, Taruscio, Domenica, Vittozzi, Luciano
Julkaistu 2014

Raising Awareness of False Positive Newborn Screening Results Arising from Pivalate-Containing Creams and Antibiotics in Europe When Screening for Isovaleric Acidaemia

Tekijä Bonham, James R., Carling, Rachel S., Lindner, Martin, Franzson, Leifur, Zetterstrom, Rolf, Boemer, Francois, Cerone, Roberto, Eyskens, Francois, Vilarinho, Laura, Hougaard, David M., Schielen, Peter C.J.I.
Julkaisussa Int J Neonatal Screen (2018)

Efficacy and outcome of expanded newborn screening for metabolic diseases - Report of 10 years from South-West Germany *

Tekijä Lindner, Martin, Gramer, Gwendolyn, Haege, Gisela, Fang-Hoffmann, Junmin, Schwab, Karl O, Tacke, Uta, Trefz, Friedrich K, Mengel, Eugen, Wendel, Udo, Leichsenring, Michael, Burgard, Peter, Hoffmann, Georg F
Julkaistu 2011

Next-generation sequencing of microbial cell-free DNA for rapid noninvasive diagnosis of infectious diseases in immunocompromised hosts

Tekijä Camargo, Jose F., Ahmed, Asim A., Lindner, Martin S., Morris, Michele I., Anjan, Shweta, Anderson, Anthony D., Prado, Clara E., Dalai, Sudeb C., Martinez, Octavio V., Komanduri, Krishna V.
Julkaisussa F1000Res (2020)

Suggested guidelines for the diagnosis and management of urea cycle disorders

Tekijä Häberle, Johannes, Boddaert, Nathalie, Burlina, Alberto, Chakrapani, Anupam, Dixon, Marjorie, Huemer, Martina, Karall, Daniela, Martinelli, Diego, Crespo, Pablo Sanjurjo, Santer, René, Servais, Aude, Valayannopoulos, Vassili, Lindner, Martin, Rubio, Vicente, Dionisi-Vici, Carlo
Julkaistu 2012

Rapid, Noninvasive Diagnosis of Balamuthia mandrillaris Encephalitis by a Plasma-Based Next-Generation Sequencing Test

Tekijä Kalyatanda, Gautam, Rand, Kenneth, Lindner, Martin S, Hong, David K, Sait Albayram, Mehmet, Gregory, Jason, Kresak, Jesse, Ibne, Karim M Ali, Cope, Jennifer R, Roy, Shantanu, Gary, Joy M, Reddy, Varalakshmi, Ahmed, Asim A
Julkaisussa Open Forum Infect Dis (2020)

Cross-sectional observational study of 208 patients with non-classical urea cycle disorders

Tekijä Rüegger, Corinne M., Lindner, Martin, Ballhausen, Diana, Baumgartner, Matthias R., Beblo, Skadi, Das, Anibh, Gautschi, Matthias, Glahn, Esther M., Grünert, Sarah C., Hennermann, Julia, Hochuli, Michel, Huemer, Martina, Karall, Daniela, Kölker, Stefan, Lachmann, Robin H., Lotz-Havla, Amelie, Möslinger, Dorothea, Nuoffer, Jean-Marc, Plecko, Barbara, Rutsch, Frank, Santer, René, Spiekerkoetter, Ute, Staufner, Christian, Stricker, Tamar, Wijburg, Frits A., Williams, Monique, Burgard, Peter, Häberle, Johannes
Julkaistu 2013

Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients

Tekijä Grünert, Sarah C, Müllerleile, Stephanie, De Silva, Linda, Barth, Michael, Walter, Melanie, Walter, Kerstin, Meissner, Thomas, Lindner, Martin, Ensenauer, Regina, Santer, René, Bodamer, Olaf A, Baumgartner, Matthias R, Brunner-Krainz, Michaela, Karall, Daniela, Haase, Claudia, Knerr, Ina, Marquardt, Thorsten, Hennermann, Julia B, Steinfeld, Robert, Beblo, Skadi, Koch, Hans-Georg, Konstantopoulou, Vassiliki, Scholl-Bürgi, Sabine, van Teeffelen-Heithoff, Agnes, Suormala, Terttu, Sperl, Wolfgang, Kraus, Jan P, Superti-Furga, Andrea, Schwab, Karl Otfried, Sass, Jörn Oliver
Julkaistu 2013

Mudd’s disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes

Tekijä Chien, Yin-Hsiu, Abdenur, Jose E., Baronio, Federico, Bannick, Allison Anne, Corrales, Fernando, Couce, Maria, Donner, Markus G., Ficicioglu, Can, Freehauf, Cynthia, Frithiof, Deborah, Gotway, Garrett, Hirabayashi, Koichi, Hofstede, Floris, Hoganson, George, Hwu, Wuh-Liang, James, Philip, Kim, Sook, Korman, Stanley H., Lachmann, Robin, Levy, Harvey, Lindner, Martin, Lykopoulou, Lilia, Mayatepek, Ertan, Muntau, Ania, Okano, Yoshiyuki, Raymond, Kimiyo, Rubio-Gozalbo, Estela, Scholl-Bürgi, Sabine, Schulze, Andreas, Singh, Rani, Stabler, Sally, Stuy, Mary, Thomas, Janet, Wagner, Conrad, Wilson, William G., Wortmann, Saskia, Yamamoto, Shigenori, Pao, Maryland, Blom, Henk J.
Julkaisussa Orphanet J Rare Dis (2015)

Classical Heroes in the 21st Century

Julkaisussa Helden - Heroisierungen - Heroismen (2023-11-20)