Works by Lindner, Martin


Results: 91
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    Molecular neonatal screening for homocystinuria in the Qatari population.

    Published in:
    Human Mutation, 2009, v. 30, n. 6, p. 1021, doi. 10.1002/humu.20994
    By:
    • Zschocke, Johannes;
    • Kebbewar, Moustafa;
    • Gan-Schreier, Hongying;
    • Fischer, Christine;
    • Fang-Hoffmann, Junmin;
    • Wilrich, Julia;
    • Abdoh, Ghassan;
    • Ben-Omran, Tawfeg;
    • Shahbek, Noora;
    • Lindner, Martin;
    • Al Rifai, Hilal;
    • Al Khal, Abdul Latif;
    • Hoffmann, Georg F.
    Publication type:
    Article
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    HiLive: real-time mapping of illumina reads while sequencing.

    Published in:
    Bioinformatics, 2017, v. 33, n. 6, p. 917, doi. 10.1093/bioinformatics/btw659
    By:
    • Lindner, Martin S.;
    • Strauch, Benjamin;
    • Schulze, Jakob M.;
    • Tausch, Simon H.;
    • Dabrowski, Piotr W.;
    • Nitsche, Andreas;
    • Renard, Bernhard Y.
    Publication type:
    Article
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    SIMA: Simultaneous Multiple Alignment of LC/MS Peak Lists.

    Published in:
    Bioinformatics, 2011, v. 27, n. 7, p. 987, doi. 10.1093/bioinformatics/btr051
    By:
    • Voss, Björn;
    • Hanselmann, Michael;
    • Renard, Bernhard Y.;
    • Lindner, Martin S.;
    • Köthe, Ullrich;
    • Kirchner, Marc;
    • Hamprecht, Fred A.
    Publication type:
    Article
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    Neurological outcome in long‐chain hydroxy fatty acid oxidation disorders.

    Published in:
    Annals of Clinical & Translational Neurology, 2024, v. 11, n. 4, p. 883, doi. 10.1002/acn3.52002
    By:
    • Mütze, Ulrike;
    • Ottenberger, Alina;
    • Gleich, Florian;
    • Maier, Esther M.;
    • Lindner, Martin;
    • Husain, Ralf A.;
    • Palm, Katja;
    • Beblo, Skadi;
    • Freisinger, Peter;
    • Santer, René;
    • Thimm, Eva;
    • vom Dahl, Stephan;
    • Weinhold, Natalie;
    • Grohmann‐Held, Karina;
    • Haase, Claudia;
    • Hennermann, Julia B.;
    • Hörbe‐Blindt, Alexandra;
    • Kamrath, Clemens;
    • Marquardt, Iris;
    • Marquardt, Thorsten
    Publication type:
    Article
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    The biochemical subtype is a predictor for cognitive function in glutaric aciduria type 1: a national prospective follow-up study.

    Published in:
    Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-98809-9
    By:
    • Märtner, E. M. Charlotte;
    • Thimm, Eva;
    • Guder, Philipp;
    • Schiergens, Katharina A.;
    • Rutsch, Frank;
    • Roloff, Sylvia;
    • Marquardt, Iris;
    • Das, Anibh M.;
    • Freisinger, Peter;
    • Grünert, Sarah C.;
    • Krämer, Johannes;
    • Baumgartner, Matthias R.;
    • Beblo, Skadi;
    • Haase, Claudia;
    • Dieckmann, Andrea;
    • Lindner, Martin;
    • Näke, Andrea;
    • Hoffmann, Georg F.;
    • Mühlhausen, Chris;
    • Walter, Magdalena
    Publication type:
    Article
    24

    Publisher Correction: The biochemical subtype is a predictor for cognitive function in glutaric aciduria type 1: a national prospective follow-up study.

    Published in:
    2021
    By:
    • Märtner, E. M. Charlotte;
    • Thimm, Eva;
    • Guder, Philipp;
    • Schiergens, Katharina A.;
    • Rutsch, Frank;
    • Roloff, Sylvia;
    • Marquardt, Iris;
    • Das, Anibh M.;
    • Freisinger, Peter;
    • Grünert, Sarah C.;
    • Krämer, Johannes;
    • Baumgartner, Matthias R.;
    • Beblo, Skadi;
    • Haase, Claudia;
    • Dieckmann, Andrea;
    • Lindner, Martin;
    • Näke, Andrea;
    • Hoffmann, Georg F.;
    • Mühlhausen, Chris;
    • Walter, Magdalena
    Publication type:
    Correction Notice
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    The biochemical subtype is a predictor for cognitive function in glutaric aciduria type 1: a national prospective follow-up study.

    Published in:
    Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-98809-9
    By:
    • Märtner, E. M. Charlotte;
    • Thimm, Eva;
    • Guder, Philipp;
    • Schiergens, Katharina A.;
    • Rutsch, Frank;
    • Roloff, Sylvia;
    • Marquardt, Iris;
    • Das, Anibh M.;
    • Freisinger, Peter;
    • Grünert, Sarah C.;
    • Krämer, Johannes;
    • Baumgartner, Matthias R.;
    • Beblo, Skadi;
    • Haase, Claudia;
    • Dieckmann, Andrea;
    • Lindner, Martin;
    • Näke, Andrea;
    • Hoffmann, Georg F.;
    • Mühlhausen, Chris;
    • Walter, Magdalena
    Publication type:
    Article
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    Newborn screening: A disease-changing intervention for glutaric aciduria type 1.

    Published in:
    2018
    By:
    • Boy, Nikolas;
    • Mengler, Katharina;
    • Thimm, Eva;
    • Schiergens, Katharina A.;
    • Marquardt, Thorsten;
    • Weinhold, Natalie;
    • Marquardt, Iris;
    • Das, Anibh M.;
    • Freisinger, Peter;
    • Grünert, Sarah C.;
    • Vossbeck, Judith;
    • Steinfeld, Robert;
    • Baumgartner, Matthias R.;
    • Beblo, Skadi;
    • Dieckmann, Andrea;
    • Näke, Andrea;
    • Lindner, Martin;
    • Heringer, Jana;
    • Hoffmann, Georg F.;
    • Mühlhausen, Chris
    Publication type:
    journal article
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    Molecular and functional characterisation of mild MCAD deficiency.

    Published in:
    Human Genetics, 2001, v. 108, n. 5, p. 404, doi. 10.1007/s004390100501
    By:
    • Zschocke, Johannes;
    • Schulze, Andreas;
    • Lindner, Martin;
    • Fiesel, Sonja;
    • Olgemöller, Katharina;
    • Hoffmann, Georg F.;
    • Penzien, Johannes;
    • Ruiter, Jos P. N.;
    • Wanders, Ronald J. A.;
    • Mayatepek, Ertan
    Publication type:
    Article
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    Mutation analysis in glycogen storage disease type 1 non-a.

    Published in:
    Human Genetics, 2000, v. 107, n. 3, p. 285, doi. 10.1007/s004390000371
    By:
    • Janecke, Andreas R.;
    • Lindner, Martin;
    • Erdel, Martin;
    • Mayatepek, Ertan;
    • Möslinger, Dorothea;
    • Podskarbi, Teodor;
    • Fresser, Friedrich;
    • Stöckler-Ipsiroglu, Silvia;
    • Hoffmann, Georg F.;
    • Utermann, Gerd
    Publication type:
    Article
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    Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients.

    Published in:
    Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-6
    By:
    • 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
    Publication type:
    Article
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    Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients.

    Published in:
    2013
    By:
    • 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
    Publication type:
    journal article
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    Outcomes after newborn screening for propionic and methylmalonic acidemia and homocystinurias.

    Published in:
    Journal of Inherited Metabolic Disease, 2024, v. 47, n. 4, p. 674, doi. 10.1002/jimd.12731
    By:
    • Reischl‐Hajiabadi, Anna T.;
    • Schnabel, Elena;
    • Gleich, Florian;
    • Mengler, Katharina;
    • Lindner, Martin;
    • Burgard, Peter;
    • Posset, Roland;
    • Lommer‐Steinhoff, Svenja;
    • Grünert, Sarah C.;
    • Thimm, Eva;
    • Freisinger, Peter;
    • Hennermann, Julia B.;
    • Krämer, Johannes;
    • Gramer, Gwendolyn;
    • Lenz, Dominic;
    • Christ, Stine;
    • Hörster, Friederike;
    • Hoffmann, Georg F.;
    • Garbade, Sven F.;
    • Kölker, Stefan
    Publication type:
    Article
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    Isovaleric aciduria identified by newborn screening: Strategies to predict disease severity and stratify treatment.

    Published in:
    Journal of Inherited Metabolic Disease, 2023, v. 46, n. 6, p. 1063, doi. 10.1002/jimd.12653
    By:
    • Mütze, Ulrike;
    • Henze, Lucy;
    • Schröter, Julian;
    • Gleich, Florian;
    • Lindner, Martin;
    • Grünert, Sarah C.;
    • Spiekerkoetter, Ute;
    • Santer, René;
    • Thimm, Eva;
    • Ensenauer, Regina;
    • Weigel, Johannes;
    • Beblo, Skadi;
    • Arélin, Maria;
    • Hennermann, Julia B.;
    • Marquardt, Iris;
    • Freisinger, Peter;
    • Krämer, Johannes;
    • Dieckmann, Andrea;
    • Weinhold, Natalie;
    • Schiergens, Katharina A.
    Publication type:
    Article
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    Recommendations for diagnosing and managing individuals with glutaric aciduria type 1: Third revision.

    Published in:
    Journal of Inherited Metabolic Disease, 2023, v. 46, n. 3, p. 482, doi. 10.1002/jimd.12566
    By:
    • Boy, Nikolas;
    • Mühlhausen, Chris;
    • Maier, Esther M.;
    • Ballhausen, Diana;
    • Baumgartner, Matthias R.;
    • Beblo, Skadi;
    • Burgard, Peter;
    • Chapman, Kimberly A.;
    • Dobbelaere, Dries;
    • Heringer‐Seifert, Jana;
    • Fleissner, Sandra;
    • Grohmann‐Held, Karina;
    • Hahn, Gabriele;
    • Harting, Inga;
    • Hoffmann, Georg F.;
    • Jochum, Frank;
    • Karall, Daniela;
    • Konstantopoulous, Vassiliki;
    • Krawinkel, Michael B.;
    • Lindner, Martin
    Publication type:
    Article
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    Impact of the SARS‐CoV‐2 pandemic on the health of individuals with intoxication‐type metabolic diseases—Data from the E‐IMD consortium.

    Published in:
    Journal of Inherited Metabolic Disease, 2023, v. 46, n. 2, p. 220, doi. 10.1002/jimd.12572
    By:
    • Mütze, Ulrike;
    • Gleich, Florian;
    • Barić, Ivo;
    • Baumgartner, Mathias;
    • Burlina, Alberto;
    • Chapman, Kimberly A.;
    • Chien, Yin‐Hsiu;
    • Cortès‐Saladelafont, Elisenda;
    • De Laet, Corinne;
    • Dobbelaere, Dries;
    • Eysken, Francois;
    • Gautschi, Matthias;
    • Santer, Rene;
    • Häberle, Johannes;
    • Joaquín, Clara;
    • Karall, Daniela;
    • Lindner, Martin;
    • Lund, Allan M.;
    • Mühlhausen, Chris;
    • Murphy, Elaine
    Publication type:
    Article
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