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  1. Opladen, Thomas [Other]; Sengupta, Devjani [Other]; Moog, Ute [Other]; Fischer, Christine [Other]; Bürger, Friederike [Other]; Haas, Dorothea [Other]; Harting, Inga [Other]; Hoffmann, Georg F. [Other]

    Aspartylglucosaminuria : unusual neonatal presentation in qatari twins with a novel aspartylglucosaminidase gene mutation and 3 new cases in a Turkish family

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    2014

    Published in: Journal of child neurology ; 29(2014), 1, Seite 36-42

  2. Boy, Nikolas [Author]; Heringer-Seifert, Jana [Author]; Seitz, Angelika [Author]; Kölker, Stefan [Author]; Harting, Inga [Author]

    Extrastriatal changes in patients with late-onset glutaric aciduria type I highlight the risk of long-term neurotoxicity

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    24 April 2017

    Published in: Orphanet journal of rare diseases ; 12(2017) Artikel-Nummer 77, 13 Seiten

  4. Haack, Tobias [Other]; Kotzaeridou, Urania [Other]; Hoffmann, Georg F. [Other]; Staufner, Christian [Other]; Straub, Beate Katharina [Other]; Kölker, Stefan [Other]; Thiel, Christian [Other]; Dikow, Nicola [Other]; Harting, Inga [Other]; Beisse, Flemming [Other]; Burgard, Peter [Other]

    Biallelic mutations in NBAS cause recurrent acute liver failure with onset in infancy

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    11 June 2015

    Published in: The American journal of human genetics ; 97(2015), 1, Seite 163-169

  5. Wick, Wolfgang [Other]; Combs, Stephanie [Other]; Wiestler, Benedikt [Other]; Schließer, Maximilian Georg [Other]; Deimling, Andreas von [Other]; Harting, Inga [Other]; Debus, Jürgen [Other]; Hartmann, Christian [Other]; Platten, Michael [Other]; Bendszus, Martin [Other]

    A phase II, randomized, study of weekly APG101+reirradiation versus reirradiation in progressive glioblastoma

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    2014

    Published in: Clinical cancer research ; 20(2014), 24, Seite 6304-6313

  6. Boy, Nikolas [Author]; Mohr, Alexander [Author]; Garbade, Sven [Author]; Freisinger, Peter [Author]; Heringer-Seifert, Jana [Author]; Seitz, Angelika [Author]; Kölker, Stefan [Author]; Harting, Inga [Author]

    Subdural hematoma in glutaric aciduria type 1 : high excreters are prone to incidental SDH despite newborn screening

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    2021

    Published in: Journal of inherited metabolic disease ; 44(2021), 6, Seite 1343-1352$10

  7. Kopajtich, Robert [Author]; Breuer, Maximilian [Author]; Harting, Inga [Author]; Kotzaeridou, Urania [Author]; Kölker, Stefan [Author]; Sauer, Sven [Author]; Carl, Matthias [Author]; Hoffmann, Georg F. [Author]; Staufner, Christian [Author]

    Biallelic IARS mutations cause growth retardation with prenatal onset, intellectual disability, muscular hypotonia, and infantile hepatopathy

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    14 July 2016

    Published in: The American journal of human genetics ; 99(2016), 2, Seite 414-422

  8. Meißner, Julia [Author]; Schmitt, Michael [Author]; Andrulis, Mindaugas [Author]; Schweizer, Leonille [Author]; Dietrich, Sascha [Author]; Alber, Bettina [Author]; Harting, Inga [Author]; Kurz, Felix T. [Author]; Martens, Uwe Marc [Author]; Ho, Anthony Dick [Author]; Müller-Tidow, Carsten [Author]; Dreger, Peter [Author]

    Cure of intravascular NK/T-cell lymphoma of the central nervous system by allogeneic hematopoietic cell transplantation

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    9 Jun 2022

    Published in: Bone marrow transplantation ; 57(2022), 9, Seite 1451-1454

  9. Schröter, Julian [Author]; Popp, Bernt [Author]; Brennenstuhl, Heiko [Author]; Driedger, Jan Henje [Author]; Jestaedt, Leonie [Author]; Arélin, Maria [Author]; Gräfe, Daniel [Author]; Neuser, Sonja Anna [Author]; Parker, Michael [Author]; Lemke, Johannes [Author]; Hoffmann, Georg F. [Author]; Kölker, Stefan [Author]; Harting, Inga [Author]; Syrbe, Steffen [Author]

    Complementing the phenotypical spectrum of TUBA1A tubulinopathy and its role in early-onset epilepsies

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    11 January 2022

    Published in: European journal of human genetics ; 30(2022), 3, Seite 298-306

  10. Kuseyri Hübschmann, Oya [Author]; Mohr, Alexander [Author]; Friedman, Jennifer [Author]; Manti, Filippo [Author]; Horvath, Gabriella [Author]; Cortès-Saladelafont, Elisenda [Author]; Mercimek-Andrews, Saadet [Author]; Yildiz, Yilmaz [Author]; Pons, Roser [Author]; Kulhánek, Jan [Author]; Oppebøen, Mari [Author]; Koht, Jeanette Aimee [Author]; Podzamczer-Valls, Inés [Author]; Domingo-Jimenez, Rosario [Author]; Ibáñez, Salvador [Author]; Alcoverro-Fortuny, Oscar [Author]; Gómez-Alemany, Teresa [Author]; de Castro, Pedro [Author]; Alfonsi, Chiara [Author]; Zafeiriou, Dimitrios I. [Author]; López-Laso, Eduardo [Author]; Guder, Philipp [Author]; Santer, René [Author]; Honzík, Tomáš [Author]; [...]

    Brain MR patterns in inherited disorders of monoamine neurotransmitters : an analysis of 70 patients

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    July 2021

    Published in: Journal of inherited metabolic disease ; 44(2021), 4 vom: Juli, Seite 1070-1082