Harting, Inga PD Dr. med.Universität HeidelbergHeidelberg
Publikationsliste einschränken
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Co-Autoren (Uni Heidelberg)
- Platten, Michael (5)
- Garbade, Sven (5)
- Staufner, Christian (5)
- Deimling, Andreas von (4)
- Burgard, Peter (4)
- Wick, Wolfgang (4)
- Opladen, Thomas (4)
- Sahm, Felix (3)
- Thiel, Christian (3)
- Straub, Beate Katharina (3)
- Debus, Jürgen (2)
- Schlemmer, Heinz-Peter (2)
- Kuseyri Hübschmann, Oya (2)
- Lenz, Dominic (2)
- Moog, Ute (2)
- Heiland, Sabine (2)
- Dikow, Nicola (2)
- Rating, Dietz (2)
- Poschke, Isabel (2)
- Beisse, Flemming (2)
- Wick, Antje (2)
- Schmitt, Michael (2)
- Mohr, Alexander (2)
- Pajtler, Kristian Wilfried (1)
- Wiestler, Benedikt (1)
- Müller-Tidow, Carsten (1)
- Radbruch, Alexander (1)
- Breckwoldt, Michael O. (1)
- Kronlage, Moritz (1)
- Dreger, Peter (1)
- Hartmann, Christian (1)
- Sauer, Sven (1)
- Pfaff, Elke (1)
- (weitere Einträge vorhanden...)
Co-Autoren (extern)
- Schnell, Oliver (1)
- Haack, Tobias (1)
- Kopajtich, Robert (1)
- Vrij-van den Bos, Suzanne (1)
- Zschocke, Johannes (1)
- Schwartz, Ida Vanessa (1)
- Manti, Filippo (1)
- Assmann, Birgit (1)
- Pouwels, Petra J. W. (1)
- Polster, Tilman (1)
- Gökçay, Gülden (1)
- Fowler, Brian (1)
- Yildiz, Yilmaz (1)
- Sivri, H. Serap (1)
- Porta, Francesco (1)
- López-Laso, Eduardo (1)
- Verhoeven, Nanda M. (1)
- Jakobs, Cornelis (1)
- Mühlhausen, Chris (1)
- Wiegand, G. (1)
- Uhlenberg, B. (1)
- Schmitt-Mechelke, T. (1)
- Pelletier, Félixe (1)
- Maier, Esther M. (1)
- Ensenauer, Regina (1)
- Lücke, Thomas (1)
- Poretti, A. (1)
- Martin, E. (1)
Publikationen in heiBIB
- Yıldız, Yılmaz: Levodopa-refractory hyperprolactinemia and pituitary findings in inherited disorders of biogenic amine metabolism / Yılmaz Yıldız, Oya Kuseyri Hübschmann, Ayça Akgöz Karaosmanoğlu, Filippo Manti, Meryem Karaca, Ida V… , 15 July 2023. - 16 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. (2023), Seite 1-16
DOI: 10.1002/jimd.12658
- Meißner, Julia: Cure of intravascular NK/T-cell lymphoma of the central nervous system by allogeneic hematopoietic cell transplantation / Julia Meissner, Michael Schmitt, Mindaugas Andrulis, Leonille Schweizer, Sascha Dietrich, Bettina Al… , 9 Jun 2022. - 4 S.
In: Bone marrow transplantation, ISSN 1476-5365. 57(2022), 9, Seite 1451-1454
DOI: 10.1038/s41409-022-01734-2
- Kuseyri Hübschmann, Oya: Brain MR patterns in inherited disorders of monoamine neurotransmitters : an analysis of 70 patients / Oya Kuseyri Hübschmann, Alexander Mohr, Jennifer Friedman, Filippo Manti, Gabriella Horvath, Elisend… , July 2021. - 13 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 44(2021), 4 vom: Juli, Seite 1070-1082
DOI: 10.1002/jimd.12360
- Boy, Nikolas: Subdural hematoma in glutaric aciduria type 1 : high excreters are prone to incidental SDH despite newborn screening / Nikolas Boy, Alexander Mohr, Sven F. Garbade, Peter Freisinger, Jana Heringer-Seifert, Angelika Seit… , 2021
In: Journal of inherited metabolic disease, ISSN 1573-2665. 44(2021), 6, Seite 1343-1352$10
DOI: 10.1002/jimd.12436
- Platten, Michael: A vaccine targeting mutant IDH1 in newly diagnosed glioma / Michael Platten, Lukas Bunse, Antje Wick, Theresa Bunse, Lucian Le Cornet, Inga Harting, Felix Sahm,… , 24 March 2021. - 6 Seiten
In: Nature, ISSN 1476-4687. 592(2021), Seite 463-468
DOI: 10.1038/s41586-021-03363-z
- Tilburg, Cornelis M. van: INFORM2 NivEnt : the first trial of the INFORM2 biomarker driven phase I/II trial series : the combination of nivolumab and entinostat in children and adolescents with refractory high-risk malignancies / Cornelis M. van Tilburg, Ruth Witt, Melanie Heiss, Kristian W. Pajtler, Christoph Plass, Isabel Posc… , 05 June 2020. - 12 S.
In: BMC cancer, ISSN 1471-2407. 20(2020) vom: Juni, Artikel-ID 523, Seite 1-12
DOI: 10.1186/s12885-020-07008-8
- Pelletier, Félixe: Endocrine and growth abnormalities in 4H leukodystrophy caused by variants in POLR3A, POLR3B, and POLR1C / Félixe Pelletier, Stefanie Perrier, Ferdy K Cayami, Amytice Mirchi, Stephan Saikali, Luan T Tran, Ni… , 2021. - 15 S.
In: The journal of clinical endocrinology & metabolism, ISSN 1945-7197. 106(2021), 2, Seite e660-e674
DOI: 10.1210/clinem/dgaa700
- Harting, Inga: Oculodentodigital dysplasia : a hypomyelinating leukodystrophy with a characteristic MRI pattern of brain stem involvement / I. Harting, S. Karch, U. Moog, A. Seitz, P.J.W. Pouwels, and N.I. Wolf, 1 May 2019. - 5 S.
In: American journal of neuroradiology, ISSN 1936-959X. 40(2019), 5, Seite 903-907
DOI: 10.3174/ajnr.A6051
- Kronlage, Moritz: Prevalence of fascicular hyperintensities in peripheral nerves of healthy individuals with regard to cerebral white matter lesions / Moritz Kronlage, Véronique Schwehr, Daniel Schwarz, Tim Godel, Inga Harting, Sabine Heiland, Martin … , 22 March 2019. - 8 S.
In: European radiology, ISSN 1432-1084. 29(2019), 7, Seite 3480-3487
DOI: 10.1007/s00330-019-06145-4
- Boy, Nikolas: Patterns, evolution, and severity of striatal injury in insidious- vs acute-onset glutaric aciduria type 1 / Nikolas Boy, Sven F. Garbade, Jana Heringer, Angelika Seitz, Stefan Kölker, Inga Harting, 11 February 2019. - 11 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 42(2019), 1, Seite 117-127
DOI: 10.1002/jimd.12033
- Vollmuth, Philipp: Automated quantitative tumour response assessment of MRI in neuro-oncology with artificial neural networks : a multicentre, retrospective study / Philipp Kickingereder, Fabian Isensee, Irada Tursunova, Jens Petersen, Ulf Neuberger, David Bonekamp… , April 2, 2019. - 13 S.
In: The lancet, ISSN 1474-5488. 20(2019), 5, Seite 728-740
DOI: 10.1016/S1470-2045(19)30098-1
- Boy, Nikolas: Patterns, evolution, and severity of striatal injury in insidious- vs acute-onset glutaric aciduria type 1 / Nikolas Boy, Sven F. Garbade, Jana Heringer, Angelika Seitz, Stefan Kölker, Inga Harting, 11 February 2019. - 11 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 42(2019), 1, Seite 117-127
DOI: 10.1002/jimd.12033
- Lenz, Dominic: SCYL1 variants cause a syndrome with low γ-glutamyl-transferase cholestasis, acute liver failure, and neurodegeneration (CALFAN) / Dominic Lenz, Patricia McClean, Aydan Kansu, Penelope E. Bonnen, Giusy Ranucci, Christian Thiel, Bea… , 08 February 2018. - 11 S.
In: Genetics in medicine, ISSN 1530-0366. 20(2018), 10, Seite 1255-1265
DOI: 10.1038/gim.2017.260
- Garbade, Sven: Age-related changes and reference values of bicaudate ratio and sagittal brainstem diameters on MRI / Sven F. Garbade, Nikolas Boy, Jana Heringer, Stefan Kölker, Inga Harting, 05. Juni 2018. - 7 S.
In: Neuropediatrics, ISSN 1439-1899. 49(2018), 04, Seite 269-275
DOI: 10.1055/s-0038-1660475
- Vrij-van den Bos, Suzanne: 4H leukodystrophy : a brain magnetic resonance imaging scoring system / Suzanne Vrij-van den Bos, Janna A. Hol, Roberta La Piana, Inga Harting, Adeline Vanderver, Frederik … , 01. März 2017. - 9 S.
In: Neuropediatrics, ISSN 1439-1899. 48(2017), 03, Seite 152-160
DOI: 10.1055/s-0037-1599141
- Wick, Wolfgang: Lomustine and bevacizumab in progressive glioblastoma / Wolfgang Wick, Thierry Gorlia, Martin Bendszus, Martin Taphoorn, Felix Sahm, Inga Harting, Alba A. B… . - 10 S.
In: The New England journal of medicine, ISSN 1533-4406. 377(2017), 20, S. 1954-1963
DOI: 10.1056/NEJMoa1707358
- Boy, Nikolas: Extrastriatal changes in patients with late-onset glutaric aciduria type I highlight the risk of long-term neurotoxicity / Nikolas Boy, Jana Heringer, Renate Brackmann, Olaf Bodamer, Angelika Seitz, Stefan Kölker and Inga H… , 24 April 2017
In: Orphanet journal of rare diseases, ISSN 1750-1172. 12(2017) Artikel-Nummer 77, 13 Seiten
DOI: 10.1186/s13023-017-0612-6
- Boy, Nikolas: Extrastriatal changes in patients with late-onset glutaric aciduria type I highlight the risk of long-term neurotoxicity / Nikolas Boy, Jana Heringer, Renate Brackmann, Olaf Bodamer, Angelika Seitz, Stefan Kölker and Inga H… . -
London: BioMed Central, 24 April 2017. - 1 Online-Ressource (13 Seiten)
DOI: 10.1186/s13023-017-0612-6
- Staufner, Christian: MRI and 1H-MRS in adenosine kinase deficiency / C. Staufner, H.J. Blom, C. Dionisi-Vici, P. Freisinger, N. Makhseed, D. Ballhausen, S. Kölker, G.F. … . - 7 S.
In: Neuroradiology, ISSN 1432-1920. 58(2016), 7, S. 697-703
DOI: 10.1007/s00234-016-1676-z
- Boy, Nikolas: Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I : second revision / Nikolas Boy, Chris Mühlhausen, Esther M. Maier, Jana Heringer, Birgit Assmann, Peter Burgard, Marjor… , 2017. - 27 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 40(2017), 1, Seite 75-101
DOI: 10.1007/s10545-016-9999-9
- Kopajtich, Robert: Biallelic IARS mutations cause growth retardation with prenatal onset, intellectual disability, muscular hypotonia, and infantile hepatopathy / Robert Kopajtich, Kei Murayama, Andreas R. Janecke, Tobias B. Haack, Maximilian Breuer, A.S. Knisely… . - 9 S.
In: The American journal of human genetics, ISSN 1537-6605. 99(2016), 2, S. 414-422
DOI: 10.1016/j.ajhg.2016.05.027
- Staufner, Christian: Recurrent acute liver failure due to NBAS deficiency : phenotypic spectrum, disease mechanisms, and therapeutic concepts / Christian Staufner, Tobias B. Haack, Marlies G. Köpke, Beate K. Straub, Stefan Kölker, Christian Thi… , 2016. - 14 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 39(2016), 1, Seite 3-16
DOI: 10.1007/s10545-015-9896-7
- Harting, Inga: 1 H-MRS in glutaric aciduria type 1 : impact of biochemical phenotype and age on the cerebral accumulation of neurotoxic metabolites / Inga Harting, Nikolas Boy, Jana Heringer, Angelika Seitz, Martin Bendszus, Petra J.W. Pouwels, Stefa… , September 2015. - 10 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 38(2015), 5, Seite 829-838
DOI: 10.1007/s10545-015-9826-8
- Haack, Tobias: Biallelic mutations in NBAS cause recurrent acute liver failure with onset in infancy / Tobias B. Haack, Christian Staufner, Marlies G. Köpke, Beate K. Straub, Stefan Kölker, Christian Thi… , 11 June 2015. - 7 S.
In: The American journal of human genetics, ISSN 1537-6605. 97(2015), 1, Seite 163-169
DOI: 10.1016/j.ajhg.2015.05.009
- Wick, Wolfgang: A phase II, randomized, study of weekly APG101+reirradiation versus reirradiation in progressive glioblastoma / Wolfgang Wick, Harald Fricke, Klaus Junge, Grigory Kobyakov, Tobias Martens, Oliver Heese, Benedikt … , 2014. - 10 S.
In: Clinical cancer research, ISSN 1557-3265. 20(2014), 24, Seite 6304-6313
DOI: 10.1158/1078-0432.CCR-14-0951-T
- Opladen, Thomas: Aspartylglucosaminuria : unusual neonatal presentation in qatari twins with a novel aspartylglucosaminidase gene mutation and 3 new cases in a Turkish family / Opladen, Thomas ; Ebinger, Friedrich ; Zschocke, Johannes ; Sengupta, Devjani ; Ben-Omran, Tawfeg ; … . - 7 S.
In: Journal of child neurology, ISSN 1708-8283. 29(2014), 1, S. 36-42
DOI: 10.1177/0883073812469049
- Harting, Inga: Interpeduncular heterotopia in Joubert Syndrome : a previously undescribed MR finding / I. Harting, U. Kotzaeridou, A. Poretti, A. Seitz, J. Pietz, M. Bendszus, E. Boltshauser, Aug 2011. - 4 S.
In: American journal of neuroradiology, ISSN 1936-959X. 32(2011), 7, Seite 1286-1289
DOI: 10.3174/ajnr.A2488
- Heringer-Seifert, Jana: Use of guidelines improves the neurological outcome in glutaric aciduria type I / Jana Heringer, S. P. Nikolas Boy, Regina Ensenauer, Birgit Assmann, Johannes Zschocke, Inga Harting,… , [November 2010]. - 10 S. : Illustrationen
In: Annals of neurology, ISSN 1531-8249. 68(2010), 5 vom: Nov., Seite 743-752
DOI: 10.1002/ana.22095
- Harting, Inga: Zur Differentialdiagnose von Erkrankungen der weißen Hirnsubstanz : charakteristische Muster in der Magnetresonanztomographie und 1 H-Magnetresonanzspektroskopie / vorgelegt von Inga Harting, 2010. - Getr. Zählung : Ill., graph. Darst.
- Wolf, Nicole: Leukoencephalopathy with ataxia, hypodontia, and hypomyelination / N.I. Wolf, I. Harting, E. Boltshauser, G. Wiegand, M.J. Koch, T. Schmitt-Mechelke, E. Martin, J. Zsc… , April 25, 2005. - 4 S.
In: Neurology, ISSN 1526-632X. 64(2005), 8, Seite 1461-1464
DOI: 10.1212/01.WNL.0000158615.56071.E3
- Schulze, Andreas: Lack of creatine in muscle and brain in an adult with GAMT deficiency / Andreas Schulze, Peter Bachert, Heinz Schlemmer, Inga Harting, Tilman Polster, Gajja S. Salomons, Na… , 23 January 2003. - 4 S.
In: Annals of neurology, ISSN 1531-8249. 53(2003), 2, Seite 248-251
DOI: 10.1002/ana.10455
- Harting, Inga: Mitochondriale Genexpression unter Hypoxie / vorgelegt von Inga Harting, 1998. - 109 Bl. : Ill., graph. Darst.
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