Auflistung nach Autor "Krägeloh-Mann, Ingeborg"

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A Mutation-Agnostic Hematopoietic Stem Cell Gene Therapy for Metachromatic Leukodystrophy

Daniel Moreno, Alberto; Raju, Janani; Kaftancioglu, Merve; Ureña Bailén, Guillermo; Rottenberger, Jennifer; Hou, Yujuan; Santhanakumaran, Vidiyaah; Lee, Jun-Hoe; Heumos, Lukas; Handgretinger, Rupert; Mezger, Markus; Selvaraj, Justin Antony; Lamsfus Calle, Andrés; Böhringer, Judith; Krägeloh-Mann, Ingeborg (2022)
Acute-onset paralytic strabismus in toddlers is important to consider as a potential early sign of late-infantile Metachromatic Leukodystrophy

Wehner, Katharina; Bender, Benjamin; Krägeloh-Mann, Ingeborg; Gröschel, Samuel (2022)
Aicardi-Goutieres syndrome due to a paternal mosaic IFIH1 mutation

Döbler-Neumann, Marion; Harmuth, Florian; Reichbauer, Jennifer; Krägeloh-Mann, Ingeborg; Schüle-Freyer, Rebecca (2020)
Arzneimittel für neuartige Therapien – Perspektiven, Chancen, Herausforderungen : Stellungnahme der Deutschen Gesellschaft für Kinder- und Jugendmedizin e. V. (DGKJ)

Krägeloh-Mann, Ingeborg (2021)
Assessing White Matter Microstructure in Brain Regions with Different Myelin Architecture Using MRI

Hagberg, Gisela; Klose, Uwe; Hauser, Till-Karsten; Scheffler, Klaus; Gröschel, Samuel; Balla, Dávid Zsolt; Nägele, Thomas; Krägeloh-Mann, Ingeborg (2016)
Association of Age at Onset and First Symptoms With Disease Progression in Patients With Metachromatic Leukodystrophy

Kehrer, Christiane; Raabe, Christa; Beck-Wödl, Stefanie; Bevot, Andrea; Kaiser, Nadja; Elgün, Saskia; Böhringer, Judith; Schöls, Ludger; Krägeloh-Mann, Ingeborg; Gröschel, Samuel (2021)
Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia

Grimmel, Mona; Bevot, Andrea; Buchert, Rebecca; Laugwitz, Lucia; Sturm, Marc; Döbler-Neumann, Marion; Beck-Wödl, Stefanie; Müller, Amelie Johanna; Nägele, Thomas; Rieß, Olaf; Krägeloh-Mann, Ingeborg; Haack, Tobias (2020)
Brain morphometry in pontocerebellar hypoplasia type 2

Ekert, Kaspar; Gröschel, Samuel; Sánchez-Albisua, Iciar; Frölich, Saskia; Engel, Corinna; Krägeloh-Mann, Ingeborg (2016)
Cerebellar Bottom-of-Fissure Dysplasia-a Novel Cerebellar Gray Matter Neuroimaging Pattern

Krägeloh-Mann, Ingeborg (2016)
Cerebellar lesions in pediatric abusive head trauma

Haas-Lude, Karin; Döbler-Neumann, Marion; Gröschel, Samuel; Nägele, Thomas; Krägeloh-Mann, Ingeborg (2019)
Cerebral gray and white matter changes and clinical course in metachromatic leukodystrophy

Krarup, Christian; Kehrer, Christiane; Wilke, Marko; Gröschel, Samuel; Krägeloh-Mann, Ingeborg; Böhringer, Judith; Clas, Philipp Matthias (2012)
Clinical application of advanced MR methods in children : points to consider

Wilke, Marko; Lorenzen, Anna; Rona, Sabine; Ernemann, Ulrike; Gröschel, Samuel; Schuhmann, Martin Ulrich; Krägeloh-Mann, Ingeborg (2018)
Comparative Analysis of Cerebral Magnetic Resonance Imaging Changes in Nontreated Infantile, Juvenile and Adult Patients with Niemann-Pick Disease Type C

Gburek-Augustat, Janina; Kern, Jan; Just, Jennifer; Harzer, Klaus; Stampfer, Miriam; Gröschel, Samuel; Beck-Wödl, Stefanie; Krägeloh-Mann, Ingeborg (2020)
Core protocol development for phase 2/3 clinical trials in the leukodystrophy vanishing white matter: a consensus statement by the VWM consortium and patient advocates

Krägeloh-Mann, Ingeborg (2023)
De novo ITPR1 variants are a recurrent cause of early-onset ataxia, acting via loss of channel function

Synofzik, Matthis; Harmuth, Florian; Gburek-Augustat, Janina; Krägeloh-Mann, Ingeborg; Bauer, Peter; Schüle-Freyer, Rebecca (2018)
De novo stop-loss variants in CLDN11 cause hypomyelinating leukodystrophy

Haack, Tobias; Krägeloh-Mann, Ingeborg (2021)
Decreasing cerebral palsy prevalence in multiple births in the modern era: a population cohort study of European data

Krägeloh-Mann, Ingeborg (2021)
Decreasing prevalence in cerebral palsy: a multi-site European population-based study, 1980 to 2003

Krägeloh-Mann, Ingeborg (2016)
Defining the phenotypical spectrum associated with variants in TUBB2A

Schäferhoff, Karin; Krägeloh-Mann, Ingeborg; Haack, Tobias (2021)
Demyelination load as predictor for disease progression in juvenile metachromatic leukodystrophy

Kehrer, Christiane; Wilke, Marko; Strölin, Manuel; Krägeloh-Mann, Ingeborg; Gröschel, Samuel (2017)

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