Publications by authors named "Florian Brackmann"

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Seizure-induced neuronal apoptosis is related to dysregulation of the RNA-edited GluR2 subunit in the developing mouse brain.
Susan Jung, Yili E Ballheimer, Florian Brackmann, Daniel Zoglauer, Carol-Immanuel Geppert

Brain Res· May 2020

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Differential regulation of angiogenesis in the developing mouse brain in response to exogenous activation of the hypoxia-inducible transcription factor system.
Regina Trollmann, Theresa Mühlberger, Mandy Richter, Gudrun Boie, Andreas Feigenspan, Florian Brackmann

Brain Res· June 2018

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Histopathological proof of the pathogenicity of a rare GFAP mutation in a patient with flaccid paraparesis.
Florian Brackmann, Roland Coras, Karl Rössler, Cornelia Kraus, Oliver Rompel

Brain Dev· April 2018

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Compound heterozygous RYR1 mutations in a preterm with arthrogryposis multiplex congenita and prenatal CNS bleeding.
Florian Brackmann, Matthias Türk, Nils Gratzki, Oliver Rompel, Heinz Jungbluth

Neuromuscul Disord· January 2018

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Rare Variant of GM2 Gangliosidosis through Activator-Protein Deficiency.
Florian Brackmann, Christiane Kehrer, Wibke Kustermann, Judith Böhringer, Ingeborg Krägeloh-Mann

Neuropediatrics· April 2017

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Hypoxia Potentiates LPS-Mediated Cytotoxicity of BV2 Microglial Cells In Vitro by Synergistic Effects on Glial Cytokine and Nitric Oxide System.
Daniel Frey, Susan Jung, Florian Brackmann, Mandy Richter-Kraus, Regina Trollmann

Neuropediatrics· October 2015

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Activin A in perinatal brain injury.
Florian A Brackmann, Christian Alzheimer, Regina Trollmann

Neuropediatrics· April 2015

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Novel MLL2 mutation in Kabuki syndrome with hypogammaglobulinemia and severe chronic thrombopenia.
Florian Brackmann, Manuela Krumbholz, Thorsten Langer, Wolfgang Rascher, Wolfgang Holter

J Pediatr Hematol Oncol· October 2013

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Activin A regulation under global hypoxia in developing mouse brain.
Florian A Brackmann, Andrea S Link, Susan Jung, Mandy Richter, Daniel Zoglauer

Brain Res· September 2013

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Ratiometric luminescence 2D in vivo imaging and monitoring of mouse skin oxygenation.
Julian Hofmann, Robert J Meier, Alexander Mahnke, Valentin Schatz, Florian Brackmann

Methods Appl Fluoresc· August 2013

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Classical MERRF phenotype associated with mitochondrial tRNA(Leu) (m.3243A>G) mutation.
Florian Brackmann, Angela Abicht, Uwe Ahting, Rolf Schröder, Regina Trollmann

Eur J Pediatr· May 2012

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Rapidly progressive phenotype of Lafora disease associated with a novel NHLRC1 mutation.
Florian A Brackmann, Alexander Kiefer, Abbas Agaimy, Martin Gencik, Regina Trollmann

Pediatr Neurol· June 2011

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