Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Florian Brackmann"'
Autor:
Andreas Feigenspan, Gudrun Boie, Regina Trollmann, M Richter, Susan Jung, Theresa Mühlberger, Florian Brackmann
Publikováno v:
Brain Research. 1688:91-102
Angiogenesis due to hypoxic-ischemic (HI) injury represents a crucial compensatory mechanism of the developing brain that is mainly regulated by hypoxia-inducible transcription factors (HIF). Pharmacological stimulation of HIF is suggested as a neuro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a23045a815f38484947c4ca77aede59b
https://doi.org/10.1016/j.brainres.2018.03.012
https://doi.org/10.1016/j.brainres.2018.03.012
Autor:
Florian Brackmann, Matthias Türk, Oliver Rompel, Regina Trollmann, Nils Gratzki, Heinz Jungbluth, Rolf Schröder
Publikováno v:
Brackmann, F, Türk, M, Gratzki, N, Rompel, O, Jungbluth, H, Schröder, R & Trollmann, R 2017, ' Compound heterozygous RYR1 mutations in a preterm with arthrogryposis multiplex congenita and prenatal CNS bleeding ', Neuromuscular Disorders . https://doi.org/10.1016/j.nmd.2017.09.009, https://doi.org/10.1016/j.nmd.2017.09.009
RYR1 mutations, the most common cause of non-dystrophic neuromuscular disorders, are associated with the malignant hyperthermia susceptibility (MHS) trait as well as congenital myopathies with widely variable clinical and histopathological manifestat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcca0aaf51dbb363c7b53a421ba73dae
https://doi.org/10.1016/j.nmd.2017.09.009
https://doi.org/10.1016/j.nmd.2017.09.009
Autor:
M. Türk, N. Gratzki, R. Schröder, Florian Brackmann, Regina Trollmann, O. Rompel, Heinz Jungbluth
Publikováno v:
Neuropediatrics. 48:S1-S45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4feb7dcfc0345baec8796e342d2b12af
https://doi.org/10.1055/s-0037-1602970
https://doi.org/10.1055/s-0037-1602970
Publikováno v:
Neuropediatrics. 48:S1-S45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d66438b2aed320b48aabcc9f056c3055
https://doi.org/10.1055/s-0037-1602941
https://doi.org/10.1055/s-0037-1602941
Autor:
Carol-Immanuel Geppert, Florian Brackmann, Yili E. Ballheimer, Regina Trollmann, Susan Jung, Daniel Zoglauer, Arndt Hartmann
Publikováno v:
Brain research. 1735
Ca2+-permeable AMPA receptors (AMPAR) which crucially modify maturational programs of the developing brain are involved in seizure-induced glutamate excitotoxicity and apoptosis. Regulatory effects on AMPAR subunit composition and RNA-editing in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bdb06a87e3d74cd163340dfb8cafc26
https://pubmed.ncbi.nlm.nih.gov/32142720
https://pubmed.ncbi.nlm.nih.gov/32142720
Autor:
Alexander Mahnke, Julian Hofmann, Florian Brackmann, Valentin Schatz, Otto S. Wolfbeis, Robert J. Meier, Gregor Liebsch, Regina Trollmann, Xu-dong Wang, Christian Bogdan, Jonathan Jantsch
Publikováno v:
Methods and applications in fluorescence. 1(4)
Tissue oxygenation plays a critical role in the pathogenesis of various diseases, but non-invasive, robust and user-friendly methods for its measurement in vivo still need to be established. Here, we are presenting an in vivo oxygen-detection system
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::192059f46f3244aa513c98bf9c30e015
https://pubmed.ncbi.nlm.nih.gov/29148451
https://pubmed.ncbi.nlm.nih.gov/29148451
Autor:
Regina Trollmann, Roland Coras, Cornelia Kraus, Florian Brackmann, Oliver Rompel, Karl Rössler
Publikováno v:
Braindevelopment. 40(4)
Infantile Alexander disease is a rare progressive leukodystrophy caused by autosomal dominant mutations in the (GFAP) gene typically presenting with psychomotor retardation, progressive macrocephaly and refractory epilepsy. Neuroradiological hallmark
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43071d6054ffa64ba5076d34bf27e6af
https://pubmed.ncbi.nlm.nih.gov/29191363
https://pubmed.ncbi.nlm.nih.gov/29191363
Autor:
Regina Trollmann, Ingeborg Krägeloh-Mann, Judith Böhringer, Florian Brackmann, Wibke Kustermann, Christiane Kehrer
Publikováno v:
Neuropediatrics. 48(2)
GM2 gangliosidosis, AB variant, is a very rare form of GM2 gangliosidosis due to a deficiency of GM2 activator protein. We report on two patients with typical clinical features suggestive of GM2 gangliosidosis, but normal results for hexosaminidase A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05a447fbce52b403b9b33ddb6a6a15de
https://pubmed.ncbi.nlm.nih.gov/28192816
https://pubmed.ncbi.nlm.nih.gov/28192816
Publikováno v:
Neuropediatrics. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f3d41fa0d0ea2a9548c5a13c91b23df
https://doi.org/10.1055/s-0036-1583707
https://doi.org/10.1055/s-0036-1583707
Autor:
T. Leis, G. Dekomien, Florian Brackmann, Ingeborg Krägeloh-Mann, W. Kustermann, G. Gusek-Schneider, Regina Trollmann
Publikováno v:
Neuropediatrics. 46
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08619d0b205d17d61fbcdbab8039f0b6
https://doi.org/10.1055/s-0035-1550688
https://doi.org/10.1055/s-0035-1550688