Search Results - "VOIGTLÄNDER, Till"

Abcd2 is a strong modifier of the metabolic impairments in peritoneal macrophages of ABCD1-deficient mice by Muneer, Zahid, Wiesinger, Christoph, Voigtländer, Till, Werner, Hauke B, Berger, Johannes, Forss-Petter, Sonja

“…The inherited peroxisomal disorder X-linked adrenoleukodystrophy (X-ALD), associated with neurodegeneration and inflammatory cerebral demyelination, is caused…”
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Multifactorial White Matter Damage in the Acute Phase and Pre-Existing Conditions May Drive Cognitive Dysfunction after SARS-CoV-2 Infection: Neuropathology-Based Evidence by Gelpi, Ellen, Klotz, Sigrid, Beyerle, Miriam, Wischnewski, Sven, Harter, Verena, Kirschner, Harald, Stolz, Katharina, Reisinger, Christoph, Lindeck-Pozza, Elisabeth, Zoufaly, Alexander, Leoni, Marlene, Gorkiewicz, Gregor, Zacharias, Martin, Haberler, Christine, Hainfellner, Johannes, Woehrer, Adelheid, Hametner, Simon, Roetzer, Thomas, Voigtländer, Till, Ricken, Gerda, Endmayr, Verena, Haider, Carmen, Ludwig, Judith, Polt, Andrea, Wilk, Gloria, Schmid, Susanne, Erben, Irene, Nguyen, Anita, Lang, Susanna, Simonitsch-Klupp, Ingrid, Kornauth, Christoph, Nackenhorst, Maja, Kläger, Johannes, Kain, Renate, Chott, Andreas, Wasicky, Richard, Krause, Robert, Weiss, Günter, Löffler-Rag, Judith, Berger, Thomas, Moser, Patrizia, Soleiman, Afshin, Asslaber, Martin, Sedivy, Roland, Klupp, Nikolaus, Klimpfinger, Martin, Risser, Daniele, Budka, Herbert, Schirmer, Lucas, Pröbstel, Anne-Katrin, Höftberger, Romana

“…There is an urgent need to better understand the mechanisms underlying acute and long-term neurological symptoms after COVID-19. Neuropathological studies can…”
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Peroxisomal Localization of the Proopiomelanocortin-Derived Peptides β-Lipotropin and β-Endorphin by Höftberger, Romana, Kunze, Markus, Voigtländer, Till, Unterberger, Ursula, Regelsberger, Günther, Bauer, Jan, Aboul-Enein, Fahmy, Garzuly, Ferenc, Forss-Petter, Sonja, Bernheimer, Hanno, Berger, Johannes, Budka, Herbert

“…The peptide hormones ACTH, MSHs, β-lipotropin (β-LPH), and β-endorphin are all derived from the precursor molecule proopiomelanocortin (POMC). Using confocal…”
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Evidence for Oxidative Stress in Experimental Prion Disease by Guentchev, Marin, Voigtländer, Till, Haberler, Christine, Groschup, Martin H., Budka, Herbert

“…Oxidative stress has been shown to be important in several neurodegenerative disorders. Previous in vitro studies have already demonstrated the ability of a…”
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Glucocorticoids in the Treatment of Children with Acute Lymphoblastic Leukemia and Hodgkin's Disease: A Pilot Study on the Adverse Psychological Reactions and Possible Associations with Neurobiological, Endocrine, and Genetic Markers by Felder-Puig, Rosemarie, Scherzer, Christiane, Baumgartner, Michaela, Ortner, Magdalena, Aschenbrenner, Claudia, Bieglmayer, Christian, Voigtländer, Till, Panzer-Grümayer, E Renate, Tissing, Wim J E, Koper, Jan W, Steinberger, Karl, Nasel, Christian, Gadner, Helmut, Topf, Reinhard, Dworzak, Michael

“…Purpose: We did a controlled study to assess adverse psychological reactions (APR) associated with high-dose glucocorticoid therapy and tried to detect somatic…”
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PrP-expressing tissue required for transfer of scrapie infectivity from spleen to brain by Aguzzi, Adriano, Blättler, Thomas, Brandner, Sebastian, Raeber, Alex J, Klein, Michael A, Voigtländer, Till, Weissmann, Charles

“…Much available evidence points to a pathological isoform of the prion protein PrP being the infectious agent that causes transmissible spongiform…”
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Pellagra encephalopathy as a differential diagnosis for Creutzfeldt-Jakob disease by Kapas, Istvan, Majtenyi, Katalin, Törö, Klara, Keller, Eva, Voigtländer, Till, Kovacs, Gabor G.

“…In the present study we evaluated cases referred as suspected Creutzfeldt-Jakob disease (CJD). Five out of 59 without prion disease showed neuropathological…”
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Accumulation of very long-chain fatty acids does not affect mitochondrial function in adrenoleukodystrophy protein deficiency by Oezen, Iris, Rossmanith, Walter, Forss-Petter, Sonja, Kemp, Stephan, Voigtländer, Till, Moser-Thier, Karin, Wanders, Ronald J., Bittner, Reginald E., Berger, Johannes

“…X-linked adrenoleukodystrophy (X-ALD, OMIM 300100) is a severe inherited neurodegenerative disease, associated with the accumulation of very long-chain fatty…”
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Selective neuronal vulnerability in human prion diseases : Fatal familial insomnia differs from other types of prion diseases by GUENTCHEV, M, WANSCHITZ, J, VOIGTLÄNDER, T, FLICKER, H, BUDKA, H

“…Human transmissible spongiform encephalopathies (TSEs) or prion diseases are neurodegenerative disorders of infectious, inherited or sporadic origin and…”
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Transcriptional Regulation of the Rat Renin Gene by Regulatory Elements in Intron I by Voigtlander, Till, Ganten, Detlev, Bader, Michael

“…Renin catalyzes the rate-limiting step in the enzymatic cascade leading to the vasoactive peptide angiotensin II. Therefore, the activity of the…”
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A Single Lung Transplant in a Patient with Fabry Disease : Causality or Far-Fetched? A Case Report by Gaggl, Martina, Kain, Renate, Jaksch, Peter, Haider, Dominik, Mundigler, Gerald, Voigtländer, Till, Sunder-Plassmann, Raute, Rommer, Paulus, Klepetko, Walter, Sunder-Plassmann, Gere

“…Introduction. Fabry disease is a rare X-linked lysosomal storage disorder, characterized by an α-galactosidase A deficiency resulting in globotriaosylceramide…”
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Zukunftsperspektiven des Nationalen Aktionsplans für seltene Erkrankungen by Voigtländer, Till

“…Zusammenfassung Im Jahr 2008 wurde das Projekt Nationaler Aktionsplan für seltene Erkrankungen (NAP.se) mit einer Petition an das Gesundheitsministerium…”
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Distribution and cellular localization of adrenoleukodystrophy protein in human tissues: Implications for X-linked adrenoleukodystrophy by Höftberger, Romana, Kunze, Markus, Weinhofer, Isabelle, Aboul-Enein, Fahmy, Voigtländer, Till, Oezen, Iris, Amann, Gabriele, Bernheimer, Hanno, Budka, Herbert, Berger, Johannes

“…Abstract Defects of adrenoleukodystrophy protein (ALDP) lead to X-linked adrenoleukodystrophy (X-ALD), a disorder mainly affecting the nervous system white…”
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Endoplasmic Reticulum Stress Features Are Prominent in Alzheimer Disease but Not in Prion Diseases In Vivo by Unterberger, Ursula, Höftberger, Romana, Gelpi, Ellen, Flicker, Helga, Budka, Herbert, Voigtländer, Till

“…Prion diseases and Alzheimer disease (AD) share a variety of clinical and neuropathologic features (e.g. progressive dementia, accumulation of abnormally…”
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Epilepsy in adult X-linked adrenoleucodystrophy due to the deletion c.1415-1416delAG in exon 5 of the ABCD1-gene by Brownstone, Eva, Voigtländer, Till, Baumhackl, Ulf, Finsterer, Josef

“…Seizures in cerebral X-linked adrenoleucodystrophy (X-ALD) more frequently occur in the early-onset compared to the late-onset form. Here we describe an adult…”
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Creutzfeldt-Jakob disease in Austria: an autopsy-controlled study by Gelpi, Ellen, Heinzl, Harald, Hoftberger, Romana, Unterberger, Ursula, Strobel, Thomas, Voigtlander, Till, Drobna, Edita, Jarius, Christa, Lang, Susanna, Waldhor, Thomas, Bernheimer, Hanno, Budka, Herbert

“…Definite diagnosis of prion diseases or transmissible spongiform encephalopathies (TSEs) requires neuropathology, usually at autopsy. Epidemiology of human…”
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Deterioration of anti-Yo-associated paraneoplastic cerebellar degeneration by Finsterer, Josef, Voigtländer, Till, Grisold, Wolfgang

“…Abstract Objectives Usually, the course of paraneoplastic cerebellar degeneration(PCD) is stable or progresses only slowly. Sudden marked progression after…”
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Fibroblasts Can Express Glial Fibrillary Acidic Protein (GFAP) In Vivo by HAINFELLNER, JOHANNES A, VOIGTLÄNDER, TILL, STRÖBEL, THOMAS, MAZAL, PETER R, MADDALENA, ALESSIA S, AGUZZI, ADRIANO, BUDKA, HERBERT

“…Neuropathologists use anti-glial fibrillary acidic protein (GFAP) antibodies as specific markers for glial cells, and neurobiologists use GFAP for targeting…”
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The lack of chromosomal protein Hmg1 does not disrupt cell growth but causes lethal hypoglycaemia in newborn mice by Voigtländer, Till, Bianchi, Marco E, Aguzzi, Adriano, Calogero, Sabina, Grassi, Fabio, Ferrier, Pierre, Ferrari, Simona

“…High mobility group 1 (HMG1) protein is an abundant component of all mammalian nuclei, and related proteins exist in all eukaryotes. HMG1 binds linear DNA with…”
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Immunohistochemical Detection of Cell Growth Fraction in Formalin-Fixed and Paraffin-Embedded Murine Tissue by Birner, Peter, Ritzi, Marion, Musahl, Christine, Knippers, Rolf, Gerdes, Johannes, Voigtländer, Till, Budka, Herbert, Hainfellner, Johannes A.

“…Monoclonal antibody MIB-1 is a reliable tool for determining proliferating cells in human tissues, but does not react with the homologous mouse antigen and is…”
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