Search Results - "Neudecker, S"

Rapid identification of goblet cells in unstained colon thin sections by means of quantum cascade laser-based infrared microspectroscopy by Kröger-Lui, N, Gretz, N, Haase, K, Kränzlin, B, Neudecker, S, Pucci, A, Regenscheit, A, Schönhals, A, Petrich, W

“…Changes in the volume covered by mucin-secreting goblet cell regions within colon thin sections may serve as a means to differentiate between ulcerative…”
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Quantification of glomerular number and size distribution in normal rat kidneys using magnetic resonance imaging by HEILMANN, Melanie, NEUDECKER, Sabine, WOLF, Ivo, GUBHAJU, Lina, STICHT, Carsten, SCHOCK-KUSCH, Daniel, KRIZ, Wilhelm, BERTRAM, John F, SCHAD, Lothar R, GRETZ, Norbert

“…Glomerular number and size are important risk factors for chronic kidney disease (CKD) and cardiovascular disease and have traditionally been estimated using…”
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High dose vitamin E therapy in amyotrophic lateral sclerosis as add-on therapy to riluzole: results of a placebo-controlled double-blind study by Graf, M, Ecker, D, Horowski, R, Kramer, B, Riederer, P, Gerlach, M, Hager, C, Ludolph, A C, Becker, G, Osterhage, J, Jost, W H, Schrank, B, Stein, C, Kostopulos, P, Lubik, S, Wekwerth, K, Dengler, R, Troeger, M, Wuerz, A, Hoge, A, Schrader, C, Schimke, N, Krampfl, K, Petri, S, Zierz, S, Eger, K, Neudecker, S, Traufeller, K, Sievert, M, Neundörfer, B, Hecht, M

“…Increasing evidence has suggested that oxidative stress may be involved in the pathogenesis of amyotrophic lateral sclerosis (ALS). The antioxidant vitamin E…”
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Automatic artifact removal from GFR measurements by Shmarlouski, A., Shulhevich, Y., Geraci, S., Friedemann, J., Gretz, N., Neudecker, S., Hesser, J., Stsepankou, D.

“…•We propose a new motion artifacts correction method for renal function measurement.•Renal function can be reliably measured in freely moving animals.•The…”
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An intronic base alteration of the CHRNE gene leading to a congenital myasthenic syndrome by MÜLLER, J. S, STUCKA, R, NEUDECKER, S, ZIERZ, S, SCHMIDT, C, HUEBNER, A, LOCHMÜLLER, H, ABICHT, A

“…Reported is a patient with a congenital myasthenic syndrome due to two compound heterozygous mutations of the CHRNE gene. The molecular consequences of a novel…”
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Central Tapia's syndrome (matador's disease) caused by metastatic hemangiosarcoma by KRASNIANSKI, M, NEUDECKER, S, SCHLÜTER, A, KRAUSE, U, WINTERHOLLER, M

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Serial magnet resonance angiography in patients with vasculitis and vasculitis-like angiopathy of the central nervous system by Krasnianski, Michael, Schlüter, A, Neudecker, S, Spielmann, R P, Stock, K

“…The purpose of the study was to examine the value of the non-invasive magnet resonance angiography (MRA) in the follow-up of cerebral vasculitis (CV) and…”
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Mitochondrial 3243 A→G mutation (MELAS mutation) associated with painful muscle stiffness by Deschauer, M., Wieser, T., Neudecker, S., Lindner, A., Zierz, S.

“…The mitochondrial mutation A→G at nucleotide position 3243 is associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes…”
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Eye camouflage and false eyespots: chaetodontid responses to predators by Neudecker, S

“…The roles of eye camouflage and eyespots are examined within the genus Chaetodon as are the various theories explaining the evolutionary significance of the…”
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Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophies by Krasnianski, Anna, Deschauer, Marcus, Neudecker, Stephan, Gellerich, Frank N., Müller, Tobias, Schoser, Benedikt G., Krasnianski, Michael, Zierz, Stephan

“…Previous findings suggested specific mitochondrial dysfunction in skeletal muscle of patients with amyotrophic lateral sclerosis (ALS). To answer the question…”
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Mitochondrial respiratory rates and activities of respiratory chain complexes correlate linearly with heteroplasmy of deleted mtDNA without threshold and independently of deletion size by Gellerich, Frank Norbert, Deschauer, Marcus, Chen, Ying, Müller, Tobias, Neudecker, Stephan, Zierz, Stephan

“…To clarify the importance of deleted protein and tRNA genes on the impairment of mitochondrial function, we performed a quantitative analysis of biochemical,…”
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Tiermodelle mit Zystennieren by Neudecker, S., Gretz, N., Hoffmann, S.

“…Polyzystische Nierenerkrankungen (PKD) sind der häufigste genetische Grund für ein terminales Nierenversagen. Flüssigkeitsgefüllte Zysten bilden sich im…”
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Gross muscle pseudohypertrophy in myeloma-associated light chain amyloidosis by WINDHAGEN, Anja, BUFLER, Johannes, NEUDECKER, Stefan

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Rimmed vacuoles in facioscapulohumeral muscular dystrophy: a unique ultrastructural feature by Neudecker, Stephan, Krasnianski, Michael, Bahn, Erik, Zierz, Stephan

“…Rimmed vacuoles (RV) are a characteristic pathological feature in inclusion body myositis, but may also occur in other neuromuscular disorders, such as distal…”
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Classical crossed pontine syndromes by Krasnianski, M, Neudecker, S, Zierz, S

“…Definitions of classical crossed brainstem syndromes in the modern neurological literature are often inaccurate and inconsistent. As a result, different…”
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Frequent low penetrance mutations in the Lamin A/C gene, causing Emery Dreifuss muscular dystrophy by Vytopil, Michal, Ricci, Enzo, Dello Russo, Antonio, Hanisch, Frank, Neudecker, Stephan, Zierz, Stephan, Ricotti, Roberta, Demay, Laurence, Richard, Pascale, Wehnert, Manfred, Bonne, Gisèle, Merlini, Luciano, Toniolo, Daniela

“…Emery Dreifuss muscular dystrophy is a genetically heterogeneous disorder characterized by the clinical triad of early onset contractures, progressive muscular…”
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Tiermodelle mit Zystennieren by Neudecker, S., Gretz, N., Hoffmann, S.

“…Zusammenfassung Polyzystische Nierenerkrankungen (PKD) sind der häufigste genetische Grund für ein terminales Nierenversagen. Flüssigkeitsgefüllte Zysten…”
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Yawning despite trismus in a patient with locked-in syndrome caused by a thrombosed megadolichobasilar artery by Krasnianski, Michael, Gaul, Charly, Neudecker, Stephan, Behrmann, Curd, Schlüter, Andreas, Winterholler, Martin

“…We report a 62-year-old woman with a locked-in syndrome with bilateral masticatory spasms and persistent trismus, who was still able to yawn. A vascular…”
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Babinski-Nageotte's syndrome and Hemimedullary (Reinhold's) syndrome are clinically and morphologically distinct conditions by Krasnianski, Michael, Neudecker, Stephan, Schluter, Andreas, Zierz, Stephan

“…A hemimedullary infarction, in which medial and lateral medullary lesions occur simultaneously, is a rare cerebrovascular disease. It has been suggested that…”
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Typical facioscapulohumeral dystrophy phenotype in patients without FSHD 4q35 deletion by KRASNIANSKI, Michael, NEUDECKER, Stephan, EGER, Katharina, JAKUBICZKA, Sibylle, ZIERZ, Stephan

“…There have been few reports on facioscapulohumeral dystrophy (FSHD) without 4q35 deletion. Most of them had either only mild FSHD phenotype or so called…”
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