Search Results - "Schnauder, Günter"

Response of Mitochondrial Respiration in Adipose Tissue and Muscle to 8 Weeks of Endurance Exercise in Obese Subjects by Hoffmann, Christoph, Schneeweiss, Patrick, Randrianarisoa, Elko, Schnauder, Günter, Kappler, Lisa, Machann, Jürgen, Schick, Fritz, Fritsche, Andreas, Heni, Martin, Birkenfeld, Andreas, Niess, Andreas M, Häring, Hans-Ulrich, Weigert, Cora, Moller, Anja

“…Abstract Context Exercise training improves glycemic control and increases mitochondrial content and respiration capacity in skeletal muscle. Rodent studies…”
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COVID-19 in persons aged 70+ in an early affected German district: Risk factors, mortality and post-COVID care needs-A retrospective observational study of hospitalized and non-hospitalized patients by Herrmann, Matthias L, Hahn, Johannes-Martin, Walter-Frank, Birgit, Bollinger, Desiree M, Schmauder, Kristina, Schnauder, Günter, Bitzer, Michael, Malek, Nisar P, Eschweiler, Gerhard W, Göpel, Siri

“…Cohorts of hospitalized COVID-19 patients have been studied in several countries since the beginning of the pandemic. So far, there is no complete survey of…”
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Insulin sensitivity predicts cognitive decline in individuals with prediabetes by Willmann, Caroline, Brockmann, Kathrin, Wagner, Robert, Kullmann, Stephanie, Preissl, Hubert, Schnauder, Günter, Maetzler, Walter, Gasser, Thomas, Berg, Daniela, Eschweiler, Gerhard W, Metzger, Florian, Fallgatter, Andreas J, Häring, Hans-Ulrich, Fritsche, Andreas, Heni, Martin

“…IntroductionEpidemiological studies indicate an association between type 2 diabetes and cognitive dysfunction that appear to start already in the prediabetic…”
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A pitfall of bilateral inferior petrosal sinus sampling in cyclic Cushing's syndrome by Albani, Adriana, Berr, Christina M, Beuschlein, Felix, Treitl, Marcus, Hallfeldt, Klaus, Honegger, Jürgen, Schnauder, Günter, Reincke, Martin

“…Clinical care of patients with cyclic Cushing's syndrome (CS) is challenging. Classical pitfalls include incorrect subtyping, unnecessary surgical procedures…”
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17α-Hydroxylase/17,20-Lyase Deficiency Caused by a Novel Homozygous Mutation (Y27Stop) in the Cytochrome CYP17 Gene by Müssig, Karsten, Kaltenbach, Simone, Machicao, Fausto, Maser-Gluth, Christiane, Hartmann, Michaela F., Wudy, Stefan A., Schnauder, Günter, Häring, Hans-Ulrich, Seif, Fritz J., Gallwitz, Baptist

“…Context: 17α-Hydroxylase/17,20-lyase deficiency, a rare autosomal recessive form of congenital adrenal hyperplasia, is caused by mutations in the cytochrome…”
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TGF-β Contributes to Impaired Exercise Response by Suppression of Mitochondrial Key Regulators in Skeletal Muscle by Böhm, Anja, Hoffmann, Christoph, Irmler, Martin, Schneeweiss, Patrick, Schnauder, Günter, Sailer, Corinna, Schmid, Vera, Hudemann, Jens, Machann, Jürgen, Schick, Fritz, Beckers, Johannes, Hrabě de Angelis, Martin, Staiger, Harald, Fritsche, Andreas, Stefan, Norbert, Nieß, Andreas M, Häring, Hans-Ulrich, Weigert, Cora

“…A substantial number of people at risk of developing type 2 diabetes could not improve insulin sensitivity by physical training intervention. We studied the…”
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TGF-[Beta] Contributes to Impaired Exercise Response by Suppression of Mitochondrial Key Regulators in Skeletal Muscle by Böhm, Anja, Hoffmann, Christoph, Irmler, Martin, Schneeweiss, Patrick, Schnauder, Günter, Sailer, Corinna, Schmid, Vera, Hudemann, Jens, Machann, Jürgen, Schick, Fritz, Beckers, Johannes, Hrabe de Angelis, Martin, Staiger, Harald, Fritsche, Andreas, Stefan, Norbert, Nieß, Andreas M, Häring, Hans-Ulrich, Weigert, Cora

“…A substantial number of people at risk of developing type 2 diabetes could not improve insulin sensitivity by physical training intervention. We studied the…”
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Hyponatremia--should it be ignored or diagnosed?--Case 8/2011 by Zürn, Christine S, Sauer-Schulz, Anja, Schnauder, Günter

“…HISTORY, CLINICAL FINDINGS: A 72-year-old dehydrated female was admitted to our emergency department. She presented with a decreased level of consciousness and…”
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17alpha-hydroxylase/17,20-lyase deficiency caused by a novel homozygous mutation (Y27Stop) in the cytochrome CYP17 gene by Müssig, Karsten, Kaltenbach, Simone, Machicao, Fausto, Maser-Gluth, Christiane, Hartmann, Michaela F, Wudy, Stefan A, Schnauder, Günter, Häring, Hans-Ulrich, Seif, Fritz J, Gallwitz, Baptist

“…17alpha-Hydroxylase/17,20-lyase deficiency, a rare autosomal recessive form of congenital adrenal hyperplasia, is caused by mutations in the cytochrome P450c17…”
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17a-hydroxylase/17,20-lyase deficiency caused by a novel homozygous mutation (Y27stop) in the cytochrome CYP17 gene by MÜSSIG, Karsten, KALTENBACH, Simone, MACHICAO, Fausto, MASER-GLUTH, Christiane, HARTMANN, Michaela F, WUDY, Stefan A, SCHNAUDER, Günter, HÄRING, Hans-Ulrich, SEIF, Fritz J, GALLWITZ, Baptist

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Can water be poisonous? by Artunc, Ferruh, Schnauder, Günter, Gallwitz, Baptist, Amend, Bastian

“…Two female patients aged over 80 years developed central nervous symptoms after drinking large amounts of water (more than 3 l per day). Both had a hypoosmolar…”
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Endocrine abnormalities in a patient with borderline personality disorder--case 8/2014 by Gassenmaier, Christoph, Schittenhelm, Jens, Selo, Nadja, Schnauder, Günter

“…We report on a 44-year-old woman who was treated for borderline personality disorder in the Department of Psychiatry. In addition, symptoms of hyperthyroidism…”
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A rare cause of thyreotoxicosis by Sauer-Schulz, Anja, Müssig, Karsten, Kurth, Ralf, Fend, Falko, Teichmann, Reinhard, Schnauder, Günter

“…Amiodarone-induced thyrotoxicosis (AIT) should be included in differential diagnoses of thyrotoxicosis in presence of a suggestive drug history. Adequate…”
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Hypothyroidism due to pseudo-malabsorption of levothyroxine--Case 12/2009 by Müssig, Karsten, Mörike, Klaus, Klein, Reinhild, Sträter, Jörn, Georges, Georg, Häring, Hans-Ulrich, Schnauder, Günter

“…Hypothyroidism is a common endocrine disorder which is easily treatable by an appropriate thyroid hormone replacement therapy in the majority of patients. In…”
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