Search Results - "Völkl, Thomas M. K."

Birth Size in Neonates with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency by Dörr, Helmuth G., Penger, Theresa, Albrecht, Andrea, Marx, Michaela, Völkl, Thomas M. K.

“…Classic congenital adrenal hyperplasia (CAH) secondary to 21-hydroxylase deficiency is characterized by increased prenatal adrenal androgen secretion. There…”
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Adrenarche and pubarche in girls with turner syndrome during growth-promoting therapy with human growth hormone by Dörr, Helmuth G, Penger, Theresa, Marx, Michaela, Rauh, Manfred, Oppelt, Patricia G, Völkl, Thomas K M

“…Data on adrenarche and pubarche in girls with Turner syndrome (TS) are inconsistent in the literature. The cohort consisted of 94 girls and young women with TS…”
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Altered 24-Hour Blood Pressure Profiles in Children and Adolescents with Classical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency by Völkl, Thomas M. K., Simm, Diemud, Dötsch, Jörg, Rascher, Wolfgang, Dörr, Helmuth G.

“…Objective: Children and adolescents with classical congenital adrenal hyperplasia have been shown to be at risk for obesity associated with higher insulin and…”
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Does an altered leptin axis play a role in obesity among children and adolescents with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency? by Völkl, Thomas M K, Simm, Diemud, Körner, Antje, Rascher, Wolfgang, Kiess, Wieland, Kratzsch, Jürgen, Dörr, Helmuth G

“…ObjectiveCongenital adrenal hyperplasia (CAH) patients are at a higher risk to develop obesity. The role of leptin in CAH is still controversial. Our study…”
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Cardiovascular anomalies in children and young adults with Ullrich‐Turner syndrome—the erlangen experience by Völkl, Thomas M. K., Degenhardt, Karin, Koch, Andreas, Simm, Diemud, Dörr, Helmuth G., Singer, Helmut

“…Background: Females with Ullrich‐Turner syndrome (UTS) have typical clinical features such as short stature, ovarian failure, visible dysmorphic stigmata, and…”
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Klinefelter syndrome and mediastinal germ cell tumors by Völkl, Thomas M.K., Langer, Thorsten, Aigner, Thomas, Greess, Holger, Beck, Jörn D., Rauch, Anita M., Dörr, Helmuth G.

“…Precocious puberty is not a typical manifestation of patients with Klinefelter syndrome (KS). However, there is an increased incidence of mediastinal germ cell…”
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Obesity Among Children and Adolescents With Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency by Volkl, Thomas M. K, Simm, Diemud, Beier, Christoph, Dorr, Helmuth G

“…Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is the most common inherited disorder of adrenal steroid biosynthesis. Patients with the…”
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2013 Lwpes/Espe 9th Joint Meeting, Milan, Italy, selected highlights by Poyrazoglu, Sukran, Völkl, Thomas M K, Karantza, Maria

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Catch-down growth during infancy of children born small (SGA) or appropriate (AGA) for gestational age with short-statured parents by Völkl, Thomas M.K., Haas, Bettina, Beier, Christoph, Simm, Diemud, Dörr, Helmuth G.

“…We analyzed postnatal growth in children with familial short stature (FSS) with regard to small (SGA) or appropriate (AGA) for gestational age status at birth…”
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Adiponectin levels are high in children with classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency by Völkl, Thomas MK, Simm, Diemud, Körner, Antje, Kiess, Wieland, Kratzsch, Jürgen, Dörr, Helmuth G

“…Objective: It has been shown that adiponectin serves as an insulin‐sensitizing adipokine. Serum concentrations of adiponectin are low in children with obesity,…”
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Statistical analysis plan for the FiO2-C trial: effects of closed-loop automatic control of the inspiratory fraction of oxygen (FiO2-C) on outcomes of extremely preterm infants—a randomized-controlled parallel group multicentre trial for safety and efficacy by König, Jochem, Stauch, Anette, Engel, Corinna, Urschitz, Michael S., Franz, Axel R., Poets, Christian F., Hummler, Helmut, Niemarkt, Hendrik J., Bassler, Dirk, Maiwald, Christian A., Bergmann, Iris, Weiss, Monika, Eichhorn, Andreas, Raubuch, Michael, Roth, Michael, Schuler, Birgit, Rötsch, Kai, Bai, Ruimiao, Fiedler, Andreas, Kapp, Sonja, Völkl, Thomas M. K., Horsinka, Sibylle C., Hammond, Edmondo N. L., von Buch, Christoph, Körner, Hans Thorsten, Tröger, Birte, Rüdiger, Mario, Seipolt, Barbara, Mense, Lars, Hoehn, Thomas, Lohmeier, Klaus, Bittrich, Hans-Jörg, Roefke, Kathrin, Niethammer, Klaus, Brenner, Britta, Raecke, Olaf, Fuchs, Hans, Klotz, Daniel, Koluch, Anna, Idel, Sandra, Lübking, Laura, Bohnhorst, Bettina, Peter, Corinna, Jacobi, Christoph, Gille, Christian, Beedgen, Bernd, Heinzmann, Tina, Meyer, Sascha, Kühr, Joachim, Holz, Sandra, Welcker, Silvia, Thome, Ulrich H., Ackermann, Benjamin W., Gebauer, Corinna, Flemmer, Andreas W., Herber-Jonat, Susanne, Kley, Adelheid, Krüger, Marcus, Reber, Daniela, Brickmann, Christian, Ackermann, Kilian, Sandkötter, Julia, Masjosthusmann, Katja, Schroth, Michael, Grillhösl, Christian, Kittel, Jochen, Michel, Holger, Schneider, Hans-Christoph, Mayer, Anja, Lode, Hans-Martin, Lorenz, Daniel, Bosk, Axel T., Gausepohl, Hans-Jürgen, Lindner, Torben, Vochem, Matthias, Strahleck, Thomas, Neuberger, Patrick, Arand, Jörg, Ehrhardt, Harald, Mendler, Marc R., Essers, Jochen, Bender, Christian, Beckmann, Jessica, Mammodova, Narmina, Rauch, Ralf, Bernbeck, Ulrich, Mohns, Thilo, Mulder, Estelle E. M., van Straaten, Henrica L. M., Hütten, Matthias, van Westering-Kroon, Elke, Nair, Vrinda

“…Abstract Background Extremely low gestational age neonates (ELGANs, i.e. those born before 28 weeks postmenstrual age (PMA)) often require supplemental oxygen…”
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Effects of closed-loop automatic control of the inspiratory fraction of oxygen (FiO 2 -C) on outcome of extremely preterm infants - study protocol of a randomized controlled parallel group multicenter trial for safety and efficacy by Maiwald, Christian A, Niemarkt, Hendrik J, Poets, Christian F, Urschitz, Michael S, König, Jochem, Hummler, Helmut, Bassler, Dirk, Engel, Corinna, Franz, Axel R

“…Most extremely low gestational age neonates (ELGANS, postmenstrual age at birth (PMA) < 28 completed weeks) require supplemental oxygen and experience frequent…”
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Seltene Differenzialdiagnose einer Gehverweigerung by Langer, Johanna, Marschal, Cordula, Endraß, Nele, Demharter, Johannes, Völkl, Thomas M. K., Schick, Christoph

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Adrenarche and puberty in children with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency by Völkl, Thomas M K, Öhl, Lisa, Rauh, Manfred, Schöfl, Christof, Dörr, Helmuth G

“…There have been only a few studies on adrenarche in girls with classic congenital adrenal hyperplasia (CAH) showing that dehydroepiandrosterone sulfate (DHEAS)…”
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McCune-Albright syndrome: clinical picture and natural history in children and adolescents by Völkl, Thomas M K, Dörr, Helmuth G

“…The classical triad of McCune-Albright syndrome (MAS) consists of polyostotic fibrous dysplasia (FD), skin hyperpigmentation (café-au-lait spots), and…”
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IGF-I–IGFBP-3–acid-labile subunit (ALS) complex in children and adolescents with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency (CAH) by Völkl, Thomas M.K, Rauh, Manfred, Schöfl, Christof, Dörr, Helmuth G

“…Abstract It has been shown that changes in IGF-I and IGFBP levels in children with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency…”
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Obesity Among Children and Adolescents With Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency by Völkl, Thomas M K, Simm, Diemud, Beier, Christoph, Dörr, Helmuth G

“…An abstract of a study about obesity among children and adolescents with classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is…”
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Spontaneous growth hormone secretion and IGF1:IGFBP3 molar ratios in children born small for gestational age (SGA) by Völkl, Thomas M.K., Schwöbel, Katja, Simm, Diemud, Beier, Christoph, Rohrer, Tilman R., Dörr, Helmuth G.

“…To analyze spontaneous nocturnal GH profiles, IGF1 and IGFBP3 serum levels, as well as IGF1:IGFBP3 molar ratios in SGA children without postnatal catch-up…”
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