Search Results - "Heubner, G"

IL-6 blockade in systemic juvenile idiopathic arthritis - achievement of inactive disease and remission (data from the German AID-registry) by Bielak, M, Husmann, E, Weyandt, N, Haas, J-P, Hügle, B, Horneff, G, Neudorf, U, Lutz, T, Lilienthal, E, Kallinich, T, Tenbrock, K, Berendes, R, Niehues, T, Wittkowski, H, Weißbarth-Riedel, E, Heubner, G, Oommen, P, Klotsche, J, Foell, Dirk, Lainka, E

“…Systemic juvenile idiopathic arthritis (sJIA) is a complex disease with an autoinflammatory component of unknown etiology related to the innate immune system…”
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Chilblain lupus erythematosus—a review of literature by Hedrich, C. M., Fiebig, B., Hauck, F. H., Sallmann, S., Hahn, G., Pfeiffer, C., Heubner, G., Gahr, M.

“…Chilblain lupus erythematosus (CHLE) is a rare, chronic form of cutaneous lupus erythematosus. Sporadic cases and two families with autosomal…”
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Good response to IL-1β blockade by anakinra in a 23-year-old CINCA/NOMID patient without mutations in the CIAS1 gene. Cytokine profiles and functional studies by HEDRICH, C. M, FIEBIG, B, SALLMANN, S, BRUCK, N, HAHN, G, ROESLER, J, ROESEN-WOLFF, A, HEUBNER, G, GAHR, M

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Wegener's granulomatosis in pediatric patients by Fiebig, B, Hedrich, C M, Heubner, G, Gahr, M

“…Wegener's Granulomatosis (WG) is a disease occurring rarely in childhood and adolescence. Together with the Churg-Strauss-Syndrome and the microscopic…”
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Chilblain lupus erythematosus—a review of literature by Hedrich, C. M., Fiebig, B., Hauck, F. H., Sallmann, S., Hahn, G., Pfeiffer, C., Heubner, G., Lee-Kirsch, M. A., Gahr, M.

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Systemic lupus erythematosus in children and adolescents by Sallmann, S, Fiebig, B, Hedrich, C M, Heubner, G, Gahr, M

“…Children and adolescents represent 15-20% of all systemic lupus erythematosus (SLE) patients. Although the clinical presentation and immunological findings are…”
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The first case of 3-methylcrotonyl-CoA carboxylase (MCC) deficiency responsive to biotin by Friebel, D, von der Hagen, M, Baumgartner, E R, Fowler, B, Hahn, G, Feyh, P, Heubner, G, Baumgartner, M R, Hoffmann, G F

“…3-Methylcrotonylglycinuria is an inborn error of leucine catabolism with an autosomal recessive pattern of inheritance that results from a deficiency of…”
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Osteoid osteomas of the fingers: an atypical localization? Two case reports and a review of the literature by Hedrich, C M, Fiebig, B, Sallmann, S, Bruck, N, Thielemann, F, Hahn, G, Heubner, G, Gahr, M

“…Osteoid osteomas are painful bone tumors that usually occur in childhood or adolescence. Despite the small size of the bony lesions osteoid osteomas can cause…”
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Osteoidosteome der Finger: eine atypische Lokalisation?: Fallberichte von zwei Patienten und Literaturübersicht by Hedrich, C.M., Fiebig, B., Sallmann, S., Bruck, N., Thielemann, F., Hahn, G., Heubner, G., Gahr, M.

“…Zusammenfassung Osteoidosteome sind schmerzhafte Tumoren vorwiegend des Kindes- und frühen Erwachsenenalters. Die genaue Pathogenese ist nach wie vor…”
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Fulminant course in a case of diffuse myelinoclastic encephalitis-- a case report by Poppe, M, Brück, W, Hahn, G, Weissbrich, B, Heubner, G, Goebel, H H, Todt, H

“…We report on a 10-year old previously healthy boy who exhibited a fulminant and nearly monophasic clinical course of demyelinating encephalitis with relapsing…”
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Mocvd process model for deposition of complex oxide ferroelectric thin films by Tompa, G. S., Colibaba-evulet, A., Cuchiaro, J. D., Provost, L. G., Hadnagy, D., Davenport, T., Sun, S., Chu, F., Fox, G., Doppelhammer, R. J., Heubner, G.

“…Thin complex oxide films, such as ferroelectrics, pyroelectrics, waveguides, superconductors, MEMS/MOEMS and piezoelectrics are experiencing rapid growth in a…”
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Epidemiology and care structures for children and adolescents and young adults up to the 26th year of life with inflammatory bowel diseases (IBD) in Leipzig/Saxony/Germany by Zurek, Marlen, Kern, Ivana, Manuwald, Ulf, Kugler, Joachim, Stange, Thoralf, Fischer, Peter, Richter, Thomas, Rothe, Ulrike

“…Aims Valid data on the incidence of inflammatory bowel disease (IBD) in children and adolescents in Germany have not yet been published. Unpublished data of…”
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Interleukin (IL)- 6 inhibition - Follow-up data of the German AID-registry1 by Bielak, M, Husmann, E, Weyandt, N, Haas, JP, Horneff, G, Lutz, T, Lilienthal, E, Kallinich, T, Tenbrock, K, Berendes, R, Dückers, G, Wittkowski, H, Weissbarth-Riedel, E, Heubner, G, Oommen, PT, Klotsche, J, Neudorf, U, Föll, D, Niehues, T, Lainka, E

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The Kleine-Levin syndrome - effects of treatment with lithium by Poppe, M, Friebel, D, Reuner, U, Todt, H, Koch, R, Heubner, G

“…Kleine-Levin syndrome (KLS) is a rare disorder which affects mainly adolescents. Periods of extreme somnolence alternate with megaphagia, psychomental changes…”
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Good response to IL-1 blockade by anakinra in a 23-year-old CINCA NOMID patient without mutations in the CIAS1 gene. Cytokine profiles and functional studies by Hedrich, C. M., Fiebig, B., Sallmann, S., Bruck, N., Hahn, G., Roesler, J., Roesen-Wolff, A., Heubner, G., Gahr, M.

“…Chronic infantile neurological cutaneous and articular (CINCA) syndrome is an autoinflammatory disease, defined by the triad of urticarial rash, neurological…”
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Periodic fever, mild arthralgias, and reversible moderate and severe organ inflammation associated with the V198M mutation in the CIAS1 gene in three German patients - expanding phenotype of CIAS1 related autoinflammatory syndrome by Pörksen, Gönke, Lohse, Peter, Rösen-Wolff, Angela, Heyden, Stefan, Förster, Theresa, Wendisch, Jörg, Heubner, Georg, von Bernuth, Horst, Sallmann, Svea, Gahr, Manfred, Roesler, Joachim

“…:  Dominant mutations in the CIAS1 gene cause a spectrum of autoinflammatory diseases such as familial cold autoinflammatory syndrome, FCAS, which is…”
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Differentiation between recurrent tumor and radiation necrosis in a child with anaplastic ependymoma after chemotherapy and radiation therapy by BEUTHIEN-BAUMANN, Bettina, HAHN, Gabriele, WINKLER, Cornelia, HEUBNER, Georg

“…In patients after treatment for malignant brain tumors, a clear distinction between tumor recurrence and radiation necrosis can be challenging. This case…”
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Good response to IL-1beta blockade by anakinra in a 23-year-old CINCA/NOMID patient without mutations in the CIAS1 gene. Cytokine profiles and functional studies by Hedrich, C M, Fiebig, B, Sallmann, S, Bruck, N, Hahn, G, Roesler, J, Roesen-Wolff, A, Heubner, G, Gahr, M

“…Chronic infantile neurological cutaneous and articular (CINCA) syndrome is an autoinflammatory disease, defined by the triad of urticarial rash, neurological…”
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Periodic fever (TRAPS) caused by mutations in the TNFα receptor 1 (TNFRSF1A) gene of three German patients by Rösen-Wolff, Angela, Kreth, Hans-Wolfgang, Hofmann, Sigrun, Höhne, Katrin, Heubner, Georg, Möbius, Dagmar, Zintl, Fritz, Gahr, Manfred, Roesler, Joachim

“…: TNF‐receptor‐associated periodic syndrome (TRAPS) is a recently recognized disorder characterized by prolonged attacks of high fever and severe localized…”
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Systemischer Lupus erythematodes im Kindes- und Jugendalter by Sallmann, Dr. S., Fiebig, B., Hedrich, C. M., Heubner, G., Gahr, M.

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