Search Results - "Padberg, W."

Intra-abdominal sepsis: new definitions and current clinical standards by Hecker, A., Reichert, M., Reuß, C. J., Schmoch, T., Riedel, J. G., Schneck, E., Padberg, W., Weigand, M. A., Hecker, M.

“…Purpose The abdomen is the second most common source of sepsis and is associated with unacceptably high morbidity and mortality. Recently, the essential…”
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Population-based incidence and prevalence of facioscapulohumeral dystrophy by Deenen, Johanna C.W, Arnts, Hisse, van der Maarel, Silvère M, Padberg, George W, Verschuuren, Jan J.G.M, Bakker, Egbert, Weinreich, Stephanie S, Verbeek, André L.M, van Engelen, Baziel G.M

“…OBJECTIVE:To determine the incidence and prevalence of facioscapulohumeral muscular dystrophy (FSHD) in the Netherlands. METHODS:Using 3-source…”
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Pancreatogastrostomy Versus Pancreatojejunostomy for RECOnstruction After PANCreatoduodenectomy (RECOPANC, DRKS 00000767): Perioperative and Long-term Results of a Multicenter Randomized Controlled Trial by Keck, Tobias, Wellner, U F, Bahra, M, Klein, F, Sick, O, Niedergethmann, M, Wilhelm, T J, Farkas, S A, Börner, T, Bruns, C, Kleespies, A, Kleeff, J, Mihaljevic, A L, Uhl, W, Chromik, A, Fendrich, V, Heeger, K, Padberg, W, Hecker, A, Neumann, U P, Junge, K, Kalff, J C, Glowka, T R, Werner, J, Knebel, P, Piso, P, Mayr, M, Izbicki, J, Vashist, Y, Bronsert, P, Bruckner, T, Limprecht, R, Diener, M K, Rossion, I, Wegener, I, Hopt, U T

“…OBJECTIVES:To assess pancreatic fistula rate and secondary endpoints after pancreatogastrostomy (PG) versus pancreatojejunostomy (PJ) for reconstruction in…”
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Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy by Lemmers, Richard J.L.F, van der Vliet, Patrick J, Klooster, Rinse, Sacconi, Sabrina, Camaño, Pilar, Dauwerse, Johannes G, Snider, Lauren, Straasheijm, Kirsten R, Jan van Ommen, Gert, Padberg, George W, Miller, Daniel G, Tapscott, Stephen J, Tawil, Rabi, Frants, Rune R, van der Maarel, Silvère M

“…Facioscapulohumeral muscular dystrophy (FSHD) is a common form of muscular dystrophy in adults that is foremost characterized by progressive wasting of muscles…”
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Morgagni−Larrey diaphragmatic hernia repair in adult patients: a retrospective single-center experience by Oppelt, P. U., Askevold, I., Bender, F., Liese, J., Padberg, W., Hecker, A., Reichert, M.

“…Purpose Morgagni−Larrey congenital diaphragmatic hernia (MLH) is rare in adult patients and surgery is performed infrequently. The evidence regarding the most…”
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Chromosome 10q-linked FSHD identifies DUX4 as principal disease gene by Lemmers, Richard J L F, van der Vliet, Patrick J, Blatnik, Ana, Balog, Judit, Zidar, Janez, Henderson, Don, Goselink, Rianne, Tapscott, Stephen J, Voermans, Nicol C, Tawil, Rabi, Padberg, George W A M, van Engelen, Baziel Gm, van der Maarel, Silvère M

“…Facioscapulohumeral dystrophy (FSHD) is an inherited muscular dystrophy clinically characterised by muscle weakness starting with the facial and upper…”
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Phosphocholine – an agonist of metabotropic but not of ionotropic functions of α9-containing nicotinic acetylcholine receptors by Richter, K., Mathes, V., Fronius, M., Althaus, M., Hecker, A., Krasteva-Christ, G., Padberg, W., Hone, A. J., McIntosh, J. M., Zakrzewicz, A., Grau, V.

“…We demonstrated previously that phosphocholine and phosphocholine-modified macromolecules efficiently inhibit ATP-dependent release of interleukin-1β from…”
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Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHD by Krom, Yvonne D, Thijssen, Peter E, Young, Janet M, den Hamer, Bianca, Balog, Judit, Yao, Zizhen, Maves, Lisa, Snider, Lauren, Knopp, Paul, Zammit, Peter S, Rijkers, Tonnie, van Engelen, Baziel G M, Padberg, George W, Frants, Rune R, Tawil, Rabi, Tapscott, Stephen J, van der Maarel, Silvère M

“…Facioscapulohumeral dystrophy (FSHD) is a progressive muscular dystrophy caused by decreased epigenetic repression of the D4Z4 macrosatellite repeats and…”
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Distinct disease phases in muscles of facioscapulohumeral dystrophy patients identified by MR detected fat infiltration by Janssen, Barbara H, Voet, Nicoline B M, Nabuurs, Christine I, Kan, Hermien E, de Rooy, Jacky W J, Geurts, Alexander C, Padberg, George W, van Engelen, Baziel G M, Heerschap, Arend

“…Facioscapulohumeral muscular dystrophy (FSHD) is an untreatable disease, characterized by asymmetric progressive weakness of skeletal muscle with fatty…”
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Commercial α1-antitrypsin preparations markedly differ in their potential to inhibit the ATP-induced release of monocytic interleukin-1β by Agné, A., Richter, K., Padberg, W., Janciauskiene, S., Grau, V.

“…The acute phase protein α1-antitrypsin (AAT) inhibits numerous proteases, specifically neutrophil elastase. Patients with an AAT deficiency due to mutations…”
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De novo mutations in PLXND1 and REV3L cause Möbius syndrome by Tomas-Roca, Laura, Tsaalbi-Shtylik, Anastasia, Jansen, Jacob G., Singh, Manvendra K., Epstein, Jonathan A., Altunoglu, Umut, Verzijl, Harriette, Soria, Laura, van Beusekom, Ellen, Roscioli, Tony, Iqbal, Zafar, Gilissen, Christian, Hoischen, Alexander, de Brouwer, Arjan P. M., Erasmus, Corrie, Schubert, Dirk, Brunner, Han, Pérez Aytés, Antonio, Marin, Faustino, Aroca, Pilar, Kayserili, Hülya, Carta, Arturo, de Wind, Niels, Padberg, George W., van Bokhoven, Hans

“…Möbius syndrome (MBS) is a neurological disorder that is characterized by paralysis of the facial nerves and variable other congenital anomalies. The aetiology…”
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When to operate after SARS-CoV-2 infection? A review on the recent consensus recommendation of the DGC/BDC and the DGAI/BDA by Noll, J., Reichert, M., Dietrich, M., Riedel, J. G., Hecker, M., Padberg, W., Weigand, M. A., Hecker, A.

“…Since the eruption of the worldwide SARS-CoV-2 pandemic in late 2019/early 2020, multiple elective surgical interventions were postponed. Through pandemic…”
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Trans-hiatal herniation following esophagectomy or gastrectomy: retrospective single-center experiences with a potential surgical emergency by Oppelt, P. U., Askevold, I., Hörbelt, R., Roller, F. C., Padberg, W., Hecker, A., Reichert, M.

“…Purpose Trans-hiatal herniation after esophago-gastric surgery is a potentially severe complication due to the risk of bowel incarceration and cardiac or…”
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Sarcopenia of kidney transplant recipients as a predictive marker for reduced graft function and graft survival after kidney transplantation by Karakizlis, H., Trudel, N., Brose, A., Reinisch, A., Reichert, M., Hecker, A., Bender, F., Askevold, I., Rainer, L., Weimer, R., Krombach, G. A., Padberg, W., Liese, J.

“…Purpose The association between sarcopenia of kidney transplant recipients and outcome after kidney transplantation (KT) has not yet been fully understood and…”
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Acute abdominal compartment syndrome: current diagnostic and therapeutic options by Hecker, A., Hecker, B., Hecker, M., Riedel, J. G., Weigand, M. A., Padberg, W.

“…Background If untreated, the abdominal compartment syndrome (ACS) has a mortality of nearly 100 %. Thus, its early recognition is of major importance for daily…”
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Characterizing the face in facioscapulohumeral muscular dystrophy by Loonen, T. G. J., Horlings, C. G. C., Vincenten, S. C. C., Beurskens, C. H. G., Knuijt, S., Padberg, G. W. A. M., Statland, J. M., Voermans, N. C., Maal, T. J. J., van Engelen, B. G. M., Mul, K.

“…Objective To evaluate facial weakness in patients with FSHD to better define clinical signs, and pilot a facial weakness severity score. Methods 87 FSHD…”
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Specific Sequence Variations within the 4q35 Region Are Associated with Facioscapulohumeral Muscular Dystrophy by Lemmers, Richard J.L.F., Wohlgemuth, Mariëlle, van der Gaag, Kristiaan J., van der Vliet, Patrick J., van Teijlingen, Corrie M.M., de Knijff, Peter, Padberg, George W., Frants, Rune R., van der Maarel, Silvère M.

“…Autosomal dominant facio scapulo humeral muscular dystrophy (FSHD) is mainly characterized by progressive wasting and weakness of the facial, shoulder, and…”
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Clinical features of facioscapulohumeral muscular dystrophy 2 by DE GREEF, J. C, LEMMERS, R. J. L. F, DESNUELLE, C, SPULER, S, TARNOPOLSKY, M, VENANCE, S. L, FRANTS, R. R, VAN DER MAAREL, S. M, TAWIL, R, CAMANO, P, DAY, J. W, SACCONI, S, DUNAND, M, VAN ENGELEN, B. G. M, KIURU-ENARI, S, PADBERG, G. W, ROSA, A. L

“…In some 5% of patients with facioscapulohumeral muscular dystrophy (FSHD), no D4Z4 repeat contraction on chromosome 4q35 is observed. Such patients, termed…”
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Sarcomeric dysfunction contributes to muscle weakness in facioscapulohumeral muscular dystrophy by LASSCHE, Saskia, STIENEN, Ger J. M, IRVING, Tom C, DER MAAREL, Silvere M. Van, VOERMANS, Nicol C, PADBERG, George W, GRANZIER, Henk, ENGELEN, Baziel G. M. Van, OTTENHEIJM, Coen A. C

“…To investigate whether sarcomeric dysfunction contributes to muscle weakness in facioscapulohumeral muscular dystrophy (FSHD). Sarcomeric function was…”
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What's in a name? The clinical features of facioscapulohumeral muscular dystrophy by Mul, Karlien, Lassche, Saskia, Voermans, Nicol C, Padberg, George W, Horlings, Corinne Gc, van Engelen, Baziel Gm

“…Facioscapulohumeral muscular dystrophy (FSHD) is an inherited and progressive muscle disorder. Although its name suggests otherwise, it comprises weakness of…”
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