Zobrazeno 1 - 10
of 27
pro vyhledávání: '"C, Tegtmeyer"'
Autor:
Kristine Nolting, Julien H. Park, Laura C. Tegtmeyer, Andrea Zühlsdorf, Marianne Grüneberg, Stephan Rust, Janine Reunert, Ingrid Du Chesne, Volker Debus, Eric Schulze-Bahr, Robert C. Baxter, Yoshinao Wada, Christian Thiel, Emile van Schaftingen, Ralph Fingerhut, Thorsten Marquardt
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 13, Iss C, Pp 33-40 (2017)
Introduction: Phosphoglucomutase 1 deficiency (PGM1 deficiency) has been identified as both, glycogenosis and congenital disorder of glycosylation (CDG). The phenotype includes hepatopathy, myopathy, oropharyngeal malformations, heart disease and gro
Externí odkaz:
https://doaj.org/article/10d9db70a03446e5b7eab4cad03b3098
Autor:
Claudia Maria Schmidt, Michael Boettcher, Michaela Klinke, Laura C. Tegtmeyer, Ingo Koenigs, Konrad Reinshagen
Publikováno v:
Klinische Pädiatrie. 230:61-67
Zusammenfassung Hintergrund Thermische Verletzungen stellen eine relevante Unfallursache im Kindesalter dar und sind häufig mit langen Krankenhausaufenthalten und schwerwiegenden physischen und psychischen Beeinträchtigungen der Patienten sowie oft
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7e660758ee78cd4b5ae2fc244bfd317
https://doi.org/10.1055/s-0043-119416
https://doi.org/10.1055/s-0043-119416
Publikováno v:
Ticks and tick-borne diseases. 10(5)
Anaplasma phagocytophilum is a tick-transmitted Gram-negative obligate intracellular bacterium that replicates in neutrophil granulocytes. It causes tick-borne fever in cattle and sheep. We report here the case of a 5-year-old cow from Germany with c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1988232e48ef69872a2780b2edd0c33
https://pubmed.ncbi.nlm.nih.gov/31171465
https://pubmed.ncbi.nlm.nih.gov/31171465
Autor:
Philip C. Tegtmeyer, Carina Helmer, M. Runge, R. Eibach, Martin Ganter, Esther Humann-Ziehank
Publikováno v:
Transboundary and Emerging Diseases. 62:425-436
Schmallenberg virus (SBV) infections can cause congenital musculoskeletal and vertebral malformations as well as neurological failures in foetuses of several ruminant species if susceptible mother animals were infected during early gestation. Blood s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b5d15134f8f8c775dcf24964aadb49d
https://doi.org/10.1111/tbed.12161
https://doi.org/10.1111/tbed.12161
Publikováno v:
Epidemiology and Infection
SUMMARYAnimal losses due to abortion and malformed offspring during the lambing period 2011/2012 amounted to 50% in ruminants in Europe. A new arthropod-borne virus, called Schmallenberg virus (SBV), was identified as the cause of these losses. Blood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5b1c2df002e1cd8230df81fe2668e06
http://europepmc.org/articles/PMC3789509
http://europepmc.org/articles/PMC3789509
Autor:
Martin Ganter, Esther Humann-Ziehank, Kathrin Mayer, Katja Voigt, Carina Helmer, Regina Eibach, Philipp Leopold Sieber, Sieglinde Stauch, Udo Moog, Heinz Strobel, Philip C. Tegtmeyer, Matthias Greiner, Daniela Bürstel
Publikováno v:
Scipedia Open Access
Scipedia SL
Veterinary Medicine and Science
Scipedia SL
Veterinary Medicine and Science
Summary Schmallenberg virus (SBV) is a member of the family Bunyaviridae and mainly affects ruminants. It is transmitted by biting midges, first and foremost Culicoides spp., and causes congenital malformations reflected in arthrogryposis–hydranenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20c24c4b7b6c6849a6ecab325c9420f5
https://www.scipedia.com/public/Helmer_et_al_2016a
https://www.scipedia.com/public/Helmer_et_al_2016a
Autor:
Georg R. Herrnstadt, Sarah L. Maier, Konrad Reinshagen, Michaela Klinke, Oliver C. Thamm, Laura C. Tegtmeyer, Ingo Koenigs
Publikováno v:
Burns : journal of the International Society for Burn Injuries. 44(1)
The purpose of this observational, multi-center study was to reveal epidemiologic, etiological and clinical aspects of hospitalized children with thermal injuries in Germany and Austria and the workup of a renewed web-based pediatric burn registry.Fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4f6736b809580b091090ed5a88e3191
https://pubmed.ncbi.nlm.nih.gov/28645714
https://pubmed.ncbi.nlm.nih.gov/28645714
Publikováno v:
Tierärztliche Praxis Ausgabe G: Großtiere / Nutztiere. 35:183-189
Zusammenfassung Gegenstand und Ziel: Der Erfolg des wiederholten metaphylaktischen Einsatzes von Praziquantel zur Bekämpfung des Moniezia-Befalls bei Schaflämmern wurde in einem siebenmonatigen (Juni bis Dezember 2004) Feldversuch geprüft. Materia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a2ccf19ed2ad8da5bb40c65ab47a5f2
https://doi.org/10.1055/s-0037-1621636
https://doi.org/10.1055/s-0037-1621636
Autor:
Gunter Simic-Schleicher, Anja Seelhöfer, Ingrid Du Chesne, Stephan Rust, Laura C. Tegtmeyer, Esther Schrapers, V. Debus, Manfred Fobker, Janine Reunert, Sebastian T. Balbach, Thorsten Marquardt, Karin Klingel
Publikováno v:
JIMD Reports ISBN: 9783662498323
Phosphoglucomutase 1 deficiency has recently been reported as a novel disease that belongs to two different classes of metabolic disorders, congenital disorders of glycosylation (CDG) and glycogen storage diseases.This paper focuses on previously rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c43630dcab6c6dfb6980c60fe40d2260
https://doi.org/10.1007/8904_2015_471
https://doi.org/10.1007/8904_2015_471
Autor:
Sharita Timal, Bobby G. Ng, Jaak Jaeken, Elżbieta Czarnowska, Emile Van Schaftingen, Anika Witten, Patricie Burda, Tanya Stojkovic, Thorsten Marquardt, Vandana Sharma, Joris A. Veltman, Ron A. Wevers, Ralph Fingerhut, Olivier Aumaître, Daisy Rymen, Gert Matthijs, Mie Ichikawa, Reuben Matalon, Stephan Rust, Pietro Vajro, François Petit, Teodor Podskarbi, Monique van Scherpenzeel, Piotr Socha, Martin Lammens, Soraya Seyyedi, Dieter Vanderschaeghe, Esther Schrapers, Yoon S. Shin, Janine Reunert, Linda De Meirleir, Eva Morava, Charles A. Stanley, Karin Huijben, Yoshinao Wada, Marie-Estelle Losfeld, Can Ficicioglu, Pascal Laforêt, Jolanta Sykut-Cegielska, Monique Piraud, Kimiyo Raymond, Maciej Adamowicz, V. Debus, Ping He, Laura C. Tegtmeyer, Francjan J. van Spronsen, Terry J. DeClue, Dirk Lefeber, Hudson H. Freeze, Nico Callewaert
Publikováno v:
The New England Journal of Medicine, 370, 533-42
The New England Journal of Medicine, 370, 6, pp. 533-42
NEW ENGLAND JOURNAL OF MEDICINE
New England Journal of Medicine, 370(6), 533-542. MASSACHUSETTS MEDICAL SOC
The New England journal of medicine
The New England Journal of Medicine, 370, 6, pp. 533-42
NEW ENGLAND JOURNAL OF MEDICINE
New England Journal of Medicine, 370(6), 533-542. MASSACHUSETTS MEDICAL SOC
The New England journal of medicine
BackgroundCongenital disorders of glycosylation are genetic syndromes that result in impaired glycoprotein production. We evaluated patients who had a novel recessive disorder of glycosylation, with a range of clinical manifestations that included he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91d19f5f94f348953f8c87c56fa6e29e
https://pubmed.ncbi.nlm.nih.gov/24849094
https://pubmed.ncbi.nlm.nih.gov/24849094