Great Ormond Street Hospital (GOSH)


Klinik

Standort der Organisation:
London, Großbritannien (UK)


Publikationen in Kooperation mit FAU-Wissenschaftlerinnen und Wissenschaftlern


Burgmaier, K., Kilian, S., Bammens, B., Benzing, T., Billing, H., Buescher, A.,... Liebau, M.C. (2019). Clinical courses and complications of young adults with Autosomal Recessive Polycystic Kidney Disease (ARPKD). Scientific Reports, 9(1), 7919-. https://dx.doi.org/10.1038/s41598-019-43488-w
Blümcke, I., Coras, R., Wefers, A.K., Capper, D., Aronica, E., Becker, A.,... Thom, M. (2019). Review: Challenges in the histopathological classification of ganglioglioma and DNT: microscopic agreement studies and a preliminary genotype-phenotype analysis. Neuropathology and Applied Neurobiology, 45(2), 95-107. https://dx.doi.org/10.1111/nan.12522
Gregor, A., Sadleir, L.G., Asadollahi, R., Azzarello-Burri, S., Battaglia, A., Ousager, L.B.,... Zweier, C. (2018). De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder. American Journal of Human Genetics, 103(2), 305-316. https://dx.doi.org/10.1016/j.ajhg.2018.07.003
Capper, D., Jones, D.T.W., Sill, M., Hovestadt, V., Schrimpf, D., Sturm, D.,... Pfister, S.M. (2018). DNA methylation-based classification of central nervous system tumours. Nature, 555(7697), 469-474. https://dx.doi.org/10.1038/nature26000
Germeshausen, M., Ancliff, P., Estrada, J., Metzler, M., Ponstingl, E., Ruetschle, H.,... Ballmaier, M. (2018). MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia. Blood Advances, 2(6), 586-596. https://dx.doi.org/10.1182/bloodadvances.2018016501
Kalwak, K., Bader, P., Styczynski, J., Gruhn, B., Patrick, K., Sedlacek, P.,... Vora, A. (2018). Prospective Clinical Phase II Results on Treosulfan-Based Conditioning Treatment of 70 Paediatric Patients with Haematological Malignancies. In BLOOD. San Diego, CA, US: WASHINGTON: AMER SOC HEMATOLOGY.
Apps, J.R., Carreno, G., Mario Gonzalez-Meljem, J., Haston, S., Guiho, R., Cooper, J.E.,... Martinez-Barbera, J.P. (2018). Tumour compartment transcriptomics demonstrates the activation of inflammatory and odontogenic programmes in human adamantinomatous craniopharyngioma and identifies the MAPK/ERK pathway as a novel therapeutic target. Acta Neuropathologica, 135(5), 757-777. https://dx.doi.org/10.1007/s00401-018-1830-2
Miera, O., Schmitt, K.R., Menon, A.K., Ersel, S., Reiprich, A., Akintuerk, H.,... Amodeo, A. (2017). Current Practice of Anticoagulation for Pediatric VAD Therapy - A Multi-Institutional European Survey of the EXCOR Pediatric Investigator Group (EEPIG). (pp. S278-S278).
Blümcke, I., Spreafico, R., Haaker, G., Coras, R., Kobow, K., Bien, C.G.,... Avanzini, G. (2017). Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery. New England Journal of Medicine, 377(17), 1648-1656. https://dx.doi.org/10.1056/NEJMoa1703784
Beniczky, S., Aurlien, H., Brogger, J.C., Hirsch, L.J., Schomer, D.L., Trinka, E.,... Herman, S.T. (2017). Standardized computer-based organized reporting of EEG: SCORE - Second version. Clinical Neurophysiology, 128(11), 2334-2346. https://dx.doi.org/10.1016/j.clinph.2017.07.418
Meyer, E., Carss, K.J., Rankin, J., Nichols, J.M.E., Grozeva, D., Joseph, A.P.,... Kurian, M.A. (2016). Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia. Nature Genetics. https://dx.doi.org/10.1038/ng.3740
Giarrana, M.L., Joset, P., Sticht, H., Robb, S., Steindl, K., Rauch, A., & Klein, A. (2015). A severe congenital myasthenic syndrome with "dropped head" caused by novel MUSK mutations. Muscle & Nerve, 52(4), 668-73. https://dx.doi.org/10.1002/mus.24687
Guerrini, R., Duchowny, M., Jayakar, P., Krsek, P., Kahane, P., Tassi, L.,... Blümcke, I. (2015). Diagnostic methods and treatment options for focal cortical dysplasia. Epilepsia, 56(11), 1669-86. https://dx.doi.org/10.1111/epi.13200
Avbersek, A., Miserocchi, A., Mcevoy, A.W., Patel, A.V., Aronica, E., Blümcke, I.,... Sisodiya, S.M. (2015). Multiphasic presentation of Rasmussen's encephalitis. Epileptic Disorders, 17(3), 315-20. https://dx.doi.org/10.1684/epd.2015.0756
Ruggieri, L., Giannuzzi, V., Baiardi, P., Bonifazi, F., Davies, E.H., Giaquinto, C.,... Ceci, A. (2015). Successful private-public funding of paediatric medicines research: lessons from the EU programme to fund research into off-patent medicines. European Journal of Pediatrics, 174(4), 481-91. https://dx.doi.org/10.1007/s00431-014-2398-z

Zuletzt aktualisiert 2016-13-12 um 07:50

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