Great Ormond Street Hospital (GOSH)


Standort der Organisation:
London, Großbritannien (UK)

Publikationen in Kooperation mit FAU-Wissenschaftern

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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.

Zuletzt aktualisiert 2016-13-12 um 07:50