Ospedale Pediatrico Bambino Gesu


Rom (Rome), Italy

Publications in cooperation with FAU scientists

Sinibaldi, L., Parisi, V., Lanciotti, S., Fontana, P., Kuechler, A., Baujat, G.,... Bernardini, L. (2019). Delineation of MidXq28-duplication syndrome distal to MECP2 and proximal to RAB39B genes. Clinical Genetics. https://dx.doi.org/10.1111/cge.13565
Zollino, M., Zweier, C., Van Balkom, I.D., Sweetser, D.A., Alaimo, J., Bijlsma, E.K.,... Hennekam, R.C. (2019). Diagnosis and management in Pitt-Hopkins syndrome: First international consensus statement. Clinical Genetics, 95(4), 462-478. https://dx.doi.org/10.1111/cge.13506
Sievers, P., Stichel, D., Schrimpf, D., Sahm, F., Koelsche, C., Reuss, D.E.,... Von Deimling, A. (2018). FGFR1:TACC1 fusion is a frequent event in molecularly defined extraventricular neurocytoma. Acta Neuropathologica, 136(2), 293-302. https://dx.doi.org/10.1007/s00401-018-1882-3
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.
Aziz, M.D., Shah, J., Kapoor, U., Dimopoulos, C.N., Ayuk, F.A., Hogan, W.J.,... Ferrara, J.L.M. (2018). Serial Biomarker Monitoring Early after HCT Identifies Different Risks for Relapse and Graft-Vs-Host Disease. In BLOOD. San Diego, CA, US: WASHINGTON: AMER SOC HEMATOLOGY.
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).
Terslev, L., Iagnocco, A., Bruyn, G.A.W., Naredo, E., Vojinovic, J., Collado, P.,... D'Agostino, M.-A. (2017). The OMERACT Ultrasound Group: A Report from the OMERACT 2016 Meeting and Perspectives. Journal of Rheumatology. https://dx.doi.org/10.3899/jrheum.161240
Wlodarski, M.W., Hirabayashi, S., Pastor, V., Stary, J., Hasle, H., Masetti, R.,... Niemeyer, C.M. (2016). Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents. Blood, 127(11), 1387-97; quiz 1518. https://dx.doi.org/10.1182/blood-2015-09-669937
Gansevoort, R.T., Arici, M., Benzing, T., Birn, H., Capasso, G., Covic, A.,... Van Biesen, W. (2016). Recommendations for the use of tolvaptan in autosomal dominant polycystic kidney disease: a position statement on behalf of the ERA-EDTA Working Groups on Inherited Kidney Disorders and European Renal Best Practice. Nephrology Dialysis Transplantation, 31(3), 337-48. https://dx.doi.org/10.1093/ndt/gfv456
Boehm, J., Chevessier, F., Koch, C., Peche, G.A., Mora, M., Morandi, L.,... Laporte, J. (2014). Clinical, histological and genetic characterisation of patients with tubular aggregate myopathy caused by mutations in STIM1. Journal of Medical Genetics, 51(12), 824-33. https://dx.doi.org/10.1136/jmedgenet-2014-102623

Last updated on 2015-09-12 at 12:12