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Number of items: 4.

Corbacioglu, S; Carreras, E; Ansari, M; Balduzzi, A; Cesaro, S; Dalle, J-H; Dignan, F; Gibson, B; Güngör, Tayfun; Gruhn, B; Lankester, A; Locatelli, F; Pagliuca, A; Peters, C; Richardson, P G; Schulz, A S; Sedlacek, P; Stein, J; Sykora, K-W; Toporski, J; Trigoso, E; Vetteranta, K; Wachowiak, J; Wallhult, E; Wynn, R; Yaniv, I; Yesilipek, A; Mohty, M; Bader, P (2018). Diagnosis and severity criteria for sinusoidal obstruction syndrome/veno-occlusive disease in pediatric patients: a new classification from the European society for blood and marrow transplantation. Bone Marrow Transplantation, 53(2):138-145.

Marquardt, L; Lacour, M; Hoernes, M; Opitz, L; Lecca, R; Volkmer, B; Reichenbach, J; Hohl, D; Ansari, M; Ozsahin, H; Güngör, T; Pachlopnik Schmid, Jana (2017). Unusual dermatological presentation and immune phenotype in SCID due to an IL7R mutation: the value of whole-exome sequencing and the potential benefit of newborn screening. Journal of the European Academy of Dermatology and Venerology, 31(3):e147-e148.

Marek, A; Stern, M; Chalandon, Y; Ansari, M; Ozsahin, H; Güngör, T; Gerber, B; Kühne, T; Passweg, J R; Gratwohl, A; Tichelli, A; Seger, R; Schanz, U; Halter, J; Stussi, G (2014). The impact of T-cell depletion techniques on the outcome after haploidentical hematopoietic SCT. Bone Marrow Transplantation, 49(1):55-61.

Gerth-Kahlert, C; Williamson, K; Ansari, M; Rainger, J K; Hingst, V; Zimmermann, T; Tech, S; Guthoff, R F; van Heyningen, V; FitzPatrick, D R (2013). Clinical and mutation analysis of 51 probands with anophthalmia and/or severe microphthalmia from a single center. Molecular Genetics & Genomic Medicine, 1(1):15-31.

This list was generated on Sat Feb 16 01:15:31 2019 CET.