Zobrazeno 1 - 5
of 5
pro vyhledávání: '"L B, Faulkner"'
Autor:
I. A. von Rosenstiel, A. Sarti, E. Monnet, Carl G.M. Weigle, E. Werner, A. Burguet, M. Calamandrei, Pedro Celiny Ramos Garcia, B. Habibi, Minke E. van der Wal, I. David Todres, Renato Fiori, Gale Pearson, C. Fromentin, A. Serrano, A. R. De Gaudio, Ayşe Korkmaz, R. Valente, H. Allemand, M. L. Dalphin, P. Habibi, M. Cavuta, D. Barata, B. Zimmermann, Sajid Maqbool, P. Martinelli, Anjum Hashmi, Ramazan Öztűrk, M. Monleón, L. E. Wilson, W. B. Vreede, Eneida Mendonça, C. Vasconcelos, R. P. G. M. Bijlmer, J. Y. Pauchard, Tony Slater, N. González Bravo, L. B. Faulkner, M. Idris Mazhar, Fan Xun-mei, Lu Zhong-yi, M. Verma, J. Jacquin, J. García Pérez, A. Menget, Delio Kipper, A. Johannes van Vught, A. Marques, Peter Tarczy-Hornoch, P. Busoni, Mary B. Zollo, Jean-Marc Treluyer, I. Fernandes, Frank Shann, J. Chhatwal, Ph. Hubert, Paulo Roberto Einloft, Reinoud J. B. J. Gemke, Jon M. Courand, J. Casado Flores, Deniz Anadol, M. Cloup, Jefferson Pedro Piva, Serap Çamur, Imran Özalp, E. Mora, L. Ventura, Simon Nadel
Publikováno v:
Intensive Care Medicine. 22:S197-S201
Autor:
S, van den Oudenrijn, M, Bruin, C C, Folman, M, Peters, L B, Faulkner, M, de Haas, A E, von dem Borne
Publikováno v:
British journal of haematology. 110(2)
Congenital amegakaryocytic thrombocytopenia (CAMT) is a rare disorder of undefined aetiology. The disease presents with severe thrombocytopenia and absence of megakaryocytes in the bone marrow. Furthermore, CAMT patients may develop bone marrow aplas
Publikováno v:
Bone marrow transplantation. 17(3)
The relative impact of age, sex, nucleated cell dose, prior chemotherapy, prior cranio-spinal irradiation (CSI) and bone marrow harvest (BMH) site on hematological recovery after ABMT were analyzed in a multivariate model. The study population compri
Autor:
L B Faulkner, G Pini
Publikováno v:
Neuropediatrics. 26(4)
Hypomelanosis of Ito (HI) (incontinentia pigmenti achromians) with cerebellar atrophy and dysmorphic features is reported in a child. The association of cerebellar anomalies and HI has been previously reported in only four cases. However, since neuro
Autor:
A P, Gillio, L B, Faulkner, B P, Alter, L, Reilly, R, Klafter, G, Heller, D C, Young, J M, Lipton, M A, Moore, R J, O'Reilly
Publikováno v:
Blood. 82(3)
This report describes the response of eighteen Diamond-Blackfan anemia (DBA) patients to recombinant human interleukin-3 (rhIL-3). rhIL-3 was administered subcutaneously once daily on an escalating dose schedule (0.5 to 10 micrograms/kg/d). The rhIL-