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252 results
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A journey of hope: lessons learned from studies on rare diseases and orphan drugs.
Wästfelt M, Fadeel B, Henter JI. Wästfelt M, et al. Among authors: fadeel b. J Intern Med. 2006 Jul;260(1):1-10. doi: 10.1111/j.1365-2796.2006.01666.x. J Intern Med. 2006. PMID: 16789973 Review.
Apoptosis: a basic biological phenomenon with wide-ranging implications in human disease.
Fadeel B, Orrenius S. Fadeel B, et al. J Intern Med. 2005 Dec;258(6):479-517. doi: 10.1111/j.1365-2796.2005.01570.x. J Intern Med. 2005. PMID: 16313474 Review.
Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis.
Rudd E, Bryceson YT, Zheng C, Edner J, Wood SM, Ramme K, Gavhed S, Gürgey A, Hellebostad M, Bechensteen AG, Ljunggren HG, Fadeel B, Nordenskjöld M, Henter JI. Rudd E, et al. Among authors: fadeel b. J Med Genet. 2008 Mar;45(3):134-41. doi: 10.1136/jmg.2007.054288. Epub 2007 Nov 9. J Med Genet. 2008. PMID: 17993578
Sequence analysis of the SRGN, AP3B1, ARF6, and SH2D1A genes in familial hemophagocytic lymphohistiocytosis.
Ma D, Rudd E, Edner J, Gavhed S, Ramme KG, Fadeel B, Nordenskjöld M, Henter JI, Zheng C. Ma D, et al. Among authors: fadeel b. Pediatr Blood Cancer. 2008 May;50(5):1067-9. doi: 10.1002/pbc.21428. Pediatr Blood Cancer. 2008. PMID: 18000860
Central nervous system involvement in severe congenital neutropenia: neurological and neuropsychological abnormalities associated with specific HAX1 mutations.
Carlsson G, van't Hooft I, Melin M, Entesarian M, Laurencikas E, Nennesmo I, Trebińska A, Grzybowska E, Palmblad J, Dahl N, Nordenskjöld M, Fadeel B, Henter JI. Carlsson G, et al. Among authors: fadeel b. J Intern Med. 2008 Oct;264(4):388-400. doi: 10.1111/j.1365-2796.2008.01982.x. Epub 2008 May 29. J Intern Med. 2008. PMID: 18513342
Syntaxin-11 is expressed in primary human monocytes/macrophages and acts as a negative regulator of macrophage engulfment of apoptotic cells and IgG-opsonized target cells.
Zhang S, Ma D, Wang X, Celkan T, Nordenskjöld M, Henter JI, Fadeel B, Zheng C. Zhang S, et al. Among authors: fadeel b. Br J Haematol. 2008 Jul;142(3):469-79. doi: 10.1111/j.1365-2141.2008.07191.x. Epub 2008 Jun 11. Br J Haematol. 2008. PMID: 18547321
Clinical presentation of Griscelli syndrome type 2 and spectrum of RAB27A mutations.
Meeths M, Bryceson YT, Rudd E, Zheng C, Wood SM, Ramme K, Beutel K, Hasle H, Heilmann C, Hultenby K, Ljunggren HG, Fadeel B, Nordenskjöld M, Henter JI. Meeths M, et al. Among authors: fadeel b. Pediatr Blood Cancer. 2010 Apr;54(4):563-72. doi: 10.1002/pbc.22357. Pediatr Blood Cancer. 2010. PMID: 19953648
Nanomedicine: reshaping clinical practice.
Fadeel B, Kasemo B, Malmsten M, Strømme M. Fadeel B, et al. J Intern Med. 2010 Jan;267(1):2-8. doi: 10.1111/j.1365-2796.2009.02186.x. J Intern Med. 2010. PMID: 20059640 No abstract available.
Familial hemophagocytic lymphohistiocytosis type 3 (FHL3) caused by deep intronic mutation and inversion in UNC13D.
Meeths M, Chiang SC, Wood SM, Entesarian M, Schlums H, Bang B, Nordenskjöld E, Björklund C, Jakovljevic G, Jazbec J, Hasle H, Holmqvist BM, Rajic L, Pfeifer S, Rosthøj S, Sabel M, Salmi TT, Stokland T, Winiarski J, Ljunggren HG, Fadeel B, Nordenskjöld M, Henter JI, Bryceson YT. Meeths M, et al. Among authors: fadeel b. Blood. 2011 Nov 24;118(22):5783-93. doi: 10.1182/blood-2011-07-369090. Epub 2011 Sep 19. Blood. 2011. PMID: 21931115
Nanosafety: towards safer design of nanomedicines.
Fadeel B. Fadeel B. J Intern Med. 2013 Dec;274(6):578-80. doi: 10.1111/joim.12137. Epub 2013 Oct 3. J Intern Med. 2013. PMID: 24102766 No abstract available.
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