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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: henter ji. 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.
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: henter ji. 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
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: henter ji. 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
Spectrum and clinical implications of syntaxin 11 gene mutations in familial haemophagocytic lymphohistiocytosis: association with disease-free remissions and haematopoietic malignancies.
Rudd E, Göransdotter Ericson K, Zheng C, Uysal Z, Ozkan A, Gürgey A, Fadeel B, Nordenskjöld M, Henter JI. Rudd E, et al. Among authors: henter ji. J Med Genet. 2006 Apr;43(4):e14. doi: 10.1136/jmg.2005.035253. J Med Genet. 2006. PMID: 16582076 Free PMC article.
Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations.
Trizzino A, zur Stadt U, Ueda I, Risma K, Janka G, Ishii E, Beutel K, Sumegi J, Cannella S, Pende D, Mian A, Henter JI, Griffiths G, Santoro A, Filipovich A, Aricò M; Histiocyte Society HLH Study group. Trizzino A, et al. Among authors: henter ji. J Med Genet. 2008 Jan;45(1):15-21. doi: 10.1136/jmg.2007.052670. Epub 2007 Sep 14. J Med Genet. 2008. PMID: 17873118
Hematopoietic stem cell transplantation in severe congenital neutropenia.
Carlsson G, Winiarski J, Ljungman P, Ringdén O, Mattsson J, Nordenskjöld M, Touw I, Henter JI, Palmblad J, Fadeel B, Hägglund H. Carlsson G, et al. Among authors: henter ji. Pediatr Blood Cancer. 2011 Mar;56(3):444-51. doi: 10.1002/pbc.22836. Pediatr Blood Cancer. 2011. PMID: 21072829
Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis.
Göransdotter Ericson K, Fadeel B, Nilsson-Ardnor S, Söderhäll C, Samuelsson A, Janka G, Schneider M, Gürgey A, Yalman N, Révész T, Egeler R, Jahnukainen K, Storm-Mathiesen I, Haraldsson A, Poole J, de Saint Basile G, Nordenskjöld M, Henter J. Göransdotter Ericson K, et al. Am J Hum Genet. 2001 Mar;68(3):590-7. doi: 10.1086/318796. Epub 2001 Feb 6. Am J Hum Genet. 2001. PMID: 11179007 Free PMC article.
Hemophagocytic lymphohistiocytosis in infants: a single center experience from India.
Ramzan M, Yadav SP, Kharya G, Chinnabhandar V, Enteserian M, Henter JI, Sachdeva A. Ramzan M, et al. Among authors: henter ji. Pediatr Hematol Oncol. 2014 Apr;31(3):285-92. doi: 10.3109/08880018.2013.862754. Epub 2014 Jan 2. Pediatr Hematol Oncol. 2014. PMID: 24383954 Clinical Trial.
Risk factors for diabetes insipidus in langerhans cell histiocytosis.
Grois N, Pötschger U, Prosch H, Minkov M, Arico M, Braier J, Henter JI, Janka-Schaub G, Ladisch S, Ritter J, Steiner M, Unger E, Gadner H; DALHX- and LCH I and II Study Committee. Grois N, et al. Among authors: henter ji. Pediatr Blood Cancer. 2006 Feb;46(2):228-33. doi: 10.1002/pbc.20425. Pediatr Blood Cancer. 2006. PMID: 16047354
Hematopoietic stem cell transplantation in children with cancer and the risk of long-term psychological morbidity in the bereaved parents.
Jalmsell L, Onelöv E, Steineck G, Henter JI, Kreicbergs U. Jalmsell L, et al. Among authors: henter ji. Bone Marrow Transplant. 2011 Aug;46(8):1063-70. doi: 10.1038/bmt.2010.287. Epub 2010 Nov 22. Bone Marrow Transplant. 2011. PMID: 21102501
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