Kostmann syndrome or infantile genetic agranulocytosis, part two: understanding the underlying genetic defects in severe congenital neutropenia
Carlsson, Göran, Melin, Malin, Dahl, Niklas, Ramme, Kim Göransdotter, Nordenskjöld, Magnus, Palmblad, Jan, Henter, Jan-Inge, Fadeel, Bengt
Published in Acta Paediatrica (01.06.2007)
Published in Acta Paediatrica (01.06.2007)
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Journal Article
Sequence analysis of the SRGN, AP3B1, ARF6, and SH2D1A genes in familial hemophagocytic lymphohistiocytosis
Ma, Daoxin, Rudd, Eva, Edner, Josefine, Gavhed, Sofie, Ramme, Kim Göransdotter, Fadeel, Bengt, Nordenskjöld, Magnus, Henter, Jan-Inge, Zheng, Chengyun
Published in Pediatric Blood & Cancer (01.05.2008)
Published in Pediatric Blood & Cancer (01.05.2008)
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Journal Article
Characterization of PRF1, STX11 and UNC13D genotype‐phenotype correlations in familial hemophagocytic lymphohistiocytosis
Horne, AnnaCarin, Ramme, Kim Göransdotter, Rudd, Eva, Zheng, Chengyun, Wali, Yasser, Al‐Lamki, Zakia, Gürgey, Aytemiz, Yalman, Nevin, Nordenskjöld, Magnus, Henter, Jan‐Inge
Published in British journal of haematology (01.10.2008)
Published in British journal of haematology (01.10.2008)
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Journal Article
Low plasma levels of the protein pro‐LL‐37 as an early indication of severe disease in patients with chronic neutropenia
Karlsson, Jenny, Carlsson, Göran, Ramme, Kim Göransdotter, Hägglund, Hans, Fadeel, Bengt, Nordenskjöld, Magnus, Henter, Jan‐Inge, Palmblad, Jan, Pütsep, Katrin, Andersson, Mats
Published in British journal of haematology (01.04.2007)
Published in British journal of haematology (01.04.2007)
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