-J I Henter Researcher Activity Profile

Research Author Detailed Information 

J I Henter Publication Rate By Year

J I Henter has published 4 paper(s) in 2007, 12 paper(s) in 2008, for a total of 16 research publications in total.

J I Ji Henter Author Information

LAST NAME: henter

FIRST NAME: J I

INITIALS: ji

AFFILIATION:

Papers

J I Henter's Publication Record

1. Assignment of the gene locus for severe congenital neutropenia to chromosome 1q22 in the original Kostmann family from Northern Sweden. Year Published: 2007
Department of Genetics and Pathology, The Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
2. Severe bacteria-associated hemophagocytic lymphohistiocytosis in an extremely premature infant. Year Published: 2007
Childhood Cancer Research Unit, Department of Women and Child Health, Karolinska University Hospital, Stockholm, Sweden.
3. VEGF reduces astrogliosis and preserves neuromuscular junctions in ALS transgenic mice. Year Published: 2007
Childhood Cancer Research Unit, Department of Woman and Child Health, Karolinska Institutet, Karolinska University Hospital, 171 76 Stockholm, Sweden.
4. VEGF reduces astrogliosis and preserves neuromuscular junctions in ALS transgenic mice. Year Published: 2007
Childhood Cancer Research Unit, Department of Woman and Child Health, Karolinska Institutet, Karolinska University Hospital, 171 76 Stockholm, Sweden.
5. Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations. Year Published: 2008
Pediatric Hematology Oncology, Ospedale dei Bambini G. Di Cristina, ARNAS Civico, Palermo, Italy.
6. Frequency and spectrum of central nervous system involvement in 193 children with haemophagocytic lymphohistiocytosis. Year Published: 2008
Childhood Cancer Research Unit, Department of Woman and Child Health, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden. annacarin.horne@karolinska.se
7. Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations. Year Published: 2008
Pediatric Hematology Oncology, Ospedale dei Bambini G. Di Cristina, ARNAS Civico, Palermo, Italy.
8. Parvovirus B19 infection in children with acute lymphoblastic leukemia is associated with cytopenia resulting in prolonged interruptions of chemotherapy. Year Published: 2008
Unit of Infectious Diseases, Department of Medicine, Solna, Center for Molecular Medicine, Stockholm, Sweden.
9. Langerhans cell histiocytosis reveals a new IL-17A-dependent pathway of dendritic cell fusion. Year Published: 2008
INSERM, U851, 21 Avenue Tony Garnier, Lyon 5-69007, France.
10. Frequency and spectrum of central nervous system involvement in 193 children with haemophagocytic lymphohistiocytosis. Year Published: 2008
Childhood Cancer Research Unit, Department of Woman and Child Health, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden. annacarin.horne@karolinska.se
11. Parvovirus B19 infection in children with acute lymphoblastic leukemia is associated with cytopenia resulting in prolonged interruptions of chemotherapy. Year Published: 2008
Unit of Infectious Diseases, Department of Medicine, Solna, Center for Molecular Medicine, Stockholm, Sweden.
12. Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations. Year Published: 2008
Pediatric Hematology Oncology, Ospedale dei Bambini G. Di Cristina, ARNAS Civico, Palermo, Italy.
13. Langerhans cell histiocytosis reveals a new IL-17A-dependent pathway of dendritic cell fusion. Year Published: 2008
INSERM, U851, 21 Avenue Tony Garnier, Lyon 5-69007, France.
14. Improved outcome in multisystem Langerhans cell histiocytosis is associated with therapy intensification. Year Published: 2008
Children's Cancer Research Institute, St Anna Children's Hospital, Vienna, Austria. h.gadner@stanna.at
15. Sequence analysis of the SRGN, AP3B1, ARF6, and SH2D1A genes in familial hemophagocytic lymphohistiocytosis. Year Published: 2008
Childhood Cancer Research Unit, Department of Woman and Child Health, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
16. Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis. Year Published: 2008
Childhood Cancer Research Unit, Department of Woman and Child Health, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden. Eva.Rudd@ki.se