Authors:
JANKA G
IMASHUKU S
ELINDER G
SCHNEIDER M
HENTER JI
Citation: G. Janka et al., INFECTION-ASSOCIATED AND MALIGNANCY-ASSOCIATED HEMOPHAGOCYTIC SYNDROMES - SECONDARY HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, Hematology/oncology clinics of North America, 12(2), 1998, pp. 435
Citation: U. Calming et Ji. Henter, ELEVATED ERYTHROCYTE SEDIMENTATION-RATE AND THROMBOCYTOSIS AS POSSIBLE INDICATORS OF ACTIVE DISEASE IN LANGERHANS CELL HISTIOCYTOSIS, Acta paediatrica, 87(10), 1998, pp. 1085-1087
Authors:
SKEPPNER G
FORESTIER E
HENTER JI
WRANNE L
Citation: G. Skeppner et al., TRANSIENT RED-CELL APLASIA IN SIBLINGS - A COMMON ENVIRONMENTAL OR A COMMON HEREDITARY FACTOR, Acta paediatrica, 87(1), 1998, pp. 43-47
Authors:
SKANSENSAPHIR U
ANDERSSON J
BJORK L
EKBERG C
FEHNIGER TE
HENTER JI
ANDERSSON U
Citation: U. Skansensaphir et al., DOWN-REGULATION OF LYMPHOKINE SYNTHESIS BY INTRAVENOUS GAMMA-GLOBULINIS DEPENDENT UPON ACCESSORY CELLS, Scandinavian journal of immunology, 47(3), 1998, pp. 229-235
Authors:
GUSTAVSSON P
WILLIG TN
VANHAERINGEN A
TCHERNIA G
DIANZANI I
DONNER M
ELINDER G
HENTER JI
NILSSON PG
GORDON L
SKEPPNER G
VANTVEERKORTHOF L
KREUGER A
DAHL N
Citation: P. Gustavsson et al., DIAMOND-BLACKFAN ANEMIA - GENETIC HOMOGENEITY FOR A GENE ON CHROMOSOME 19Q13 RESTRICTED TO 1.8 MB, Nature genetics, 16(4), 1997, pp. 368-371
Citation: A. Hedman et al., PREVALENCE AND TREATMENT OF CHRONIC IDIOPATHIC THROMBOCYTOPENIC PURPURA OF CHILDHOOD IN SWEDEN, Acta paediatrica, 86(2), 1997, pp. 226-227
Authors:
FAVARA BE
FELLER AC
PAULI M
JAFFE ES
WEISS LM
ARICO M
BUCSKY P
EGELER RM
ELINDER G
GADNER H
GRESIK M
HENTER JI
IMASHUKU S
JANKASCHAUB G
JAFFE R
LADISCH S
NEZELOF C
PRITCHARD J
Citation: Be. Favara et al., CONTEMPORARY CLASSIFICATION OF HISTIOCYTIC DISORDERS, Medical and pediatric oncology, 29(3), 1997, pp. 157-166
Authors:
HENTER JI
ARICO M
EGELER RM
ELINDER G
FAVARA BE
FILIPOVICH AH
GADNER H
IMASHUKU S
JANKASCHAUB G
KOMP D
LADISCH S
WEBB D
Citation: Ji. Henter et al., HLH-94 - A TREATMENT PROTOCOL FOR HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, Medical and pediatric oncology, 28(5), 1997, pp. 342-347
Citation: Ji. Henter et I. Nennesmo, NEUROPATHOLOGIC FINDINGS AND NEUROLOGIC SYMPTOMS IN 23 CHILDREN WITH HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, The Journal of pediatrics, 130(3), 1997, pp. 358-365
Authors:
ARICO M
JANKA G
FISCHER A
HENTER JI
BLANCHE S
ELINDER G
MARTINETTI M
RUSCA MP
Citation: M. Arico et al., HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS - REPORT OF 122 CHILDREN FROM THE INTERNATIONAL REGISTRY, Leukemia, 10(2), 1996, pp. 197-203
Authors:
HENTER JI
WINIARSKI J
LJUNGMAN P
RINGDEN O
OST A
Citation: Ji. Henter et al., BONE-MARROW TRANSPLANTATION IN 2 CHILDREN WITH CONGENITAL AMEGAKARYOCYTIC THROMBOCYTOPENIA (VOL 15, PG 799, 1995), Bone marrow transplantation, 18(2), 1996, pp. 487-487
Authors:
HENTER JI
ANDERSSON B
ELINDER G
JAKOBSON A
LUBECK PO
SODER O
Citation: Ji. Henter et al., ELEVATED CIRCULATING LEVELS OF INTERLEUKIN-1 RECEPTOR ANTAGONIST BUT NOT IL-1 AGONISTS IN HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, Medical and pediatric oncology, 27(1), 1996, pp. 21-25
Authors:
BOLME P
HENTER JI
WINIARSKI J
ELINDER G
LJUNGMAN P
LONNERHOLM G
RINGDEN O
Citation: P. Bolme et al., ALLOGENEIC BONE-MARROW TRANSPLANTATION FOR HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS IN SWEDEN, Bone marrow transplantation, 15(3), 1995, pp. 331-335
Citation: Ji. Henter et G. Elinder, HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS - AN INHERITED PRIMARY FORM AND A REACTIVE SECONDARY FORM, British Journal of Haematology, 91(3), 1995, pp. 774-775
Authors:
ARICO M
JANKA G
FISCHER A
HENTER JI
BLANCHE S
ELINDER G
MARTINETTI M
RUSCA MP
Citation: M. Arico et al., HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS - REPORT OF 122 CHILDREN FROM THE INTERNATIONAL REGISTRY, Blood, 86(10), 1995, pp. 189-189
Citation: Ji. Henter et al., MYELODYSPLASTIC SYNDROME FOLLOWING EPIPODOPHYLLOTOXIN THERAPY IN FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, Pediatric hematology and oncology, 10(2), 1993, pp. 163-168
Citation: C. Granert et al., KALA-AZAR IN A ONE-YEAR-OLD SWEDISH CHILD - DIAGNOSTIC DIFFICULTIES BECAUSE OF ACTIVE HEMOPHAGOCYTOSIS, Acta paediatrica, 82(9), 1993, pp. 794-796
Citation: B. Landin et Ji. Henter, A NOVEL SPLICE JUNCTION MUTATION (IVS-2 NT-1 G-]T) PRESENTING WITH DOMINANT BETA-THALASSEMIA IN A SCANDINAVIAN FAMILY, Blood, 82(10), 1993, pp. 10000361-10000361