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About me

Earned an MD from Uppsala University 1980 and after internship in Uppsala completed a fellowship in Pediatrics (1987) in Stockholm. Defended a PhD-thesis at Karolinska Institutet in 1990, with focus on hemophagocytic lymphohistiocytosis (HLH).

Specialized clinically in Pediatric Hematology and Oncology, and became Professor at Karolinska Institutet in 2004.

Director of Research and Education at Karolinska University Hospital since 2012.  

Education

1973-1980 University Medical Degree (M.D.), University of Uppsala     

1976-1979 Bachelor of Science in Economics (B. Sc.), University of Uppsala

1980-1981 Licensed physician.

1982-1987 Board Certified Specialist in Pediatrics

1986-1990 Dr Med Sci (Ph.D.), Dept of Pediatrics, Karolinska Institutet

Research description

The main research interest is within the histiocytic disorders, including Hemophagocytic Lymphohistiocytosis (HLH) and Langerhans cell histiocytosis (LCH).

In addition to developing the first diagnostic criteria for HLH,  PI of HLH-94 as well as HLH-2004. Studied underlying biological and genetic defects in HLH. Another interest is the secondary forms of HLH.

Increasingly interested in clinical and biological studies of Langerhans cell histiocytosis (LCH), with the ultimate aim to reduce morbidity and mortality.

In addition, interests in many other fields including End-of-Life Care and Rare Diseases.

President of the Histiocyte Society 2004-2007, and the Founding President of the International Conference for Rare Diseases and Orphan Drugs (ICORD).

Academic honours, awards and prizes

2002: Jubilee Prize Winner of the Children´s Cancer Foundation of Sweden. (“Barncancerfondens Jubileumspris”)

2003: Alvarengas Prize, awarded by the Swedish Society of Medicine.

2011: Lennander’s Award, awarded by the Swedish Society of Medicine.

2011: The Jubilee Prize awarded by the Swedish Society of Medicine 2011 (“Svenska Läkaresällskapets Jubileumspriset 2011”)

Links

Publications

Gain-of-function mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms
Tesi B, Davidsson J, Voss M, Rahikkala E, Holmes Td, Chiang Scc, et al
Blood 2017;129(16):2266-2279

How to Treat Involvement of the Central Nervous System in Hemophagocytic Lymphohistiocytosis?
Horne A, Wickström R, Jordan Mb, Yeh Ea, Naqvi A, Henter Ji, et al
Current treatment options in neurology 2017;19(1):3-

Targeting SAMHD1 with the Vpx protein to improve cytarabine therapy for hematological malignancies
Herold N, Rudd Sg, Ljungblad L, Sanjiv K, Myrberg Ih, Paulin Cb, et al
Nature medicine 2017;23(2):256-263

2016 Classification Criteria for Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis: A European League Against Rheumatism/American College of Rheumatology/Paediatric Rheumatology International Trials Organisation Collaborative Initiative
Ravelli A, Minoia F, Davì S, Horne A, Bovis F, Pistorio A, et al
Arthritis & rheumatology (Hoboken, N.J.) 2016;68(3):566-76

2016 Classification Criteria for Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis: A European League Against Rheumatism/American College of Rheumatology/Paediatric Rheumatology International Trials Organisation Collaborative Initiative
Ravelli A, Minoia F, Davì S, Horne A, Bovis F, Pistorio A, et al
Annals of the rheumatic diseases 2016;75(3):481-9

Adsorptive depletion of blood monocytes reduces the levels of circulating interleukin-17A in Langerhans cell histiocytosis
Lourda M, Olsson-Åkefeldt S, Gavhed D, Axdorph Nygell U, Berlin G, Laurencikas E, et al
Blood 2016;128(9):1302-5

Adult hemophagocytic lymphohistiocytosis causing multi organ dysfunction in a patient with multiple autoimmune disorders: when the immune system runs amok
Fleischmann R, Böhmerle W, Von Laffert M, Jöhrens K, Mengel A, Hotter B, et al
Clinical case reports 2016;4(2):165-70

Children with cancer share their views: tell the truth but leave room for hope
Jalmsell L, Lövgren M, Kreicbergs U, Henter Ji, Frost Bm
Acta paediatrica (Oslo, Norway : 1992) 2016;105(9):1094-9

Clinical presentation of hemophagocytic lymphohistiocytosis in adults is less typical than in children
Zhang Z, Wang J, Ji B, Bahr Greenwood Tv, Zhang Y, Wang Y, et al
Clinics (Sao Paulo, Brazil) 2016;71(4):205-9

Expert consensus on dynamics of laboratory tests for diagnosis of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis
Ravelli A, Minoia F, Davì S, Horne A, Bovis F, Pistorio A, et al
RMD open 2016;2(1):e000161-

Revised classification of histiocytoses and neoplasms of the macrophage-dendritic cell lineages
Emile Jf, Abla O, Fraitag S, Horne A, Haroche J, Donadieu J, et al
Blood 2016;127(22):2672-81

Successful Hematopoietic Stem Cell Transplantation in a Patient with LPS-Responsive Beige-Like Anchor (LRBA) Gene Mutation
Tesi B, Priftakis P, Lindgren F, Chiang Sc, Kartalis N, Löfstedt A, et al
Journal of clinical immunology 2016;36(5):480-9

The minimum required level of donor chimerism in hereditary hemophagocytic lymphohistiocytosis
Hartz B, Marsh R, Rao K, Henter Ji, Jordan M, Filipovich L, et al
Blood 2016;127(25):3281-90

Tissue-infiltrating neutrophils represent the main source of IL-23 in the colon of patients with IBD
Kvedaraite E, Lourda M, Ideström M, Chen P, Olsson-Åkefeldt S, Forkel M, et al
Gut 2016;65(10):1632-41

Cancer risk in relatives of patients with a primary disorder of lymphocyte cytotoxicity: a retrospective cohort study
Lofstedt A, Chiang Scc, Onelov E, Bryceson Yt, Meeths M, Henter Ji
LANCET HAEMATOLOGY 2015;2(12):E536-E542

Cancer risk in relatives of patients with a primary disorder of lymphocyte cytotoxicity: a retrospective cohort study
Löfstedt A, Chiang Sc, Onelöv E, Bryceson Yt, Meeths M, Henter Ji
The Lancet. Haematology 2015;2(12):e536-42

Cladribine and cytarabine in refractory multisystem Langerhans cell histiocytosis: results of an international phase 2 study
Donadieu J, Bernard F, Van Noesel M, Barkaoui M, Bardet O, Mura R, et al
Blood 2015;126(12):1415-23

Consensus recommendations for the diagnosis and management of hemophagocytic lymphohistiocytosis associated with malignancies
Lehmberg K, Nichols Ke, Henter Ji, Girschikofsky M, Greenwood T, Jordan M, et al
Haematologica 2015;100(8):997-1004

Hemophagocytic lymphohistiocytosis in 2 patients with underlying IFN-γ receptor deficiency
Tesi B, Sieni E, Neves C, Romano F, Cetica V, Cordeiro Ai, et al
The Journal of allergy and clinical immunology 2015;135(6):1638-41

Incidence and Clinical Presentation of Primary Hemophagocytic Lymphohistiocytosis in Sweden
Meeths M, Horne A, Sabel M, Bryceson Yt, Henter Ji
PEDIATRIC BLOOD & CANCER 2015;62(2):346-352

Lack of bone lesions at diagnosis is associated with inferior outcome in multisystem langerhans cell histiocytosis of childhood
Histiocyte Soc, Arico M, Astigarraga I, Braier J, Donadieu J, Gadner H, et al
BRITISH JOURNAL OF HAEMATOLOGY 2015;169(2):241-8

On the Child's Own Initiative: Parents Communicate with Their Dying Child About Death
Jalmsell L, Kontio T, Stein M, Henter Ji, Kreicbergs U
Death studies 2015;39(1-5):111-7

Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense Mutations
Tesi B, Chiang Sc, El-ghoneimy D, Hussein Aa, Langenskiöld C, Wali R, et al
Pediatric blood & cancer 2015;62(12):2094-100

Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis
Tesi B, Lagerstedt-robinson K, Chiang Sc, Ben Bdira E, Abboud M, Belen B, et al
Genome medicine 2015;7():130-

An N-Terminal Missense Mutation in STX11 Causative of FHL4 Abrogates Syntaxin-11 Binding to Munc18-2
Müller Ml, Chiang Sc, Meeths M, Tesi B, Entesarian M, Nilsson D, et al
Frontiers in immunology 2014;4():515-

Bortezomib and IL-12 produce synergetic anti-multiple myeloma effects with reduced toxicity to natural killer cells
Wang X, Feng X, Wang J, Shao N, Ji C, Ma D, et al
Anti-cancer drugs 2014;25(3):282-8

Combined newborn screening for familial hemophagocytic lymphohistiocytosis and severe T- and B-cell immunodeficiencies
Borte S, Meeths M, Liebscher I, Krist K, Nordenskjöld M, Hammarström L, et al
The Journal of allergy and clinical immunology 2014;134(1):226-8

Detection of IL-17A-producing peripheral blood monocytes in Langerhans cell histiocytosis patients
Lourda M, Olsson-Åkefeldt S, Gavhed D, Björnfot S, Clausen N, Hjalmars U, et al
Clinical immunology (Orlando, Fla.) 2014;153(1):112-22

Hemophagocytic Lymphohistiocytosis in Infants: A Single Center Experience from India
Ramzan M, Yadav Sp, Kharya G, Chinnabhandar V, Enteserian M, Henter Ji, et al
PEDIATRIC HEMATOLOGY AND ONCOLOGY 2014;31(3):285-92

High Systemic Levels of the Cytokine-Inducing HMGB1 Isoform Secreted in Severe Macrophage Activation Syndrome
Palmblad K, Schierbeck H, Sundberg E, Horne Ac, Harris He, Henter Ji, et al
MOLECULAR MEDICINE 2014;:538-47

Pathophysiology and spectrum of diseases caused by defects in lymphocyte cytotoxicity
Meeths M, Chiang Sc, Löfstedt A, Müller Ml, Tesi B, Henter Ji, et al
Experimental cell research 2014;325(1):10-7

Pediatric Crohn's disease from onset to adulthood: granulomas are associated with an early need for immunomodulation
Ideström M, Rubio Ca, Onelöv E, Henter Ji, Fagerberg Ul, Finkel Y
Scandinavian journal of gastroenterology 2014;49(8):950-7

Polyclonal T-cells express CD1a in Langerhans cell histiocytosis (LCH) lesions
West Ja, Olsen Sl, Mitchell Jm, Priddle Re, Luke Jm, Akefeldt So, et al
PloS one 2014;9(10):e109586-

Chemoresistance of human monocyte-derived dendritic cells is regulated by IL-17A
Olsson Åkefeldt S, Maisse C, Belot A, Mazzorana M, Salvatore G, Bissay N, et al
PloS one 2013;8(2):e56865-

Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine production
Chiang Sc, Theorell J, Entesarian M, Meeths M, Mastafa M, Al-herz W, et al
Blood 2013;121(8):1345-56

Development of classical Hodgkin's lymphoma in an adult with biallelic STXBP2 mutations
Machaczka M, Klimkowska M, Chiang Sc, Meeths M, Müller Ml, Gustafsson B, et al
Haematologica 2013;98(5):760-4

Novel deep intronic and missense UNC13D mutations in familial haemophagocytic lymphohistiocytosis type 3
Entesarian M, Chiang Sc, Schlums H, Meeths M, Chan My, Mya Sn, et al
British journal of haematology 2013;162(3):415-8

Ovarian failure in HAX1-deficient patients: is there a gender-specific difference in pubertal development in severe congenital neutropenia or Kostmann disease?
Carlsson G, Kriström B, Nordenskjöld M, Henter Ji, Fadeel B
Acta paediatrica (Oslo, Norway : 1992) 2013;102(1):78-82

Targeting BCL2 family in human myeloid dendritic cells: a challenge to cure diseases with chronic inflammations associated with bone loss
Olsson Åkefeldt S, Ismail Mb, Valentin H, Aricò M, Henter Ji, Delprat C
Clinical & developmental immunology 2013;2013():701305-

Therapy prolongation improves outcome in multisystem Langerhans cell histiocytosis
Histiocyte Soc, Gadner H, Minkov M, Grois N, Potschger U, Thiem E, et al
BLOOD 2013;121(25):5006-14

Transition to noncurative end-of-life care in paediatric oncology--a nationwide follow-up in Sweden
Jalmsell L, Forslund M, Hansson Mg, Henter Ji, Kreicbergs U, Frost Bm
Acta paediatrica (Oslo, Norway : 1992) 2013;102(7):744-8

A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromes
Bryceson Yt, Pende D, Maul-pavicic A, Gilmour Kc, Ufheil H, Vraetz T, et al
Blood 2012;119(12):2754-63

Duration and morbidity of chronic immune thrombocytopenic purpura in children: five-year follow-up of a Nordic cohort
Nopho Itp Working Grp, Rosthoj S, Rajantie J, Treutiger I, Zeller B, Tedgard U, et al
ACTA PAEDIATRICA 2012;101(7):761-6

Incidence of severe congenital neutropenia in Sweden and risk of evolution to myelodysplastic syndrome/leukaemia
Carlsson G, Fasth A, Berglöf E, Lagerstedt-robinson K, Nordenskjöld M, Palmblad J, et al
British journal of haematology 2012;158(3):363-9

Killer cell immunoglobulin-like receptor gene polymorphisms predispose susceptibility to Epstein-Barr virus associated hemophagocytic lymphohistiocytosis in Chinese children
Qiang Q, Xie Zd, Liu Cy, Huang Zz, Xu Jm, Ai Jh, et al
MICROBIOLOGY AND IMMUNOLOGY 2012;56(6):378-84

Langerhans cell histiocytosis in children born 1982-2005 after in vitro fertilization
Akefeldt So, Finnström O, Gavhed D, Henter Ji
Acta paediatrica (Oslo, Norway : 1992) 2012;101(11):1151-5

Risk factors for early death in children with haemophagocytic lymphohistiocytosis
Trottestam H, Berglof E, Horne A, Onelov E, Beutel K, Lehmberg K, et al
ACTA PAEDIATRICA 2012;101(3):313-8

Syntaxin 11 marks a distinct intracellular compartment recruited to the immunological synapse of NK cells to colocalize with cytotoxic granules
Dabrazhynetskaya A, Ma Jx, Guerreiro-cacais Ao, Arany Z, Rudd E, Henter Ji, et al
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE 2012;16(1):129-41

The need for worldwide policy and action plans for rare diseases
Int Conference Rare Dis Orphan, Forman J, Taruscio D, Llera Va, Barrera La, Cote Tr, et al
ACTA PAEDIATRICA 2012;101(8):805-7

Treatment of familial hemophagocytic lymphohistiocytosis with third-party mesenchymal stromal cells
Mougiakakos D, Machaczka M, Jitschin R, Klimkowska M, Entesarian M, Bryceson Yt, et al
Stem cells and development 2012;21(17):3147-51

Chemoimmunotherapy for hemophagocytic lymphohistiocytosis: long-term results of the HLH-94 treatment protocol
Histiocyte Soc, Trottestam H, Horne A, Arico M, Egeler Rm, Filipovich Ah, et al
BLOOD 2011;118(17):4577-84

Familial hemophagocytic lymphohistiocytosis type 3 (FHL3) caused by deep intronic mutation and inversion in UNC13D
Meeths M, Chiang Scc, Wood Sm, Entesarian M, Schlums H, Bang B, et al
BLOOD 2011;118(22):5783-93

Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis type 3
Sieni E, Cetica V, Santoro A, Beutel K, Mastrodicasa E, Meeths M, et al
JOURNAL OF MEDICAL GENETICS 2011;48(5):343-52

Hematopoietic stem cell transplantation in children with cancer and the risk of long-term psychological morbidity in the bereaved parents
Jalmsell L, Onelov E, Steineck G, Henter Ji, Kreicbergs U
BONE MARROW TRANSPLANTATION 2011;46(8):1063-70

Hematopoietic Stem Cell Transplantation in Severe Congenital Neutropenia
Carlsson G, Winiarski J, Ljungman P, Ringden O, Mattsson J, Nordenskjold M, et al
PEDIATRIC BLOOD & CANCER 2011;56(3):444-51

Incidence and Pattern of Radiological Central Nervous System Langerhans Cell Histiocytosis in Children: A Population Based Study
Laurencikas E, Gavhed D, Stalemark H, Van't Hooft I, Prayer D, Grois N, et al
PEDIATRIC BLOOD & CANCER 2011;56(2):250-7

Anxiety is Contagious-Symptoms of Anxiety in the Terminally Ill Child Affect Long-Term Psychological Well-Being in Bereaved Parents
Jalmsell L, Kreicbergs U, Onelov E, Steineck G, Henter Ji
PEDIATRIC BLOOD & CANCER 2010;54(5):751-7

Central Nervous System Disease in Langerhans Cell Histiocytosis
Histiocyte Soc Cns Lch Study Grp, Grois N, Fahrner B, Arceci Rj, Henter Ji, Mcclain K, et al
JOURNAL OF PEDIATRICS 2010;156(6):873-81

Clinical Presentation of Griscelli Syndrome Type 2 and Spectrum of RAB27A Mutations
Meeths M, Bryceson Yt, Rudd E, Zheng Cy, Wood Sm, Ramme K, et al
PEDIATRIC BLOOD & CANCER 2010;54(4):563-72

Evaluation of Parvovirus B19 Infection in Children with Malignant or Hematological Disorders
Gustafsson I, Kaldensjo T, Lindblom A, Norbeck O, Henter Ji, Tolfvenstam T, et al
CLINICAL INFECTIOUS DISEASES 2010;50(10):1426-7

Frequency and Development of CNS Involvement in Chinese Children With Hemophagocytic Lymphohistiocytosis
Yang S, Zhang L, Jia Cg, Ma Hh, Henter Ji, Shen Kl
PEDIATRIC BLOOD & CANCER 2010;54(3):408-15

Spectrum of clinical presentations in familial hemophagocytic lymphohistiocytosis type 5 patients with mutations in STXBP2
Meeths M, Entesarian M, Al-herz W, Chiang Scc, Wood Sm, Al-ateeqi W, et al
BLOOD 2010;116(15):2635-43

The proteasome inhibitor bortezomib disrupts tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) expression and natural killer (NK) cell killing of TRAIL receptor-positive multiple myeloma cells
Feng Xl, Yan J, Wang Yb, Zierath Jr, Nordenskjold M, Henter Ji, et al
MOLECULAR IMMUNOLOGY 2010;47(14):2388-96

Biomarkers in the Cerebrospinal Fluid and Neurodegeneration in Langerhans Cell Histiocytosis
Gavhed D, Akefeldt So, Osterlundh G, Laurencikas E, Hjorth L, Blennow K, et al
PEDIATRIC BLOOD & CANCER 2009;53(7):1264-70

Different NK cell-activating receptors preferentially recruit Rab27a or Munc13-4 to perforin-containing granules for cytotoxicity
Wood Sm, Meeths M, Chiang Scc, Bechensteen Ag, Boelens Jj, Heilmann C, et al
BLOOD 2009;114(19):4117-27

Fatal Hemophagocytic Lymphohistiocytosis in X-Linked Chronic Granulomatous Disease Associated With a Perforin Gene Variant
Van Montfrans Ja, Rudd E, Van De Corput L, Henter Ji, Nikkels P, Wulffraat N, et al
PEDIATRIC BLOOD & CANCER 2009;52(4):527-9

Interleukin-17A is not expressed by CD207(+) cells in Langerhans cell histiocytosis lesions reply
Arico M, Henter Ji, Egeler Rm, Delprat C
NATURE MEDICINE 2009;15(5):484-485

Multiple inherited sequence variations in two disease-causing genes in familial haemophagocytic lymphohistiocytosis
Rudd E, Meeths M, Uysal Z, Nordenskjod M, Henter Ji, Fadeel B
BRITISH JOURNAL OF HAEMATOLOGY 2009;146(2):218-20

Proteasome inhibition induces apoptosis in primary human natural killer cells and suppresses NKp46-mediated cytotoxicity
Wang Xl, Ottosson A, Ji Cy, Feng Xl, Nordenskjold M, Henter Ji, et al
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL 2009;94(4):470-8

Survivin expression in the bone marrow of patients with severe congenital neutropenia
Carlsson G, Boxhammer S, Garwicz D, Henter Ji, Palmblad J, Nordenskjold M, et al
LEUKEMIA 2009;23(3):622-5

Treatment of the X-Linked Lymphoproliferative, Griscelli and Chediak-Higashi Syndromes by HLH Directed Therapy
Trottestam H, Beutel K, Meeths M, Carlsen N, Heilmann C, Pasic S, et al
PEDIATRIC BLOOD & CANCER 2009;52(2):268-72

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, et al
JOURNAL OF INTERNAL MEDICINE 2008;264(4):388-400

Characterization of PRF1, STX11 and UNC13D genotype-phenotype correlations in familial hemophagocytic lymphohistiocytosis
Horne A, Ramme Kg, Rudd E, Zheng Cy, Wali Y, Al-lamki Z, et al
BRITISH JOURNAL OF HAEMATOLOGY 2008;143(1):75-83

Frequency and spectrum of central nervous system involvement in 193 children with haemophagocytic lymphohistiocytosis
Histiocyte Soc, Horne A, Trottestam H, Arico M, Egeler Rm, Filipovich Ah, et al
BRITISH JOURNAL OF HAEMATOLOGY 2008;140(3):327-35

Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations
Histiocyte Soc Hlh Study Grp, Trizzino A, Stadt Uz, Ueda I, Risma K, Janka G, et al
JOURNAL OF MEDICAL GENETICS 2008;45(1):15-21

Improved outcome in multisystem Langerhans cell histiocytosis is associated with therapy intensification
Histiocyte Soc, Gadner H, Grois N, Potschger U, Minkov M, Arico M, et al
BLOOD 2008;111(5):2556-62

Incidence of Langerhans cell histiocytosis in children: A population-based study
Stalemark H, Laurencikas E, Karis J, Gavhed D, Fadeel B, Henter Ji
PEDIATRIC BLOOD & CANCER 2008;51(1):76-81

[Langerhans cell histiocytosis: new light over pathogenesis. 75 years since Sture Siwe's classic work on "systemic reticuloendotheliosis"]
Fadeel B, Olsson S, Jakobson A, Hjorth L, Osterlundh G, Henter Ji
Lakartidningen 2008;105(51-52):3737-42

Langerhans cell histiocytosis reveals a new IL-17A dependent pathway of dendritic cell fusion
Coury F, Annels N, Rivollier A, Olsson S, Santoro A, Speziani C, et al
NATURE MEDICINE 2008;14(1):81-7

Neuropsychological sequelae in patients with neurodegenerative Langerhans cell histiocytosis
Van't Hooft I, Gavhed D, Laurencilkas E, Henter Ji
PEDIATRIC BLOOD & CANCER 2008;51(5):669-74

Parvovirus B19 infection in children with acute lymphoblastic leukemia is associated with cytopenia resulting in prolonged interruptions of chemotherapy
Lindblom A, Heyman M, Gustafsson I, Norbeck O, Kaldensjo T, Vernby A, et al
CLINICAL INFECTIOUS DISEASES 2008;46(4):528-36

Reactivations in Multisystem Langerhans Cell Histiocytosis: Data of the International LCH Registry
Int Lch Study Grp, Minkov M, Steiner M, Potschger U, Arico M, Braier J, et al
JOURNAL OF PEDIATRICS 2008;153(5):700-5

Sequence analysis of the SRGN, AP3B1, ARF6, and SH2D1A genes in familial hemophagocytic lymphohistiocytosis
Ma Dx, Rudd E, Edner J, Gavhed S, Ramme Kg, Fadeel B, et al
PEDIATRIC BLOOD & CANCER 2008;50(5):1067-9

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, et al
JOURNAL OF MEDICAL GENETICS 2008;45(3):134-41

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 St, Ma Dx, Wang Xl, Celkan T, Nordenskjoeld M, Henter Ji, et al
BRITISH JOURNAL OF HAEMATOLOGY 2008;142(3):469-79

Why rare diseases are an important medical and social issue
Schieppati A, Henter Ji, Daina E, Aperia A
LANCET 2008;371(9629):2039-41

Assignment of the gene locus for severe congenital neutropenia to chromosome 1q22 in the original Kostmann family from Northern Sweden
Melin M, Entesarian M, Carlsson G, Garwicz D, Klein C, Fadeel B, et al
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 2007;353(3):571-5

Brief reports - Pulmonary function testing and pulmonary Langerhans cell histiocytosis
Bernstrand C, Cederlund K, Henter Ji
PEDIATRIC BLOOD & CANCER 2007;49(3):323-8

Defective cytotoxic lymphocyte degranulation in syntaxin-11-deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients
Bryceson Yt, Rudd E, Zheng Cy, Edner J, Ma D, Wood Sm, et al
BLOOD 2007;110(6):1906-15

Does treatment of newly diagnosed idiopathic thrombocytopenic purpura reduce morbidity?
Nopho Itp Study Grp, Treutiger I, Rajantie J, Zeller B, Henter Ji, Elinder G, et al
ARCHIVES OF DISEASE IN CHILDHOOD 2007;92(8):704-7

Fatal agranulocytosis after deferiprone therapy in a child with Diamond-Blackfan anemia
Henter Ji, Karlen J
BLOOD 2007;109(12):5157-9

Fetal hemolytic anemia and intrauterine death caused by anti-M immunization
Wikman A, Edner A, Gryfelt G, Jonsson B, Henter Ji
TRANSFUSION 2007;47(5):911-7

HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)
Klein C, Grudzien M, Appaswamy G, Germeshausen M, Sandrock I, Schaffer Aa, et al
NATURE GENETICS 2007;39(1):86-92

HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis
Histiocyte Soc, Henter Ji, Horne A, Arico M, Egeler Rm, Filipovich Ah, et al
PEDIATRIC BLOOD & CANCER 2007;48(2):124-31

Kostmann syndrome or infantile genetic agranulocytosis, part two: understanding the underlying genetic defects in severe congenital neutropenia
Carlsson G, Melin M, Dahl N, Ramme Kg, Nordenskjold M, Palmblad J, et al
ACTA PAEDIATRICA 2007;96(6):813-9

Low plasma levels of the protein pro-LL-37 as an early indication of severe disease in patients with chronic neutropenia
Karlsson J, Carlsson G, Ramme Kg, Hagglund H, Nordenskjold M, Henter Ji, et al
BRITISH JOURNAL OF HAEMATOLOGY 2007;137(2):166-9

Parents' intellectual and emotional awareness of their child's impending death to cancer: a population-based long-term follow-up study
Vaidimarsdottir U, Kreicbergs U, Hauksdottir A, Hunt H, Onelov E, Henter Jl, et al
LANCET ONCOLOGY 2007;8(8):706-14

Severe bacteria-associated hemophagocytic lymphohistiocytosis in an extremely premature infant
Edner J, Rudd E, Zheng Cy, Dahlander A, Eksborg S, Schneider Em, et al
ACTA PAEDIATRICA 2007;96(11):1703-6

Simultaneous manifestation of fulminant infectious mononucleosis with haemophagocytic syndrome and B-cell lymphoma in X-linked lymphoproliferative disease
Hugle B, Astigarraga I, Henter Ji, Porwit-macdonald A, Meindl A, Schuster V
EUROPEAN JOURNAL OF PEDIATRICS 2007;166(6):589-93

VEGF reduces astrogliosis and preserves neuromuscular junctions in ALS transgenic mice
Zheng C, Skold Mk, Li H, Nennesmo I, Fadeel B, Henter Ji
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 2007;363(4):989-93

A journey of hope: lessons learned from studies on rare diseases and orphan drugs
Wastfelt M, Fadeel B, Henter Ji
JOURNAL OF INTERNAL MEDICINE 2006;260(1):1-10

Betulinic acid, a natural cytotoxic agent, fails to trigger apoptosis in human Burkitt's lymphoma-derived B-cell lines
Karpova Mb, Sanmun D, Henter Ji, Smirnov Af, Fadeel B
INTERNATIONAL JOURNAL OF CANCER 2006;118(1):246-52

[Can cytostatics be effective in severe avian influenza? The disease picture has similarities with hemophagocytic lymphohistiocytosis]
Henter Ji
Lakartidningen 2006;103(15-16):1180-1

Combined spectral karyotyping, comparative genomic hybridization, and in vitro apoptyping of a panel of Burkitt's lymphoma-derived B cell lines reveals an unexpected complexity of chromosomal aberrations and a recurrence of specific abnormalities in chemoresistant cell lines
Karpova Mb, Schoumans J, Blennow E, Ernberg I, Henter Ji, Smirnov Af, et al
INTERNATIONAL JOURNAL OF ONCOLOGY 2006;28(3):605-17

Cytotoxic therapy for severe avian influenza A (H5N1) infection
Henter Ji, Chow Cb, Leung Cw, Lau Yl
LANCET 2006;367(9513):870-3

Elevated serum levels of the decoy receptor osteoprotegerin in children with langerhans cell histiocytosis
Rosso Da, Karis J, Braier Jl, Henter Ji, Fadeel B
PEDIATRIC RESEARCH 2006;59(2):281-6

[Kostmann's syndrome largely elucidated--by Swedish research. 50 years since Rolf Kostmann's pioneering work on severe congenital neutropenia]
Carlsson G, Garwicz D, Nordenskjöld M, Fadeel B, Palmblad J, Henter Ji
Lakartidningen 2006;103(50-52):4022-7

Kostmann syndrome or infantile genetic agranulocytosis, part one: Celebrating 50 years of clinical and basic research on severe congenital neutropenia
Carlsson G, Andersson M, Putsep K, Garwicz D, Nordenskjold M, Henter Ji, et al
ACTA PAEDIATRICA 2006;95(12):1526-32

Neutrophil elastase and granulocyte colony-stimulating factor receptor mutation analyses and leukemia evolution in severe congenital neutropenia patients belonging to the original Kostmann family in northern Sweden
Carlsson G, Aprikyan Aag, Ericson Kg, Stein S, Makaryan V, Dale Dc, et al
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL 2006;91(5):589-95

Periodontal disease in patients from the original Kostmann family with severe congenital neutropenia
Carlsson G, Wahlin Yb, Johansson A, Olsson A, Eriksson T, Claesson R, et al
JOURNAL OF PERIODONTOLOGY 2006;77(4):744-51

Risk factors for diabetes insipidus in langerhans cell histiocytosis
Dalhx Lch I Ii Study Comm, Grois N, Potschger U, Prosch H, Minkov M, Arico M, et al
PEDIATRIC BLOOD & CANCER 2006;46(2):228-33

Spectrum and clinical implications of syntaxin 11 gene mutations in familial haemophagocytic lymphohistiocytosis: association with disease-free remissions and haematopoietic malignancies
Rudd E, Ericson Kg, Zheng C, Uysal Z, Ozkan A, Gurgey A, et al
JOURNAL OF MEDICAL GENETICS 2006;43(4):e14-

Symptoms affecting children with malignancies during the last month of life: A nationwide follow-up
Jalmsell L, Kreicbergs U, Onelov E, Steineck G, Henter Ji
PEDIATRICS 2006;117(4):1314-20

Age-dependent differences in Nordic children with ITP
Nopho Working Grp, Rosthoj S, Hedlund-treutiger I, Rajantie J, Zeller B, Jonsson Og, et al
JOURNAL OF PEDIATRICS 2005;146(1):151-2

Care-related distress: A nationwide study of parents who lost their child to cancer
Kreicbergs U, Valdimarsdottir U, Onelov E, Bjork O, Steineck G, Henter Ji
JOURNAL OF CLINICAL ONCOLOGY 2005;23(36):9162-71

Childhood idiopathic thrombocytopenic purpura in the Nordic countries: Epidemiology and predictors of chronic disease
Nopho Itp Working Grp, Five Natl Study Grps, Zeller B, Rajantie J, Hedlund-treutiger I, Tedgard U, et al
ACTA PAEDIATRICA 2005;94(2):178-84

[Enigmatic diseases in children. Still a lot of questions left in spite of great research progress on LCH and HLH]
Fadeel B, Trottestam H, Löfstedt M, Gavhed D, Henter Ji
Lakartidningen 2005;102(18-19):1444-6

Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis
Histiocyte Soc, Horne A, Janka G, Egeler Rm, Gadner H, Imashuku S, et al
BRITISH JOURNAL OF HAEMATOLOGY 2005;129(5):622-30

Immunohistochemical detection of the apoptosis-related proteins FADD, FLICE, and FLIP in langerhans cell histiocytosis
Bank Mi, Gudbrand C, Rengtved P, Carstensen H, Fadeel B, Henter Ji, et al
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY 2005;27(6):301-6

Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11
Zur Stadt U, Schmidt S, Diler As, Henter Ji, Kabisch H, Schneppenheim R, et al
HUMAN MOLECULAR GENETICS 2005;14(6):827-34

Long-term follow-up of Langerhans cell histiocytosis: 39 years' experience at a single centre
Bernstrand C, Sandstedt B, Ahstrom L, Henter Ji
ACTA PAEDIATRICA 2005;94(8):1073-84

Raji revisited: cytogenetics of the original Burkitt's lymphoma cell line
Karpova Mb, Schoumans J, Ernberg I, Henter Ji, Nordenskjold M, Fadeel B
LEUKEMIA 2005;19(1):159-61

Subtyping of natural killer cell cytotoxicity deficiencies in haemophagocytic lymphohistocytosis provides therapeutic guidance
Horne A, Zheng Cy, Lorenz I, Lofstedt M, Montgomery Sm, Janka G, et al
BRITISH JOURNAL OF HAEMATOLOGY 2005;129(5):658-66

Anxiety and depression in parents 4-9 years after the loss of a child owing to a malignancy: a population-based follow-up
Kreicbergs U, Valdimarsdottir U, Onelov E, Henter Ji, Steineck G
PSYCHOLOGICAL MEDICINE 2004;34(8):1431-41

A population-based nationwide study of parents' perceptions of a questionnaire on their child's death due to cancer
Kreicbergs U, Valdimarsdottir U, Steineck G, Henter Ji
LANCET 2004;364(9436):787-9

Efficacy and safety of two different rG-CSF preparations in the treatment of patients with severe congenital neutropenia
Carlsson G, Ahlin A, Dahllof G, Elinder G, Henter Ji, Palmblad J
BRITISH JOURNAL OF HAEMATOLOGY 2004;126(1):127-32

Histiocyte disorders
Henter Ji, Tondini C, Pritchard J
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY 2004;50(2):157-74

Kostmann syndrome: severe congenital neutropenia associated with defective expression of Bcl-2, constitutive mitochondrial release of cytochrome c, and excessive apoptosis of myeloid progenitor cells
Carlsson G, Aprikyan Aag, Tehranchi R, Dale Dc, Porwit A, Hellstrom-lindberg E, et al
BLOOD 2004;103(9):3355-61

Longitudinal follow-up of patients with Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis
Imashuku S, Teramura T, Tauchi H, Ishida Y, Otoh Y, Sawada M, et al
HAEMATOLOGICA 2004;89(2):183-8

Talking about death with children who have severe malignant disease
Kreicbergs U, Valdimarsdottir U, Onelov E, Henter Ji, Steineck G
NEW ENGLAND JOURNAL OF MEDICINE 2004;351(12):1175-86

Tumor necrosis factor, interleukin 11, and leukemia inhibitory factor produced by Langerhans cells in Langerhans cell histiocytosis
By Ua, Tani E, Andersson U, Henter Ji
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY 2004;26(11):706-11

Vascular endothelial growth factor prolongs survival in a transgenic mouse model of ALS
Zheng Cy, Nennesmo I, Fadeel B, Henter Ji
ANNALS OF NEUROLOGY 2004;56(4):564-7

Clinical and genetic studies of familial hemophagocytic lymphohistiocytosis in Oman: Need for early treatment
Al-lamki Z, Wali Ya, Pathare A, Ericson Kg, Henter Ji
PEDIATRIC HEMATOLOGY AND ONCOLOGY 2003;20(8):603-9

Duration and morbidity of newly diagnosed idiopathic thrombocytopenic purpura in children: A prospective Nordic study of an unselected cohort
Nopho Itp Working Group, Rosthoj S, Hedlund-treutiger R, Rajantie J, Zeller B, Jonsson Og, et al
JOURNAL OF PEDIATRICS 2003;143(3):302-7

Immunogenetic heterogeneity in single-system and multisystem Langerhans cell histiocytosis
Bernstrand C, Carstensen H, Jakobsen B, Svejgaard A, Henter Ji, Olerup O
PEDIATRIC RESEARCH 2003;54(1):30-6

Langerhans-cell histiocytosis: neoplasia or unbridled inflammation?
Fadeel B, Henter Ji
TRENDS IN IMMUNOLOGY 2003;24(8):409-10

Randomized study of IVIg and high-dose dexamethasone therapy for children with chronic idiopathic thrombocytopenic purpura
Hedlund-treutiger I, Henter Ji, Elinder G
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY 2003;25(2):139-44

Sequence analysis of the granulysin and granzyme B genes in familial hemophagocytic lymphohistiocytosis
Ericson Kg, Fadeel B, Andersson M, Gudmundsson Gh, Gurgey A, Yalman N, et al
HUMAN GENETICS 2003;112(1):98-9

Biology and treatment of familial hemophagocytic lymphohistiocytosis: Importance of perforin in lymphocyte-mediated cytotoxicity and triggering of apoptosis
Henter Ji
MEDICAL AND PEDIATRIC ONCOLOGY 2002;38(5):305-9

Brain 18-FDG PET scan in central nervous system Langerhans cell histiocytosis
Calming U, Bemstrand C, Mosskin M, Elander Ss, Ingvar M, Henter Ji
JOURNAL OF PEDIATRICS 2002;141(3):435-40

Familial transient erythroblastopenia of childhood is associated with the chromosome 19q13.2 region but not caused by mutations in coding sequences of the ribosomal protein S19 (RPS19) gene
Gustavsson P, Klar J, Matsson H, Forestier E, Henter Ji, Rao S, et al
BRITISH JOURNAL OF HAEMATOLOGY 2002;119(1):261-4

Findings in familial haemophagocytic lymphohistiocytosis prior to symptomatic presentation
Hafsteinsdottir S, Jonmundsson Gk, Kristinsson Jr, Winiarski J, Henter Ji, Haraldsson A
ACTA PAEDIATRICA 2002;91(8):974-7

Prenatal diagnosis of perforin gene mutations in familial hemophagocytic lymphohistiocytosis (FHLH)
Zur Stadt U, Pruggmayer M, Jung H, Henter Ji, Schneider M, Kabisch H, et al
PRENATAL DIAGNOSIS 2002;22(1):80-1

Treatment of hemophagocytic lymphohistiocytosis with HLH-94 immunochemotherapy and bone marrow transplantation
Histiocyte Soc, Henter Ji, Samuelsson-horne A, Arico M, Egeler Rm, Elinder G, et al
BLOOD 2002;100(7):2367-73

Familial hemophagocytic lymphohistiocytosis: Too little cell death can seriously damage your health
Fadeel B, Orrenius S, Henter Ji
LEUKEMIA & LYMPHOMA 2001;42(1-2):13-20

Pulmonary abnormalities at long-term follow-up of patients with Langerhans cell histiocytosis
Bernstrand C, Cederlund K, Sandstedt B, Ahstrom L, Lundell M, Dahlquist G, et al
MEDICAL AND PEDIATRIC ONCOLOGY 2001;36(4):459-68

Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis
Ericson Kg, Fadeel B, Nilsson-ardnor S, Soderhall C, Samuelsson A, Janka G, et al
AMERICAN JOURNAL OF HUMAN GENETICS 2001;68(3):590-7

Successful treatment of Langerhans'-cell histiocytosis with etanercept
Henter Ji, Karlen J, Calming U, Bernstrand C, Andersson U, Fadeel B
NEW ENGLAND JOURNAL OF MEDICINE 2001;345(21):1577-8

[Apoptosis required for maintenance of homeostasis: familial hemophagocytic lymphohistiocytosis caused by too little cell death]
Fadeel B, Henter Ji, Orrenius S
Lakartidningen 2000;97(12):1395-400

Detection of langerhans cell histiocytosis lesions with somatostatin analogue scintigraphy - A preliminary report
Calming U, Jacobsson H, Henter Ji
MEDICAL AND PEDIATRIC ONCOLOGY 2000;35(5):462-7

[Familial hemophagocytic lymphohistiocytosis: diagnosis, treatment and pathophysiological mechanisms]
Henter Ji, Samuelsson A, Ericson K, Nilsson-ardnor S, Elinder G, Fadeel B
Lakartidningen 2000;97(12):1405-8

[Parvovirus B19 infection--an incidious chameleon]
Broliden K, Tolfvenstam T, Papadogiannakis N, Westgren M, Matt P, Lundqvist A, et al
Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke 2000;120(4):455-8

Smoking preceded pulmonary involvement in adults with Langerhans cell histiocytosis diagnosed in childhood
Bernstrand C, Cederlund K, Ahstrom L, Henter Ji
ACTA PAEDIATRICA 2000;89(11):1389-92

Cleavage of Bcl-2 is an early event in chemotherapy-induced apoptosis of human myeloid leukemia cells
Fadeel B, Hassan Z, Hellstrom-lindberg E, Henter Ji, Orrenius S, Zhivotovsky B
LEUKEMIA 1999;13(5):719-28

Effective control of Epstein-Barr virus-related hemophagocytic lymphohistiocytosis with immunochemotherapy
Histiocyte Soc, Imashuku S, Hibi S, Ohara T, Iwai A, Sako M, et al
BLOOD 1999;93(6):1869-74

Induction of apoptosis and caspase activation in cells obtained from familial haemophagocytic lymphohistiocytosis patients
Fadeel B, Orrenius S, Henter Ji
BRITISH JOURNAL OF HAEMATOLOGY 1999;106(2):406-15

[Parvovirus B19 infection--an insidious chameleon]
Broliden K, Tolfvenstam T, Papadogiannakis N, Westgren M, Matt P, Lundqvist A, et al
Lakartidningen 1999;96(46):5066-9

Perforin gene defects in familiar hemophagocytic lymphohistiocytosis
Stepp Se, Dufourcq-lagelouse R, Le Deist F, Bhawan S, Certain S, Mathew Pa, et al
SCIENCE 1999;286(5446):1957-9

Phosphatidylserine exposure during apoptosis is a cell-type-specific event and does not correlate with plasma membrane phospholipid scramblase expression
Fadeel B, Gleiss B, Hogstrand K, Chandra J, Wiedmer T, Sims Pj, et al
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 1999;266(2):504-11

Successful extracorporeal membrane oxygenation in four children with malignant disease and severe Pneumocystis carinii pneumonia
Linden V, Karlen J, Olsson M, Palmer K, Ehren H, Henter Ji, et al
MEDICAL AND PEDIATRIC ONCOLOGY 1999;32(1):25-31

Autopsy findings in 27 children with haemophagocytic lymphohistiocytosis
Ost A, Nilsson-ardnor S, Henter Ji
HISTOPATHOLOGY 1998;32(4):310-6

Down-regulation of lymphokine synthesis by intravenous gammaglobulin is dependent upon accessory cells
Skansen-saphir U, Andersson J, Bjork L, Ekberg C, Fehniger Te, Henter Ji, et al
SCANDINAVIAN JOURNAL OF IMMUNOLOGY 1998;47(3):229-35

Elevated erythrocyte sedimentation rate and thrombocytosis as possible indicators of active disease in Langerhans' cell histiocytosis
Calming U, Henter Ji
ACTA PAEDIATRICA 1998;87(10):1085-7

Familial hemophagocytic lymphohistiocytosis - Primary hemophagocytic lymphohistiocytosis
Henter Ji, Arico M, Elinder G, Imashuku S, Janka G
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA 1998;12(2):417-33

Infection- and malignancy-associated hemophagocytic syndromes - Secondary hemophagocytic lymphohistiocytosis
Janka G, Imashuku S, Elinder G, Schneider M, Henter Ji
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA 1998;12(2):435-44

Involvement of caspases in neutrophil apoptosis: Regulation by reactive oxygen species
Fadeel B, Ahlin A, Henter Ji, Orrenius S, Hampton Mb
BLOOD 1998;92(12):4808-18

Persistent B19 parvovirus infection in pediatric malignancies
Broliden K, Tolfvenstam T, Ohlsson S, Henter Ji
MEDICAL AND PEDIATRIC ONCOLOGY 1998;31(2):66-72

Transient red cell aplasia in siblings: a common environmental or a common hereditary factor?
Skeppner G, Forestier E, Henter Ji, Wranne L
ACTA PAEDIATRICA 1998;87(1):43-7

Contemporary classification of histiocytic disorders
Favara Be, Feller Ac, Pauli M, Jaffe Es, Weiss Lm, Arico M, et al
MEDICAL AND PEDIATRIC ONCOLOGY 1997;29(3):157-66

Diamond-Blackfan anaemia: Genetic homogeneity for a gene on chromosome 19q13 restricted to 1.8 Mb
Gustavsson P, Willig Tn, Vanhaeringen A, Tchernia G, Dianzani I, Donner M, et al
NATURE GENETICS 1997;16(4):368-71

HLH-94: A treatment protocol for hemophagocytic lymphohistiocytosis
Henter Ji, Arico M, Egeler Rm, Elinder G, Favara Be, Filipovich Ah, et al
MEDICAL AND PEDIATRIC ONCOLOGY 1997;28(5):342-7

Neuropathologic findings and neurologic symptoms in twenty-three children with hemophagocytic lymphohistiocytosis
Henter Ji, Nennesmo I
JOURNAL OF PEDIATRICS 1997;130(3):358-65

Prevalence and treatment of chronic idiopathic thrombocytopenic purpura of childhood in Sweden
Hedman A, Henter Ji, Hedlund I, Elinder G
ACTA PAEDIATRICA 1997;86(2):226-7

Elevated circulating levels of interleukin-1 receptor antagonist but not IL-1 agonists in hemophagocytic lymphohistiocytosis
Henter Ji, Andersson B, Elinder G, Jakobson A, Lubeck Po, Soder O
MEDICAL AND PEDIATRIC ONCOLOGY 1996;27(1):21-5

Hemophagocytic lymphohistiocytosis. Report of 122 children from the international Registry
Arico M, Janka G, Fischer A, Henter Ji, Blanche S, Elinder G, et al
LEUKEMIA 1996;10(2):197-203

Intralesional steroids in Langerhans cell histiocytosis of bone
Bernstrand C, Bjork O, Ahstrom L, Henter Ji
ACTA PAEDIATRICA 1996;85(4):502-4

[Thalassemia, heading for Sweden. A new patient group at Swedish pediatric clinics]
Sandström L, Ljung R, Henter Ji, Elinder G
Lakartidningen 1996;93(1-2):26-30

Transient hypertriglyceridemia of infancy
Nilsson A, Ortqvist E, Lagercrantz H, Nilssonehle P, Henter Ji
ACTA PAEDIATRICA 1996;85(12):1508-10

ALLOGENEIC BONE-MARROW TRANSPLANTATION FOR HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS IN SWEDEN
Bolme P, Henter Ji, Winiarski J, Elinder G, Ljungman P, Lonnerholm G, et al
BONE MARROW TRANSPLANTATION 1995;15(3):331-5

BONE-MARROW TRANSPLANTATION IN 2 CHILDREN WITH CONGENITAL AMEGAKARYOCYTIC THROMBOCYTOPENIA
Henter Jj, Winiarski J, Ljungman P, Ringden O, Ost A
BONE MARROW TRANSPLANTATION 1995;15(5):799-801

HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS - AN INHERITED PRIMARY FORM AND A REACTIVE SECONDARY FORM
Henter Ji, Elinder G
BRITISH JOURNAL OF HAEMATOLOGY 1995;91(3):774-5

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