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List of works by Jan-Inge Henter

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 Coll

scientific article published on 28 August 2015

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 Coll

scientific article published on March 2016

A RAB27A 5' untranslated region structural variant associated with late-onset hemophagocytic lymphohistiocytosis and normal pigmentation.

scientific article published on 6 March 2018

A population-based nationwide study of parents' perceptions of a questionnaire on their child's death due to cancer

scientific article

A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromes

scientific article published on 31 January 2012

Adsorptive depletion of blood monocytes reduces the levels of circulating interleukin-17A in Langerhans cell histiocytosis

scientific article

Age-dependent differences in Nordic children with ITP

scientific article published on 01 January 2005

Allogeneic bone marrow transplantation for hemophagocytic lymphohistiocytosis in Sweden

scientific article published on 01 March 1995

An N-Terminal Missense Mutation in STX11 Causative of FHL4 Abrogates Syntaxin-11 Binding to Munc18-2.

scientific article published on 14 January 2014

Anxiety and depression in parents 4-9 years after the loss of a child owing to a malignancy: a population-based follow-up

scientific article published in November 2004

Anxiety is contagious-symptoms of anxiety in the terminally ill child affect long-term psychological well-being in bereaved parents

scientific article published in May 2010

Autopsy findings in 27 children with haemophagocytic lymphohistiocytosis.

scientific article published in April 1998

Betulinic acid, a natural cytotoxic agent, fails to trigger apoptosis in human Burkitt's lymphoma-derived B-cell lines

scientific article published on January 2006

Biology and treatment of familial hemophagocytic lymphohistiocytosis: importance of perforin in lymphocyte-mediated cytotoxicity and triggering of apoptosis

scientific article

Biomarkers in the cerebrospinal fluid and neurodegeneration in Langerhans cell histiocytosis

scientific article published in December 2009

Bone marrow transplantation in two children with congenital amegakaryocytic thrombocytopenia.

scientific article

Bortezomib and IL-12 produce synergetic anti-multiple myeloma effects with reduced toxicity to natural killer cells

scientific article published on March 2014

Brain 18-FDG PET scan in central nervous system langerhans cell histiocytosis

scientific article

Cancer risk in relatives of patients with a primary disorder of lymphocyte cytotoxicity: a retrospective cohort study.

scientific article published on 3 December 2015

Care-related distress: a nationwide study of parents who lost their child to cancer

scientific article published on 19 September 2005

Central nervous system disease in Langerhans cell histiocytosis

scientific article

Characterization of PRF1, STX11 and UNC13D genotype-phenotype correlations in familial hemophagocytic lymphohistiocytosis

scientific article published in October 2008

Chemoimmunotherapy for hemophagocytic lymphohistiocytosis: long-term results of the HLH-94 treatment protocol

scientific article published on 6 September 2011

Chemoresistance of human monocyte-derived dendritic cells is regulated by IL-17A.

scientific article published on 18 February 2013

Childhood idiopathic thrombocytopenic purpura in the Nordic countries: epidemiology and predictors of chronic disease.

scientific article

Children with cancer share their views: tell the truth but leave room for hope

scientific article published on 7 June 2016

Cladribine and cytarabine in refractory multisystem Langerhans cell histiocytosis: results of an international phase 2 study.

scientific article

Clinical and Genetic Studies of Familial Hemophagocytic Lymphohistiocytosis in Oman: Need for Early Treatment ⬇️

scientific article published on December 1, 2003

Clinical presentation of Griscelli syndrome type 2 and spectrum of RAB27A mutations

scientific article published on April 2010

Clinical presentation of hemophagocytic lymphohistiocytosis in adults is less typical than in children

scientific article

Combined newborn screening for familial hemophagocytic lymphohistiocytosis and severe T- and B-cell immunodeficiencies

scientific article

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

scientific article published on March 2006

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

scientific article published on 2 January 2013

Confirmed efficacy of etoposide and dexamethasone in HLH treatment: long-term results of the cooperative HLH-2004 study

scientific article published on 21 September 2017

Consensus recommendations for the diagnosis and management of hemophagocytic lymphohistiocytosis associated with malignancies

scientific article published on August 2015

Cytotoxic therapy for severe avian influenza A (H5N1) infection.

scientific article

Cytotoxic therapy for severe swine flu A/H1N1.

scientific article published on December 2010

Defective cytotoxic lymphocyte degranulation in syntaxin-11 deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients

scientific article published on 15 September 2007

Detection of IL-17A-producing peripheral blood monocytes in Langerhans cell histiocytosis patients.

scientific article published on 15 April 2014

Detection of Langerhans cell histiocytosis lesions with somatostatin analogue scintigraphy--a preliminary report

scientific article published on 01 November 2000

Development of classical Hodgkin's lymphoma in an adult with biallelic STXBP2 mutations

scientific article published on 25 October 2012

Diamond-Blackfan anaemia: genetic homogeneity for a gene on chromosome 19q13 restricted to 1.8 Mb ⬇️

scientific article (publication date: August 1997)

Differences in Granule Morphology yet Equally Impaired Exocytosis among Cytotoxic T Cells and NK Cells from Chediak-Higashi Syndrome Patients

scientific article published on 18 April 2017

Different NK cell-activating receptors preferentially recruit Rab27a or Munc13-4 to perforin-containing granules for cytotoxicity

scientific article

Does treatment of newly diagnosed idiopathic thrombocytopenic purpura reduce morbidity?

scientific article

Down-regulation of lymphokine synthesis by intravenous gammaglobulin is dependent upon accessory cells

scientific article published on 01 March 1998

Duration and morbidity of chronic immune thrombocytopenic purpura in children: five-year follow-up of a Nordic cohort

scientific article

Duration and morbidity of newly diagnosed idiopathic thrombocytopenic purpura in children: a prospective nordic study of an unselected cohort ⬇️

scientific article published on September 1, 2003

Efficacy and safety of two different rG-CSF preparations in the treatment of patients with severe congenital neutropenia

scientific article published in July 2004

Elevated erythrocyte sedimentation rate and thrombocytosis as possible indicators of active disease in Langerhans' cell histiocytosis

scientific article published on 01 October 1998

Elevated serum levels of the decoy receptor osteoprotegerin in children with Langerhans cell histiocytosis

scientific article published on 01 February 2006

Evaluation of Parvovirus B19 Infection in Children with Malignant or Hematological Disorders

scientific article published on 15 May 2010

Expert consensus on dynamics of laboratory tests for diagnosis of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis.

scientific article published on 19 January 2016

Familial Hemophagocytic Lymphohistiocytosis: Too Little Cell Death Can Seriously Damage Your Health ⬇️

scientific article published on June 1, 2001

Familial hemophagocytic lymphohistiocytosis type 3 (FHL3) caused by deep intronic mutation and inversion in UNC13D

scientific article published on 19 September 2011

Familial hemophagocytic lymphohistiocytosis. Primary hemophagocytic lymphohistiocytosis ⬇️

scientific article published on April 1, 1998

Familial hemophagocytic lymphohistiocytosis: diagnosis, treatment and pathophysiological mechanisms

scientific article published on March 2000

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

scientific article published on 01 October 2002

Fatal agranulocytosis after deferiprone therapy in a child with Diamond-Blackfan anemia.

scientific article published on 7 March 2007

Fatal hemophagocytic lymphohistiocytosis in X-linked chronic granulomatous disease associated with a perforin gene variant

scientific article

Fetal hemolytic anemia and intrauterine death caused by anti-M immunization

scientific article published in May 2007

Fifteen years of treatment with intravenous immunoglobulin in central nervous system Langerhans cell histiocytosis

scientific article published on 11 January 2011

Findings in familial haemophagocytic lymphohistiocytosis prior to symptomatic presentation.

scientific article published on January 2002

Frequency and development of CNS involvement in Chinese children with hemophagocytic lymphohistiocytosis

scientific article published in March 2010

Frequency and spectrum of central nervous system involvement in 193 children with haemophagocytic lymphohistiocytosis

scientific article published on 10 December 2007

Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms

scientific article published on 15 February 2017

Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations.

scientific article

Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis type 3

scientific article

HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)

scientific article

HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis.

scientific article

HLH-94: a treatment protocol for hemophagocytic lymphohistiocytosis. HLH study Group of the Histiocyte Society

scientific article published on 01 May 1997

Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis

scientific article published in June 2005

Haemophagocytic lymphohistiocytosis: an inherited primary form and a reactive secondary form

scientific article published on 01 November 1995

Healing hemophagocytosis

scientific article published in November 2005

Hematopoietic stem cell transplantation in children with cancer and the risk of long-term psychological morbidity in the bereaved parents.

scientific article

Hematopoietic stem cell transplantation in severe congenital neutropenia

scientific article published on 11 November 2010

Hemophagocytic lymphohistiocytosis in 2 patients with underlying IFN-γ receptor deficiency

scientific article published on 13 January 2015

Hemophagocytic lymphohistiocytosis in infants: a single center experience from India

scientific article published on 2 January 2014

Hemophagocytic lymphohistiocytosis. Report of 122 children from the International Registry. FHL Study Group of the Histiocyte Society.

scientific article published on February 1996

High systemic levels of the cytokine-inducing HMGB1 isoform secreted in severe macrophage activation syndrome

scientific article

Histiocyte disorders

scientific article published on 01 May 2004

How to Treat Involvement of the Central Nervous System in Hemophagocytic Lymphohistiocytosis?

scientific article published on January 2017

Immunogenetic heterogeneity in single-system and multisystem langerhans cell histiocytosis

scientific article published on 16 April 2003

Immunohistochemical detection of the apoptosis-related proteins FADD, FLICE, and FLIP in Langerhans cell histiocytosis

scientific article published on 01 June 2005

Improved outcome in multisystem Langerhans cell histiocytosis is associated with therapy intensification

scientific article

Incidence and clinical presentation of primary hemophagocytic lymphohistiocytosis in Sweden

scientific article published on 8 November 2014

Incidence and pattern of radiological central nervous system Langerhans cell histiocytosis in children: a population based study

scientific article published in February 2011

Incidence of Langerhans cell histiocytosis in children: a population-based study

scientific article published on 01 July 2008

Incidence of severe congenital neutropenia in Sweden and risk of evolution to myelodysplastic syndrome/leukaemia

scholarly article by Göran Carlsson et al published 25 May 2012 in British Journal of Haematology

Infection- and malignancy-associated hemophagocytic syndromes. Secondary hemophagocytic lymphohistiocytosis ⬇️

scientific article published on April 1, 1998

Intralesional steroids in Langerhans cell histiocytosis of bone.

scientific article

Involvement of caspases in neutrophil apoptosis: regulation by reactive oxygen species

scientific article published on 01 December 1998

Killer cell immunoglobulin-like receptor gene polymorphisms predispose susceptibility to Epstein-Barr virus associated hemophagocytic lymphohistiocytosis in Chinese children

scientific article published in June 2012

Kostmann syndrome or infantile genetic agranulocytosis, part one: celebrating 50 years of clinical and basic research on severe congenital neutropenia

scientific article published on December 2006

Kostmann syndrome or infantile genetic agranulocytosis, part two: Understanding the underlying genetic defects in severe congenital neutropenia

scientific article published on June 2007

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

scientific article published on 05 February 2004

Lack of bone lesions at diagnosis is associated with inferior outcome in multisystem langerhans cell histiocytosis of childhood

scientific article published on 18 December 2014

Langerhans cell histiocytosis in children born 1982-2005 after in vitro fertilization

scientific article published on 11 September 2012

Langerhans cell histiocytosis reveals a new IL-17A-dependent pathway of dendritic cell fusion

scientific article published on 23 December 2007

Langerhans-cell histiocytosis: neoplasia or unbridled inflammation?

scientific article published on 01 August 2003

Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11

scientific article

Long-term follow-up of Langerhans cell histiocytosis: 39 years' experience at a single centre

scientific article published on 01 August 2005

Longitudinal follow-up of patients with Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis.

scientific article published in February 2004

Low plasma levels of the protein pro-LL-37 as an early indication of severe disease in patients with chronic neutropenia

scientific article published in April 2007

Multiple inherited sequence variations in two disease-causing genes in familial haemophagocytic lymphohistiocytosis

scientific article published on 19 May 2009

Neuropathologic findings and neurologic symptoms in twenty-three children with hemophagocytic lymphohistiocytosis.

scientific article published on March 1997

Neuropsychological sequelae in patients with neurodegenerative Langerhans cell histiocytosis

scientific article published in November 2008

Novel deep intronic and missense UNC13D mutations in familial haemophagocytic lymphohistiocytosis type 3.

scientific article published on 14 May 2013

On the Child's Own Initiative: Parents Communicate with Their Dying Child About Death.

scientific article

Ovarian failure in HAX1-deficient patients: is there a gender-specific difference in pubertal development in severe congenital neutropenia or Kostmann disease?

scientific article published in January 2013

Parents' intellectual and emotional awareness of their child's impending death to cancer: a population-based long-term follow-up study

scientific article published in August 2007

Parvovirus B19 infection in children with acute lymphoblastic leukemia is associated with cytopenia resulting in prolonged interruptions of chemotherapy

scientific article published in February 2008

Pathophysiology and spectrum of diseases caused by defects in lymphocyte cytotoxicity.

scientific article published on 28 March 2014

Pediatric Crohn's disease from onset to adulthood: granulomas are associated with an early need for immunomodulation

scientific article published on 27 May 2014

Perforin gene defects in familial hemophagocytic lymphohistiocytosis.

scientific article

Periodontal disease in patients from the original Kostmann family with severe congenital neutropenia

scientific article published in April 2006

Phosphatidylserine exposure during apoptosis is a cell-type-specific event and does not correlate with plasma membrane phospholipid scramblase expression

scientific article published on 01 December 1999

Polyclonal T-cells express CD1a in Langerhans cell histiocytosis (LCH) lesions

scientific article

Prenatal diagnosis of perforin gene mutations in familial hemophagocytic lymphohistiocytosis (FHLH)

scientific article published on 01 January 2002

Pronounced hyperferritinemia: expanding the field of hemophagocytic lymphohistiocytosis

scientific article published on 01 June 2008

Proteasome inhibition induces apoptosis in primary human natural killer cells and suppresses NKp46-mediated cytotoxicity

scientific article published on 19 February 2009

Pulmonary abnormalities at long-term follow-up of patients with Langerhans cell histiocytosis

scientific article published on 01 April 2001

Pulmonary function testing and pulmonary Langerhans cell histiocytosis

scientific article

Reactivations in multisystem Langerhans cell histiocytosis: data of the international LCH registry

scientific article

Revised classification of histiocytoses and neoplasms of the macrophage-dendritic cell lineages

scientific article published on 10 March 2016

Ribonucleotide reductase inhibitors suppress SAMHD1 ara-CTPase activity enhancing cytarabine efficacy

scientific article published on 17 January 2020

Risk factors for diabetes insipidus in langerhans cell histiocytosis.

scientific article

Risk factors for early death in children with haemophagocytic lymphohistiocytosis

scientific article

SAMHD1 protects cancer cells from various nucleoside-based antimetabolites

scientific article

Sequence analysis of the granulysin and granzyme B genes in familial hemophagocytic lymphohistiocytosis

scientific article (publication date: 2003)

Sequence analysis of theSRGN, AP3B1, ARF6, andSH2D1A genes in familial hemophagocytic lymphohistiocytosis

article

Severe bacteria-associated hemophagocytic lymphohistiocytosis in an extremely premature infant

scientific article published on 19 September 2007

Simultaneous manifestation of fulminant infectious mononucleosis with haemophagocytic syndrome and B-cell lymphoma in X-linked lymphoproliferative disease

scientific article published on 21 October 2006

Smoking preceded pulmonary involvement in adults with Langerhans cell histiocytosis diagnosed in childhood

scientific article published on 01 November 2000

Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense Mutations

scientific article published on 16 July 2015

Spectrum of clinical presentations in familial hemophagocytic lymphohistiocytosis type 5 patients with mutations in STXBP2.

scientific article published on 17 June 2010

Subtyping of natural killer cell cytotoxicity deficiencies in haemophagocytic lymphohistocytosis provides therapeutic guidance

scientific article published in June 2005

Successful Hematopoietic Stem Cell Transplantation in a Patient with LPS-Responsive Beige-Like Anchor (LRBA) Gene Mutation.

scientific article published on 4 May 2016

Successful treatment of Langerhans'-cell histiocytosis with etanercept

scientific article published on 01 November 2001

Symptoms Affecting Children With Malignancies During the Last Month of Life: A Nationwide Follow-up

scientific article published on 01 April 2006

Syntaxin 11 marks a distinct intracellular compartment recruited to the immunological synapse of NK cells to colocalize with cytotoxic granules

scientific article published on January 2012

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

scientific article published on 11 June 2008

Talking about death with children who have severe malignant disease

scientific article published in September 2004

Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis

scientific article published on 18 December 2015

Targeting BCL2 family in human myeloid dendritic cells: a challenge to cure diseases with chronic inflammations associated with bone loss

scientific article published on 22 May 2013

Targeting SAMHD1 with the Vpx protein to improve cytarabine therapy for hematological malignancies

scientific article

Thalassemia, heading for Sweden. A new patient group at Swedish pediatric clinics

scientific article published in January 1996

The minimum required level of donor chimerism in hereditary hemophagocytic lymphohistiocytosis

scientific article published on 20 April 2016

The need for worldwide policy and action plans for rare diseases

scientific article

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

scientific article published on 9 June 2010

Therapy prolongation improves outcome in multisystem Langerhans cell histiocytosis

scientific article published on 15 April 2013

Tissue-infiltrating neutrophils represent the main source of IL-23 in the colon of patients with IBD.

scientific article

Transient hypertriglyceridemia of infancy

scientific article published on 01 December 1996

Transient red cell aplasia in siblings: a common environmental or a common hereditary factor?

scientific article published on 01 January 1998

Transition to noncurative end-of-life care in paediatric oncology--a nationwide follow-up in Sweden

scientific article published on 16 April 2013

Treatment of familial hemophagocytic lymphohistiocytosis with third-party mesenchymal stromal cells

scientific article published on 30 July 2012

Treatment of hemophagocytic lymphohistiocytosis with HLH-94 immunochemotherapy and bone marrow transplantation

scientific article published on October 2002

Treatment of the X-linked lymphoproliferative, Griscelli and Chédiak-Higashi syndromes by HLH directed therapy

scientific article published on 01 February 2009

Tumor necrosis factor, interleukin 11, and leukemia inhibitory factor produced by Langerhans cells in Langerhans cell histiocytosis

scientific article published on 01 November 2004

VEGF reduces astrogliosis and preserves neuromuscular junctions in ALS transgenic mice

scientific article published on 01 October 2007

Vascular endothelial growth factor prolongs survival in a transgenic mouse model of ALS.

scientific article published in October 2004

Why rare diseases are an important medical and social issue

scientific article published on June 2008

With me or against me: Tumor suppressor and drug resistance activities of SAMHD1.

scientific article published on 11 May 2017

[Apoptosis required for maintenance of homeostasis: familial hemophagocytic lymphohistiocytosis caused by too little cell death]

scientific article published on 01 March 2000

[Can cytostatics be effective in severe avian influenza? The disease picture has similarities with hemophagocytic lymphohistiocytosis]

scientific article published on 01 April 2006

[Enigmatic diseases in children. Still a lot of questions left in spite of great research progress on LCH and HLH]

scientific article published on 01 May 2005

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