Lista de obras -

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

artículo científico publicado en 2012

A treatment protocol for infants younger than 1 year with acute lymphoblastic leukaemia (Interfant-99): an observational study and a multicentre randomised trial.

artículo científico publicado en 2007

A91V is a polymorphism in the perforin gene not causative of an FHLH phenotype

artículo científico publicado en 2004

Almost normal cognitive function in patients during therapy for childhood acute lymphoblastic leukemia without cranial irradiation according to ALL-BFM 95 and COALL 06-97 protocols: results of an Austrian-German multicenter longitudinal study and im

artículo científico publicado en 2007

Amsacrine combined with etoposide and high-dose methylprednisolone as salvage therapy in acute lymphoblastic leukemia in children

artículo científico publicado en 2005

An aggressive systemic juvenile xanthogranuloma clonally related to a preceding T‐cell acute lymphoblastic leukemia ⬇️

artículo científico publicado el 16 de septiembre de 2010

Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases

artículo científico publicado en 2010

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

artículo científico publicado en 2011

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

artículo científico publicado en 2017

Differentiating macrophage activation syndrome in systemic juvenile idiopathic arthritis from other forms of hemophagocytic lymphohistiocytosis

artículo científico publicado en 2013

Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5).

artículo científico publicado en 2012

Effective Immunological Guidance of Genetic Analyses Including Exome Sequencing in Patients Evaluated for Hemophagocytic Lymphohistiocytosis.

artículo científico publicado en 2017

Familial and acquired hemophagocytic lymphohistiocytosis

artículo científico publicado en 2005

Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11

artículo científico publicado en 2009

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

artículo científico publicado en 2007

Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis type 3

artículo científico publicado en 2011

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

artículo científico publicado en 2007

Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis

artículo científico publicado en 2005

Hemophagocytic Lymphohistiocytosis in Critically Ill Patients

artículo científico publicado en 2019

Hemophagocytic lymphohistiocytosis and Kawasaki disease: combined manifestation and differential diagnosis

artículo científico publicado en 2009

Hemophagocytic lymphohistiocytosis in adults: collaborative analysis of 137 cases of a nationwide German registry

artículo científico publicado en 2020

Hemophagocytic lymphohistiocytosis in critically ill patients: diagnostic reliability of HLH-2004 criteria and HScore

scientific article published on 24 May 2020

Hemophagocytic lymphohistiocytosis in imported pediatric visceral leishmaniasis in a nonendemic area.

artículo científico publicado en 2014

Hemophagocytic lymphohistiocytosis in syntaxin-11-deficient mice: T-cell exhaustion limits fatal disease

scientific journal article

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

artículo científico publicado en 2017

Hyperferritinemia in Critically Ill Patients

artículo científico publicado en 2020

Infection of T lymphocytes in Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis in children of non-Asian origin

artículo científico publicado en 2009

Is an infectious trigger always required for primary hemophagocytic lymphohistiocytosis? Lessons from in utero and neonatal disease

scientific article published on 01 August 2018

Italian Society of Hematology guidelines for thalassemia and non-invasive iron measurements

artículo científico publicado en 2008

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 (LCH): guidelines for diagnosis, clinical work-up, and treatment for patients till the age of 18 years

artículo científico publicado en 2012

Late-onset hemophagocytic lymphohistiocytosis (HLH) in an adult female with Griscelli syndrome type 2 (GS2).

artículo científico publicado en 2014

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

artículo científico publicado en 2005

Mutating heme oxygenase-1 into a peroxidase causes a defect in bilirubin synthesis associated with microcytic anemia and severe hyperinflammation

artículo científico publicado en 2016

Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A

artículo científico publicado en 2006

Neonatal cholestasis and glucose-6-P-dehydrogenase deficiency.

artículo científico publicado en 2010

Outcome of congenital acute lymphoblastic leukemia treated on the Interfant-99 protocol.

artículo científico publicado en 2009

Pancytopenia in a 4-year-old boy. 22q11.2 microdeletion syndrome

scientific article published on 01 May 2009

Parental informed consent in pediatric cancer trials: a population-based survey in Germany

artículo científico publicado en 2012

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

artículo científico publicado en 2002

Primary and secondary hemophagocytic lymphohistiocytosis have different patterns of T-cell activation, differentiation and repertoire.

artículo científico publicado en 2016

Pulmonary involvement in pediatric-onset multisystem Langerhans cell histiocytosis: effect on course and outcome

artículo científico publicado en 2012

Rapid LightCycler assay for identification of the perforin codon 374 Trp --> stop mutation in patients and families with hemophagocytic lymphohistiocytosis (HLH)

scientific article published on 01 July 2003

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

artículo científico publicado en 2008

Recent advances in the diagnosis and treatment of hemophagocytic lymphohistiocytosis.

artículo científico publicado en 2012

Recommendations for the Use of Etoposide-Based Therapy and Bone Marrow Transplantation for the Treatment of HLH: Consensus Statements by the HLH Steering Committee of the Histiocyte Society

scientific article published on 04 July 2018

Recommendations for the management of hemophagocytic lymphohistiocytosis in adults

scientific article published on 16 April 2019

Risk factors for early death in children with haemophagocytic lymphohistiocytosis

artículo científico publicado en 2011

Risk factors for mixed chimerism in children with hemophagocytic lymphohistiocytosis after reduced toxicity conditioning

artículo científico publicado en 2020

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

artículo científico publicado en 2003

Similar but not the same: Differential diagnosis of HLH and sepsis

artículo científico publicado en 2017

Stem cell transplantation for children with hemophagocytic lymphohistiocytosis: results from the HLH-2004 study

scientific article published on 01 August 2020

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

artículo científico publicado en 2005

The minimum required level of donor chimerism in hereditary hemophagocytic lymphohistiocytosis

artículo científico publicado en 2016

The risk of hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type 2

artículo científico publicado en 2013

Treatment and Mortality of Hemophagocytic Lymphohistiocytosis in Adult Critically Ill Patients: A Systematic Review With Pooled Analysis

artículo científico publicado en 2020

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

artículo científico publicado en 2002

Treosulfan-based conditioning regimen for children and adolescents with hemophagocytic lymphohistiocytosis

artículo científico publicado en 2013

Variant alleles of cytokine genes influence risk and clinical course of Langerhans cell histiocytosis

scientific article published on 16 August 2011

Your critical care patient may have HLH (hemophagocytic lymphohistiocytosis)

artículo científico publicado en 2016

Lista de obras de

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

A treatment protocol for infants younger than 1 year with acute lymphoblastic leukaemia (Interfant-99): an observational study and a multicentre randomised trial.

A91V is a polymorphism in the perforin gene not causative of an FHLH phenotype

Almost normal cognitive function in patients during therapy for childhood acute lymphoblastic leukemia without cranial irradiation according to ALL-BFM 95 and COALL 06-97 protocols: results of an Austrian-German multicenter longitudinal study and im

Amsacrine combined with etoposide and high-dose methylprednisolone as salvage therapy in acute lymphoblastic leukemia in children

An aggressive systemic juvenile xanthogranuloma clonally related to a preceding T‐cell acute lymphoblastic leukemia ⬇️

Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases

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

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

Differentiating macrophage activation syndrome in systemic juvenile idiopathic arthritis from other forms of hemophagocytic lymphohistiocytosis

Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5).

Effective Immunological Guidance of Genetic Analyses Including Exome Sequencing in Patients Evaluated for Hemophagocytic Lymphohistiocytosis.

Familial and acquired hemophagocytic lymphohistiocytosis

Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11

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

Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis type 3

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

Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis

Hemophagocytic Lymphohistiocytosis in Critically Ill Patients

Hemophagocytic lymphohistiocytosis and Kawasaki disease: combined manifestation and differential diagnosis

Hemophagocytic lymphohistiocytosis in adults: collaborative analysis of 137 cases of a nationwide German registry

Hemophagocytic lymphohistiocytosis in critically ill patients: diagnostic reliability of HLH-2004 criteria and HScore

Hemophagocytic lymphohistiocytosis in imported pediatric visceral leishmaniasis in a nonendemic area.

Hemophagocytic lymphohistiocytosis in syntaxin-11-deficient mice: T-cell exhaustion limits fatal disease

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

Hyperferritinemia in Critically Ill Patients

Infection of T lymphocytes in Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis in children of non-Asian origin

Is an infectious trigger always required for primary hemophagocytic lymphohistiocytosis? Lessons from in utero and neonatal disease

Italian Society of Hematology guidelines for thalassemia and non-invasive iron measurements

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

Langerhans cell histiocytosis (LCH): guidelines for diagnosis, clinical work-up, and treatment for patients till the age of 18 years

Late-onset hemophagocytic lymphohistiocytosis (HLH) in an adult female with Griscelli syndrome type 2 (GS2).

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

Mutating heme oxygenase-1 into a peroxidase causes a defect in bilirubin synthesis associated with microcytic anemia and severe hyperinflammation

Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A

Neonatal cholestasis and glucose-6-P-dehydrogenase deficiency.

Outcome of congenital acute lymphoblastic leukemia treated on the Interfant-99 protocol.

Pancytopenia in a 4-year-old boy. 22q11.2 microdeletion syndrome

Parental informed consent in pediatric cancer trials: a population-based survey in Germany

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

Primary and secondary hemophagocytic lymphohistiocytosis have different patterns of T-cell activation, differentiation and repertoire.

Pulmonary involvement in pediatric-onset multisystem Langerhans cell histiocytosis: effect on course and outcome

Rapid LightCycler assay for identification of the perforin codon 374 Trp --> stop mutation in patients and families with hemophagocytic lymphohistiocytosis (HLH)

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

Recent advances in the diagnosis and treatment of hemophagocytic lymphohistiocytosis.

Recommendations for the Use of Etoposide-Based Therapy and Bone Marrow Transplantation for the Treatment of HLH: Consensus Statements by the HLH Steering Committee of the Histiocyte Society

Recommendations for the management of hemophagocytic lymphohistiocytosis in adults

Risk factors for early death in children with haemophagocytic lymphohistiocytosis

Risk factors for mixed chimerism in children with hemophagocytic lymphohistiocytosis after reduced toxicity conditioning

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

Similar but not the same: Differential diagnosis of HLH and sepsis

Stem cell transplantation for children with hemophagocytic lymphohistiocytosis: results from the HLH-2004 study

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

The minimum required level of donor chimerism in hereditary hemophagocytic lymphohistiocytosis

The risk of hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type 2

Treatment and Mortality of Hemophagocytic Lymphohistiocytosis in Adult Critically Ill Patients: A Systematic Review With Pooled Analysis

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

Treosulfan-based conditioning regimen for children and adolescents with hemophagocytic lymphohistiocytosis

Variant alleles of cytokine genes influence risk and clinical course of Langerhans cell histiocytosis

Your critical care patient may have HLH (hemophagocytic lymphohistiocytosis)