Langerhans' cell histiocytosis: is there a role for genetics?

Bamlanivimab and Etesevimab administered in an outpatient setting for SARS-CoV-2 infection.

Pathogens and global health·2022

Recommendations for pre-symptomatic genetic testing for hereditary transthyretin amyloidosis in the era of effective therapy: a multicenter Italian consensus.

Orphanet journal of rare diseases·2020

Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations.

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society·2020

Primary mediastinal large B-cell lymphoma: Outcome of a series of pediatric patients treated with high-dose methotrexate and cytarabine plus anti-CD20.

Pediatric blood & cancer·2017

Late-onset Pompe disease: a genetic-radiological correlation on cerebral vascular anomalies.

Journal of neurology·2017

Nasal powders of thalidomide for local treatment of nose bleeding in persons affected by hereditary hemorrhagic telangiectasia.

International journal of pharmaceutics·2016

The use of MYD88 and IGH polymerase chain reaction in the diagnosis and follow-up of Bing-Neel syndrome.

Haematologica·2026

CD19 antigen: from tumor target to safety switch in CAR-T cell therapy.

Haematologica·2026

Adult-onset activated PI3Kδ syndrome presenting with HLH-like hyperinflammation, autoimmunity, and thrombosis: an underrecognized inborn error of immunity.

Haematologica·2026

Divergent roles of interleukin-12p40 and interleukin-18 in severe fibrosing chronic graft-versus-host-disease, immunity, and post-transplant outcomes.

Haematologica·2026

Response to comment on: "Ligature-induced periodontitis promotes Dnmt3aR878H-driven clonal hematopoiesis".

Haematologica·2026

Optimizing exposure: the case for dose-dense CAR T-cell administration.

Haematologica·2026

Genetic Modifiers of Cardiac Remodeling Severity in IVS4+919G>A-Associated Fabry Cardiomyopathy.

International journal of molecular sciences·2026

Dissecting Missing Heritability in Rare Inherited Macular Dystrophies.

Genes·2026

Site-Resolved Plasma-Protein Architecture of Infection Susceptibility: A Cis-pQTL Mendelian Randomization and Colocalization Study.

Genes·2026

Socioeconomic and Migration-Related Determinants of Newborn Metabolic Screening Uptake: A Case-Control Study in Urban Iran.

Journal of immigrant and minority health·2026

Generation of two induced pluripotent stem cell lines from Fabry disease patients carrying GLA mutations.

Stem cell research·2026

Variable Expressiveness of a Novel Pathogenic SETD1A Missense Variant Linked to FLOS Domain Haploinsufficiency in a Mexican Pedigree.

Diseases (Basel, Switzerland)·2026

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Langerhans' cell histiocytosis: is there a role for genetics?

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Bamlanivimab and Etesevimab administered in an outpatient setting for SARS-CoV-2 infection.

Recommendations for pre-symptomatic genetic testing for hereditary transthyretin amyloidosis in the era of effective therapy: a multicenter Italian consensus.

Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations.

Primary mediastinal large B-cell lymphoma: Outcome of a series of pediatric patients treated with high-dose methotrexate and cytarabine plus anti-CD20.

Late-onset Pompe disease: a genetic-radiological correlation on cerebral vascular anomalies.

Nasal powders of thalidomide for local treatment of nose bleeding in persons affected by hereditary hemorrhagic telangiectasia.

The use of MYD88 and IGH polymerase chain reaction in the diagnosis and follow-up of Bing-Neel syndrome.

CD19 antigen: from tumor target to safety switch in CAR-T cell therapy.

Adult-onset activated PI3Kδ syndrome presenting with HLH-like hyperinflammation, autoimmunity, and thrombosis: an underrecognized inborn error of immunity.

Divergent roles of interleukin-12p40 and interleukin-18 in severe fibrosing chronic graft-versus-host-disease, immunity, and post-transplant outcomes.

Response to comment on: "Ligature-induced periodontitis promotes Dnmt3aR878H-driven clonal hematopoiesis".

Optimizing exposure: the case for dose-dense CAR T-cell administration.

Genetic Modifiers of Cardiac Remodeling Severity in IVS4+919G>A-Associated Fabry Cardiomyopathy.

Dissecting Missing Heritability in Rare Inherited Macular Dystrophies.

Site-Resolved Plasma-Protein Architecture of Infection Susceptibility: A Cis-pQTL Mendelian Randomization and Colocalization Study.

Socioeconomic and Migration-Related Determinants of Newborn Metabolic Screening Uptake: A Case-Control Study in Urban Iran.

Generation of two induced pluripotent stem cell lines from Fabry disease patients carrying GLA mutations.

Variable Expressiveness of a Novel Pathogenic SETD1A Missense Variant Linked to FLOS Domain Haploinsufficiency in a Mexican Pedigree.

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Langerhans' cell histiocytosis: is there a role for genetics?

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