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International expert consensus recommendations for the diagnosis and treatment of Langerhans cell histiocytosis in adults

Blood, 2022-04, Vol.139 (17), p.2601-2621

2022

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Prior viral infection primes cross-reactive CD8+ T cells that respond to mouse heart allografts

Frontiers in immunology, 2023-12, Vol.14, p.1287546-1287546

2023

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Self-Reported Napping and Duration and Quality of Sleep in the Lifestyle Interventions and Independence for Elders Pilot Study

Journal of the American Geriatrics Society (JAGS), 2008-09, Vol.56 (9), p.1674-1680

2008

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Improving Medical Students’ Understanding of Pediatric Diseases through an Innovative and Tailored Web-based Digital Pathology Program with Philips Pathology Tutor (Formerly PathXL)

Journal of pathology informatics, 2019-01, Vol.10 (1), p.18-18, Article 18

2019

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Circulating senescent myeloid cells infiltrate the brain and cause neurodegeneration in histiocytic disorders

Immunity (Cambridge, Mass.), 2023-12, Vol.56 (12), p.2790-2802.e6

2023

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Molecular Characterization of Sporadic Pediatric Thyroid Carcinoma with the DNA/RNA ThyroSeq v2 Next-Generation Sequencing Assay

Pediatric and developmental pathology, 2016-03, Vol.19 (2), p.115-122

2016

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Identification of Unique, Heterozygous Germline Mutation, STK11 (p.F354L), in a Child with an Encapsulated Follicular Variant of Papillary Thyroid Carcinoma within Six Months of Completing Treatment for Neuroblastoma

Pediatric and developmental pathology, 2015-07, Vol.18 (4), p.318-323

2015

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Mutations in the nuclear bile acid receptor FXR cause progressive familial intrahepatic cholestasis

Nature communications, 2016-02, Vol.7 (1), p.10713-10713, Article 10713

2016

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Dedication

Hematology/oncology clinics of North America, 2015-10, Vol.29 (5), p.xi-xii

2015

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Self-reported Napping, Sleep Duration and Quality in the Lifestyle Interventions and Independence for Elders Pilot (LIFE-P) Study

Journal of the American Geriatrics Society (JAGS), 2008-07, Vol.56 (9), p.1674-1680

2008

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Consensus recommendations for the diagnosis and clinical management of Rosai-Dorfman-Destombes disease

Blood, 2018-06, Vol.131 (26), p.2877-2890

2018

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

Blood, 2016-06, Vol.127 (22), p.2672

2016

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ALK-positive histiocytosis: a new clinicopathologic spectrum highlighting neurologic involvement and responses to ALK inhibition

Blood, 2022-01, Vol.139 (2), p.256-280

2022

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Histiocytic disorders

Nature reviews. Disease primers, 2021-10, Vol.7 (1), p.73-73, Article 73

2021

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CNS Langerhans cell histiocytosis: Common hematopoietic origin for LCH‐associated neurodegeneration and mass lesions

Cancer, 2018-06, Vol.124 (12), p.2607-2620

2018

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BRAF-V600E–mutated Rosai-Dorfman-Destombes disease and Langerhans cell histiocytosis with response to BRAF inhibitor

Blood advances, 2019-06, Vol.3 (12), p.1848-1853

2019

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RARE-40. CASE REPORT: LONG-TERM SURVIVOR OF A RARE, PEDIATRIC PRIMARY HISTIOCYTIC SARCOMA (HS) OF THE CENTRAL NERVOUS SYSTEM (CNS) FOLLOWING COMPLETE RESECTION, CHEMOTHERAPY AND ALLOGENEIC HEMATOPOIETIC CELL TRANSPLANTATION (ALLO-HCT)

Neuro-oncology (Charlottesville, Va.), 2020-12, Vol.22 (Supplement_3), p.iii451-iii451

2020

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Activating Mutations in CSF1R and Additional Receptor Tyrosine Kinases in Sporadic and Familial Histiocytic Neoplasms

Blood, 2018-11, Vol.132 (Supplement 1), p.49-49

2018

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International expert consensus recommendations for the diagnosis and treatment of Langerhans cell histiocytosis in adults

Prior viral infection primes cross-reactive CD8+ T cells that respond to mouse heart allografts

Self-Reported Napping and Duration and Quality of Sleep in the Lifestyle Interventions and Independence for Elders Pilot Study

Improving Medical Students’ Understanding of Pediatric Diseases through an Innovative and Tailored Web-based Digital Pathology Program with Philips Pathology Tutor (Formerly PathXL)

Circulating senescent myeloid cells infiltrate the brain and cause neurodegeneration in histiocytic disorders

Molecular Characterization of Sporadic Pediatric Thyroid Carcinoma with the DNA/RNA ThyroSeq v2 Next-Generation Sequencing Assay

Identification of Unique, Heterozygous Germline Mutation, STK11 (p.F354L), in a Child with an Encapsulated Follicular Variant of Papillary Thyroid Carcinoma within Six Months of Completing Treatment for Neuroblastoma

Mutations in the nuclear bile acid receptor FXR cause progressive familial intrahepatic cholestasis

Dedication

Self-reported Napping, Sleep Duration and Quality in the Lifestyle Interventions and Independence for Elders Pilot (LIFE-P) Study

Consensus recommendations for the diagnosis and clinical management of Rosai-Dorfman-Destombes disease

Erdheim-Chester disease: consensus recommendations for evaluation, diagnosis, and treatment in the molecular era

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

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

Childhood-onset Erdheim-Chester disease in the molecular era: clinical phenotypes and long-term outcomes of 21 patients

Activating mutations in CSF1R and additional receptor tyrosine kinases in histiocytic neoplasms

ALK-positive histiocytosis: a new clinicopathologic spectrum highlighting neurologic involvement and responses to ALK inhibition

Histiocytic disorders

CNS Langerhans cell histiocytosis: Common hematopoietic origin for LCH‐associated neurodegeneration and mass lesions

Langerhans cell histiocytosis: NACHO update on progress, chaos, and opportunity on the path to rational cures

BRAF-V600E–mutated Rosai-Dorfman-Destombes disease and Langerhans cell histiocytosis with response to BRAF inhibitor

RARE-40. CASE REPORT: LONG-TERM SURVIVOR OF A RARE, PEDIATRIC PRIMARY HISTIOCYTIC SARCOMA (HS) OF THE CENTRAL NERVOUS SYSTEM (CNS) FOLLOWING COMPLETE RESECTION, CHEMOTHERAPY AND ALLOGENEIC HEMATOPOIETIC CELL TRANSPLANTATION (ALLO-HCT)

BRAFV600E-induced senescence drives Langerhans cell histiocytosis pathophysiology

Activating Mutations in CSF1R and Additional Receptor Tyrosine Kinases in Sporadic and Familial Histiocytic Neoplasms

Activating mutations in CSF-1R and additional receptor tyrosine kinases in histiocytic neoplasms

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