Results 271 to 280 of about 9,263,948 (394)

Molestia de Hodgkin Hodgkin's disease

open access: yesMemorias do Instituto Oswaldo Cruz, 1929
José Guilherme Lacorte
doaj   +1 more source

A Comprehensive Review of Kimura Disease. [PDF]

open access: yesHead Neck Pathol
Lagerstrom IT   +5 more
europepmc   +1 more source

Atypical hodgkin and reed-sternberg cells in peripheral blood of a patient with advanced stage of Hodgkin's disease - a case report

open access: diamond, 2003
Rajko Milošević   +4 more
openalex   +2 more sources

Final Results From a Large, Non‐Interventional, Phase 4 Study of Ruxolitinib for the Treatment of Myelofibrosis in Clinical Routine

open access: yesEuropean Journal of Haematology, EarlyView.
ABSTRACT JAKoMo was a long‐term, multicenter, non‐interventional study observing the efficacy, safety, and quality of life (QOL) effects of ruxolitinib (RUX), managed per clinical routine at investigator discretion, for treatment of 943 patients with myelofibrosis (MF) in 122 German centers.
Steffen Koschmieder   +15 more
wiley   +1 more source

Machine Learning for Prediction of High‐Risk Hospitalizations in Lymphoma Patients: A Danish Population‐Based Study

open access: yesEuropean Journal of Haematology, EarlyView.
ABSTRACT Objective Infections are a leading cause of hospitalization in patients treated for lymphoma and can be life‐threatening. This study developed a machine learning (ML)‐based risk stratification method to classify infection‐related hospitalizations (IRH) into serious‐IRH (S‐IRH) and non‐serious‐IRH (NS‐IRH).
Alexander Djupnes Fuglkjaer   +11 more
wiley   +1 more source

Incremental immunogenicity of multiple doses of SARS‐CoV‐2 vaccination in patients with haematological malignancies

open access: yes
British Journal of Haematology, EarlyView.
Abi Vijenthira   +23 more
wiley   +1 more source

Rare dysfunctional SCN2A variants are associated with malformation of cortical development

open access: yesEpilepsia, Volume 66, Issue 3, Page 914-928, March 2025.
Abstract Objective SCN2A encodes the voltage‐gated sodium (Na+) channel α subunit NaV1.2, which is important for the generation and forward and back propagation of action potentials in neurons. Genetic variants in SCN2A are associated with a spectrum of neurodevelopmental disorders.
Jérôme Clatot   +19 more
wiley   +1 more source

A Rare Case of Hodgkin Lymphoma With Isolated Epitrochlear Lymphadenopathy. Our Experience and Main Differential Diagnosis. [PDF]

open access: yesCase Rep Med
Cea L   +8 more
europepmc   +1 more source

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