Anne Pagnier
Grenoble, France
Last Updated: 09/26/2026
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Found 49 publications
French protocol for the diagnosis and management of hereditary angioedema.
Journal: La Revue de medecine interne
Published: September 01, 2025
Neurofilament as a biomarker of neurodegeneration in childhood Langerhans cell histiocytosis: A feasibility study on 273 patients.
Journal: British journal of haematology
Published: July 28, 2025
A de novo dominant-negative PSMB8 mutation causes severe CANDLE/PRAAS due to arrested proteasome biogenesis.
Journal: Annals of the rheumatic diseases
Published: July 24, 2025
YAP1::MAML2 fusion, a newly identified genetic anomaly in a posterior fossa infant tumor, associated with the methylation class "embryonal tumor with multilayered rosettes, non-C19MC-altered" in the Heidelberg central nervous system tumor classifier and "embryonal tumor with multilayered rosettes-DICER" in the NIH classifier.
Journal: Acta neuropathologica communications
Published: July 23, 2025
Desmoid-Type Fibromatosis Tumors in Children After First-Line Failure: Clinical Aspects and Approaches for Subsequent Therapeutic Lines.
Journal: Pediatric blood & cancer
Published: July 03, 2025
Feasibility and efficacy of MEMMAT-like regimen in heavily pretreated adult patients with recurrent malignant embryonal brain tumors: A series of 6 cases.
Journal: Neuro-oncology advances
Published: June 27, 2025
Oral berotralstat for hereditary angioedema prophylaxis in patients aged 2 to <12 years: APeX-P interim results.
Journal: Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology
Published: June 03, 2025
Pediatric eosinophilic fasciitis: similarities and differences with adult forms.
Journal: European journal of pediatrics
Published: October 11, 2024
Last Updated: 09/26/2026