Centre Hospitalier Universitaire de Caen

Hospital


Location: Caen, France (FR) FR

ISNI: 0000000404720160

ROR: https://ror.org/027arzy69

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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

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To

Abstract

Journal

Salvage total glossectomy and total glosso-laryngectomy: Are they worth it? A GETTEC French multicenter study. (2022) Mazerolle P, Fuchsmann C, Schultz P, Benmoussa N, Malard O, Bozec A, Deneuve S, et al. Journal article Ultrasensitive molecular imaging of intestinal mucosal inflammation using leukocyte-mimicking particles targeted to MAdCAM-1 in mice (2020) Fournier AP, De Lizarrondo SM, Rateau A, Gerard-Brisou A, Waldner M, Neurath M, Vivien D, et al. Journal article Mutations in the BAF-complex subunit DPF2 are associated with Coffin-Siris syndrome (2019) Vasileiou G, Vergarajauregui S, Endele S, Popp B, Büttner C, Ekici AB, Gerard M, et al. Conference contribution A Phase 2 Study of Galunisertib (TGF-beta 1 Receptor Type I Inhibitor) and Sorafenib in Patients With Advanced Hepatocellular Carcinoma (2019) Kelley RK, Gane E, Assenat E, Galle PR, Merle P, Hourmand IO, Cleverly A, et al. Journal article BRAF inhibitor treatment in hairy cell leukemia: a long-term follow up study (2019) Liebers N, Roider T, Bohn JP, Pircher A, Ferstl B, Ebnoether M, Perker M, et al. Conference contribution BRAF inhibitor treatment in classic hairy cell leukemia: a long-term follow-up study of patients treated outside clinical trials (2019) Liebers N, Roider T, Bohn JP, Haberbosch I, Pircher A, Ferstl B, Ebnöther M, et al. Journal article Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris Syndrome (2018) Vasileiou G, Vergarajauregui S, Endele S, Popp B, Büttner C, Ekici AB, Gerard M, et al. Journal article Association of Cerebral Amyloid-? Aggregation With Cognitive Functioning in Persons Without Dementia (2018) Jansen WJ, Ossenkoppele R, Tijms BM, Fagan AM, Hansson O, Klunk WE, Van Der Flier WM, et al. Journal article PDE3A mutations cause autosomal dominant hypertension with brachydactyly (2015) Maass PG, Aydin A, Luft FC, Schaechterle C, Weise A, Stricker S, Lindschau C, et al. Journal article Hereditary myopathy with early respiratory failure: occurrence in various populations (2014) Palmio J, Evila A, Chapon F, Tasca G, Xiang F, Bradvik B, Eymard B, et al. Journal article