Výsledky vyhledávání - "Marie Odile Joly"

Akademický článek

A case report of Muir-Torre syndrome in a woman with breast cancer and MSI-Low skin squamous cell carcinoma

Autor: Caroline Kientz, Marie-Odile Joly, Laurence Faivre, Alix Clemenson, Sophie Dalac, Côme Lepage, Caroline Chapusot, Caroline Jacquot, Renaud Schiappa, Marine Lebrun

Publikováno v: Hereditary Cancer in Clinical Practice, Vol 15, Iss 1, Pp 1-4 (2017)

Abstract Background The tumor spectrum in the Lynch syndrome is well defined, comprising an increased risk of developing colonic and extracolonic malignancies. Muir-Torre syndrome is a variant with a higher risk of skin disease. Patients have been de

Externí odkaz: https://doaj.org/article/7d02ade405f34cb29ce637ad88e533e9

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Characteristics of H3 K27M-mutant gliomas in adults

Autor: Jacques Guyotat, Véronique Bourg, Anne Jouvet, François Ducray, Fanny Burel-Vandenbos, Jérôme Honnorat, Fabien Forest, Alexandra Amiel-Benouaich, David Meyronet, Tanguy Fenouil, Maud Esteban-Mader, Charlotte Bonnet, Emmanuelle Uro-Coste, Cécilia Rousselot-Denis, Marie-Odile Joly

Publikováno v: Neuro-Oncology. 19:1127-1134

Background Diffuse H3 K27M-mutant gliomas occur primarily in children but can also be encountered in adults. The aim of this study was to describe the characteristics of H3 K27M-mutant gliomas in adults. Methods We analyzed the characteristics of 21

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b100e6ae55183ab519310c6393e65e06
https://doi.org/10.1093/neuonc/now274

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Type 1 serrated polyposis represents a predominantly female disease with a high prevalence of dysplastic serrated adenomas, without germline mutation in MUTYH, APC , and PTEN genes

Autor: Valérie Hervieu, Marie-Odile Joly, Thomas Walter, Jean-Christophe Saurin, Marco Petronio, Stéphane Pinson, Julien Forestier

Publikováno v: United European Gastroenterology Journal. 4:305-313

The aim of this article is to clarify the epidemiologic, clinical, endoscopic, biological and genetic characteristics of type 1 serrated polyposis patients.Consecutive patients responding to the WHO definition of type 1 serrated polyposis in one refe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeae2fd0d8fe9d768d4c2bce814ca230
https://doi.org/10.1177/2050640615594939

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The axon guidance molecule semaphorin 3F is a negative regulator of tumor progression and proliferation in ileal neuroendocrine tumors

Autor: Marie-Odile Joly, Colette Roche, Valérie Hervieu, Patrick Massoma, Thomas Walter, Nicolas Gadot, Julien Bollard, Martine Blanc, Florian Lepinasse, Christophe Couderc, Jean-Yves Scoazec, Cécile Vercherat, Gilles Poncet

Publikováno v: Oncotarget

// Julien Bollard 1, * , Patrick Massoma 1, * , Cecile Vercherat 1 , Martine Blanc 1 , Florian Lepinasse 2 , Nicolas Gadot 3 , Christophe Couderc 1 , Gilles Poncet 4 , Thomas Walter 4 , Marie-Odile Joly 1, 2, 5 , Valerie Hervieu 1, 2, 5 , Jean-Yves S

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f22db8e1cc9ed8f358a6abb4b0465a4
https://doi.org/10.18632/oncotarget.5481

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Gemcitabine and oxaliplatin or alkylating agents for neuroendocrine tumors: Comparison of efficacy and search for predictive factors guiding treatment choice

Autor: Julien Forestier, Jean-Yves Scoazec, Cécile Vercherat, Valérie Hervieu, Thomas Walter, Marie-Odile Joly, Catherine Lombard-Bohas, Anne-Sophie Dussol

Publikováno v: Cancer. 121:3428-3434

BACKGROUND The alkylating agents (ALKYs) streptozotocin, dacarbazine, and temozolomide currently are the main drugs used in systemic chemotherapy for neuroendocrine tumors (NETs). The promising activity shown by gemcitabine and oxaliplatin (GEMOX) in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::597ee7c0f8c8850b7de80fe06717b355
https://doi.org/10.1002/cncr.29517

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A case report of Muir-Torre syndrome in a woman with breast cancer and MSI-Low skin squamous cell carcinoma

Autor: Sophie Dalac, Laurence Faivre, Renaud Schiappa, Alix Clemenson, Marie-Odile Joly, Côme Lepage, Marine Lebrun, Caroline Kientz, Caroline Chapusot, Caroline Jacquot

Publikováno v: Hereditary Cancer in Clinical Practice
Hereditary Cancer in Clinical Practice, BioMed Central, 2017, 15 (1), pp.6. ⟨10.1186/s13053-017-0066-9⟩
Hereditary Cancer in Clinical Practice, BioMed Central, 2017, 15 (1), pp.6. 〈https://hccpjournal.biomedcentral.com/articles/10.1186/s13053-017-0066-9〉. 〈10.1186/s13053-017-0066-9〉
Hereditary Cancer in Clinical Practice, Vol 15, Iss 1, Pp 1-4 (2017)

IF 1.590; International audience; Background: The tumor spectrum in the Lynch syndrome is well defined, comprising an increased risk of developing colonic and extracolonic malignancies. Muir-Torre syndrome is a variant with a higher risk of skin dise

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ca8f11ddad5673a992a7190e085bef4
https://hal.archives-ouvertes.fr/hal-01541073

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Gangliocytome du cervelet chez un enfant de 11ans

Autor: Françoise Cattin, Marie Odile Joly, Alexandre Vasiljevic, Séverine Valmary-Degano, Gabriel Viennet, Anne Jouvet

Publikováno v: Annales de Pathologie. 34:477-480

Cerebellar gangliocytoma can correspond to Lhermitte-Duclos disease, a benign hamartomatous malformation encountered in young adults. It can also be a part of gangliogliomas/gangliocytomas family, which usually encompasses temporal pediatric neoplasm

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::fddc58e2f5b9f845be0ccfdb25689600
https://doi.org/10.1016/j.annpat.2014.09.008

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