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Automated evaluation with deep learning of total interstitial inflammation and peritubular capillaritis on kidney biopsies.
Published in:
Nephrology Dialysis Transplantation, 2023, v. 38, n. 12, p. 2786, doi. 10.1093/ndt/gfad094
By:
- Jacq, Amélie;
- Tarris, Georges;
- Jaugey, Adrien;
- Paindavoine, Michel;
- Maréchal, Elise;
- Bard, Patrick;
- Rebibou, Jean-Michel;
- Ansart, Manon;
- Calmo, Doris;
- Bamoulid, Jamal;
- Tinel, Claire;
- Ducloux, Didier;
- Crepin, Thomas;
- Chabannes, Melchior;
- Vega, Mathilde Funes de la;
- Felix, Sophie;
- Martin, Laurent;
- Legendre, Mathieu
Publication type:
Article
Deep learning automation of MEST-C classification in IgA nephropathy.
Published in:
Nephrology Dialysis Transplantation, 2023, v. 38, n. 7, p. 1741, doi. 10.1093/ndt/gfad039
By:
- Jaugey, Adrien;
- Maréchal, Elise;
- Tarris, Georges;
- Paindavoine, Michel;
- Martin, Laurent;
- Chabannes, Melchior;
- Vega, Mathilde Funes de la;
- Chaintreuil, Mélanie;
- Robier, Coline;
- Ducloux, Didier;
- Crépin, Thomas;
- Felix, Sophie;
- Jacq, Amélie;
- Calmo, Doris;
- Tinel, Claire;
- Zanetta, Gilbert;
- Rebibou, Jean-Michel;
- Legendre, Mathieu
Publication type:
Article
Dramatic Efficacy of Interferon and Vemurafenib on Psychiatric Symptoms Revealing BRAF<sup>V600E</sup>Mutated Erdheim-Chester Disease: A Case Report.
Published in:
2022
By:
- Razanamahery, Jérôme;
- Abdallahoui, Maroua;
- Chabridon, Guillaume;
- Fromont, Agnès;
- Tarris, Georges;
- Idbaih, Ahmed;
- Comby, Pierre Olivier;
- Godard, Francois;
- Haroche, Julien;
- Audia, Sylvain;
- Bonnotte, Bernard
Publication type:
Case Study
Cardiomyopathy due to PRDM16 mutation: First description of a fetal presentation, with possible modifier genes.
Published in:
American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2020, v. 184, n. 1, p. 129, doi. 10.1002/ajmg.c.31766
By:
- Delplancq, Geoffroy;
- Tarris, Georges;
- Vitobello, Antonio;
- Nambot, Sophie;
- Sorlin, Arthur;
- Philippe, Christophe;
- Carmignac, Virginie;
- Duffourd, Yannis;
- Denis, Charlotte;
- Eicher, Jean Christophe;
- Chevarin, Martin;
- Millat, Gilles;
- Khallouk, Bouchra;
- Rousseau, Thierry;
- Falcon‐Eicher, Sylvie;
- Vasiljevic, Alexandre;
- Harizay, Fara T.;
- Thauvin‐Robinet, Christel;
- Faivre, Laurence;
- Kuentz, Paul
Publication type:
Article
Epidemiological Impact of GII.17 Human Noroviruses Associated With Attachment to Enterocytes.
Published in:
Frontiers in Microbiology, 2022, v. 13, p. 1, doi. 10.3389/fmicb.2022.858245
By:
- Estienney, Marie;
- Tarris, Georges;
- Abou-Hamad, Nicole;
- Rouleau, Alain;
- Boireau, Wilfrid;
- Chassagnon, Rémi;
- Ayouni, Siwar;
- Daval-Frerot, Philippe;
- Martin, Laurent;
- Bouyer, Frédéric;
- Le Pendu, Jacques;
- de Rougemont, Alexis;
- Belliot, Gael
Publication type:
Article
Temporal Artery Vascular Diseases.
Published in:
Journal of Clinical Medicine, 2022, v. 11, n. 1, p. 275, doi. 10.3390/jcm11010275
By:
- Greigert, Hélène;
- Ramon, André;
- Tarris, Georges;
- Martin, Laurent;
- Bonnotte, Bernard;
- Samson, Maxime
Publication type:
Article
Case Report: Giant insulinoma, a very rare tumor causing hypoglycemia.
Published in:
Frontiers in Endocrinology, 2023, p. 1, doi. 10.3389/fendo.2023.1125772
By:
- Tarris, Georges;
- Rouland, Alexia;
- Guillen, Kévin;
- Loffroy, Romaric;
- Lariotte, Anne-Cécile;
- Rat, Patrick;
- Bouillet, Benjamin;
- Andrianiaina, Haingo;
- Petit, Jean-Michel;
- Martin, Laurent
Publication type:
Article
Chronic kidney disease linked to SARS-CoV-2 infection: a case report.
Published in:
2021
By:
- Tarris, Georges;
- de Rougemont, Alexis;
- Estienney, Marie-Anaïs;
- Journet, Julien;
- Lariotte, Anne-Cécile;
- Aubignat, Damien;
- Rebibou, Jean-Michel;
- De La Vega, Mathilde Funes;
- Legendre, Mathieu;
- Belliot, Gael;
- Martin, Laurent
Publication type:
journal article
Recognition of intraglomerular histological features with deep learning in protocol transplant biopsies and their association with kidney function and prognosis.
Published in:
Clinical Kidney Journal, 2024, v. 17, n. 2, p. 1, doi. 10.1093/ckj/sfae019
By:
- Farhat, Imane;
- Maréchal, Elise;
- Calmo, Doris;
- Ansart, Manon;
- Paindavoine, Michel;
- Bard, Patrick;
- Tarris, Georges;
- Ducloux, Didier;
- Felix, Sophie Adrian;
- Martin, Laurent;
- Tinel, Claire;
- Gibier, Jean-Baptiste;
- Vega, Mathilde Funes de la;
- Rebibou, Jean-Michel;
- Bamoulid, Jamal;
- Legendre, Mathieu
Publication type:
Article
Heamatological malignancies in giant cell arteritis: a French population-based study.
Published in:
Rheumatology, 2021, v. 60, n. 11, p. 5408, doi. 10.1093/rheumatology/keab328
By:
- Greigert, Hélène;
- Mounier, Morgane;
- Arnould, Louis;
- Creuzot-Garcher, Catherine;
- Ramon, André;
- Martin, Laurent;
- Tarris, Georges;
- Ponnelle, Tibor;
- Audia, Sylvain;
- Bonnotte, Bernard;
- Maynadie, Marc;
- Samson, Maxime
Publication type:
Article
Sudden Infant Death Associated with Rhinovirus Infection.
Published in:
Viruses (1999-4915), 2024, v. 16, n. 4, p. 518, doi. 10.3390/v16040518
By:
- Auvray, Christelle;
- Perez-Martin, Stéphanie;
- Schuffenecker, Isabelle;
- Pitoiset, Cécile;
- Tarris, Georges;
- Ambert-Balay, Katia;
- Martin, Laurent;
- Dullier-Taillefumier, Nathalie;
- Bour, Jean-Baptiste;
- Manoha, Catherine
Publication type:
Article
Enteric Viruses and Inflammatory Bowel Disease.
Published in:
Viruses (1999-4915), 2021, v. 13, n. 1, p. 104, doi. 10.3390/v13010104
By:
- Tarris, Georges;
- de Rougemont, Alexis;
- Charkaoui, Maëva;
- Michiels, Christophe;
- Martin, Laurent;
- Belliot, Gaël;
- Guix, Susana
Publication type:
Article
Allelic heterogeneity in a patient with postzygotic MTOR‐related hypomelanosis of Ito with neurodevelopmental abnormalities.
Published in:
Clinical Genetics, 2024, v. 105, n. 5, p. 581, doi. 10.1111/cge.14511
By:
- Engel, Camille;
- Chevarin, Martin;
- Piard, Juliette;
- Abad, Marine;
- Thomas, Quentin;
- Carmignac, Virginie;
- Duffourd, Yannis;
- Lemesle‐Martin, Martine;
- Tarris, Georges;
- Thauvin‐Robinet, Christel;
- Vabres, Pierre;
- Faivre, Laurence;
- Kuentz, Paul
Publication type:
Article
Early prenatal diagnosis of causative homozygous variants in ASCC1 in a fetus with cystic hygroma and additional homozygous variants of unknown significance associated with a neurological phenotype not visible in early gestation: Dual diagnosis or not?
Published in:
Prenatal Diagnosis, 2024, v. 44, n. 3, p. 352, doi. 10.1002/pd.6519
By:
- Favier, Maud;
- Delanne, Julian;
- Gorincour, Guillaume;
- Faivre, Laurence;
- Racine, Caroline;
- Philippe, Christophe;
- Duffourd, Yannis;
- Vitobello, Antonio;
- Rousseau, Thierry;
- Martz, Olivia;
- Tarris, Georges;
- Oualiken, Camélia;
- Thauvin‐Robinet, Christel;
- Mau‐Them, Frédéric Tran
Publication type:
Article

Found: 14