Výsledky vyhledávání

[Sporadic kidney cancer of young subjects: Study of the clinical and pathological features of a bicentric cohort]

Autor: J, Cohen, M O, Timsit, O D, Zerbib, M, Rouprêt, V, Verkarre, E, Comperat, A, Mejean, M O, Bitker

Publikováno v: Progres en urologie : journal de l'Association francaise d'urologie et de la Societe francaise d'urologie. 28(2)

The epidemiology of kidney cancer is evolving with a net increase in the incidence of renal tumors, globally, and in young people in particular.To evaluate the incidence and clinical and pathological characteristics of sporadic renal tumors in young

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f78dd69ccb2b6fed5cdc4919b8354dfc
https://pubmed.ncbi.nlm.nih.gov/29170016

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[Tubulocystic renal cell carcinoma with poorly differentiated foci]

Autor: Fanny, Derquin, S, Moreau, F, Dargent, N, Rioux Leclercq, V, Verkarre

Publikováno v: Annales de pathologie. 37(4)

Tubulocystic renal cell carcinoma is a rare tumor with an indolent behavior in the majority of cases. In contrast, tubulocystic renal cell carcinoma with poorly differentiated foci has a bad prognosis with an aggressive and metastatic behavior. We pr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::078adf2329903a72ad909604eda82546
https://pubmed.ncbi.nlm.nih.gov/28732560

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Diagnostic fortuit d’une forme rare de duplication urétérale congénitale asymptomatique en TEP/TDM : à propos d’un cas

Autor: H. Slimani, A. Chaput, P.M. David, V. Verkarre, Danielle Canioni, P. Weinmann, J. Rossignol

Publikováno v: Médecine Nucléaire. 42:160-161

Introduction Nous rapportons le cas d’un patient suivi pour un lymphome B diffus a grandes cellules (DLBCL) de localisation ORL chez qui la TEP/TDM a revele une malformation congenitale urogenitale tres rare, qui a initialement ete interpretee comm

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::72016f92e8f8d5990091f3d206adc629
https://doi.org/10.1016/j.mednuc.2018.03.072

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Le diagnostic histologique de la maladie cœliaque

Autor: N. Brousse, V. Verkarre

Publikováno v: Pathologie Biologie. 61:e13-e19

Coeliac disease is a common disease, affecting 1% of the population. Clinical manifestations are multiple. The diagnosis requires serologic testing and a duodenal biopsy that shows the characteristic findings of intraepithelial lymphocytosis, crypt h

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e9d7d5d1d3473c69070494efcf30c541
https://doi.org/10.1016/j.patbio.2011.03.003

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Chromosome 11p15 Paternal Isodisomy in Focal Forms of Neonatal Hyperinsulinism

Autor: P de Lonlay, Serge Romana, F. Jaubert, C. Werl, C. Bellanné-Chantelot, V. Verkarre, Laurence Hubert, M. le Lorch, Claire Nihoul-Fékété, Lena Damaj, Y de Keyzer, Y. Aigrain

Publikováno v: The Journal of Clinical Endocrinology & Metabolism. 93:4941-4947

Focal forms of congenital hyperinsulinism are due to a constitutional heterozygous mutation of paternal origin in the ABCC8 gene, more often than the KCNJ11 gene, located in the 11p15.1 region. This mutation is associated with the loss of the materna

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04298cf6c0065d36d3412d0900d4e287
https://doi.org/10.1210/jc.2008-0673

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[Cancer genetic screening for patient with multiple renal tumors: What is the current practice for what results?]

Autor: A, Beaugerie, V, Verkarre, F, Audenet, T, Le Guilchet, S, Hurel, S, Richard, J M, Corréas, E, Fontaine, A, Méjean, M O, Timsit

Publikováno v: Progres en urologie : journal de l'Association francaise d'urologie et de la Societe francaise d'urologie. 26(8)

To evaluate in a high volume center the practice and the performance of cancer genetic screening for patients with multiple renal tumors without a predisposition to kidney tumors known at the time of surgery.All patients treated for multiple renal tu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::cb96891389659f18e500b6a1c093ca20
https://pubmed.ncbi.nlm.nih.gov/27473786

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