日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Localized chromophobe carcinomas treated by nephron-sparing surgery have excellent oncologic outcomes

采用保留肾单位手术治疗的局限性嫌色细胞癌具有极佳的肿瘤学疗效。

Bigot, Pierre; Bernhard, Jean-Christophe; Flamand, Vincent; Gill, Inderbir; Verhoest, Grégory; Beauval, Jean Baptiste; Nouhaud, François Xavier; Suer, Evren; Ploussard, Guillaume; Hetet, Jean François; Rigaud, Jérôme; Baco, Eduard; Larré, Stéphane; Sebe, Philippe; Koutlidis, Nicolas; Descazeaud, Aurélien; Eto, Masatoshi; Doerfler, Arnaud; Roupret, Morgan; Vuong, Nam Son; Reix, Boris; Matsugasumi, Toru; Bakri, Adnan El; Albiges, Laurence; Soulié, Michel; Patard, Jean-Jacques; Méjean, Arnaud; Bensalah, Karim

The subclassification of papillary renal cell carcinoma does not affect oncological outcomes after nephron sparing surgery

乳头状肾细胞癌的亚型分类并不影响肾单位保留手术后的肿瘤学预后。

Bigot, Pierre; Bernhard, Jean-Christophe; Gill, Inderbir S; Vuong, Nam Son; Verhoest, Grégory; Flamand, Vincent; Reix, Boris; Suer, Evren; Gökce, Ilker; Beauval, Jean Baptiste; Nouhaud, François Xavier; Eto, Masatoshi; Baco, Eduard; Matsugasumi, Toru; Chowaniec, Yvonne; Rigaud, Jérôme; Lenormand, Claire; Pfister, Christian; Hetet, Jean François; Ploussard, Guillaume; Roupret, Morgan; Léon, Priscilla; Bakri, Adnan El; Larré, Stéphane; Tillou, Xavier; Doerfler, Arnaud; Descazeaud, Aurélien; Koutlidis, Nicolas; Schneider, Alexandre; Sebe, Philippe; Ingels, Alexandre; Azzouzi, Abdel Rahmène; Soulié, Michel; Méjean, Arnaud; Bensalah, Karim; Patard, Jean-Jacques

Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemia

SLC25A38错义变异在常染色体隐性遗传性铁粒幼细胞性贫血中起着重要作用

Kannengiesser, Caroline; Sanchez, Mayka; Sweeney, Marion; Hetet, Gilles; Kerr, Briedgeen; Moran, Erica; Fuster Soler, Jose L; Maloum, Karim; Matthes, Thomas; Oudot, Caroline; Lascaux, Axelle; Pondarré, Corinne; Sevilla Navarro, Julian; Vidyatilake, Sudharma; Beaumont, Carole; Grandchamp, Bernard; May, Alison

A new missense mutation in the L ferritin coding sequence associated with elevated levels of glycosylated ferritin in serum and absence of iron overload

铁蛋白编码序列中发现一种新的错义突变,该突变与血清中糖基化铁蛋白水平升高和无铁过载相关。

Kannengiesser, Caroline; Jouanolle, Anne-Marie; Hetet, Gilles; Mosser, Annick; Muzeau, Françoise; Henry, Dominique; Bardou-Jacquet, Edouard; Mornet, Martine; Brissot, Pierre; Deugnier, Yves; Grandchamp, Bernard; Beaumont, Carole

Wild-type and mutant ferroportins do not form oligomers in transfected cells

野生型和突变型铁转运蛋白在转染细胞中均不形成寡聚体。

Gonçalves, Ana Sofia; Muzeau, Françoise; Blaybel, Rand; Hetet, Gilles; Driss, Fathi; Delaby, Constance; Canonne-Hergaux, François; Beaumont, Carole

Idiopathic dilated cardiomyopathy: lack of association with haemochromatosis gene in the CARDIGENE study

特发性扩张型心肌病:CARDIGENE 研究中未发现与血色素沉着症基因存在关联

G Hetet, B Grandchamp, C Bouchier, V Nicaud, L Tiret, G Roizès, M Desnos, K Schwartz, R Dorent, M Komajda; CARDIGENE Group

Identification of four novel PMM2 mutations in congenital disorders of glycosylation (CDG) Ia French patients

在法国先天性糖基化障碍 (CDG) Ia 患者中鉴定出四种新的 PMM2 突变

Vuillaumier-Barrot, S; Hetet, G; Barnier, A; Dupré, T; Cuer, M; de Lonlay, P; Cormier-Daire, V; Durand, G; Grandchamp, B; Seta, N