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

A retrospective study on the prognostic factors and success, survival, and failure outcomes of treated endodontic-periodontal lesions

回顾性研究根管治疗后牙周病变的预后因素及治疗成功率、存活率和失败率

Wong, Ingar; Ton, An; Cassidy, Amiel J; Fozzard, Nicolette; Sharma, Lavanya Ajay; Love, Robert M; Sharma, Ajay

SATB2-associated syndrome: characterization of skeletal features and of bone fragility in a prospective cohort of 19 patients

SATB2相关综合征:一项前瞻性队列研究(纳入19例患者)中骨骼特征和骨脆性的特征分析

Mouillé, M; Rio, M; Breton, S; Piketty, M L; Afenjar, A; Amiel, J; Capri, Y; Goldenberg, A; Francannet, C; Michot, C; Mignot, C; Perrin, L; Quelin, C; Van Gils, J; Barcia, G; Pingault, V; Maruani, G; Koumakis, E; Cormier-Daire, V

Induction of Repeated Social Defeat Stress in Rats

诱导大鼠产生重复性社会挫败应激

Munshi, Soumyabrata; Ritger, Alexandra; Rosenkranz, Amiel J

Innovative image-guided CyberKnife stereotactic radiotherapy for bladder cancer

用于膀胱癌的创新型图像引导CyberKnife立体定向放射治疗

Thariat, J; Trimaud, R; Angellier, G; Caullery, M; Amiel, J; Bondiau, P-Y; Gerard, J-P

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

基于芯片的比较基因组杂交技术在综合征型自闭症谱系障碍患者中发现了高频率的隐匿性染色体重排。

Jacquemont, M-L; Sanlaville, D; Redon, R; Raoul, O; Cormier-Daire, V; Lyonnet, S; Amiel, J; Le Merrer, M; Heron, D; de Blois, M-C; Prieur, M; Vekemans, M; Carter, N P; Munnich, A; Colleaux, L; Philippe, A

Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development

胎儿期 CHD7 截断突变所致 CHARGE 综合征的表型谱与人类发育过程中的表达相关

Sanlaville, D; Etchevers, H C; Gonzales, M; Martinovic, J; Clément-Ziza, M; Delezoide, A-L; Aubry, M-C; Pelet, A; Chemouny, S; Cruaud, C; Audollent, S; Esculpavit, C; Goudefroye, G; Ozilou, C; Fredouille, C; Joye, N; Morichon-Delvallez, N; Dumez, Y; Weissenbach, J; Munnich, A; Amiel, J; Encha-Razavi, F; Lyonnet, S; Vekemans, M; Attié-Bitach, T

Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome

人类MID1基因的胚胎表达及其在奥皮茨综合征中的突变

Pinson, L; Augé, J; Audollent, S; Mattéi, G; Etchevers, H; Gigarel, N; Razavi, F; Lacombe, D; Odent, S; Le Merrer, M; Amiel, J; Munnich, A; Meroni, G; Lyonnet, S; Vekemans, M; Attié-Bitach, T

Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation

自动荧光基因分型可检测出特发性综合征性智力低下患者中10%的隐匿性亚端粒重排。

Rio, M; Molinari, F; Heuertz, S; Ozilou, C; Gosset, P; Raoul, O; Cormier-Daire, V; Amiel, J; Lyonnet, S; Le Merrer, M; Turleau, C; de Blois, M-C; Prieur, M; Romana, S; Vekemans, M; Munnich, A; Colleaux, L

Towards a suggestive facial dysmorphism in adenylosuccinate lyase deficiency?

腺苷酸琥珀酸裂解酶缺乏症是否可能伴有面部畸形?

Holder-Espinasse, M; Marie, S; Bourrouillou, G; Ceballos-Picot, I; Nassogne, M-C; Faivre, L; Amiel, J; Munnich, A; Vincent, M-F; Cormier-Daire, V

Establishment of two new human bladder carcinoma cell lines, CAL 29 and CAL 185. Comparative study of cell scattering and epithelial to mesenchyme transition induced by growth factors.

建立了两种新的人类膀胱癌细胞系,CAL 29 和 CAL 185比较研究了生长因子诱导的细胞扩散和上皮间质转化

Cattan N, Rochet N, Mazeau C, Zanghellini E, Mari B, Chauzy C, Stora de Novion H, Amiel J, Lagrange J L, Rossi B, Gioanni J