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

Ex vivo culture of human fetal gonads: manipulation of meiosis signalling by retinoic acid treatment disrupts testis development.

人类胎儿性腺的体外培养:视黄酸处理操纵减数分裂信号会破坏睾丸发育

Jørgensen A, Nielsen J E, Perlman S, Lundvall L, Mitchell R T, Juul A, Rajpert-De Meyts E

Frontotemporal dementia caused by CHMP2B mutations

由CHMP2B基因突变引起的额颞叶痴呆

Isaacs, A M; Johannsen, P; Holm, I; Nielsen, J E

Genome-wide gene expression profiling of testicular carcinoma in situ progression into overt tumours

睾丸原位癌进展为明显肿瘤的全基因组基因表达谱分析

Almstrup, K; Hoei-Hansen, C E; Nielsen, J E; Wirkner, U; Ansorge, W; Skakkebaek, N E; Rajpert-De Meyts, E; Leffers, H

Motor evoked potentials from the external anal sphincter in patients with autosomal dominant pure spastic paraplegia linked to chromosome 2p

2p染色体连锁的常染色体显性纯痉挛性截瘫患者的肛门外括约肌运动诱发电位

Jennum, P; Neerup Jensen, L; Fenger, K; Nielsen, J E; Fuglsang-Frederiksen, A; Nielsen, J E

Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study

常染色体显性纯痉挛性截瘫:一项临床、辅助临床和遗传学研究

Nielsen, J E; Krabbe, K; Jennum, P; Koefoed, P; Jensen, L N; Fenger, K; Eiberg, H; Hasholt, L; Werdelin, L; Sørensen, S A

Urodynamic evaluation of patients with autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24

对患有与 2p21-p24 染色体相关的常染色体显性纯痉挛性截瘫的患者进行尿动力学评估

Jensen, L N; Gerstenberg, T; Kallestrup, E B; Koefoed, P; Nordling, J; Nielsen, J E

Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome

遗传性血色素沉着症:一例基底神经节铁沉积伴帕金森综合征的病例

Nielsen, J E; Jensen, L N; Krabbe, K