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

Ultrasound Super-Resolution Imaging of Neonatal Cerebral Vascular Reorganization

新生儿脑血管重组的超声超分辨率成像

Schwarz, Simone; Denis, Louise; Nedoschill, Emmanuel; Buehler, Adrian; Danko, Vera; Hilger, Alina C; Brevis Nuñez, Francisco; Dürr, Nikola R; Schlunz-Hendann, Martin; Brassel, Friedhelm; Felderhoff-Müser, Ursula; Reutter, Heiko; Woelfle, Joachim; Jüngert, Jörg; Dohna-Schwake, Christian; Bruns, Nora; Regensburger, Adrian P; Couture, Olivier; Mandelbaum, Henriette; Knieling, Ferdinand

Neonatal Long-Chain 3-Ketoacyl-CoA Thiolase deficiency: Clinical-biochemical phenotype, sodium-D,L-3-hydroxybutyrate treatment experience and cardiac evaluation using speckle echocardiography

新生儿长链 3-酮脂酰辅酶 A 硫解酶缺乏症:临床生化表型、D、L-3-羟基丁酸钠治疗经验及斑点超声心动图心脏评估

Annemarijne R J Veenvliet, Mark R Garrelfs, Floris E A Udink Ten Cate, Sacha Ferdinandusse, Simone Denis, Sabine A Fuchs, Marit Schwantje, Rosa Geurtzen, Annemiek M J van Wegberg, Marleen C D G Huigen, Leo A J Kluijtmans, Ronald J A Wanders, Terry G J Derks, Lonneke de Boer, Riekelt H Houtkooper, Ma

Cardiolipin-induced activation of pyruvate dehydrogenase links mitochondrial lipid biosynthesis to TCA cycle function

心磷脂诱导的丙酮酸脱氢酶激活将线粒体脂质生物合成与 TCA 循环功能联系起来

Yiran Li, Wenjia Lou, Vaishnavi Raja, Simone Denis, Wenxi Yu, Michael W Schmidtke, Christian A Reynolds, Michael Schlame, Riekelt H Houtkooper, Miriam L Greenberg

A novel case of ACOX2 deficiency leads to recognition of a third human peroxisomal acyl-CoA oxidase

ACOX2 缺乏症的新病例导致对第三种人类过氧化物酶体酰基辅酶 A 氧化酶的识别

Sacha Ferdinandusse, Simone Denis, Carlo W T van Roermund, Mary Anne Preece, Janet Koster, Merel S Ebberink, Hans R Waterham, Ronald J A Wanders

Mannose-binding lectin is required for the effective clearance of apoptotic cells by adipose tissue macrophages during obesity

甘露糖结合凝集素是肥胖过程中脂肪组织巨噬细胞有效清除凋亡细胞所必需的

Rinke Stienstra, Wieneke Dijk, Lianne van Beek, Henry Jansen, Mattijs Heemskerk, Riekelt H Houtkooper, Simone Denis, Vanessa van Harmelen, Ko Willems van Dijk, Cees J Tack, Sander Kersten

Genetic basis of hyperlysinemia

高赖氨酸血症的遗传基础

Sander M Houten, Heleen Te Brinke, Simone Denis, Jos Pn Ruiter, Alida C Knegt, Johannis Bc de Klerk, Persephone Augoustides-Savvopoulou, Johannes Häberle, Matthias R Baumgartner, Turgay Coşkun, Johannes Zschocke, Jörn Oliver Sass, Bwee Tien Poll-The, Ronald Ja Wanders, Marinus Duran