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

Personalized Genotype-Based Approach for Treatment of Phenylketonuria

基于基因型的个性化苯丙酮尿症治疗方法

Gundorova, Polina; Yousefi, Behnam; Woidy, Mathias; Rose-Heine, Malcolm Summer; Khatri, Robin; Kasten, Viviane; Bonn, Stefan; Muntau, Ania Carolina; Gersting, Soeren Waldemar

Successful Pregnancy Management of a Woman With Severe Methylmalonic Acidemia

成功管理一名患有严重甲基丙二酸血症的女性的妊娠

Woidy, M; Tsiakas, K; Mahmud, M; Eich, G; Loos, S; Lisfeld, J; Schultz, S; Tallarek, A C; Hecher, K; Huber, T B; Muntau, A C; Gramer, G

Accumulation of α-synuclein mediates podocyte injury in Fabry nephropathy

α-突触核蛋白的积累介导法布里肾病中的足细胞损伤

Fabian Braun, Ahmed Abed, Dominik Sellung, Manuel Rogg, Mathias Woidy, Oysten Eikrem, Nicola Wanner, Jessica Gambardella, Sandra D Laufer, Fabian Haas, Milagros N Wong, Bernhard Dumoulin, Paula Rischke, Anne Mühlig, Wiebke Sachs, Katharina von Cossel, Kristina Schulz, Nicole Muschol, Sören W Gerstin

Long-Term Antibody Response to SARS-CoV-2 in Children

儿童对SARS-CoV-2的长期抗体反应

Dunay, Gabor A; Barroso, Madalena; Woidy, Mathias; Danecka, Marta K; Engels, Geraldine; Hermann, Katharina; Neumann, Friederike S; Paul, Kevin; Beime, Jan; Escherich, Gabriele; Fehse, Kristin; Grinstein, Lev; Haniel, Franziska; Haupt, Luka J; Hecher, Laura; Kehl, Torben; Kemen, Christoph; Kemper, Markus J; Kobbe, Robin; Kohl, Aloisa; Klokow, Thomas; Nörz, Dominik; Olfe, Jakob; Schlenker, Friderike; Schmiesing, Jessica; Schrum, Johanna; Sibbertsen, Freya; Stock, Philippe; Tiede, Stephan; Vettorazzi, Eik; Zazara, Dimitra E; Zapf, Antonia; Lütgehetmann, Marc; Oh, Jun; Mir, Thomas S; Muntau, Ania C; Gersting, Søren W

Specific CD4+ T Cell Responses to Ancestral SARS-CoV-2 in Children Increase With Age and Show Cross-Reactivity to Beta Variant

儿童对祖先 SARS-CoV-2 的特异性 CD4+ T 细胞反应随年龄增长而增加,并与 β 变体表现出交叉反应

Kevin Paul, Freya Sibbertsen, Daniela Weiskopf, Marc Lütgehetmann, Madalena Barroso, Marta K Danecka, Laura Glau, Laura Hecher, Katharina Hermann, Aloisa Kohl, Jun Oh, Julian Schulze Zur Wiesch, Alessandro Sette, Eva Tolosa, Eik Vettorazzi, Mathias Woidy, Antonia Zapf, Dimitra E Zazara, Thomas S Mir

Production of sealed rod sources made from epoxy resin for the Saint-Petersburg brick phantom for the calibration of whole-body counters

生产用于圣彼得堡砖形体模型的环氧树脂密封棒状光源,该模型用于校准全身计数器

Woidy, Patrick; Meisenberg, Oliver

Dominant KPNA3 Mutations Cause Infantile-Onset Hereditary Spastic Paraplegia

KPNA3 显性突变导致婴儿发病的遗传性痉挛性截瘫

Claudia Schob, Maja Hempel, Dana Safka Brozkova, Huafang Jiang, Soo Yeon Kim, Nurit Assia Batzir, Naama Orenstein, Tatjana Bierhals, Jessika Johannsen, Anna Uhrova Meszarosova, Jong-Hee Chae, Pavel Seeman, Mathias Woidy, Fang Fang, Christian Kubisch, Stefan Kindler, Jonas Denecke

Edgetic Perturbations Contribute to Phenotypic Variability in PEX26 Deficiency

边缘扰动导致 PEX26 缺陷的表型变异

Lotz-Havla, Amelie S; Woidy, Mathias; Guder, Philipp; Schmiesing, Jessica; Erdmann, Ralf; Waterham, Hans R; Muntau, Ania C; Gersting, Søren W

Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder

双等位基因 MADD 变异可导致一系列表型,从发育迟缓到多系统疾病

Pauline E Schneeberger, Fanny Kortüm, Georg Christoph Korenke, Malik Alawi, René Santer, Mathias Woidy, Daniela Buhas, Stephanie Fox, Jane Juusola, Majid Alfadhel, Bryn D Webb, Emanuele G Coci, Rami Abou Jamra, Manuela Siekmeyer, Saskia Biskup, Corina Heller, Esther M Maier, Poupak Javaher-Haghighi,

Inborn errors of metabolism and the human interactome: a systems medicine approach

先天性代谢缺陷与人类相互作用组:系统医学方法

Woidy, Mathias; Muntau, Ania C; Gersting, Søren W