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

Severe Prenatal Presentation of Adenylosuccinate Lyase Deficiency Caused by a Synonymous ADSL Variant Inducing Aberrant Splicing

由同义ADSL变异引起的腺苷酸琥珀酸裂解酶缺乏症的严重产前表现,该变异导致异常剪接

Klapperich, Aysegül; Skopova, Vaclava; Karakaya, Mert; Velmans, Clara; Netzer, Christian; Strizek, Brigitte; Mrazova, Lenka Steiner; Zikanova, Marie

Expanding clinical spectrum of PAICS deficiency: Comprehensive analysis of two sibling cases.

PAICS 缺陷的临床谱系不断扩大:对两例同胞病例的综合分析

Weng Wen-Chin, Skopova Vaclava, Baresova Veronika, Liu Yao-Lin, Hsueh Hsueh-Wen, Chien Yin-Hsiu, Hwu Wuh-Liang, Souckova Olga, Hnizda Ales, Kmoch Stanislav, Lee Ni-Chung, Zikanova Marie

Phosphoribosylformylglycinamidine Synthase (PFAS) Deficiency: Clinical, Genetic and Metabolic Characterisation of a Novel Defect in Purine de Novo Synthesis

磷酸核糖甲酰甘氨酰胺合成酶(PFAS)缺乏症:嘌呤从头合成中一种新型缺陷的临床、遗传和代谢特征

Zikanova, Marie; Skopova, Vaclava; Stuurman, Kyra E; Baresova, Veronika; Souckova, Olga; Hnizda, Ales; Krijt, Matyas; Bleyer, Anthony J; Zeman, Jiri; Kmoch, Stanislav

Metabolites of De Novo Purine Synthesis: Metabolic Regulators and Cytotoxic Compounds

从头嘌呤合成的代谢产物:代谢调节剂和细胞毒性化合物

Souckova, Olga; Skopova, Vaclava; Baresova, Veronika; Sedlak, David; Bleyer, Anthony J; Kmoch, Stanislav; Zikanova, Marie

Adenylosuccinate lyase deficiency

腺苷酸琥珀酸裂解酶缺乏症

Jurecka, Agnieszka; Zikanova, Marie; Kmoch, Stanislav; Tylki-Szymańska, Anna