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Molecular and Cellular Pediatrics

IF
论文数42
被引数
期刊论文 42
发表时间
Caffeine citrate increases ciliary beat frequency in human respiratory epithelial cells枸橼酸咖啡因增加人呼吸道上皮细胞的纤毛摆动频率
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deleteCindric, Sandra; Bodenbeck, Laura; Hjeij, Rim; Loges, Niki Tomas; Edelbusch, Christine; George, Sebastian; Pennekamp, Petra; Rieger-Fackeldey, Esther; Omran, Heymut
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Preventive application of lung growth factors and lack of attenuation of phenotype disruption of lung resident MSC from preterm infants by hyperoxia预防性应用肺生长因子及高氧未能减轻早产儿肺驻留间充质干细胞的表型破坏
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deleteHolzfurtner, Lena; Behnke, Judith; Korte, Pauline; Goetz, Maurizio J.; Petzinger, Jutta; Windhorst, Anita C.; Shahzad, Tayyab; Rivetti, Stefano; Dong, Ying; Bellusci, Saverio; Ehrhardt, Harald
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Sex differences in the long-term tolerability of BNT162b2 in children and adolescentsBNT162b2在儿童和青少年中长期耐受性的性别差异
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deleteMoor, Jeanne; Grieshaber, Vivien; Toepfner, Nicole; Holzwarth, Sarah; Moor, Matthias B.; Kublickiene, Karolina; Strumann, Christoph; Chao, Cho-Ming
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Priming innate immunity and long-term outcome先天免疫的预激活与长期预后
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deletePradler, Victoria; Wright, Clyde J.; Kazemi-Butterfield, Nazanin; Glaser, Kirsten
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LEF1 gene mutation impairs the intestinal barrier and causes diarrheaLEF1基因突变损害肠道屏障并导致腹泻
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deleteJie, Jianan; Qiu, Mengling; Liu, Xing; Zhang, Qingqing; Xie, Jing; Geng, Lanlan; Gong, Sitang; Cheng, Yang
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Phenocopies of 22q11.2DS: revealing genetic diversity in clinically suspected 22q11.2 deletion syndrome22q11.2DS的表型复制:揭示临床疑似22q11.2缺失综合征中的遗传多样性
delete2026-04-30
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deleteSzumutku, Fanni; Lengyel, Anna; Pinti, Eva; Kun, Ilona; Nemeth, Krisztina; Abonyi, Tunde; Gal, Fanni; Ryu, Seung Woo; Song, Yongjun; Ujfalusi, Aniko; Kadar, Krisztina; Javorszky, Eszter; Tory, Kalman; Kis, Eva; Goda, Vera; Krivan, Gergely; Kovacs, Arpad Ferenc; Haltrich, Iren
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Protein-truncating variants in APBA1 in minors with severe, early-onset obesity: implications for genetic testingAPBA1基因中的蛋白质截断变异在重度、早发性肥胖的少数民族中的发现:对遗传检测的启示
delete2026-04-22
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deleteLerner, Joanna; Moawia, Abubakar; Zorn, Stefanie; Kloker, Simone; Klehr-Martinelli, Margit; Winner, Kay; Penfold, Denisa; Volkl, Thomas M. K.; Krausnick, Miriam; Siebert, Reiner; Wabitsch, Martin
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Diagnoses of double heterozygous NF1 variants and dual RASopathy双重杂合NF1变异和双重RASopathy的诊断
delete2026-04-15
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deleteAngelova-Toshkina, Daniela; Schanze, Denny; Vaassen, Pia; Fruhwald, Michael C.; Rosenbaum, Thorsten; Zenker, Martin; Kuhlen, Michaela
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Efficacy of azacitidine and trametinib against leptomeningeal melanosis associated with congenital melanocytic nevus syndrome阿扎胞苷和曲美替尼对先天性黑色素细胞痣综合征相关软脑膜黑色素沉着症的治疗效果
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deleteRaljevic, Lina; Komlosi, Katalin; Feige, Ursula; Eckenweiler, Matthias; Lassmann, Silke; Jrad, Haroun Bel Hadj; Werner, Martin; Fischer, Judith; Has, Cristina; Feuchtinger, Tobias; Uhl, Markus; Niemeyer, Charlotte M.; Hettmer, Simone
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Phenotypic variability in female individuals with the NAA10 missense variants p.(L126R), p.(L126V), or p.(F128L) leading to NAA10-related syndrome携带NAA10错义变异p.(L126R)、p.(L126V)或p.(F128L)的女性个体中与NAA10相关综合征相关的表型变异
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deleteBuhler, Anja; Aigner-Radakovics, Katharina; Diofano, Federica; Marchi, Elaine; Weinmann-Emhardt, Karolina; Paquay, Amina; Lilja, Stephanie V.; Rosensteiner, Bernhard; Harpell, Randie; Bernard, Ewelina; Just, Steffen; Bittner, Reginald E.; Lyon, Gholson J.; Kustermann, Monika
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Retrospective screening for congenital cytomegalovirus infection in the Survey of Neonates in Pomerania shows very low disease burden对波美拉尼亚新生儿调查中先天性巨细胞病毒感染的回顾性筛查显示疾病负担极低
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deleteBaier, Jan; Konrad, Chiara; Groffmann, Maximilian; Ittermann, Till; Allenberg, Heike; Asmus, Maria; Ihler, Friedrich; Busch, Chia-Jung; Lehmann, Kathrin; Becker, Karsten; Lange, Anja; Heckmann, Matthias
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Sepsis profile among preterm infants with enterostomy and fecal transfer: a multicenter retrospective cohort study早产儿肠造口术与粪便移植患者的脓毒症特征:一项多中心回顾性队列研究
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deleteAl-Kudsi, Zeina; Wieg, Christian; Fortmann, Mats Ingmar; Faust, Kirstin; Herting, Egbert; Linnemann, Knud; Weller, Ursula; Potratz, Jenny; Gopel, Wolfgang; Humberg, Alexander
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Risk factors and outcomes of delayed completion of the hexavalent 3+1 immunisation series in German preterm infants - an observational study德国早产儿六价3+1免疫接种系列延迟完成的风险因素及结局:一项观察性研究
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deleteKraft, Hannah; Dammann, Marie-Theres; Hanke, Kathrin; Zemlin, Michael; Wenglein, Janina Soler; Rohde, Jule; Lasserre, Desiree; Humberg, Alexander; Roll, Claudia; Hartel, Christoph; Rupp, Jan; Brinkmann, Folke; Pirr, Sabine; Jensen, Reinhard; Odendahl, Rainer; Ahrens, Peter; Silwedel, Christine; Liese, Johannes; Gopel, Wolfgang; Herting, Egbert; Stichtenoth, Guido; Fortmann, Ingmar
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Next-generation sequencing of cell-free microbial DNA in blood samples of critically ill children: a single-center experience血液样本中细胞外微生物DNA的下一代测序研究:一项单中心经验
delete2026-04-08
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deleteAdolph, Jonas E.; Pentek, Christina; Bauch, Thomas; Held, Clara; Brenner, Thorsten; Felderhoff-Muser, Ursula; Grumaz, Silke; Horvatek, Petra; Steindor, Mathis; Asar, Lucia; Voigt, Sebastian; Dziobaka, Jan; Dohna-Schwake, Christian; Goretzki, Sarah C.
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