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

Performance of cellulose-based card for direct genetic testing of spinal muscular atrophy

用于脊髓性肌萎缩症直接基因检测的纤维素基卡片的性能

Wijaya, Yogik Onky Silvana; Ar Rochmah, Mawaddah; Nurputra, Dian Kesumapramudya; Farmawati, Arta

Identification of volatile organic compound as a novel modality for cervical cancer detection

挥发性有机化合物作为一种新型宫颈癌检测方法的鉴定

Zucha, Muhammad Ary; Nurputra, Dian Kesumapramudya; Kusumanto, Ardhanu; Hidayat, Shidiq Nur; Triyana, Kuwat; Priadi, Widha Apriani; Yasmine, Nadia; Emilia, Ova

Expression of Human Myxovirus Resistance Protein 1 (MxA) in Shunt Infections

分流感染中人粘液病毒抵抗蛋白1 (MxA) 的表达

Syahputra, Reza; Nurputra, Dian Kesumapramudya; Triono, Agung; Herini, Elisabeth Siti

Development of a Mobile-Based Personal Health Record for Pediatric Attention-Deficit/Hyperactivity Disorder Management: Protocol for a Study Based on Action Research Design

开发基于移动设备的儿童注意力缺陷/多动障碍个人健康记录:基于行动研究设计的研究方案

Santoso, Dian Budi; Kristanti, Martina Sinta; Nurputra, Dian Kesumapramudya; Sutomo, Retno

Fast and noninvasive electronic nose for sniffing out COVID-19 based on exhaled breath-print recognition

基于呼出气体指纹识别技术的快速无创电子鼻,可用于检测新冠病毒。

Nurputra, Dian Kesumapramudya; Kusumaatmaja, Ahmad; Hakim, Mohamad Saifudin; Hidayat, Shidiq Nur; Julian, Trisna; Sumanto, Budi; Mahendradhata, Yodi; Saktiawati, Antonia Morita Iswari; Wasisto, Hutomo Suryo; Triyana, Kuwat

Managing pregnancy in a spinal muscular atrophy type III patient in Indonesia: a case report

印度尼西亚脊髓性肌萎缩症III型患者妊娠管理:病例报告

Setyaningrum, Cempaka Thursina Srie; Harahap, Indra Sari Kusuma; Nurputra, Dian Kesumapramudya; Rachman, Irwan Taufiqur; Harahap, Nur Imma Fatimah

Hybrid learning method based on feature clustering and scoring for enhanced COVID-19 breath analysis by an electronic nose

基于特征聚类和评分的混合学习方法,用于增强电子鼻对新冠病毒呼吸的分析。

Hidayat, Shidiq Nur; Julian, Trisna; Dharmawan, Agus Budi; Puspita, Mayumi; Chandra, Lily; Rohman, Abdul; Julia, Madarina; Rianjanu, Aditya; Nurputra, Dian Kesumapramudya; Triyana, Kuwat; Wasisto, Hutomo Suryo

Birth of spinal muscular atrophy unaffected baby from genetically at-risk parents following a pre-implantation genetic screening: A case report

父母在接受胚胎植入前遗传学筛查后,产下未患脊髓性肌萎缩症的婴儿:病例报告

Adrainus Polim, Arie; Handayani, Nining; Kesumapramudya Nurputra, Dian; Melanie Lubis, Anggia; Sirait, Batara; Jakobus, Dennis; Boediono, Arief; Sini, Ivan

Assessment of Spinal Muscular Atrophy Carrier Status by Determining SMN1 Copy Number Using Dried Blood Spots

利用干血斑测定SMN1拷贝数评估脊髓性肌萎缩症携带者状态

Wijaya, Yogik Onky Silvana; Purevsuren, Jamiyan; Harahap, Nur Imma Fatimah; Niba, Emma Tabe Eko; Bouike, Yoshihiro; Nurputra, Dian Kesumapramudya; Rochmah, Mawaddah Ar; Thursina, Cempaka; Hapsara, Sunartini; Yamaguchi, Seiji; Nishio, Hisahide; Shinohara, Masakazu

Determining the association between polymorphisms of the DAT1 and DRD4 genes with attention deficit hyperactivity disorder in children from Java Island

确定爪哇岛儿童DAT1和DRD4基因多态性与注意力缺陷多动障碍之间的关联

Thursina, Cempaka; Nurputra, Dian Kesumapramudya; Harahap, Indra Sari Kusuma; Harahap, Nur Imma Fatimah; Sa'adah, Nihayatus; Wibowo, Samekto; Sutarni, Sri; Sadewa, Ahmad Hamim; Hanjaya, Hermawan; Nishio, Hisahide