Nurputra DK - Search Results

1

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

Hidayat SN, Julian T, Dharmawan AB, Puspita M, Chandra L, Rohman A, Julia M, Rianjanu A, Nurputra DK, Triyana K, Wasisto HS. Hidayat SN, et al. Among authors: nurputra dk. Artif Intell Med. 2022 Jul;129:102323. doi: 10.1016/j.artmed.2022.102323. Epub 2022 May 17. Artif Intell Med. 2022. PMID: 35659391 Free PMC article.

2

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

Nurputra DK, Kusumaatmaja A, Hakim MS, Hidayat SN, Julian T, Sumanto B, Mahendradhata Y, Saktiawati AMI, Wasisto HS, Triyana K. Nurputra DK, et al. NPJ Digit Med. 2022 Aug 16;5(1):115. doi: 10.1038/s41746-022-00661-2. NPJ Digit Med. 2022. PMID: 35974062 Free PMC article.

3

Dried Blood Spot Screening System for Spinal Muscular Atrophy with Allele-Specific Polymerase Chain Reaction and Melting Peak Analysis.

Wijaya YOS, Nishio H, Niba ETE, Shiroshita T, Kato M, Bouike Y, Tode C, Ar Rochmah M, Harahap NIF, Nurputra DK, Okamoto K, Saito T, Takeuchi A, Lai PS, Yamaguchi S, Shinohara M. Wijaya YOS, et al. Among authors: nurputra dk. Genet Test Mol Biomarkers. 2021 Apr;25(4):293-301. doi: 10.1089/gtmb.2020.0312. Genet Test Mol Biomarkers. 2021. PMID: 33877896

4

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

Setyaningrum CTS, Harahap ISK, Nurputra DK, Rachman IT, Harahap NIF. Setyaningrum CTS, et al. Among authors: nurputra dk. J Med Case Rep. 2022 Jan 16;16(1):14. doi: 10.1186/s13256-021-03226-1. J Med Case Rep. 2022. PMID: 35033190 Free PMC article.

5

Clinical characterizations of three adults with genetically confirmed spinal muscular atrophy: a case series.

Setyaningrum CTS, Harahap ISK, Nurputra DK, Ar Rochmah M, Sadewa AH, Alkarani GH, Harahap NIF. Setyaningrum CTS, et al. Among authors: nurputra dk. J Med Case Rep. 2022 Nov 15;16(1):435. doi: 10.1186/s13256-022-03633-y. J Med Case Rep. 2022. PMID: 36376972 Free PMC article.

6

The analysis of DMD gene deletions by multiplex PCR in Indonesian DMD/BMD patients: the era of personalized medicine.

Iskandar K, Dwianingsih EK, Pratiwi L, Kalim AS, Mardhiah H, Putranti AH, Nurputra DK, Triono A, Herini ES, Malueka RG, Gunadi, Lai PS, Sunartini. Iskandar K, et al. Among authors: nurputra dk. BMC Res Notes. 2019 Oct 28;12(1):704. doi: 10.1186/s13104-019-4730-1. BMC Res Notes. 2019. PMID: 31661024 Free PMC article.

7

[No title available]

[No authors listed] [No authors listed] PMID: 33561069

8

Paramyotonia congenita: from clinical diagnosis to in silico protein modeling analysis.

Nurputra DK, Nakagawa T, Takeshima Y, Harahap IS, Morikawa S, Sakaeda T, Lai PS, Matsuo M, Takaoka Y, Nishio H. Nurputra DK, et al. Pediatr Int. 2012 Oct;54(5):602-12. doi: 10.1111/j.1442-200X.2012.03646.x. Epub 2012 Jul 10. Pediatr Int. 2012. PMID: 22507243

9

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

Thursina C, Nurputra DK, Harahap ISK, Harahap NIF, Sa'adah N, Wibowo S, Sutarni S, Sadewa AH, Hanjaya H, Nishio H. Thursina C, et al. Among authors: nurputra dk. Neurol Int. 2020 Jul 10;12(1):8292. doi: 10.4081/ni.2020.8292. eCollection 2020 Jul 10. Neurol Int. 2020. PMID: 32774820 Free PMC article.

10

Valproic acid increases SMN2 expression and modulates SF2/ASF and hnRNPA1 expression in SMA fibroblast cell lines.

Harahap IS, Saito T, San LP, Sasaki N, Gunadi, Nurputra DK, Yusoff S, Yamamoto T, Morikawa S, Nishimura N, Lee MJ, Takeshima Y, Matsuo M, Nishio H. Harahap IS, et al. Among authors: nurputra dk. Brain Dev. 2012 Mar;34(3):213-22. doi: 10.1016/j.braindev.2011.04.010. Epub 2011 May 11. Brain Dev. 2012. PMID: 21561730

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