Results 1-3 of 3 (Search time: 0.014 seconds).
Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link | |
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1 | 2020 | AKR1D1 and CYP7B1 mutations in patients with inborn errors of bile acid metabolism: Possibly underdiagnosed diseases | Chen J.-Y.; JIA-FENG WU ; Kimura A.; Nittono H.; Liou B.-Y.; Lee C.-S.; HO-SHENG CHEN ; YU-CHUN CHIU ; YEN-HSUAN NI ; STEVEN SHINN-FORNG PENG ; WANG-TSO LEE ; I-JUNG TSAI ; MEI-HWEI CHANG ; HUEY-LING CHEN | Pediatrics and Neonatology | 13 | 10 | |
2 | 2012 | A novel 3670-base pair mitochondrial DNA deletion resulting in multi-systemic manifestations in a child | Liu H.-M.; Tsai L.-P.; YIN-HSIU CHIEN ; JIA-FENG WU ; WEN-CHIN WENG ; STEVEN SHINN-FORNG PENG ; EN-TING WU ; PEI-HSIN HUANG ; WANG-TSO LEE ; I-JUNG TSAI ; WUH-LIANG HWU ; NI-CHUNG LEE | Pediatrics and Neonatology | 10 | 9 | |
3 | 2003 | Neurofibromatosis Type I and Intestinal Neuronal Dysplasia Type B in a Child: Report of One Case | JIA-FENG WU ; HUEY-LING CHEN ; STEVEN SHINN-FORNG PENG ; Yu T.-W.; WANG-TSO LEE ; MEI-HWEI CHANG | Acta Paediatrica Taiwanica | 4 | 0 |