Chen PJ - Search Results

1

Application of massively parallel sequencing to genetic diagnosis in multiplex families with idiopathic sensorineural hearing impairment.

Wu CC, Lin YH, Lu YC, Chen PJ, Yang WS, Hsu CJ, Chen PL. Wu CC, et al. Among authors: chen pl, chen pj. PLoS One. 2013;8(2):e57369. doi: 10.1371/journal.pone.0057369. Epub 2013 Feb 22. PLoS One. 2013. PMID: 23451214 Free PMC article.

2

Chromosomal changes and clonality relationship between primary and recurrent hepatocellular carcinoma.

Chen YJ, Yeh SH, Chen JT, Wu CC, Hsu MT, Tsai SF, Chen PJ, Lin CH. Chen YJ, et al. Among authors: chen jt, chen pj. Gastroenterology. 2000 Aug;119(2):431-40. doi: 10.1053/gast.2000.9373. Gastroenterology. 2000. PMID: 10930378

3

Common clinical features of children with enlarged vestibular aqueduct and Mondini dysplasia.

Wu CC, Chen YS, Chen PJ, Hsu CJ. Wu CC, et al. Among authors: chen ys, chen pj. Laryngoscope. 2005 Jan;115(1):132-7. doi: 10.1097/01.mlg.0000150691.85387.3f. Laryngoscope. 2005. PMID: 15630381

4

Specificity of SLC26A4 mutations in the pathogenesis of inner ear malformations.

Wu CC, Chen PJ, Hsu CJ. Wu CC, et al. Among authors: chen pj. Audiol Neurootol. 2005 Jul-Aug;10(4):234-42. doi: 10.1159/000085825. Epub 2005 May 18. Audiol Neurootol. 2005. PMID: 15905611

5

Prevalent SLC26A4 mutations in patients with enlarged vestibular aqueduct and/or Mondini dysplasia: a unique spectrum of mutations in Taiwan, including a frequent founder mutation.

Wu CC, Yeh TH, Chen PJ, Hsu CJ. Wu CC, et al. Among authors: chen pj. Laryngoscope. 2005 Jun;115(6):1060-4. doi: 10.1097/01.MLG.0000163339.61909.D0. Laryngoscope. 2005. PMID: 15933521

6

Serum adiponectin correlates with viral characteristics but not histologic features in patients with chronic hepatitis C.

Liu CJ, Chen PJ, Jeng YM, Huang WL, Yang WS, Lai MY, Kao JH, Chen DS. Liu CJ, et al. Among authors: chen ds, chen pj. J Hepatol. 2005 Aug;43(2):235-42. doi: 10.1016/j.jhep.2005.02.044. J Hepatol. 2005. PMID: 15964656

7

Adiponectin levels among patients with chronic hepatitis B and C infections and in response to IFN-alpha therapy.

Lu JY, Chuang LM, Yang WS, Tai TY, Lai MY, Chen PJ, Kao JH, Lee CZ, Lee HS. Lu JY, et al. Among authors: chen pj. Liver Int. 2005 Aug;25(4):752-9. doi: 10.1111/j.1478-3231.2005.1007.x. Liver Int. 2005. PMID: 15998426 Clinical Trial.

8

Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families.

Wu CC, Chiu YH, Chen PJ, Hsu CJ. Wu CC, et al. Among authors: chen pj. Ear Hear. 2007 Jun;28(3):332-42. doi: 10.1097/AUD.0b013e318047941e. Ear Hear. 2007. PMID: 17485982

9

Prospective mutation screening of three common deafness genes in a large Taiwanese Cohort with idiopathic bilateral sensorineural hearing impairment reveals a difference in the results between families from hospitals and those from rehabilitation facilities.

Wu CC, Chen PJ, Chiu YH, Lu YC, Wu MC, Hsu CJ. Wu CC, et al. Among authors: chen pj. Audiol Neurootol. 2008;13(3):172-81. doi: 10.1159/000112425. Epub 2007 Dec 13. Audiol Neurootol. 2008. PMID: 18075246

10

Predominance of genetic diagnosis and imaging results as predictors in determining the speech perception performance outcome after cochlear implantation in children.

Wu CC, Lee YC, Chen PJ, Hsu CJ. Wu CC, et al. Among authors: chen pj. Arch Pediatr Adolesc Med. 2008 Mar;162(3):269-76. doi: 10.1001/archpediatrics.2007.59. Arch Pediatr Adolesc Med. 2008. PMID: 18316665

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