Hsiao HP - Search Results

1

Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Beckwith-Wiedemann Syndrome.

Lin HY, Lee CL, Fran S, Tu RY, Chang YH, Niu DM, Chang CY, Chiu PC, Chou YY, Hsiao HP, Yang CF, Tsai MC, Chu TH, Chuang CK, Lin SP. Lin HY, et al. Among authors: hsiao hp. J Pers Med. 2021 Oct 22;11(11):1066. doi: 10.3390/jpm11111066. J Pers Med. 2021. PMID: 34834418 Free PMC article.

2

Mutations in pseudohypoparathyroidism 1a and pseudopseudohypoparathyroidism in ethnic Chinese.

Wu YL, Hwang DY, Hsiao HP, Ting WH, Huang CY, Tsai WY, Chen HC, Chao MC, Lo FS, Tsai JD, Yang S, Shih SL, Lin SP, Lin CL, Lee YJ. Wu YL, et al. Among authors: hsiao hp. PLoS One. 2014 Mar 20;9(3):e90640. doi: 10.1371/journal.pone.0090640. eCollection 2014. PLoS One. 2014. PMID: 24651309 Free PMC article.

3

Epigenotype, Genotype, and Phenotype Analysis of Taiwanese Patients with Silver-Russell Syndrome.

Lin HY, Lee CL, Fran S, Tu RY, Chang YH, Niu DM, Chang CY, Chiu PC, Chou YY, Hsiao HP, Tsai MC, Chao MC, Tsai LP, Yang CF, Su PH, Pan YW, Lee CH, Chu TH, Chuang CK, Lin SP. Lin HY, et al. Among authors: hsiao hp. J Pers Med. 2021 Nov 13;11(11):1197. doi: 10.3390/jpm11111197. J Pers Med. 2021. PMID: 34834549 Free PMC article.

4

Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Silver-Russell Syndrome.

Lin HY, Lee CL, Tu YR, Chang YH, Niu DM, Chang CY, Chiu PC, Chou YY, Hsiao HP, Tsai MC, Chao MC, Tsai LP, Yang CF, Su PH, Pan YW, Lee CH, Chu TH, Chuang CK, Lin SP. Lin HY, et al. Among authors: hsiao hp. Int J Med Sci. 2024 Jan 1;21(1):8-18. doi: 10.7150/ijms.84154. eCollection 2024. Int J Med Sci. 2024. PMID: 38164354 Free PMC article.

5

Spectrum of PHEX Mutations and FGF23 Profiles in a Taiwanese Cohort With X-Linked Hypophosphatemia Including 102 Patients.

Su PH, Yu JS, Wu YZ, Tsai YS, Lo FS, Lin JL, Chao MC, Hsu CC, Ke YY, Chiu PC, Chen JC, Huang YH, Lin SP, Chou YY, Ting WH, Wang SY, Chiu CF, Huang YC, Hsiao HP, Lin CH, Wang CH, Bau DT, Lin CY. Su PH, et al. Among authors: hsiao hp. In Vivo. 2024 Jan-Feb;38(1):341-350. doi: 10.21873/invivo.13444. In Vivo. 2024. PMID: 38148081 Free PMC article.

6

Impaired glucose homeostasis and a novel HLCS pathogenic variant in holocarboxylase synthetase deficiency: a report of two cases and brief review.

Wu HR, Chen KJ, Hsiao HP, Chao MC. Wu HR, et al. Among authors: hsiao hp. J Pediatr Endocrinol Metab. 2020 Nov 26;33(11):1481-1486. doi: 10.1515/jpem-2020-0106. J Pediatr Endocrinol Metab. 2020. PMID: 32841162 Review.

7

RBM15-MKL1 (OTT-MAL) fusion transcript in an adult acute myeloid leukemia patient.

Hsiao HH, Yang MY, Liu YC, Hsiao HP, Tseng SB, Chao MC, Liu TC, Lin SF. Hsiao HH, et al. Among authors: hsiao hp. Am J Hematol. 2005 May;79(1):43-5. doi: 10.1002/ajh.20298. Am J Hematol. 2005. PMID: 15849773 Free article.

8

Feminizing adrenocortical adenoma presenting as heterosexual precocious puberty: report of one case.

Hsiao HP, Chao MC, Lin CY, Chen HL, Chiou SS, Chen BH. Hsiao HP, et al. Acta Paediatr Taiwan. 2005 Mar-Apr;46(2):97-100. Acta Paediatr Taiwan. 2005. PMID: 16302588

9

Novel SOX9 gene mutation in campomelic dysplasia with autosomal sex reversal.

Hsiao HP, Tsai LP, Chao MC, Tseng HI, Chang YC. Hsiao HP, et al. J Formos Med Assoc. 2006 Dec;105(12):1013-6. doi: 10.1016/S0929-6646(09)60286-2. J Formos Med Assoc. 2006. PMID: 17185244 Free article.

10

Growth hormone deficiency in a case of crouzon syndrome with hydrocephalus.

Wen MH, Hsiao HP, Chao MC, Tsai FJ. Wen MH, et al. Among authors: hsiao hp. Int J Pediatr Endocrinol. 2010;2010:876514. doi: 10.1155/2010/876514. Epub 2010 May 30. Int J Pediatr Endocrinol. 2010. PMID: 20585360 Free PMC article.

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