Niu DM - Search Results

1

Survival and diagnostic age of 175 Taiwanese patients with mucopolysaccharidoses (1985-2019).

Lin HY, Lee CL, Chang CY, Chiu PC, Chien YH, Niu DM, Tsai FJ, Hwu WL, Lin SJ, Lin JL, Chao MC, Chang TM, Tsai WH, Wang TJ, Chuang CK, Lin SP. Lin HY, et al. Among authors: niu dm. Orphanet J Rare Dis. 2020 Nov 7;15(1):314. doi: 10.1186/s13023-020-01598-z. Orphanet J Rare Dis. 2020. PMID: 33160388 Free PMC article.

2

A pilot study of neonatal screening by electrospray ionization tandem mass spectrometry in Taiwan.

Lin WD, Wu JY, Lai CC, Tsai FJ, Tsai CH, Lin SP, Niu DM. Lin WD, et al. Among authors: niu dm. Acta Paediatr Taiwan. 2001 Jul-Aug;42(4):224-30. Acta Paediatr Taiwan. 2001. PMID: 11550411

3

Clinical features of Ehlers-Danlos syndrome.

Yen JL, Lin SP, Chen MR, Niu DM. Yen JL, et al. Among authors: niu dm. J Formos Med Assoc. 2006 Jun;105(6):475-80. doi: 10.1016/S0929-6646(09)60187-X. J Formos Med Assoc. 2006. PMID: 16801035 Free article.

4

Prader-Willi syndrome in Taiwan.

Lin HY, Lin SP, Yen JL, Lee YJ, Huang CY, Hung HY, Hsu CH, Kao HA, Chang JH, Chiu NC, Ho CS, Chao MC, Niu DM, Tsai LP, Kuo PL. Lin HY, et al. Among authors: niu dm. Pediatr Int. 2007 Jun;49(3):375-9. doi: 10.1111/j.1442-200X.2007.02368.x. Pediatr Int. 2007. PMID: 17532839

5

Genotype and phenotype in patients with Prader-Willi syndrome in Taiwan.

Lin HY, Lin SP, Chuang CK, Chen MR, Yen JL, Lee YJ, Huang CY, Tsai LP, Niu DM, Chao MC, Kuo PL. Lin HY, et al. Among authors: niu dm. Acta Paediatr. 2007 Jun;96(6):902-5. doi: 10.1111/j.1651-2227.2007.00284.x. Acta Paediatr. 2007. PMID: 17537021

6

Low frequency of the CYP21A2 deletion in ethnic Chinese (Taiwanese) patients with 21-hydroxylase deficiency.

Lee HH, Lee YJ, Wang YM, Chao HT, Niu DM, Chao MC, Tsai FJ, Lo FS, Lin SJ. Lee HH, et al. Among authors: niu dm. Mol Genet Metab. 2008 Apr;93(4):450-7. doi: 10.1016/j.ymgme.2007.10.008. Epub 2007 Nov 26. Mol Genet Metab. 2008. PMID: 18039588

7

The gene founder effect of two spontaneous mutations in ethnic Chinese (Taiwanese) CAH patients with 21-hydroxylase deficiency.

Lee YJ, Tsai LP, Niu DM, Shu SG, Chao MC, Lee HH. Lee YJ, et al. Among authors: niu dm. Mol Genet Metab. 2009 May;97(1):75-9. doi: 10.1016/j.ymgme.2009.01.001. Epub 2009 Feb 6. Mol Genet Metab. 2009. PMID: 19201236

8

Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis.

Hung CC, Lin SY, Lee CN, Cheng HY, Lin CY, Chang CH, Chiu HH, Yu CC, Lin SP, Cheng WF, Ho HN, Niu DM, Su YN. Hung CC, et al. Among authors: niu dm. Anal Biochem. 2009 Jun 15;389(2):102-6. doi: 10.1016/j.ab.2009.03.032. Epub 2009 Mar 27. Anal Biochem. 2009. PMID: 19328768

9

Incidence of the mucopolysaccharidoses in Taiwan, 1984-2004.

Lin HY, Lin SP, Chuang CK, Niu DM, Chen MR, Tsai FJ, Chao MC, Chiu PC, Lin SJ, Tsai LP, Hwu WL, Lin JL. Lin HY, et al. Among authors: niu dm. Am J Med Genet A. 2009 May;149A(5):960-4. doi: 10.1002/ajmg.a.32781. Am J Med Genet A. 2009. PMID: 19396827

10

Clinical features of osteogenesis imperfecta in Taiwan.

Lin HY, Lin SP, Chuang CK, Chen MR, Chang CY, Niu DM. Lin HY, et al. Among authors: niu dm. J Formos Med Assoc. 2009 Jul;108(7):570-6. doi: 10.1016/S0929-6646(09)60375-2. J Formos Med Assoc. 2009. PMID: 19586831 Free article.

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