Niu DM - Search Results

1

Two frequent mutations associated with the classic form of propionic acidemia in Taiwan.

Chiu YH, Liu YN, Liao WL, Chang YC, Lin SP, Hsu CC, Chiu PC, Niu DM, Wang CH, Ke YY, Chien YH, Hsiao KJ, Liu TT. Chiu YH, et al. Among authors: niu dm. Biochem Genet. 2014 Oct;52(9-10):415-29. doi: 10.1007/s10528-014-9657-6. Epub 2014 May 27. Biochem Genet. 2014. PMID: 24863100

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

Alpha-galactosidase activity should be examined in patients with proteinuria: what have we learned from a family affected with Fabry disease?

Lee NC, Niu DM, Lin CY, Hsiao KJ, Yang AH, Ng YY. Lee NC, et al. Among authors: niu dm. Nephrol Dial Transplant. 2006 Feb;21(2):549-50. doi: 10.1093/ndt/gfi191. Epub 2005 Oct 12. Nephrol Dial Transplant. 2006. PMID: 16221700 No abstract available.

4

Long-term follow-up of Chinese patients who received delayed treatment for 6-pyruvoyl-tetrahydropterin synthase deficiency.

Lee NC, Cheng LY, Liu TT, Hsiao KJ, Chiu PC, Niu DM. Lee NC, et al. Among authors: niu dm. Mol Genet Metab. 2006 Feb;87(2):128-34. doi: 10.1016/j.ymgme.2005.09.028. Epub 2005 Dec 20. Mol Genet Metab. 2006. PMID: 16364672

5

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.

6

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

7

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

8

Long-term follow-up of Taiwanese Chinese patients treated early for 6-pyruvoyl-tetrahydropterin synthase deficiency.

Liu KM, Liu TT, Lee NC, Cheng LY, Hsiao KJ, Niu DM. Liu KM, et al. Among authors: niu dm. Arch Neurol. 2008 Mar;65(3):387-92. doi: 10.1001/archneur.65.3.387. Arch Neurol. 2008. PMID: 18332253 Clinical Trial.

9

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

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

207 results

Search Page

Filters