Niu DM - Search Results

1

Contributions of bone maturation measurements to the differential diagnosis of neonatal transient hypothyroidism versus dyshormonogenetic congenital hypothyroidism.

Niu DM, Hwang B, Tiu CM, Tsai LP, Yen JL, Lee NC, Lin CY. Niu DM, et al. Acta Paediatr. 2004 Oct;93(10):1301-6. Acta Paediatr. 2004. PMID: 15499948

2

Comparison of radioisotopic and ultrasonic scanning in the evaluation of neonatal hypothyroidism.

Niu DM, Chao T, Tiu CM, Chou YH, Chu YK, Hwang B. Niu DM, et al. Zhonghua Yi Xue Za Zhi (Taipei). 1995 Nov;56(5):345-50. Zhonghua Yi Xue Za Zhi (Taipei). 1995. PMID: 8605650 Clinical Trial.

3

Congenital hypothyroidism with multiple ovarian cysts.

Chen CH, Tiu CM, Chou YH, Chen WY, Hwang B, Niu DM. Chen CH, et al. Among authors: niu dm. Eur J Pediatr. 1999 Oct;158(10):851-2. doi: 10.1007/s004310051221. Eur J Pediatr. 1999. PMID: 10486092

4

DiGeorge syndrome with microdeletion of chromosome 22q11.2: report of one case.

Wang JL, Chen SJ, Chung MY, Niu DM, Lin CY, Hwang BT, Lu JH. Wang JL, et al. Among authors: niu dm. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1997 Sep-Oct;38(5):385-9. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1997. PMID: 9401184

5

[Maturation of ganglioneuroblastoma to ganglioneuroma: a case report].

Niu DM, Chang TK, Liu SM, Hwang B. Niu DM, et al. Zhonghua Yi Xue Za Zhi (Taipei). 1993 Apr;51(4):318-21. Zhonghua Yi Xue Za Zhi (Taipei). 1993. PMID: 8481854 Chinese.

6

Identification of CpG methylation of the SNRPN gene by methylation-specific multiplex PCR.

Hung CC, Lin SY, Lin SP, Niu DM, Lee NC, Cheng WF, Chen CP, Lin WL, Lee CN, Su YN. Hung CC, et al. Among authors: niu dm. Electrophoresis. 2009 Jan;30(2):410-6. doi: 10.1002/elps.200800225. Electrophoresis. 2009. PMID: 19137525

7

Diagnosis of congenital hypothyroidism from human anagen scalp hair by infrared microspectroscopy.

Lin SY, Niu DM, Tu CP, Lin HL, Li MJ, Cheng YD. Lin SY, et al. Among authors: niu dm. Ultrastruct Pathol. 2001 Sep-Oct;25(5):357-60. doi: 10.1080/019131201317101225. Ultrastruct Pathol. 2001. PMID: 11758716

8

Differentiation of hair growth cycle from scalp hair roots for the diagnosis of glucose-6-phosphate dehydrogenase deficiency in neonates.

Lin SY, Niu DM, Li MJ, Tu CP, Lin HL. Lin SY, et al. Among authors: niu dm. J Inherit Metab Dis. 2000 Nov;23(7):693-704. doi: 10.1023/a:1005622728805. J Inherit Metab Dis. 2000. PMID: 11117431

9

Chinese achondroplasia is also defined by recurrent G380R mutations of the fibroblast growth factor receptor-3 gene.

Niu DM, Hsiao KJ, Wang NH, Chin LS, Chen CH. Niu DM, et al. Hum Genet. 1996 Jul;98(1):65-7. doi: 10.1007/s004390050161. Hum Genet. 1996. PMID: 8682509

10

Recurrent rhabdomyolysis caused by palmitoyltransferase II (CPT-2) deficiency but complete normal acylcarnitine profile: A patient presentation and review of the literature.

Lu CH, Yang CF, Chen YR, Chen YJ, Lu YH, Niu DM. Lu CH, et al. Among authors: niu dm. Mol Genet Metab Rep. 2024 Oct 5;41:101151. doi: 10.1016/j.ymgmr.2024.101151. eCollection 2024 Dec. Mol Genet Metab Rep. 2024. PMID: 39429887 Free PMC article.

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