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Zhonghua Yi Xue Za Zhi = Chinese Medical Journal; Free China Ed|November 1, 1990
[Propionic acidemia: report of a case that is successfully managed by peritoneal dialysis and sodium benzoate therapy]W C Hsu, S P Lin, F Y Huang, et al.
Human Genetics|August 1, 1992
Identification of a missense phenylketonuria mutation at codon 408 in ChineseC H Lin, K J Hsiao, T F Tsai, et al.
European Journal of Pediatrics|October 1, 1986
A Chinese family with phenylketonuria and maternal phenylketonuria detected by family screeningK J Hsiao, C H Chen, P C Chiu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|June 1, 1995
Fabry's disease: report of a caseH S Chang, L S Ro, S T Chen, et al.
Taiwan Yi Xue Hui Za Zhi. Journal of the Formosan Medical Association|January 1, 1989
Screening of congenital hypothyroidism, phenylketonuria, galactosemia, homocystinuria, and maple syrup urine disease in moderate to severe mentally retarded Chinese childrenK J Hsiao, C H Chen, T T Liu, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui|February 2, 1999
The effect of povidone-iodine on thyroid function of neonates with different birth sizesM J Jeng, C Y Lin, W J Soong, et al.
Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui|January 1, 1997
Neonatal thyroid function is unaffected by single treatment with different preparations of povidone-iodine on a wide skin surfaceM J Jeng, C Y Lin, W J Soong, et al.
American Journal of Medical Genetics|March 15, 1991
DNA polymorphisms and deletion analysis of the Duchenne-Becker muscular dystrophy gene in the ChineseB W Soong, T F Tsai, C H Su, et al.
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