Molecular genetic study of Pompe disease in Chinese patients in Taiwan
Ko, Tsang-Ming, Hwu, Wuh-Liang, Lin, Yu-Wan, Tseng, Li-Hui, Hwa, Hsiao-Lin, Wang, Tso-Ren, Chuang, Sou-Ming
Published in Human mutation (1999)
Published in Human mutation (1999)
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Allele distribution at the FMR1 locus in the general Chinese population
Chiang, Shu-Chuan, Lee, Yu-May, Wang, Tso-Ren, Hwu, Wuh-Liang
Published in Clinical genetics (01.05.1999)
Published in Clinical genetics (01.05.1999)
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Dopamine Receptor D2 Gene Polymorphisms Are Associated in Taiwanese Children With Tourette Syndrome
Lee, Cheng-Chun, Chou, I.-Ching, Tsai, Chang-Hai, Wang, Tso-Ren, Li, Tsai-Chung, Tsai, Fuu-Jen
Published in Pediatric neurology (01.10.2005)
Published in Pediatric neurology (01.10.2005)
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Molecular identification of combined homozygous and compound heterozygous mutations in the CYP21 gene in simple virilizing congenital adrenal hyperplasia in Taiwan
Wang, Hsu-Hui, Lee, Hsien-Hsiung, Wu, Du-An, Lee, Yann-Jin, Chung, Bon-Chu, Wang, Tso-Ren
Published in Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi (01.11.2003)
Published in Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi (01.11.2003)
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Cranial MR Spectroscopy of Tetrahydrobiopterin Deficiency
Chien, Yin-Hsiu, Peng, Shiin-Feng, Wang, Tso-Ren, Hwu, Wuh-Liang
Published in American journal of neuroradiology : AJNR (01.06.2002)
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Published in American journal of neuroradiology : AJNR (01.06.2002)
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Neonatal type of nonketotic hyperglycinemia
Lu, Frank L, Wang, Pen-Jung, Hwu, Wuh-Liang, Tsou Yau, Kuo-Inn, Wang, Tso-Ren
Published in Pediatric neurology (01.04.1999)
Published in Pediatric neurology (01.04.1999)
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Neonatal Hepatitis: A Follow-up Study
Chang, Mei-Hwei, Hsu, Hey-Chi, Lee, Chin-Yun, Wang, Tso-Ren, Kao, Chuan-Liang
Published in Journal of pediatric gastroenterology and nutrition (01.03.1987)
Published in Journal of pediatric gastroenterology and nutrition (01.03.1987)
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Duplication of proteolipid protein gene: A possible major cause of Pelizaeus-Merzbacher disease
Wang, Pen-Jung, Hwu, Wuh-Liang, Lee, Wang-Tso, Wang, Tso-Ren, Shen, Yu-Zen
Published in Pediatric neurology (01.09.1997)
Published in Pediatric neurology (01.09.1997)
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Phenylalanine hydroxylase deficiency: intelligence of patients after early dietary treatment
Chien, Yin-Hsiu, Chiang, Shu-Chuan, Huang, Aichu, Lin, Jing-Meei, Chiu, Yen-Nan, Chou, Shi-Ping, Wang, Tso-Ren, Hwu, Wuh-Liang
Published in Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi (01.11.2004)
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Published in Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi (01.11.2004)
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Glucose-6-phosphatase gene G327A mutation is common in Chinese patients with glycogen storage disease type Ia
Hwu, W L, Chuang, S C, Tsai, L P, Chang, M H, Chuang, S M, Wang, T R
Published in Human molecular genetics (01.06.1995)
Published in Human molecular genetics (01.06.1995)
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In Vitro DNA Methylation Inhibits FMR-1 Promoter
Hwu, W.L., Lee, Y.M., Lee, S.C., Wang, T.R.
Published in Biochemical and biophysical research communications (28.05.1993)
Published in Biochemical and biophysical research communications (28.05.1993)
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Kleine-Levin syndrome in a boy with Prader-Willi syndrome
Gau, S F, Soong, W T, Liu, H M, Hou, J W, Tsai, W Y, Chiu, Y N, Yeh, Y C, Wang, P J, Wang, T R
Published in Sleep (New York, N.Y.) (1996)
Published in Sleep (New York, N.Y.) (1996)
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Homocystinuria presenting as fatal common carotid artery occlusion
LU, C.-Y, HOU, J.-W, WANG, P.-J, CHIU, H.-H, WANG, T.-R
Published in Pediatric neurology (01.09.1996)
Published in Pediatric neurology (01.09.1996)
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