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Shuan-Pei Lin

Showing results (51-60 of 281) with videos related to

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Taiwanese Journal of Obstetrics & Gynecology|April 4, 2013
Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicismChih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 4, 2013
Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcomeChih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, et al.
Prenatal Diagnosis|April 2, 2004
Detection of a homozygous D645E mutation of the acid alpha-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type IIChih-Ping Chen, Shuan-Pei Lin, Chin-Yuan Tzen, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 7, 2023
Genetic counseling of a prenatally detected familial 18.79-kb Xp21.1 microduplication encompassing exon 13 of DMD in a pregnancy with no apparent phenotypic abnormalities in the male carriers in the familyChih-Ping Chen, Shuan-Pei Lin, Fang-Tzu Wu, et al.
Journal of Personalized Medicine|July 27, 2022
Surgical Strategy to Decrease the Revision Rate of Fassier-Duval Nailing in the Lower Limbs of Osteogenesis ImperfectaYi-Chi Hung, Kai-Yuan Cheng, Hsiang-Yu Lin, et al.
Orphanet Journal of Rare Diseases|June 10, 2017
Transcranial pulsed ultrasound facilitates brain uptake of laronidase in enzyme replacement therapy for Mucopolysaccharidosis type I diseaseYu-Hone Hsu, Ren-Shyan Liu, Win-Li Lin, et al.
The Kaohsiung Journal of Medical Sciences|December 3, 2009
Lafora disease and congenital generalized lipodystrophy: a case reportChih-Fan Tseng, Che-Sheng Ho, Nan-Chang Chiu, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|June 28, 2008
Non-ketotic hyperglycinemia with a novel GLDC mutation in a Taiwanese childChia-Ying Chang, Shuan-Pei Lin, Hsiang-Yu Lin, et al.
Journal of Microbiology, Immunology, and Infection = Wei Mian Yu Gan Ran Za Zhi|June 30, 2005
A seroepidemiologic study of Helicobacter pylori and hepatitis A virus infection in primary school students in TaipeiHsiang-Yu Lin, Chih-Kuang Chuang, Hung-Chang Lee, et al.
Orphanet Journal of Rare Diseases|September 3, 2014
A modified liquid chromatography/tandem mass spectrometry method for predominant disaccharide units of urinary glycosaminoglycans in patients with mucopolysaccharidosesChih-Kuang Chuang, Hsiang-Yu Lin, Tuen-Jen Wang, et al.
Pageof 29

Showing results (51-60 of 281) with videos related to

Sort By:
Pageof 29
Taiwanese Journal of Obstetrics & Gynecology|April 4, 2013
Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicismChih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 4, 2013
Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcomeChih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, et al.
Prenatal Diagnosis|April 2, 2004
Detection of a homozygous D645E mutation of the acid alpha-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type IIChih-Ping Chen, Shuan-Pei Lin, Chin-Yuan Tzen, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 7, 2023
Genetic counseling of a prenatally detected familial 18.79-kb Xp21.1 microduplication encompassing exon 13 of DMD in a pregnancy with no apparent phenotypic abnormalities in the male carriers in the familyChih-Ping Chen, Shuan-Pei Lin, Fang-Tzu Wu, et al.
Journal of Personalized Medicine|July 27, 2022
Surgical Strategy to Decrease the Revision Rate of Fassier-Duval Nailing in the Lower Limbs of Osteogenesis ImperfectaYi-Chi Hung, Kai-Yuan Cheng, Hsiang-Yu Lin, et al.
Orphanet Journal of Rare Diseases|June 10, 2017
Transcranial pulsed ultrasound facilitates brain uptake of laronidase in enzyme replacement therapy for Mucopolysaccharidosis type I diseaseYu-Hone Hsu, Ren-Shyan Liu, Win-Li Lin, et al.
The Kaohsiung Journal of Medical Sciences|December 3, 2009
Lafora disease and congenital generalized lipodystrophy: a case reportChih-Fan Tseng, Che-Sheng Ho, Nan-Chang Chiu, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|June 28, 2008
Non-ketotic hyperglycinemia with a novel GLDC mutation in a Taiwanese childChia-Ying Chang, Shuan-Pei Lin, Hsiang-Yu Lin, et al.
Journal of Microbiology, Immunology, and Infection = Wei Mian Yu Gan Ran Za Zhi|June 30, 2005
A seroepidemiologic study of Helicobacter pylori and hepatitis A virus infection in primary school students in TaipeiHsiang-Yu Lin, Chih-Kuang Chuang, Hung-Chang Lee, et al.
Orphanet Journal of Rare Diseases|September 3, 2014
A modified liquid chromatography/tandem mass spectrometry method for predominant disaccharide units of urinary glycosaminoglycans in patients with mucopolysaccharidosesChih-Kuang Chuang, Hsiang-Yu Lin, Tuen-Jen Wang, et al.
Pageof 29