Search Results - "Lin, Po-Te" :: K.UTB vyhledávací portál

Inherited coagulation factor VII deficiency in Taiwan: Two novel F7 variants with relevant regional features in 33 patients

by Lin, Hsuan‐Yu, Lin, Ching‐Yeh, Kuo, Su‐Feng, Lin, Jen‐Shiou, Lin, Po‐Te, Huang, Ying‐Chih, Hsieh, Han‐Ni, Shen, Ming‐Ching
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.07.2024)

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A distinct common p.Gln317 mutation among causative LMAN1 genetic mutations of combined factor V and factor VIII deficiency in five Taiwanese families

by Lin, Hsuan‐Yu, Lin, Jen‐Shiou, Tsay, Woei, Lin, Po‐Te, Huang, Ying‐Chih, Shen, Ming‐Ching
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.01.2022)

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Relationships between depression and anxiety symptoms and adipocyte-derived proteins in postmenopausal women

by Wu, Yu-Ting, Huang, Wan-Yu, Kor, Chew-Teng, Liu, Ko-Hung, Chen, Ting-Yu, Lin, Po-Te, Wu, Hung-Ming
Published in PloS one (05.03.2021)

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Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population

by Shen, Ming‐Ching, Wang, Jiaan‐Der, Tsai, Woei, Lin, Ching‐Yeh, Lin, Jen‐Shiou, Kuo, Su‐Feng, Lin, Po‐Te, Huang, Ying‐Chih, Hung, Mei‐Hua
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.11.2021)

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Characterization of congenital factor XII deficiency in Taiwanese patients: identification of one novel and one common mutation

by Chou, Sheng-Chieh, Lin, Ching-Yeh, Lin, Hsuan-Yu, Pai, Chen-Hsueh, Yu, Cheng-Ye, Kuo, Su-Feng, Lin, Jen-Shiou, Lin, Po-Te, Hung, Mei-Hua, Hsieh, Han-Ni, Liu, Hsiang-Chun, Shen, Ming-Ching
Published in International journal of hematology (01.10.2022)

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Relationships between Follicle-Stimulating Hormone and Adiponectin in Postmenopausal Women

by Huang, Wan-Yu, Chen, Dar-Ren, Kor, Chew-Teng, Chen, Ting-Yu, Lin, Po-Te, Tseng, Joseph Ta Chien, Wu, Hung-Ming
Published in Metabolites (19.10.2020)

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Segmental uniparental disomy as a rare cause of congenital severe factor XIII deficiency in a girl with only one heterozygous carrier parent

by Shen, Ming-Ching, Chen, Ming, Chang, Shung-Ping, Lin, Po-Te, Hsieh, Han-Ni, Lin, Kai-Hsin
Published in Pediatric hematology and oncology (17.11.2018)

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Congenital factor V deficiency in Taiwan: identification of a novel variant p.Tyr1813 ∗ and two variants specific to East Asians

by Lin, Hsuan-Yu, Lin, Ching-Yeh, Kuo, Su-Feng, Lin, Jen-Shiou, Lin, Po-Te, Huang, Ying-Chih, Hsieh, Han-Ni, Shen, Ming-Ching
Published in Blood coagulation & fibrinolysis (01.01.2023)

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