Su-Feng Kuo

Critical Test Result Recall Supporting System (CTR RSS) Improves Follow-Up among Patients in the Community

Chew-Teng Kor, C. Twu, Yuan-Ting Yang, 2022, Diagnostics.

Characterization of hereditary factor XI deficiency in Taiwanese patients: identification of three novel and two common mutations

M. Shen, Hsuan-Yu Lin, Ching-Yeh Lin, 2020, International Journal of Hematology.

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

M. Shen, Hsuan-Yu Lin, Ching-Yeh Lin, 2022, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

A family with an MYH9-related disorder with different phenotypes masquerading as immune thrombocytopaenia: an underreported disorder in Taiwan

P. Chiu, M. Shen, Ching-Yeh Lin, 2020, International Journal of Hematology.

Absence of hypercoagulability in acute Kawasaki disease

Ming-Tsan Lin, Yu-Jun Chang, L. Tsao, 2005, Pediatrics international : official journal of the Japan Pediatric Society.

A Case Report of a 3-Year-Old Child With Anaphylactic Shock After a Diclofenac Suppository Confirmed by Serial Tryptase and a Basophil Activation Test

Y. Tsai, Tsu-Man Chiu, W. Chung, 2022, Frontiers in Pediatrics.

A large family of hereditary spherocytosis and a rare case of hereditary elliptocytosis with a novel SPTA1 mutation underdiagnosed in Taiwan: A case report and literature review

Hsuan-Yu Lin, Ching-Yeh Lin, Jen‐Shiou Lin, 2023, Medicine.

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

M. Shen, Ching-Yeh Lin, Jiaan-Der Wang, 2021, Haemophilia : the official journal of the World Federation of Hemophilia.

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

M. Shen, Hsuan-Yu Lin, Ching-Yeh Lin, 2022, International Journal of Hematology.