Time |
Topic |
13:00-13:05 |
Opening Remarks |
|
Moderator:彭慶添理事長 |
13:05-13:55 |
特別演講 The origin and occurrence of de novo mutation in hemophilia A without prior family history 沈銘鏡教授/彰化基督教醫院 |
|
Moderator:邱世欣、王建得 |
13:55-14:10 |
Clinical manifestations and genetic studies of hereditary hemorrhagic telangiectasia patients seen in middle part of Taiwan 林敬業醫師/彰化基督教醫院 |
14:10-14:25 |
Compound heterozygous mutations including one novel mutation in PROC gene causing severe phenotype in a patient presenting with neonatal purpura fulminans 邱世欣醫師/高雄醫學大學附設醫院 |
14:25-14:40 |
Overview of rFVIIIfc : the novel role for hemophilia management 王建得醫師/台中榮總 |
14:40-14:55 |
Acquired Platelet Dysfunction with Eosinophilia (APDE) Syndrome: Two Case Reports 施銘洋醫師/台中榮總 |
14:55-15:15 |
Coffee break |
|
Moderator:彭慶添、陳宇欽 |
15:15-15:30 |
Successful Treatment of Refractory Pancreatic Hemorrhage in a Severe-type Hemophilia A Patient with Chronic Pancreatitis and Pseudoaneurysm 蔡佳叡醫師/台北醫學大學附設醫院 |
15:30-15:45 |
Midnight shift-related recurrent midcycle pain and corpus luteum rupture bleeding during ovulation resulting in massive hemoperitoneum in a female with severe type 1 von Willebrand disease 張家堯醫師/台北醫學大學附設醫院 |
15:45-16:00 |
Pulmonary Embolisms in A Child with Chronic Myeloid Leukemia treated with Dasatinib 翁德甫醫師/中國醫藥大學兒童醫院 |
16:00-16:15 |
Generation of Mouse model of bleeding disorder by CRISPR 林淑華教授/台灣大學醫技系 |
16:15-16:30 |
Podoplanin promotes oral cancer progression by disrupting hemostatic balance 李星瑩博士/長庚大學生物醫學研究所 |
16:30-16:45 |
Phenotype and genotype of two brothers with inherited coagulation factor XIII deficiency 陳宇欽醫師/三軍總醫院 |
16:45-17:00 |
Closing remarks 沈銘鏡教授 |
教育積分: |
中國民國血液病學會1.5學分、台灣兒科醫學會學分申請中。 |