½Ã°£ | ÇÁ·Î±×·¥ | ¿¬ÀÚ |
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09:10~09:20 | °³È¸»ç | |
¥°. Genetics in neuromuscular disorder | <ÁÂÀå: ±è´ë¼º(ºÎ»êÀÇ´ë), ±Ç±âÇÑ(ÇѸ²ÀÇ´ë)> | |
09:20~09:50 | Basic genetics and next-generation sequencing application in neuromuscular disease | ±è¿µÀº(ÇѾçÀÇ´ë, Áø´Ü°Ë»çÀÇÇаú) |
09:50~10:20 | Practical diagnostic approach in myopathy : Tips to set up genetic approach for myopathy in your clinic |
ÀÌÁ¾¸ñ(°æºÏÀÇ´ë, ½Å°æ°ú) |
10:20~10:50 | Practical diagnostic approach in inherited motor neuron disease (Hereditary spastic paraplegia (HSP) and spinal muscular atrophy (SMA)) : Tips to set up genetic approach for HSP and SMA in your clinic |
ÃÖ¼®Áø(¼¿ïÀÇ´ë, ½Å°æ°ú) |
10:50~11:30 | Gene therapy in transthyretin-mediated amyloidosis (Case-based learning) | Lucia Galan (Hospital Clinico San Carlos, Spain) |
11:30~11:40 | Q & A | |
11:40~11:50 | Intermission | |
¥±. Recently updated guideline & clinical scales for neuromuscular disorder | <ÁÂÀå: ±èº´ÁØ(¼º±Õ°üÀÇ´ë), ±èÁ¾±¹(µ¿¾ÆÀÇ´ë)> | |
11:50~12:10 | EAN/PNS guideline in diagnosis & management of Guillain-Barre syndrome | À±º°¾Æ(µ¿¾ÆÀÇ´ë, ½Å°æ°ú) |
12:10~12:30 | EAN/PNS guideline in diagnosis & management of chronic inflammatory demyelinating polyneuropathy | ±èÁöÀº(ÀÌÈÀÇ´ë, ½Å°æ°ú) |
12:30~13:00 | Clinical scales for neuromuscular disorder | ±è½Â¿ì(¿¬¼¼ÀÇ´ë, ½Å°æ°ú) |
13:00~13:10 | Q & A | |
13:10~ | Æóȸ»ç |