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- Abstract：Objective To explore the clinical features and pathologyical changes of amyloid polyneuropathy. 摘 要：目的 探討類澱粉性周圍神經病的臨床特點及病理改變。
- Objective To explore the clinical features and pathologyical changes of amyloid polyneuropathy. 目的探討類澱粉性周圍神經病的臨床特點及病理改變。
- Abstract： Objective To make clear the real type of the first familial amyloid polyneuropathy(FAP) family in China. 摘 要： 目的 對我國首次報道的家族性澱粉樣多發性神經病（FAP）家系進行各項研究，以期發現其真正類型。
- Grafts used in Domino lier transplantation (LT) obtained from liing donor lier transplantation (LDLT) for familial amyloid polyneuropathy (FAP) patients hae been mainly used as reduced grafts. 源於家族性澱粉樣多發神經病(FAP)活體供肝肝移植(LDLT)患者的供肝一直主要以減體積移植肝用於"多米諾"肝移植.
- Conclusion Diagnose this disease according to clinical features and biopsy of peripheral nerves and skin,the liver transplantation is an future treatment for amyloid polyneuropathy. 結論 根據臨床特點及周圍神經皮膚活檢進行診斷，肝移植是治療本病最有前途的方法。
- Portuguese type familial amyloid polyneuropathy 葡萄牙型家族性澱粉樣多神經病
- Rukavina type familial amyloid polyneuropathy 路卡維納型家族性澱粉樣多神經病
- Van Allen type familial amyloid polyneuropathy 凡愛倫型家族性澱粉樣多神經病
- hereditary amyloid polyneuropathy 遺傳性澱粉樣多神經病
- Hereditary amyloid polyneuropathy Portuguese type 遺傳性澱粉樣多神經病, 葡萄牙型
- Liver transplantation for familial amyloid polyneuropathy 肝移植治療家族性澱粉樣變多發性神經病
- Results Amyloid polyneuropathy is chronic progressive peripheral neuropathy,can be accompanied by injured of cardiovascular system, gastrointestinal tract and kidneys; 結果本病為慢性進行性周圍神經病，可伴有心、胃腸、腎等損傷。
- Containing amyloid deposits, as an organ. 蠟樣的器官等含澱粉蛋白沉積的
- familial amyloid polyneuropathy 家族性澱粉樣多神經病
- amyloid polyneuropathy 澱粉樣多神經病
- Every RCS on one AP has a mate RCS on its pair AP. AP 上的每個 RCS 在其配對 AP 上都有一個配對 RCS。
- She repeated the gist of the AP bulletin. 她把美聯社電訊的要點又講了一遍。
- An AP is characterized as online or offline. 在線或離線也可以作為刻畫 AP 的特徵。
- The meters show your HP, MP, and "AP". 在四處奔走的時候，你將隨機遇敵，進行戰鬥。
- The AP in the GUI will be a lighter gray. GUI 中的 AP 將會是淺灰色。
