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Skin amyloid deposits and nerve fiber loss as markers of neuropathy onset and progression in hereditary transthyretin amyloidosis
European Journal of Neurology ( IF 4.5 ) Pub Date : 2022-01-31 , DOI: 10.1111/ene.15268 Luca Leonardi 1, 2 , Clovis Adam 1, 3, 4 , Guillemette Beaudonnet 1, 5 , Diane Beauvais 1 , Cécile Cauquil 1 , Adeline Not 1 , Olivier Morassi 1 , Anouar Benmalek 6 , Olivier Trassard 4 , Andoni Echaniz-Laguna 1, 3 , David Adams 1, 3 , Céline Labeyrie 1, 3, 4
European Journal of Neurology ( IF 4.5 ) Pub Date : 2022-01-31 , DOI: 10.1111/ene.15268 Luca Leonardi 1, 2 , Clovis Adam 1, 3, 4 , Guillemette Beaudonnet 1, 5 , Diane Beauvais 1 , Cécile Cauquil 1 , Adeline Not 1 , Olivier Morassi 1 , Anouar Benmalek 6 , Olivier Trassard 4 , Andoni Echaniz-Laguna 1, 3 , David Adams 1, 3 , Céline Labeyrie 1, 3, 4
Affiliation
This study was undertaken to assess skin biopsy as a marker of disease onset and severity in hereditary transthyretin amyloidosis with polyneuropathy (ATTRv-PN), a treatable disease.
中文翻译:
皮肤淀粉样蛋白沉积和神经纤维丢失作为遗传性转甲状腺素蛋白淀粉样变性神经病变发作和进展的标志物
本研究旨在评估皮肤活检作为遗传性转甲状腺素蛋白淀粉样变性伴多发性神经病 (ATTRv-PN) 疾病发作和严重程度的标志物,这是一种可治疗的疾病。
更新日期:2022-01-31
中文翻译:
皮肤淀粉样蛋白沉积和神经纤维丢失作为遗传性转甲状腺素蛋白淀粉样变性神经病变发作和进展的标志物
本研究旨在评估皮肤活检作为遗传性转甲状腺素蛋白淀粉样变性伴多发性神经病 (ATTRv-PN) 疾病发作和严重程度的标志物,这是一种可治疗的疾病。