Lv1
46 积分 2025-09-12 加入
A case of familial amyloidotic polyneuropathy with a rare Phe33Leu mutation in the TTR gene
2个月前
已完结
Clinical and genetic findings in eight Israeli patients with transthyretin-associated familial amyloid polyneuropathy
2个月前
已关闭
TRANSTHYRETIN FAMILIAL AMYLOID POLYNEUROPATHY – THREE HUNGARIAN CASES WITH RARE MUTATIONS (His88Arg AND Phe33Leu)
2个月前
已完结
Genetically confirmed transthyretin amyloidosis primarily referred as hypertrophic cardiomyopathy
2个月前
已完结
Nexiguran Ziclumeran Gene Editing in Hereditary ATTR with Polyneuropathy
2个月前
已完结
Pain‐Related Evoked Potentials in Hereditary Transthyretin Amyloidosis With Polyneuropathy
2个月前
已完结
Quantitative sensory testing: a good tool to identify subclinical neuropathy in ATTRV30M amyloidosis patients?
2个月前
已完结
Rac1 inhibition prevents axonal cytoskeleton dysfunction in transthyretin amyloid polyneuropathy
2个月前
已完结
Functional and morphometric assessment of small-fibre damage in late-onset hereditary transthyretin amyloidosis with polyneuropathy: the controversial relation between small-fibre-related symptoms and diagnostic test findings
2个月前
已完结
Transthyretin amyloid polyneuropathy in France: A cross-sectional study with 413 patients and real-world tafamidis meglumine use (2009–2019)
2个月前
已完结
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