Results 221 to 230 of about 61,872 (307)
ABSTRACT Background Amyloidosis is a rare, multisystem disorder characterized by extracellular deposition of misfolded protein fibrils. Gastrointestinal (GI) amyloidosis is uncommon but under‐recognized due to nonspecific symptoms, but early diagnosis is critical to improve quality of life and prognosis.
Myo Jin Tang +3 more
wiley +1 more source
Polyneuropathy in Wild-Type Transthyretin Amyloidosis. [PDF]
Sciarrone MA +14 more
europepmc +1 more source
Hepatocyte-like cells reveal novel role of SERPINA1 in transthyretin amyloidosis [PDF]
Christoph Niemietz +5 more
openalex +1 more source
Nodular amyloid deposits with collagen fibre rupture in tenosynovial carpal tissues are associated with transthyretin cardiomyopathy: a single-centre prospective diagnostic study. [PDF]
Zustin J +7 more
europepmc +1 more source
Early nociceptive evoked potentials in symptomatic and asymptomatic transthyretin mutation carriers. [PDF]
Massucco S +9 more
europepmc +1 more source
Discontinuation of Tafamidis in Wild-Type Transthyretin Amyloid Cardiomyopathy Patients. [PDF]
Baba Y +5 more
europepmc +1 more source
Trends in diagnostic testing in Medicare patients with wild-type transthyretin amyloid cardiomyopathy. [PDF]
Witteles RM +7 more
europepmc +1 more source

