amyloidotic

amyloidotic

adjective Referring to amyloid or amyloidosis.
References in periodicals archive ?
2015), has been implemented and adapted for other late-onset diseases around the world (Hawkins, Ho, & Hayden, 2011), namely, Machado-Joseph disease (MJD) and Familial Amyloidotic Polyneuropathy (FAP), two Portuguese monogenic, autosomal and dominant diseases (Sequeiros et al.
Risk perception in subjects at-risk for Familial Amyloidotic Polyneuropathy
Vitreous opacities and outcome of vitreous surgery in patients with familial amyloidotic polyneuropathy.
The product is intended for the treatment of mediated amyloidosis in patients with familial amyloidotic polyneuropathy (FAP).
alcohol), hypothyroidism, amyloidotic peripheral neuropathy, vitamin B12 deficiency, connective tissue disease, infection, hereditary disease, and so on.
These include Nor98 or atypical scrapie in sheep (1) and 2 prion diseases of cattle, bovine amyloidotic spongiform encephalopathy or L-type BSE (2) and H-type BSE (3), both of which have a pathology and epidemiology distinct from classical or C-type BSE (4).
Alnylam will initiate a phase II study on ALN-TTRsc (familial amyloidotic cardiomyopathy) later this year as per the successful completion of the phase I study.
Left ventricular dyssynchrony is associated with reduced heart rate variability in familial amyloidotic polyneuropathy.
2] found that the median duration of time from first symptom to diagnosis of AL amyloidosis was longer in patients whose first symptom was neuropathy (48 versus 12 months) which can precede amyloidotic infiltration of vital organs.
Familial amyloidotic polyneuropathy with severe renal involvement in association with transthyretin Gly47Glu in Dutch, British and American-Finnish families.
They have found a process by which proteins with a tendency to cause conformational diseases such as amyotrophic lateral sclerosis, familial amyloidotic polyneuropathy, familial amyloidotic cardiomyopathy, etc.
The long-term impact of liver transplantation on kidney function in familiar amyloidotic polyneuropathy patients.