TY - JOUR
AU - Borbujo, J.
AB - 1400 Correspondence disease is characterized by amyloid deposition of mutated 2 Schulze PC, Maurer MS. Transthyretin Val30Met mutation in an African American with cardiac amyloidosis. Congest Heart Fail 2010; fibrillar TTR. 16:73–6. The Val30Met mutation is very unusual in patients of Afri- 3 Plante ´-Bordeneuve V, Ferreira A, Lalu T et al. Diagnostic pitfalls in can origin and has been reported only once in an African sporadic transthyretin familial amyloid polyneuropathy (TTR-FAP). American patient. Diagnosis of TTR familial polyneuropathy Neurology 2007; 69:693–8. can be problematic, especially in sporadic cases such as ours. 4 Herlenius G, Wilczek HE, Larsson M, Ericzon BG. Familial Amyloi- The clinical phenotype can vary greatly depending on the site dotic Polyneuropathy World Transplant Registry. Ten years of inter- national experience with liver transplantation for familial of involvement of amyloid deposits. The main clinical expres- amyloidotic polyneuropathy: results from the Familial Amyloidotic sion is a peripheral sensory neuropathy which progresses Polyneuropathy World Transplant Registry. Transplantation 2004; towards autonomic and motor neuropathy that typically starts 77:64–71. in the lower extremities. Late in the disease progression, car- 5 Holmgren G, Ericzon BG, Groth CG et al. Clinical improvement and diac conduction abnormalities are common. The disease may amyloid 
TI - Unilateral livedo reticularis after kidney graft embolization with polyvinyl alcohol microspheres
JF - British Journal of Dermatology
DO - 10.1111/j.1365-2133.2011.10256.x
DA - 2011-06-01
UR - https://www.deepdyve.com/lp/oxford-university-press/unilateral-livedo-reticularis-after-kidney-graft-embolization-with-vo0G6lsxac
SP - 1400
EP - 1402
VL - 164
IS - 6
DP - DeepDyve
ER -