none4noneE. Pilato; A. Dell'Amore; L. Botta; G. ArpesellaE. Pilato; A. Dell'Amore; L. Botta; G. Arpesell
Familial amyloidotic polyneuropathy (FAP) is an inherited disorder with the systemic deposition of a...
Transplant Proc. 2003 May;35(3):1116-20. End-stage renal disease in familial amyloidosis ATTR Val...
Familial amyloidotic polyneuropathy (FAP), found in the northernmost counties in Sweden, is a rare, ...
none8noneDell'Amore A.; Pilato E.; Martin-Suarez S.; Botta L.; Mikus E.; Mikus P. M.; Leone O.; Arpe...
There are few reports of combined heart and liver transplantation (CHLT) for familial amyloidotic po...
Familial amyloidotic polyneuropathy (FAP) is an inherited disease characterized by an abnormal syste...
FAMILIAL amyloidotic polyneuropathy (FAP) is aninherited autosomal dominant systemic disease cause
Abstract Introduction Hereditary amyloidodis is a rare disease process with a propensity to cause po...
FAMILIAL amyloid polyneuropathy (FAP) is the mostcommon form of herederitary amyloidosis. Initial cl...
none10noBackground and Objective. Although combined heart and liver transplantation (CHLT) is an ac...
Liver transplantation is a standard treatment for patients with familial amyloidotic polyneuropathy ...
OBJECTIVE: To review our experience of liver transplantation (LT) for patients with non-Val30Met fam...
A 32-year-old Portuguese with hereditary amyloidosis had been suffering from polyneuropathy for 9 ye...
none8noBackground. Although orthotopic liver transplantation (OLT) and combined heart and liver tran...
Liver transplantation is a standard treatment for patients with familial amyloidotic polyneuropathy ...
Familial amyloidotic polyneuropathy (FAP) is an inherited disorder with the systemic deposition of a...
Transplant Proc. 2003 May;35(3):1116-20. End-stage renal disease in familial amyloidosis ATTR Val...
Familial amyloidotic polyneuropathy (FAP), found in the northernmost counties in Sweden, is a rare, ...
none8noneDell'Amore A.; Pilato E.; Martin-Suarez S.; Botta L.; Mikus E.; Mikus P. M.; Leone O.; Arpe...
There are few reports of combined heart and liver transplantation (CHLT) for familial amyloidotic po...
Familial amyloidotic polyneuropathy (FAP) is an inherited disease characterized by an abnormal syste...
FAMILIAL amyloidotic polyneuropathy (FAP) is aninherited autosomal dominant systemic disease cause
Abstract Introduction Hereditary amyloidodis is a rare disease process with a propensity to cause po...
FAMILIAL amyloid polyneuropathy (FAP) is the mostcommon form of herederitary amyloidosis. Initial cl...
none10noBackground and Objective. Although combined heart and liver transplantation (CHLT) is an ac...
Liver transplantation is a standard treatment for patients with familial amyloidotic polyneuropathy ...
OBJECTIVE: To review our experience of liver transplantation (LT) for patients with non-Val30Met fam...
A 32-year-old Portuguese with hereditary amyloidosis had been suffering from polyneuropathy for 9 ye...
none8noBackground. Although orthotopic liver transplantation (OLT) and combined heart and liver tran...
Liver transplantation is a standard treatment for patients with familial amyloidotic polyneuropathy ...
Familial amyloidotic polyneuropathy (FAP) is an inherited disorder with the systemic deposition of a...
Transplant Proc. 2003 May;35(3):1116-20. End-stage renal disease in familial amyloidosis ATTR Val...
Familial amyloidotic polyneuropathy (FAP), found in the northernmost counties in Sweden, is a rare, ...