Search for dissertations about: "Familial amyloid polyneuropathy"
Showing result 6 - 10 of 17 swedish dissertations containing the words Familial amyloid polyneuropathy.
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6. Two Types of Fibrils in ATTR Amyloidosis : Implications for Clinical Phenotype and Treatment Outcome
Abstract : Systemic amyloidoses are a group of lethal diseases where proteins aggregate into fibrillar structures, called amyloid fibrils, that deposits throughout the body. Transthyretin (TTR) causes one type of amyloidosis, in which the aggregates mainly infiltrate nervous and cardiac tissue. READ MORE
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7. Cardiac involvement in familial amyloidosis with polyneuropathy
Abstract : Familial amyloidosis with polyneuropathy (FAP) is a neuropathic form of heredofamilial systemic amyloidosis. Clusters of patients have been reported predominantly from Portugal, Japan and Sweden. The present study examines the involvement of the heart in individuals with the Swedish variety of FAP. READ MORE
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8. Gastrointestinal involvement in familial amyloidosis with polyneuropathy : a clinical study
Abstract : Familial Amyloidosis with Polyneuropathy was first recognized in Portugal and reported by Andrade in 1952. The disease is rare, but clustering of the patients has been reported from Portugal, Japan and northern Sweden. The gastrointestinal involvement in the Swedish form of the disease was studied in this investigation. READ MORE
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9. Cardio-pulmonary function in familial amyloidosis with polyneuropathy : a clinical study of cases from northern Sweden
Abstract : Familial amyloidosis with polyneuropathy (FAP) was first reported from Portugal in 1952, but since then this syndrome has been recognized in many countries including Sweden. In this investigation cardiac and pulmonary functions in the Swedish variety of FAP were studied. READ MORE
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10. Transthyretin in senile systemic amyloidosis and familial amyloidotic polyneuropathy
Abstract : The amyloidoses comprise a heterogeneous group of disorders characterized by the deposition of fibrillar, proteinaceous amyloid deposits in various organs and tissues. To date, 17 different proteins of various sizes have been identified as amyloid proteins. READ MORE