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Journal of the American College of Cardiology, ISSN 0735-1097, 07/2016, Volume 68, Issue 2, pp. 161 - 172
Background Transthyretin amyloidosis (ATTR) is a heterogeneous disorder with multiorgan involvement and a genetic or nongenetic basis. Objectives The goal of... 
transthyretin | amyloid | aging | DIAGNOSIS | POLYNEUROPATHY | CARDIAC & CARDIOVASCULAR SYSTEMS | ACID SCINTIGRAPHY | HEART-FAILURE | PRESERVED EJECTION FRACTION | PREDICTIVE-VALUE | BLACK-AMERICANS | TC-99M-DPD SCINTIGRAPHY | SYSTEMIC AMYLOIDOSIS | MYOCARDIAL-CONTRACTION FRACTION | Peptides | Transplants & implants | Pulmonary arteries | United States--US | Diabetic neuropathy | Family medical history | Multivariate analysis | Quality of life | Confidence intervals | Body mass index | Genotype & phenotype | Mutation | Heart | Demography | ROW other regions of the world | Val122Ile valine-to-isoleucine substitution at position 122 | wt-ATTR wild-type transthyretin amyloidosis | mBMI modified body mass index | TTR-CM transthyretin cardiomyopathy | LVEDD left ventricular end-diastolic dimension | Pain | ATTR transthyretin amyloidosis | Blood pressure | Amyloid | QOL quality of life | Age | Genotypes | BMI body mass index | MCF myocardial contraction fraction | SV stroke volume | Mortality | EDV end-diastolic volume | Data processing | LV left ventricular | Survival | Walking | HFpEF heart failure in the setting of a preserved ejection fraction | TTR transthyretin | mt-ATTR mutated or hereditary transthyretin amyloidosis | Amyloidosis | Amyloid - genetics | Prealbumin - genetics | United States - epidemiology | Prognosis | Survival Rate - trends | Amyloid Neuropathies, Familial - genetics | Amyloid Neuropathies, Familial - metabolism | Humans | Middle Aged | Genotype | Male | Amyloid Neuropathies, Familial - epidemiology | Incidence | Cardiomyopathies - genetics | Cardiomyopathies - epidemiology | Phenotype | Amyloid - metabolism | Prealbumin - metabolism | Cardiomyopathies - metabolism | Female | Registries | Surveys and Questionnaires | Aged | Index Medicus | Abridged Index Medicus | Clinical Medicine | Neurology | Neurologi | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin
Journal Article
European Heart Journal, ISSN 0195-668X, 06/2016, Volume 37, Issue 23, pp. 1826 - 1834
Journal Article
Journal Article
Neuroepidemiology, ISSN 0251-5350, 11/2018, Volume 51, Issue 3-4, pp. 177 - 182
Background: Transthyretin-associated familial amyloid polyneuropathy (TTR-FAP) is a rare, hereditary, progressive and neurodegenerative disease. We aimed to... 
Original Paper | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | Prevalence | MANAGEMENT | FAP | TAFAMIDIS | Amyloidosis | Transthyretin familial amyloid polyneuropathy | Epidemiology | Portugal | CLINICAL NEUROLOGY | Incidence
Journal Article
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2010, Volume 18, Issue 8, pp. 948 - 952
The Val30Met transthyretin familial amyloid polyneuropathy (TTR-V30M-FAP) is the most frequent familial amyloidosis, with autosomal dominant transmission. This... 
transthyretin amyloid polyneuropathy | mitochondria | penetrance | parent-of-origin | PORTUGAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | PEDIGREE DATA | VAL30MET | DISEASE | JAPAN | GENETICS & HEREDITY | LATE-ONSET | PROTEINS | SWEDISH | Haplotypes | Humans | Middle Aged | DNA, Mitochondrial | Male | Mitochondrial DNA | Gender | Polyneuropathy | Gene polymorphism | Portugal | Mitochondria | Sweden | Maternal inheritance | Prealbumin | Genetics | Adult | Female | Amyloid | France | Age | Deoxyribonucleic acid--DNA | Japan | Phenotypic variations | Transthyretin | Penetrance | Heredity | Polymorphism, Genetic | Hypotheses | Disease transmission | Age of Onset | Amyloid Neuropathies, Familial | Amyloidosis | Genetic testing | Mutation | transthyretin | Prealbumin - genetics | Amyloid Neuropathies, Familial - genetics | Mitochondria - metabolism | Sweden - epidemiology | Amyloid Neuropathies, Familial - epidemiology | DNA, Mitochondrial - genetics | Mitochondria - genetics | Portugal - epidemiology | Index Medicus | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | MEDICINE | Klinisk genetik | Dermatology and venerology,clinical genetics, internal medicine | Medical Genetics | Medicinsk genetik | Clinical genetics | MEDICIN | Medicinska och farmaceutiska grundvetenskaper | genetik | Dermatologi och venerologi, klinisk genetik, invärtesmedicin
Journal Article
Journal Article