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DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT, ISSN 0012-0472, 09/2018, Volume 143, Issue 18, pp. 1335 - 1343
Journal Article
European Heart Journal - Cardiovascular Imaging, ISSN 2047-2404, 10/2017, Volume 18, Issue 10, pp. 1128 - 1137
Journal Article
Amyloid, ISSN 1350-6129, 07/2019, Volume 26, Issue 3, pp. 118 - 124
Objectives: Previous clinical studies have shown frequent cardiac symptoms in patients with hereditary gelsolin (AGel) amyloidosis, possibly related to amyloid... 
hereditary amyloidosis | AGel | Meretoja disease | Gelsolin | heart | MEDICINE, RESEARCH & EXPERIMENTAL | TRANSTHYRETIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | INVOLVEMENT | BIOPSY | FEATURES | MEDICINE, GENERAL & INTERNAL | FINNISH-TYPE | FAMILIAL AMYLOIDOSIS | DYSTROPHY | MUTATION | Index Medicus
Journal Article
JACC: Cardiovascular Imaging, ISSN 1936-878X, 2014, Volume 7, Issue 5, pp. 502 - 510
Journal Article
Deutsche Medizinische Wochenschrift, ISSN 0012-0472, 01/2018, Volume 143, Issue 2, pp. 101 - 109
Journal Article
Medicine, ISSN 0025-7974, 03/2017, Volume 96, Issue 10, pp. e5737 - e5737
Journal Article
American Journal of Ophthalmology, ISSN 0002-9394, 08/2018, Volume 192, pp. 169 - 177
To describe abnormalities in choroidal and retinal vasculature associated with Val30Met familial transthyretin amyloidosis (V30M-FTA) using fluorescein and... 
VITREOUS AMYLOIDOSIS | POLYNEUROPATHY | HEREDITARY | INVOLVEMENT | OPHTHALMOLOGY | NEUROPATHIES | OCULAR MANIFESTATIONS | NONFAMILIAL AMYLOIDOSIS | Glaucoma | Genetic aspects | Amyloidosis | Ophthalmology | Neovascularization | Fluorescein | Hypertension | Walking | Medical imaging | Statistical analysis | Mutation | Age
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 04/2014, Volume 9, Issue 1, pp. 61 - 61
Background: Transthyretin amyloidosis is a systemic disorder caused by amyloid deposits formed by misfolded transthyretin monomers. Two main forms exist:... 
Functional | Secondary | Transthyretin | Cardiomyopathies | Amyloid | Amyloidosis | Gastrointestinal disorders | Hereditary | Amyloid neuropathies | Nutritional status | Quality of life | MEDICINE, RESEARCH & EXPERIMENTAL | FECAL INCONTINENCE | POLYNEUROPATHY | LIVER-TRANSPLANTATION | OCULOLEPTOMENINGEAL AMYLOIDOSIS | CLINICAL-FEATURES | LEPTOMENINGEAL AMYLOIDOSIS | ATTR VAL30MET | FAMILIAL AMYLOIDOSIS | GENETICS & HEREDITY | LATE-ONSET | ENDOCRINE-CELLS | Prealbumin - genetics | Gastrointestinal Diseases - physiopathology | Humans | Amyloid Neuropathies, Familial - complications | Quality of Life | Female | Gastrointestinal Diseases - complications | Male | Nutritional Status | Mutation | Amyloid Neuropathies, Familial - physiopathology | Complications and side effects | Care and treatment | Gene mutations | Gastrointestinal diseases | Cardiac patients | Development and progression | Research | Health aspects | Risk factors | Surveys | Albumin | Medicine, Experimental | Medical research | Pharmaceutical industry | Analysis | Transplants & implants | Review boards | Cardiomyopathy | Mortality | Clinical trials | Diarrhea | Nausea | Proteins | Studies | Confidence intervals | Body mass index | Biopsy | Vomiting | Drug therapy | Constipation | Age | Index Medicus | Medical and Health Sciences | Medicin och hälsovetenskap | Gastroenterologi | Klinisk medicin | Clinical Medicine | Gastroenterology and Hepatology
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 08/2019, Volume 403, pp. 1 - 6
Despite growing numbers of patients diagnosed with late-onset hereditary ATTR V30M amyloidosis with polyneuropathy (ATTRv-PN), this condition remains poorly... 
Hereditary transthyretin amyloidosis | Early-onset ATTRv-PN | Polyneuropathy | Late-onset ATTRv-PN | Familial amyloid polyneuropathy | Polyneuropathies | Amyloidosis
Journal Article